Hostname: page-component-cd9895bd7-dzt6s Total loading time: 0 Render date: 2024-12-28T13:14:05.523Z Has data issue: false hasContentIssue false

Harnessing the bilingual descent down the mountain of life: Charting novel paths for Cognitive and Brain Reserves research

Published online by Cambridge University Press:  13 March 2024

Jason Rothman*
Affiliation:
UiT, the Arctic University of Norway, Tromsø, Norway and Nebrija Research Centre in Cognition, University Nebrija, Madrid, Spain
*
Author for correspondence: Jason Rothman; Email: jason.rothman@uit.no
Rights & Permissions [Opens in a new window]

Abstract

Evidence from various empirical study types have converged to show bilingualism's potential for serving as a cognitive and brain reserves contributor. In this article, I contextualize, frame the need for and offer some expanding questions in this endeavor, inclusive of empirical pathways to address them. While the set of variables and questions discussed herein are definitively incomplete, they embody a good starting point for shaping future directions in research that considers the role bilingual language engagement can have for the developing mind and brain, inclusive of how various, non-linear factors impact the descent bilinguals of various types take down the proverbial mountain of life.

Type
Research Article
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
Copyright © The Author(s), 2024. Published by Cambridge University Press

Introduction

If we view life as a mountain and our lifespans as a climb, anecdotal observation alone leads to what developmental and aging sciences have documented and endeavored to explain for quite some time: the journey is flanked by periods where our minds and bodies are not – as nature would intend – at their prime. In children, the process of development towards the peak is one of patient, yet exciting anticipation. Barring pathology and notwithstanding individual genetic and important (inequitable) environmental differences, all children mature to a state where their bodies and cognitive functions are gradually more developed than the days, months and years before. After individuals reach the pinnacle and surpass a plateaued stretch, one naturally commences the processes of physical and cognitive descent over the course of the aging process. While the early and later years of life share overlapping signs of off-peak abilities, they are not equalFootnote 1. As the youth ascend towards cognitive and physical crescendos, their bodies, including the brain, undergo vital physical development in parallel with the expanding of social and family networks, the attaining of independence, the experiencing of (more easily) high degrees of mental stimulation and more. Conversely, having left the heights behind, aging adults progressively go through a reversal of sorts: their fully developed bodies and minds atrophy while social networks, mental activities and eventually independence decrease as a function of various milestones associated with increasing age. The adult's off-peak state is, thus, distinguished by tradeoffs from a unique vantage point of experience and its resulting heuristic proficiency.

Of particular interest herein is a subset of consequences the descent has for the mind/brain specifically. Cognitive aging (CA) refers to the naturally occurring (i.e., it is definitively not a disease), progressive attenuation of cognitive abilities (e.g., memory, decision making, attention) and deterioration of the physical brain (structure and function) over the lifespan (Salthouse, Reference Salthouse2004, Reference Salthouse2019). While CA is a lifelong process, our focus herein is primarily on the part that exists within later years of life. To experience CA for as long as possible, is simultaneously a privilege and misfortune. After all, to do so means one has survived the gauntlet of life that paves the path to the top of the proverbial mountain and are well engaged with the ups and downs of the descending journey. Moreover, for a majority of older aged people, CA is not excessively cumbersome or infringing (e.g., Dumas, Reference Dumas2015; Harada et al., Reference Harada, Love and Triebel2013; Salthouse, Reference Salthouse2019). While one notices changes in mental sharpness, the extent to which they drastically alter one's lifestyle is typically not severe insofar as they do not outpace other natural progressive declines with the aging body overall (e.g., mobility issues, decline in sight/hearing).

While normal CA is inevitable, it is not uniform. To begin with, generally speaking, CA effects in older age manifest differentially across distinct cognitive abilities. For older adults affected more by CA, there is significant individual variation in timing onset, progressivity rate and severity of symptoms (Stern, Reference Stern2002; Tucker-Drob, Reference Tucker-Drob2019). In the case that particular symptoms of CA present earlier and/or more severely than normal, one has reason for concern. Such symptoms can find their roots in various types of atypical neurodegeneration, either with or without co-morbidity of other primary neurological disorders such as Parkinson's and Huntington's diseases (Aarsland et al., Reference Aarsland, Zaccai and Brayne2005; Martinez-Horta et al., Reference Martinez-Horta, Sampedro, Horta-Barba, Perez-Perez, Pagonabarraga, Gomez-Anson and Kulisevsky2020). Minor, yet abnormal cognitive senescence is often diagnosed as Mild Cognitive Impairment (MCI), which may or may not develop into dementia later on. In the case of severe symptoms, various types of dementias are diagnosed as the source cause. Even still, for severe CA associated with pathological neurodegeneration there is still considerable variation in timing onset, progressivity rate and severity of symptoms. Understanding how and why these variations come to be is the topic of much research and of particular interest here: what variables contribute to why some people have later and/or less CA symptoms when increasing age is controlled for?

Neuroscience, cognitive/psychological science, genetics, gerontology, exercise science, nutrition science among many other disciplines have addressed questions of the above type. Amongst other important insights, accumulating evidence points in the following directions: (i) individual differences in how normal and pathological CA manifest are not random and (ii) various (naturally occurring) lifestyle enrichment factors have significant impact on and explanatory power for how symptoms play out. Couched within the cognitive and brain reserves hypotheses (Stern, Reference Stern2002, Reference Stern2009; Stern et al., Reference Stern, Arenaza-Urquijo, Bartrés-Faz, Belleville, Cantilon, Chetelat, Ewers, Franzmeier, Kempermann, Kremen, Okonkwo, Scarmeas, Soldan, Udeh-Momoh, Valenzuela, Vemuri and Vuoksimaa2020) – the idea that over the course of life individuals can differentially accrue via life-style enrichment experiences natural protection against loss of brain structure (brain reserve, BR) and/or cognitive function (cognitive reserve, CR) related to aging or disease – the present paper zooms in on one particular lifestyle factor: bilingualismFootnote 2.

At present, a critical mass of research shows, at least under conditions of active multilingual language engagement and/or over the cognitively demanding process of additional language learning itself, the juggling of more than one language in a single mind can have consequences for various domains of cognition and the brain structures and networks that subserve them (see DeLuca et al., Reference DeLuca, Segaert, Mazaheri and Krott2020; Grundy, Reference Grundy2020; Pliatsikas, Reference Pliatsikas2019, Reference Pliatsikas2020; Prat et al., Reference Prat, Yamasaki and Peterson2019). The leading hypotheses for these effects link them to the (degree of) demands placed on cognitive-processing systems needed to manage more than one language (see Bialystok, Reference Bialystok2017; Bialystok & Craik, Reference Bialystok and Craik2022 for review). If so, bilingualism has all the hallmarks of a potential cognitive reserve (CR) and brain reserve (BR) contributor, which research with elderly populations corroborates (e.g., Anderson et al., Reference Anderson, Grundy, Grady, Craik and Bialystok2021; Bialystok, Reference Bialystok2021; Calvo et al., Reference Calvo, García, Manoiloff and Ibáñez2016, Reference Calvo, Anderson, Berkes, Freedman, Craik and Bialystok2023a; Gallo et al., Reference Gallo, DeLuca, Prystauka, Voits, Rothman and Abutalebi2022a; Guzmán-Vélez & Tranel, Reference Guzmán-Vélez and Tranel2015; Voits et al., Reference Voits, DeLuca and Abutalebi2022a). Although for context we will go through the main arguments and constructs from the relevant literatures in greater detail below, the purpose and ultimate value of the present paper are definitively not to repeat or merely highlight why bilingualism is likely to serve as a CR and BR contributor. Rather, the goal is to unpack important considerations of investigating bilingualism as a potential reserve contributor, specifically highlighting various new directions for empirical research working with older bilinguals. In doing so, we will primarily tackle why and precisely how leveraging/juxtaposing a wider, untapped spectrum of naturally occurring, dynamic laboratories of bilingualism as they exist differentially in the real world of older adults globally can open up novel questions while contributing to better addressing and answering existing ones in the bilingualism and aging literature. Consequentially, additional insights regarding the very nature of CR and BR more generally will materialize.

We will do the above by articulating questions that give rise to new directions in empirical and longitudinal research programs working with older bilinguals. The argument will be made that of the known environmental factors for reserve accrual, the dynamic nature of bilingualism, when operationalized and capitalized on with appropriate nuance and care, provides the requisite variation essential for: (i) teasing out how language experience contributes independently to and/or interacts with other factors for CR and BR accrual, (ii) revealing novel insights into the very constructs of CR and BR themselves and (iii) advancements specifically in the neurocognitive study of bilingualism and aging, if not the neurocognition of bilingualism more generally.

The argumentation will be predicated on the considerable spectrum of (circumstances leading to) changes in bilingual engagement behavior (linguistic exposure and usage patterns) that naturally exists globally (and locally) in the latter years of life for some (crucially not all) bilingual communities and the subgroups and individuals that comprise them. Exploiting and manipulating to our advantage the heterogeneity of these naturally occurring shifts in bilingual usage/engagement “maintenance” specifically in older age when reserve deposits begin to be used, on the scale that already exists, renders bilingualism truly special as a testing ground. The potential hyperbole of such a claim is tempered by the fact that well over half the world's population is multilingual (De Houwer, Reference De Houwer2021; Grosjean, Reference Grosjean1982; Rothman et al., Reference Rothman, Alonso and Puig-Mayenco2019). While the ratio/distribution of (functional) monolinguals to multilinguals comply with geographic and sociopolitical tendencies, there is no corner of the inhabited earth where multilingualism is absent. Its distribution defies not only geography, but class, age, sex/gender and wealth. As a result, arguments can be made that bilingualism is uniquely equitable compared to other lifestyle reserve contributor factors, which otherwise can be highly co-linear with high socio-economic status (Gallo et al., Reference Gallo, DeLuca, Prystauka, Voits, Rothman and Abutalebi2022a). And yet, despite the ubiquity and favorable, equitable coverage of multilingualism, no two multilingual contexts are exactly the same. Its diversity and variation, useful empirical ingredients, as well as the factors underlying them are abundant, definable and measurable.

What is the global reality of Aging?

Since the later part of the 1800s, many countries have seen over a doubling of their 65 years-and-older populations (Kinsella & He, Reference Kinsella and He2009). According to a World Health Organization 2021 report, in 2020 there was roughly 1 billion people over the age of 60 globally. By 2050, this number is expected to more than double. Between 2020-2050, the number of individuals over the age of 80 are expected to triple, reaching nearly half a billion. Not only is the global population increasing, but current gains in life expectancy are outpacing the already upward trends in population growth. To be sure, this reality marks progress on many fronts for science and humanity. However, it also entails the three “c”s: real societal and personal costs, concerns and challenges, not least because the resources required to functionally, ethically and compassionately manage increased age on such a scale in our societies – let alone at the individual (family) level – are staggering.

While neurodegeneration is not the only inherent health-related concern of aging, the economic and personal reality of it and its ubiquity make it stand out. The World Health Organization 2021 report claims that more than 55 million adults currently suffer from various types of dementia worldwide. This report also suggests that year-on-year 10 million new cases of dementia are expected. Global estimates in 2016 suggested then that the total economic costs of caring for elderly people with dementia was approaching the trillion dollar mark (Xu et al., Reference Xu, Zhang and Wu2017). The Xu et al. systematic review indicated that by 2017 the average cost in Europe had risen to just over €32,500 per case. For sake of comparison, the average annual median equivalized income in the EU-27 in 2018 was just under €17,000 (even at the top end of the range, Luxembourg, it was just over €32,500).

The economic burden of cognitive decline is undeniable and will only continue to grow. But not all parts of the world are equally positioned. According to the same World Health Organization report, of the 55 million cases of dementia globally, roughly 60% reside in low and middle-income countries. And yet, 74% of the costs related to care occur in high-income countries. Even if economic resources were boundless, never mind equitably distributed, societies would still need to confront serious limitations with respect to what the current state of health science offers for quality-of-life issues in our senior populations. Indeed, current pharmacological treatments for many cognitive/ neuro-degeneration ailments are scarce and inadequate (Briggs et al., Reference Briggs, Kennelly and O'Neill2016; Fish et al., Reference Fish, Steadman, Bayle and Whiting2019). For example, the best available drug treatments for Alzheimer's disease, effective at an efficacy rate barely scratching 50%, compensate for cognitive decline symptoms on the order of months.

While atypical pathological neurodegeneration is and should remain a primary concern, one should not ignore what the three Cs (costs, concerns and challenges) bring to bear for normal CA. After all, estimates indicate that by 2050 there will be at least 2 billion people in the thick of either typical or atypical CA. It seems that presently, the best prevention/treatment options for symptom onset/severity for pathological and typical CA available are lifestyle enrichment factors that stretch neuroplasticity, such as physical exercise, healthy diet and a range of activities/therapies that challenge, strain and thus train the brain (Klimova et al., Reference Klimova, Maresova and Kuca2016, Reference Klimova, Valis and Kuca2017; Teixeira et al., Reference Teixeira, Gobbi, Corazza, Stella, Costa and Gobbi2012; Wang et al., Reference Wang, Pei, Zhan and Cai2020). What role does/can bilingualism play in this space?

Reserves: How does our lifestyle contribute to them and what role do they play in cognitive aging?

Behaviorally, normal CA is associated with a decrease in overall processing speed, certain types of memory (e.g., short term and episodic), language, visuospatial and executive functions (EFs) and is marked by significant individual variation in cognitive performance (Salthouse, Reference Salthouse2000, Reference Salthouse2004, Reference Salthouse2019). At the neural level, CA is perhaps most clearly identifiable in anatomical changes in gray matter (GM) and white matter (WM) integrity, particularly in the prefrontal cortex and hippocampus, paired with decreased efficiency (i.e., increased requirements of implicated networks) in task performance (e.g., Farokhian et al., Reference Farokhian, Yang, Beheshti, Matsuda and Wu2017; MacPherson & Cox, Reference MacPherson, Cox and Riby2017; Persson et al., Reference Persson, Nyberg, Lind, Larsson, Nilsson, Ingvar and Buckner2006). Symptomatically at the behavioral level and neurologically, Mild Cognitive Impairment (MCI) and dementias of various types associate similarly, the main differences relating to progression rate, pervasiveness, severity and specificity of cognitive impairments and neurological damage as well as the potential for various bio/neuro-markers for (predictive) diagnosis. Among other ways, normal CA and related clinical pathologies can be assessed at the level of functional neural connectivity, the integrated relationship between separated brain regions, as measured by Resting State EEG/MEG (RS-EEG; Babiloni et al., Reference Babiloni, Del Percio, Lizio, Noce, Lopez, Soricelli, Ferri, Nobili, Arnaldi, Famà, Aarsland, Orzi, Buttinelli, Giubilei, Onofrj, Stocchi, Stirpe, Fuhr, Gschwandtner, Ransmayr and Bonanni2018; Fleck et al., Reference Fleck, Kuti, Mercurio, Mullen, Austin and Pereira2017) and/or on-task performance with EEG/MEG (Jauny et al., Reference Jauny, Eustache and Hinault2022; Miraglia et al., Reference Miraglia, Vecchio and Rossini2017; Polich, Reference Polich1997). For example, in older age, greater mean coherence (neural connectivity) in RS-EEG at the individual level correlates with higher levels of cognitive/brain reserves (Fleck et al., Reference Fleck, Kuti, Mercurio, Mullen, Austin and Pereira2017). In the present context, one wonders under what degrees of bilingual experience does better (preserved) mean coherence obtain (Bice et al., Reference Bice, Yamasaki and Prat2020; Calvo et al., Reference Calvo, Grundy and Bialystok2023b; Pereira Soares et al., Reference Pereira Soares, Kubota, Rossi and Rothman2021) and, if so, how does that translate to older age?

In the context of the discussions herein, we can understand Cognitive Reserve (CR) as a protective mechanism related to efficient connectivity among the neural circuits supporting sustained cognitive function following damage to the physical brain associated with age, injury, disease or a combination thereof. Similarly, Brain Reserve (BR) refers to the protective potential of anatomical features such as neuronal density and synaptic connectivity. According to the reserve hypothesis (see Stern et al., Reference Stern, Arenaza-Urquijo, Bartrés-Faz, Belleville, Cantilon, Chetelat, Ewers, Franzmeier, Kempermann, Kremen, Okonkwo, Scarmeas, Soldan, Udeh-Momoh, Valenzuela, Vemuri and Vuoksimaa2020 for review), using accrued reserves in later age provides compensation for natural degenerative and neuropathological damage, accounting for significant (and often highly beneficial) individual variation in onset and degree of normal CA, MCI, and dementia, despite neurodegenerative changes that are underlyingly similar in nature and extent (Perneczky et al., Reference Perneczky, Kempermann, Korczyn, Matthews, Ikram, Scarmeas, Chetelat, Stern and Ewers2019; Petrosini et al., Reference Petrosini, De Bartolo, Foti, Gelfo, Cutuli, Leggio and Mandolesi2009; Villeneuve, Reference Villeneuve2019). How do these reserves build up? While genetic factors can be determinants of individual differences, research shows that lifestyle factors such as higher levels/more years of education, healthy nutrition, occupational attainment, engagement with leisure activities that promote cognitive and/or physical excursion correlate in older age to degree of cognitive and brain reserves (Stern et al., Reference Stern, Arenaza-Urquijo, Bartrés-Faz, Belleville, Cantilon, Chetelat, Ewers, Franzmeier, Kempermann, Kremen, Okonkwo, Scarmeas, Soldan, Udeh-Momoh, Valenzuela, Vemuri and Vuoksimaa2020) – for example, greater RS-EEG mean coherence as referenced above (e.g., Fleck et al., Reference Fleck, Kuti, Mercurio, Mullen, Austin and Pereira2017).

Why should lifestyle factors matter? Let us unpack how this process is hypothesized to work using a factor with robust predictive validity for augmented resilience to the symptoms of CA and clinical dementia: Physical Exercise (PE) (e.g., Campbell et al., Reference Campbell, Grace, Ritchie, Beaumont and Sculthorpe2019; Yaffe et al., Reference Yaffe, Fiocco, Lindquist, Vittinghoff, Simonsick, Newman, Satterfield, Rosano, Rubin, Ayonayon, Harris and Study2009). Conceptually, how this works is not qualitatively different from the much more commonly discussed case of cardiovascular health. PE renders the heart muscle efficient in doing its intended job for longer: pushing out more blood, which lowers resting beat-rate and keeps blood pressure optimally regulated. Similarly, PE is argued to be deterministic for structural changes in the brain such as increased gray matter volume in frontal and hippocampal regions (e.g., Erickson et al., Reference Erickson, Leckie and Weinstein2014) and reduced gray and white matter degradation (Burzynska et al., Reference Burzynska, Chaddock-Heyman, Voss, Wong, Gothe, Olson, Knecht, Lewis, Monti, Cooke, Wojcicki, Fanning, Chung, Awick, McAuley and Kramer2014) in older populations. Like the case of the heart, engagement in good-measured PE strains and trains the cerebrovascular system. This, in turn, conditions benefits on glucose and lipid metabolism carrying “food” to the brain (Mandolesi et al., Reference Mandolesi, Polverino, Montuori, Foti, Ferraioli, Sorrentino and Sorrentino2018), leaving reserve deposits over time that later correlate to more favorable onsets, progression and symptom severity for CA and neurodegeneration.

Can bilingualism contribute to reserve accrual?

In this section, we contextualize and summarize the evidence supporting the position that, like PE, engagement with the (mundane) activities required for bilingual language control demands, at least under specific intensities, provides stretched neuroplasticity related to CR and BR accrual. To begin with, many studies have shown older bilinguals outperform monolinguals (often better than young bilinguals) on cognitive control and memory tasks, behaviorally and at the brain level (e.g., Bialystok et al., Reference Bialystok, Craik, Klein and Viswanathan2004; Grant et al., Reference Grant, Dennis and Li2014; Kousaie & Phillips, Reference Kousaie and Phillips2017). Older bilinguals also show better preserved brain structure across white matter and grey matter (Perani & Abutalebi, Reference Perani and Abutalebi2015; Pliatsikas, Reference Pliatsikas2020) increasingly as a function of increased bilingual engagement (DeLuca & Voits, Reference DeLuca and Voits2022), lower activation while performing executive control tasks (Gold et al., Reference Gold, Kim, Johnson, Kryscio and Smith2013), superior resting state functional connectivity, suggesting increased neural efficiency (Pliatsikas & Luk, Reference Pliatsikas and Luk2016) and degree of bilingual engagement correlating with hippocampal adaptations in typical aging and with those diagnosed with MCI (Voits et al., Reference Voits, Robson, Rothman and Pliatsikas2022b, Reference Voits, Rothman, Calabria, Robson, Aguirre, Cattaneo, Costumero, Hernández, Juncadella Puig, Marín-Marín, Suades, Costa and Pliatsikas2023). Several recent meta-analyses bringing together relevant studies from the past two decades point in the same direction: bilingualism correlates with later onset of symptoms and, thus, diagnosis of dementia by as much as 5-7 years relative to comparable monolinguals (Anderson et al., Reference Anderson, Hawrylewicz and Grundy2020; Brini et al., Reference Brini, Sohrabi, Hebert, Forrest, Laine, Hämäläinen, Karrasch, Peiffer, Martins and Fairchild2020, although other factors can mitigate such as SES indicators, e.g., Gollan et al., Reference Gollan, Salmon, Montoya and Galasko2011). A recent paper worthy of specific mention cleverly matched brain pathology via MRI scanning across bilinguals and monolinguals, effectively showing that brain-matched older monolinguals display significantly more behavioral deficiencies in cognitive functioning (Berkes et al., Reference Berkes, Calvo, Anderson and Bialystok2021). Another noteworthy recent study focused on conversion rates from MCI to Alzheimer's Disease (AD), showing that while bilinguals attending a memory clinic are older than monolinguals when diagnosed with MCI by a differential of 3 years, bilinguals have an increased MCI-to-AD conversion rate of a year (Berkes et al., Reference Berkes, Bialystok, Craik, Troyer and Freedman2020). This is not surprising when one considers that bilingualism (any reserve contributor factor for that matter) does not stop or necessarily slow down the actual neurological erosion of degenerative disorders, but rather masks/compensates for the behavioral symptoms that lead to diagnosis until a breaking point. In any case, all of these observations from the literature – and more – lead not only to the conclusion that bilingualism can have a particularly strong effect on the aging mind/brain, but that it serves as a significant CR and BR contributor.

How does bilingualism contribute to the building up of reserves in the brain? While the precise mechanisms are not entirely clear – as is the case for all proposed CR and BR life-style enrichment factors – a crucial, shared commonality with other potential contributor factors is the cognitively demanding nature of bilingualism. The presence of more than one language introduces competition in several overlapping cognitive systems (Green & Abutalebi, Reference Green and Abutalebi2013; Jared & Kroll, Reference Jared and Kroll2001; Marian & Spivey, Reference Marian and Spivey2003; Spivey & Marian, Reference Spivey and Marian1999). As all languages are simultaneously activated in the mind, even when the context calls for a unilingual mode, there is a pressing and ubiquitous need to regulate interference. Bilingualism, especially under certain conditions, requires constant and often unpredictable selection between the two (or more) languages (Abutalebi & Green, Reference Abutalebi and Green2016). After all, one could be using language X at any given time, but someone associated with language Y unexpectedly enters a room where instantaneous switching becomes necessary. The resolution of this competition requires increased engagement of cognitive control functions, under the more general umbrella of attention, including inhibition, particular types of memory, monitoring and updating for successful communication to take place. The degree to which one's circumstances requires dynamic multilingual engagement is thought to “train” related cognitive skills and brain networks, making them more efficient. Research such as that presented above suggests that these effects extend beyond language control to domain-general cognition and that adaptations in cognition are supported by corresponding changes in the brain, specifically brain networks and areas underlying cognitive control functions that overlap with language control. Crucially, the functions and brain regions argued to be enhanced by bilingualism over the lifespan (Pliatsikas, Reference Pliatsikas2019) are not random, but largely overlap with those that decline due to CA, MCI, and dementia (Voits et al., Reference Voits, Pliatsikas, Robson and Rothman2020).

How can we move forward with novel direction?

As we have seen above, while evidence from complimentary angles converges and is convincing, it is gathered and framed to effectively serve the singular question of whether or not bilingualism can be considered a genuine CR and BR contributor. There are conspiring reasons for this. To begin with, the original question had to be asked before any others could make sense. Only by having obtained the available evidence in pursuit of addressing the original question is the foundation now set for asking further ones. Moreover, a sizable portion of the available data used to address the basic question is unnuanced with respect to how bilingualism is qualified/quantified at the intersection of at least two axioms: (a) degree of engagement with bilingualism over (b) the time domain. For some study types, there is simply no way to (have) avoid(ed) this, effectively delimiting the possible set of askable questions from the outset. For example, in cohort studies showing that bilinguals, over monolinguals, are diagnosed with dementia with as much as 5-7 years delay, the data used are from preexisting medical records from which one is lucky to have had any indication of mono- vs. bilingual status at all. In many cases, this dichotomous categorization is all that is available in the relevant sense, thus essentially forcing the formation of broad groups for relatively simple statistical comparisons. And still, the fact that bilingualism emerges with good predictive validity in so many of these studies across broad geographic and sociodemographic coverage is all the more impressive.

Having a relatively unnuanced monolingualism vs. bilingualism comparison is not always a forced choice of the data at hand. And yet, even in purposefully designed empirical studies, a more-or-less dichotomous comparison still dominates the bilingualism and (neurocognitive) aging literature, as true of bilingualism studies in general. Given argumentation for why simple monolingual vs. bilingual comparisons are potentially problematic for bilingualism research in general (e.g., De Houwer, Reference De Houwer2023; Rothman et al., Reference Rothman, Bayram, DeLuca, Di Pisa, Dunabeitia, Gharibi, Hao, Kolb, Kubota, Kupisch, Laméris, Luque, van Osch, Pereira Soares, Prystauka and Wulff2023) and especially insufficient for questions related to neurocognition by failing to consider the impact of individual differences in bilingual experience (e.g., DeLuca et al., Reference DeLuca, Rothman, Bialystok and Pliatsikas2019; Titone & Tiv, Reference Titone and Tiv2022), it seems incongruous to not adapt accordingly in the aging and bilingualism literature. To be fair and clear, it should not be understood from the present argumentation that monolingual-to-bilingual aggregate comparisons, even relatively simplistic ones depending on the question, have no use in the present space. The majority of the studies reviewed throughout this article thus far speak well to the contrary. Rather, a better framing is to ask what the field has been missing out on by not having pursued alternatives. In other words, what questions have not yet been properly framed/addressed as a result?

While research clearly shows that bilingualism can correlate to behavioral and neurological exponents understood as embodiments of CR and BR, in my view, there is very little from the existing literature that speaks to the relative weighting of (real world diversity in) bilingual experiences themselves in relation to CR and BR. This means that what could be a mutually beneficial, bidirectional road has essentially been a one-way highway: bilingualism research couched within the CR and BR reserve hypothesis has not contributed much back to the theory from which it draws, despite potentially being its largest testing ground. For those primarily interested in bilingualism and aging, this also means that we know much less about how bilingualism actually functions for CR and BR accrual and subsequent deployment then we ought to.

To begin to fill some of the gaps of missed opportunities, several questions – not a complete list to be sure – immediately come to mind. To start, it seems worth considering the following interrelated questions: What is the nature of reserve accrual in the shorter term – for example, when language learning is used as an intervention in the older age? and (how) does it differ when older monolinguals are first introduced to bilingualism (true L2 learning in the elderly) via language learning as compared to when preexisting older bilinguals learn additional languages? Although, space does not permit a deep dive here, given the theoretical and practical promise of older age language learning interventions in the general topical space of the present discussion and its emerging prominence in the empirical landscape (Klimova, Reference Klimova2018), a few thoughts are befitting.

Research already exists showing that novel language learning in older ages changes the structure of the brain (Li et al., Reference Li, Legault and Litcofsky2014; Nilsson et al., Reference Nilsson, Berggren, Garzón, Lebedev and Lövdén2021; Schlegel et al., Reference Schlegel, Rudelson and Tse2012), pondering/proposing it as a potential reserve building intervention (Antoniou et al., Reference Antoniou, Gunasekera and Wong2013; Kliesch et al., Reference Kliesch, Pfenninger, Wieling, Stark and Meyer2022; Klimova, Reference Klimova2018; Wong et al., Reference Wong, Ou, Pang, Zhang, Tse, Lam and Antoniou2019). And yet, such research mainly addresses the “can X result in Y” question, offering little insights on the nature of bilingual-induced reserve accrual itself. For example, what do such changes tell us about any specificity of later language learning over the learning of anything else that involves complex cognitive processing? Are correlations merely a reflection of learning that happens to be targeted with language or is there something related to introducing/augmenting bilingualism specifically? At first glance, such a query can (and has been attempted to) be controlled for via the inclusion of comparison groups with non-linguistic, but equally demanding cognitive training. And while doing so offers better control for answering the “can X result in Y” question, it only partially addresses the spirit of actual expansion questions we have posed above.

Of course, no one is suggesting that bilingualism or language specifically has any special characteristic as a cognitive flexor accruing BR and CR over other potential lifestyle factors. And yet, things related to language are not inconsequential, specifically the degree of dual language engagement in the usage tug-of-war of the available languages over time and its ubiquity in the real world of so many. This consequential part of bilingualism is greatly reduced, if not removed from the learning-as-intervention empiricism. And so, while it is incredibly promising that language learning in later life shows signs of neurological adaptation in similar areas to real world bilingualism in its various forms, it cannot be taken for granted that what seems to be similar CR and BR in both cases is in fact the same. After all, what can be captured via language learning-as-intervention studies could only ever be a sub-part of the CR and BR accrual potential of the case of bilingualism in the “wild” over time, that corresponds with the expansion phase – where the brain adapts to handle the demands presented by the learning context itself – of the Dynamic Restructuring Model (DRM, Pliatsikas, Reference Pliatsikas2020). For particular questions, that is enough. Ultimately, however, we are interested in understanding bilingual induced CR and BR more broadly, which includes how they come to manifest and are sustained/used after the intensity of language learning itself ceases. That is, what can studying the longevity of bilingualism tell us in stages the DRM describes as points where normalization of brain matter or even reductions are expected, notwithstanding maintained or enhanced corresponding cognitive performance, a CR sign of efficiency. While existing studies have independent theoretical and practical value, it is not clear how they bring us closer to a more complete, nuanced picture of the mechanisms at play in bilingualism neurocognition per se, much less a better understanding of how bilingualism research contributes back to the construct validity of CR and BR more specifically.

Let us consider and, in fact, dedicate the remaining space to the following set of questions then: (1) What is the independent value of bilingualism in CR and BR accrual, that is, factoring out other lifestyle enrichment contributions? (2) How do the patterns of bilingual engagement, more and less stable, over the lifespan relate to availability of reserve “funds” later in life? and (3) How do changes – gradual and abrupt – specifically in the later years of life affect the sustained availability and deployment of reserves in the older age? As should be evident, these questions differ from previous ones in two important ways. First, they do not seek nor contribute to querying if bilingualism is a CR and BR contributor. Rather, they start from the premise that it can be. Secondly, these questions are apt, if not designed, to shed light on the mechanistic aspects underlying the interfaces between bilingualism, neurocognition and aging as well as shedding some unique light on the construct nature of CR and BR. What remains, then, is to provide, question by question, better context for how each pushes the general program in novel directions, underscoring what is gained by doing so and how one can begin to do it.

With Question 1 in mind, it must be acknowledged that no lifestyle enrichment factor exists in a vacuum. In fact, some are highly correlated. For example, a person who engages in high degrees of exercise is more likely to eat a healthier diet, have a better sleep balance, and, on average come from higher SES. And yet, variation in how even these correlated factors present at the individual level are sufficient to tease them apart in carefully designed research. While some nods to bilingualism potentially being a CR and BR contributor can be found in the general cognitive neuroscience literature (typically mere mentions in reviews and white papers – e.g., Stern et al., Reference Stern, Arenaza-Urquijo, Bartrés-Faz, Belleville, Cantilon, Chetelat, Ewers, Franzmeier, Kempermann, Kremen, Okonkwo, Scarmeas, Soldan, Udeh-Momoh, Valenzuela, Vemuri and Vuoksimaa2020), bilingualism – least qualitatively nuanced variables that proxy for its degree of engagement/usage patterns – is a factor that is essentially never included as a co-variable in such empirical studies. Alternatively, while studies, review papers and metanalyses that hone in on the role of bilingualism in the CR and BR space typically review at length research done with other lifestyle enrichment factors, the opposite is true: with few expectations (Gallo et al., Reference Gallo, Kubiak and Myachykov2022b) empirically all other known factors that could be confounded are effectively ignored. As a result, we have no way to know what role, if any, bilingualism might be playing in studies focusing on other lifestyle factors as much as not controlling for these other factors in bilingualism-focused studies compromises determining the unmoderated role bilingualism is actually playing as an independent factor. Given the ubiquity and dynamicity of bilingualism world-wide and how it interacts with the spectra of other lifestyle factors, the above scenario means that some level of undesirable noise is floating around un(der)acknowledged in many, if not most available studies from all literatures working on CR and BR. This makes it all the more essential to do two things: (a) understand the moderated relationship between clusters of lifestyle enrichment factors, including bilingualism and (b) support research that can tease their independence apart meaningfully.

Some notable steps in this direction are beginning to emerge of which the Fitness, Aging and Bilingualism (FAB) project lead by Linda Wheeldon in Norway and Katrien Segaert in the UK and a project within our lab, at UiT, the Arctic University of Norway, EEG-Cognitive Aging Project (EEG-CAP) are good examples. EEG-CAP, while measuring bilingualism as a spectrum of experiences, includes a set of measures tapping into individuals’ physical exercise, dietary patterns, social networks, general life satisfaction, and a composite proxy for lifetime accrual of CR (engagement in cognitively engaging activities). With the goal of a sample size in the several hundreds (n = approximately 150 presently), the detailed background information pertaining to many life-style factors will be used to unpack individual patterns in brain (rs-EEG and on-task EEG) and behavioral data tapping into various executive functions and different types of memory. Structural equation modelling will be applied to understand the moderative relationships of all these factors. Work like EEG-CAP is not only welcome but introduces new frontiers for expanding questions in bilingualism and aging research as well as bridging it with the cognitive neuroscience of aging more generally.

Addressing question 2 begins to reveal the latent potential for bilingualism to shed specific light on the nature of BR and CR. Using the metaphor of a bank account, the idea here is to utilize the dynamic nature of bilingualism in well-designed empirical studies to understand what types of bank accounts CR and BR represent. But how can one go about testing how more and less stable patterns of bilingual engagement over the lifespan relate to availability of reserve “funds”, which, in turn, tells us something about their very nature? I would like to suggest that scenarios of real-world, major shifts in societal bilingualism that have happened over the past few decades present a good place to start. Under scenarios where a society (or major parts of it) was (functionally) bilingual, but no longer is or the opposite – resurgences of societal bilingualism that was (for a period) not supported – cohort studies with now aging adults who lived through periods where major changes out of their control resulted in increasingly less or more societal bilingualism and whose individual engagement with bilingualism shifted or not in parallel – so-called increasers/maintainers vs. attriters – such a complex question can be meaningfully put to test. Let us consider a project I have recently framed with Tom Voits, which seeks to examine older adults in the former Soviet Union republics as a case in point. Take for example, the Latvian society. Prior to the early 1990s, either Russian or Russian/Latvian bilingualism was the expected norm for many decades, reenforced by the necessity of Russian in all domains of the public sphere. While it is true that large sections of the Latvian population still report dominance in Russian, for most Latvian native speakers a dramatic shift linguistically took place in parallel to Latvia's gaining independence in the early 1990s. Rather quickly, Russian was replaced by Latvian in the public sector and with it the need to maintain usage of Russian fell off drastically for many, but not all Latvians and, crucially, the degree of this shift is not absolute but continuous at the measurable individual level. For many in the target age-range of our studies, dramatic shifting will have taken place after having lived as much as 50 plus years in default bilingualism. The degree of Russian loss – from nothing to complete and all points in-between – at the individual level on the scale of hundreds of thousands of people provides both the numbers and diversity needed to capitalize on this reality to test the waters of how degree of maintenance /attrition of bilingual engagement plays out. Our idea, in scenarios of this type, is to do a very similar study in method as described for EEG-CAP. To address question 2, we will take blocks of people currently at three age groups 60-69, 70-79 and 80-89 and develop bespoke questionnaires to augment the battery described for EEG-CAP to tap into their maintenance/ attrition/increase of Russian/Latvian engagement since the early 1990s to begin to understand what role this plays. Doing so will be the first attempt at charting and factoring the ebbs and flows of bilingual language engagement as a proxy for the deterministic role of its dynamicity, on scale and with ecologically valid control. Peeling back the layers of impact degree of bilingual engagement shifting over the lifespan might have, where it naturally ranges from potentially little to dramatic after decades of previous stability, is non-trivial. In the bank account metaphor, such work will offer insights into what types of accounts reserves represent: are they interest bearing, if so, is the interest compounded or simple, do they have caps for deposits and what happens to large deposits made that are not added to at all, added to little or suddenly augmented to over stretches of time?

While research designed around scenarios such as the Latvian one are well-positioned to frame and address Question 2, informing both the reserve hypothesis directly and our own theory internal questions related to CR and BR in the real world of bilingualism, they do not afford the control needed to ask Question 3: How do changes – gradual and abrupt – specifically in the later years of life affect the sustained availability and deployment of reserves in older age? This is so because individual level shifting is motivated and, thus, significantly impacted by an unpredictable event at the societal level where, as time from the precipitating point of sudden changes moves on, there are various implications that result in continuity losses related to other variables making replication of conditions a priori impossible. That is, 1991 – the point that Russian changes dramatically in the Latvian landscape – is fixed in time and the pool of participants for such studies is fixed at that point (1991) and limited to those that happened to be there at whatever age one was at that time, having been bilingual under whatever intensity they were for as long as they were at the time. Of course, as each year passes from 1991 the ensuing societal changes and attitudes stemming from that abrupt change can also have an effect and present, today over 30 years (and growing), potential noise for particular questions. These facts can be manipulated advantageously in pursuit of addressing Question 2, but pose obstacles for precisely determining what shifting in older age specifically entails since this would require seemingly replicable conditions from the same fixed point in time of all participants.

So, how can we go about addressing Question 3 then? In our lab here in Norway, we are framing a series of studies that side steps at least some of the issues discussed immediately above by harnessing the almost default status of bilingualism that exists in our country given the presence and status of English for much of the lifetime of our aging population and the very high proficiency in and functional use of it in this population. With nearly a million people over the age of 65 in Norway alone, such a project provides the scale needed to be meaningful. However, Norway's relationship with English is not so unique in that it presents rather similarly in much of Northern Europe – for example, other Nordic countries (Denmark, Sweden, Iceland and Finland) and the Netherlands. Of course, this might also be true in other parts of the world and certainly for languages other than English that enjoy nearly universally high proficiency in places where it is not the native language and also has high functional use in the same society. While it is true that Norwegians generally have good English proficiency, the degree to which they use it can range dramatically. In some public and professional sectors, it would not be a stretch to say that English has a similar functional usage pattern to that of Norwegian – e.g., people who work in jobs that are international facing. For example, while Norwegian is clearly the dominant language in our context, many, if not most, of our colleagues at the university use English daily as they engage with the international landscape of many groups. English can be and often is the default language for particular functions. As a result, for native Norwegians in this context, they are not merely extremely proficient in English but they are highly and continuously engaging with English all the time. But what happens when they retire? While their proficiency might be impacted little, their usage patterns might or might not change dramatically. One can imagine that some will hardly ever need to use English again, others will maintain relationships and habits that result in less dramatic changes whereas others might not reduce English engagement at all. We plan to chart this by tracking individuals longitudinally, starting just prior to retirement (providing a baseline) and for 5 years (at least) after. We are able to plan for this well as in Norway – as in much of the region – retirement comes at a predictable age: currently 67. The idea is to again use the battery of tests developed in EEG-CAP iteratively over time, as well as track information related to diagnosis of MCI and potential conversion rate to dementia with such individuals over this 5 year period – longer should funding exist – whereby we can track in real time starting just prior to and onwards from the very point where dramatic change in bilingualism engagement sets in. We will document the individual degree of change in bilingual engagement alongside any changes in other lifestyle enrichment factor behaviors to both tease apart bilingualism from other factors and understand better what change in engagement entails for CR and BR deployment specifically in the very years where it is needed most.

Conclusion

In this article, I have framed the need and potential for expanding questions related to bilingualism and (neurocognitive) aging. While the set of variables and questions discussed are certainly not exhaustive, they constitute a beginning for what should form part of the next frontier in the legacy and value of considering the role bilingual language engagement has for the developing mind and brain, inclusive of how it impacts the descent from the proverbial mountain of life.

Competing interests

The author declares none.

Footnotes

1 It is important to offer some clarification with respect to the “mountain” analogy offered herein, inclusive of some terms used in appealing to it metaphorically. This analogy in no way ignores the ebs and flows that exist in development and aging, that is, points in both childhood and in older age that are nonlinear. Rather, the intention is to appeal to what a simple hike on any mountain evidences: mountains in the real world never have perfectly flat inclines and declines—these only exist in cartoonish renderings and/or can seem as such in photos when the offered perspective comes from a vantage point that is significantly zoomed out. In fact, more generally speaking, it is likely that inconsistencies in heralding the relative zoomed perspective of particular bilingualism and neurocognition studies themselves contribute to misunderstandings that circulate through several debates within the field (Leivada et al., Reference Leivada, Duñabeitia, Westergaard and Rothman2021, Reference Leivada, Dentella, Masullo and Rothman2023). In any case, the real nature of mountainous climbs and descents entail a series of peaks and valleys, iterative ups and downs taking place along what is otherwise clearly the ascent or the descent. In this sense, the mountain metaphor is apt to capture the actual non-linear reality of cognitive development across the lifespan. In the context of the present article, highlighting this is especially important in keeping with current discourses in aging sciences, which endeavor to inject distance from a an overly simplistic view of aging based on cognitive decline solely and/or comparisons between so-called healthy aging and neurodegenerative pathology first and foremost (Rowe & Kahn, Reference Rowe and Kahn1997; Schulz & Heckhausen, Reference Schulz and Heckhausen1996). The “mountain”, is precisely used herein to recognize the descriptive observation that CA includes moments of growth and arrests and that these actually occur throughout the lifespan.

2 I use the term bilingualism as a catch-all label, intending to cover multilingualism as well. Such a position does not ignore or preclude the possibility that bilingualism and multilingualism could have distinct outcomes for the relevant domains and theoretical issues discussed herein, however, this is largely a question of degree. For ease of exposition and clarity, it is my view that using a single term is better than interchanging them or creating a new one, such as bi-multilingualism. Given that many researchers and especially non-researchers take the term multilingualism to apply only in the case where at least three languages are at play, I opted to use the term bilingual throughout viewing it as more inclusive such that anyone that requires multilingualism to include three languages would know that the present discussion and claims refer also to people for which only two are in play.

References

Aarsland, D., Zaccai, J., & Brayne, C. (2005). A systematic review of prevalence studies of dementia in Parkinson's disease. Movement disorders: official journal of the Movement Disorder Society, 20(10), 12551263.CrossRefGoogle ScholarPubMed
Abutalebi, J., & Green, D. W. (2016). Neuroimaging of language control in bilinguals: neural adaptation and reserve. Bilingualism: Language and cognition, 19(4), 689698CrossRefGoogle Scholar
Anderson, J. A., Hawrylewicz, K., & Grundy, J. G. (2020). Does bilingualism protect against dementia? A meta-analysis. Psychonomic Bulletin & Review, 27(5), 952965. https://doi.org/10.3758/s13423-020-01736-5CrossRefGoogle ScholarPubMed
Anderson, J. A., Grundy, J. G., Grady, C. L., Craik, F. I., & Bialystok, E. (2021). Bilingualism contributes to reserve and working memory efficiency: Evidence from structural and functional neuroimaging. Neuropsychologia, 163, 108071.CrossRefGoogle ScholarPubMed
Antoniou, M., Gunasekera, G. M., & Wong, P. C. (2013). Foreign language training as cognitive therapy for age-related cognitive decline: A hypothesis for future research. Neuroscience & Biobehavioral Reviews, 37(10), 26892698.CrossRefGoogle ScholarPubMed
Babiloni, C., Del Percio, C., Lizio, R., Noce, G., Lopez, S., Soricelli, A., Ferri, R., Nobili, F., Arnaldi, D., Famà, F., Aarsland, D., Orzi, F., Buttinelli, C., Giubilei, F., Onofrj, M., Stocchi, F., Stirpe, P., Fuhr, P., Gschwandtner, U., Ransmayr, G., … Bonanni, L. (2018). Abnormalities of resting-state functional cortical connectivity in patients with dementia due to Alzheimer's and Lewy body diseases: an EEG study. Neurobiology of aging, 65, 1840. https://doi.org/10.1016/j.neurobiolaging.2017.12.023CrossRefGoogle ScholarPubMed
Berkes, M., Bialystok, E., Craik, F. I., Troyer, A., & Freedman, M. (2020). Conversion of mild cognitive impairment to alzheimer's disease in monolingual and bilingual patients. Alzheimer disease and associated disorders, 34(3), 225.CrossRefGoogle ScholarPubMed
Berkes, M., Calvo, N., Anderson, J. A., Bialystok, E., & Alzheimer's Disease Neuroimaging Initiative. (2021). Poorer clinical outcomes for older adult monolinguals when matched to bilinguals on brain health. Brain Structure and Function, 226, 415424.CrossRefGoogle ScholarPubMed
Bialystok, E. (2017). The bilingual adaptation: How minds accommodate experience. Psychological bulletin, 143(3), 233CrossRefGoogle ScholarPubMed
Bialystok, E. (2021). Bilingualism: Pathway to cognitive reserve. Trends in cognitive sciences, 25(5), 355364.CrossRefGoogle ScholarPubMed
Bialystok, E., & Craik, F. I. (2022). How does bilingualism modify cognitive function? Attention to the mechanism. Psychonomic Bulletin & Review, 29(4), 12461269.CrossRefGoogle ScholarPubMed
Bialystok, E., Craik, F. I., Klein, R., & Viswanathan, M. (2004). Bilingualism, aging, and cognitive control: evidence from the Simon task. Psychology and aging, 19(2), 290.CrossRefGoogle ScholarPubMed
Bice, K., Yamasaki, B. L., & Prat, C. S. (2020). Bilingual language experience shapes resting-state brain rhythms. Neurobiology of Language, 1(3), 288318.CrossRefGoogle ScholarPubMed
Briggs, R., Kennelly, S. P., & O'Neill, D. (2016). Drug treatments in Alzheimer's disease. Clinical medicine, 16(3), 247.CrossRefGoogle ScholarPubMed
Brini, S., Sohrabi, H. R., Hebert, J. J., Forrest, M. R. L., Laine, M., Hämäläinen, H., Karrasch, M., Peiffer, J. J., Martins, R. N., & Fairchild, T. J. (2020). Bilingualism is associated with a delayed onset of dementia but not with a lower risk of developing it: a systematic review with meta-analyses. Neuropsychology Review, 30, 124.CrossRefGoogle Scholar
Burzynska, A. Z., Chaddock-Heyman, L., Voss, M. W., Wong, C. N., Gothe, N. P., Olson, E. A., Knecht, A., Lewis, A., Monti, J. M., Cooke, G. E., Wojcicki, T. R., Fanning, J., Chung, H. D., Awick, E., McAuley, E., & Kramer, A. F. (2014). Physical activity and cardiorespiratory fitness are beneficial for white matter in low-fit older adults. PloS one, 9(9), e107413. https://doi.org/10.1371/journal.pone.0107413CrossRefGoogle ScholarPubMed
Calvo, N., García, A. M., Manoiloff, L., & Ibáñez, A. (2016). Bilingualism and cognitive reserve: a critical overview and a plea for methodological innovations. Frontiers in aging neuroscience, 7, 249.CrossRefGoogle Scholar
Calvo, N., Anderson, J. A., Berkes, M., Freedman, M., Craik, F. I., & Bialystok, E. (2023a). Gray matter volume as evidence for cognitive Reserve in Bilinguals with Mild Cognitive Impairment. Alzheimer Disease & Associated Disorders, 37(1), 712.CrossRefGoogle ScholarPubMed
Calvo, N., Grundy, J. G., & Bialystok, E. (2023b). Bilingualism modulates neural efficiency at rest through alpha reactivity. Neuropsychologia, 180, 108486.CrossRefGoogle ScholarPubMed
Campbell, A., Grace, F., Ritchie, L., Beaumont, A., & Sculthorpe, N. (2019). Long-term aerobic exercise improves vascular function into old age: a systematic review, meta-analysis and meta regression of observational and interventional studies. Frontiers in physiology, 31.Google Scholar
De Houwer, A. (2021). Bilingual development in childhood. Cambridge University Press.CrossRefGoogle Scholar
De Houwer, A. (2023). The danger of bilingual–monolingual comparisons in applied psycholinguistic research. Applied Psycholinguistics, 44(3), 343357.CrossRefGoogle Scholar
DeLuca, V., & Voits, T. (2022). Bilingual experience affects white matter integrity across the lifespan. Neuropsychologia, 169, 108191.CrossRefGoogle ScholarPubMed
DeLuca, V., Rothman, J., Bialystok, E., & Pliatsikas, C. (2019). Redefining bilingualism as a spectrum of experiences that differentially affects brain structure and function. Proceedings of the National Academy of Sciences, 116(15), 75657574.CrossRefGoogle ScholarPubMed
DeLuca, V., Segaert, K., Mazaheri, A., & Krott, A. (2020). Understanding bilingual brain function and structure changes? U bet! A unified bilingual experience trajectory model. Journal of Neurolinguistics, 56, 100930.CrossRefGoogle Scholar
Dumas, J. A. (2015). What is normal cognitive aging? Evidence from task-based functional neuroimaging. Current behavioral neuroscience reports, 2, 256261.CrossRefGoogle ScholarPubMed
Erickson, K. I., Leckie, R. L., & Weinstein, A. M. (2014). Physical activity, fitness, and gray matter volume. Neurobiology of aging, 35, S20S28.CrossRefGoogle ScholarPubMed
Farokhian, F., Yang, C., Beheshti, I., Matsuda, H., & Wu, S. (2017). Age-related gray and white matter changes in normal adult brains. Aging and disease, 8(6), 899.CrossRefGoogle ScholarPubMed
Fish, P. V., Steadman, D., Bayle, E. D., & Whiting, P. (2019). New approaches for the treatment of Alzheimer's disease. Bioorganic & medicinal chemistry letters, 29(2), 125133.CrossRefGoogle ScholarPubMed
Fleck, J. I., Kuti, J., Mercurio, J., Mullen, S., Austin, K., & Pereira, O. (2017). The impact of age and cognitive reserve on resting-state brain connectivity. Frontiers in aging neuroscience, 9, 392.CrossRefGoogle ScholarPubMed
Gallo, F., DeLuca, V., Prystauka, Y., Voits, T., Rothman, J., & Abutalebi, J. (2022a). Bilingualism and aging: implications for (delaying) neurocognitive decline. Frontiers in Human Neuroscience, 16, 22.CrossRefGoogle ScholarPubMed
Gallo, F., Kubiak, J., & Myachykov, A. (2022b). Add bilingualism to the Mix: L2 proficiency modulates the effect of cognitive reserve proxies on executive performance in healthy aging. Frontiers in Psychology, 13, 780261.CrossRefGoogle Scholar
Gold, B. T., Kim, C., Johnson, N. F., Kryscio, R. J., & Smith, C. D. (2013). Lifelong bilingualism maintains neural efficiency for cognitive control in aging. Journal of Neuroscience, 33(2), 387396.CrossRefGoogle ScholarPubMed
Gollan, T. H., Salmon, D. P., Montoya, R. I., & Galasko, D. R. (2011). Degree of bilingualism predicts age of diagnosis of Alzheimer's disease in low-education but not in highly educated Hispanics. Neuropsychologia, 49(14), 38263830.CrossRefGoogle ScholarPubMed
Grant, A., Dennis, N. A., & Li, P. (2014). Cognitive control, cognitive reserve, and memory in the aging bilingual brain. Frontiers in psychology, 5, 1401.CrossRefGoogle ScholarPubMed
Green, D. W., & Abutalebi, J. (2013). Language control in bilinguals: The adaptive control hypothesis. Journal of cognitive psychology, 25(5), 515530.CrossRefGoogle ScholarPubMed
Grosjean, F. (1982). Life with two languages: An introduction to bilingualism. Harvard University Press.Google Scholar
Grundy, J. G. (2020). The effects of bilingualism on executive functions: An updated quantitative analysis. Journal of Cultural Cognitive Science, 4(2), 177199.CrossRefGoogle Scholar
Guzmán-Vélez, E., & Tranel, D. (2015). Does bilingualism contribute to cognitive reserve? Cognitive and neural perspectives. Neuropsychology, 29(1), 139.CrossRefGoogle ScholarPubMed
Harada, C. N., Love, M. C. N., & Triebel, K. L. (2013). Normal cognitive aging. Clinics in geriatric medicine, 29(4), 737752.CrossRefGoogle ScholarPubMed
Jared, D., & Kroll, J. F. (2001). Do bilinguals activate phonological representations in one or both of their languages when naming words?. Journal of memory and language, 44(1), 231.CrossRefGoogle Scholar
Jauny, G., Eustache, F., & Hinault, T. T. (2022). M/EEG dynamics underlying reserve, resilience, and maintenance in aging: a review. Frontiers in Psychology, 13, 861973.CrossRefGoogle ScholarPubMed
Kinsella, K., & He, W. (2009). An aging world: 2008: International population reports (pp. 5172). Washington DC: US Government Printing Office.Google Scholar
Kliesch, M., Pfenninger, S. E., Wieling, M., Stark, E., & Meyer, M. (2022). Cognitive benefits of learning additional languages in old adulthood? insights from an intensive longitudinal intervention study. Applied Linguistics, 43(4), 653676.CrossRefGoogle Scholar
Klimova, B. (2018). Learning a foreign language: A review on recent findings about its effect on the enhancement of cognitive functions among healthy older individuals. Frontiers in human neuroscience, 12, 305.CrossRefGoogle Scholar
Klimova, B., Maresova, P., & Kuca, K. (2016). Non-pharmacological approaches to the prevention and treatment of Alzheimer's disease with respect to the rising treatment costs. Current Alzheimer Research, 13(11), 12491258.CrossRefGoogle Scholar
Klimova, B., Valis, M., & Kuca, K. (2017). Cognitive decline in normal aging and its prevention: a review on non-pharmacological lifestyle strategies. Clinical interventions in aging, 903910.CrossRefGoogle ScholarPubMed
Kousaie, S., & Phillips, N. A. (2017). A behavioural and electrophysiological investigation of the effect of bilingualism on aging and cognitive control. Neuropsychologia, 94, 2335CrossRefGoogle ScholarPubMed
Leivada, E., Duñabeitia, J. A., Westergaard, M., & Rothman, J. (2021). On the phantom-like appearance of bilingualism effects on neurocognition: (How) should we proceed? Bilingualism: Language and Cognition. https://doi.org/10.1017/S1366728920000358CrossRefGoogle Scholar
Leivada, E., Dentella, V., Masullo, C., & Rothman, J. (2023). On trade-offs in bilingualism and moving beyond the stacking the deck fallacy. Bilingualism: Language and Cognition, 1- 6. doi:10.1017/S1366728922000761Google Scholar
Li, P., Legault, J., & Litcofsky, K. A. (2014). Neuroplasticity as a function of second language learning: Anatomical changes in the human brain. Cortex, 58, 301324.CrossRefGoogle ScholarPubMed
MacPherson, S., & Cox, S. (2017). The frontal ageing hypothesis: Evidence from normal ageing and dementia. In Riby, L. (Ed.), Handbook of gerontology research methods: Understanding successful ageing (pp. 139158). Routledge/Taylor & Francis Group.Google Scholar
Mandolesi, L., Polverino, A., Montuori, S., Foti, F., Ferraioli, G., Sorrentino, P., & Sorrentino, G. (2018). Effects of physical exercise on cognitive functioning and wellbeing: biological and psychological benefits. Frontiers in psychology, 509.Google Scholar
Marian, V., & Spivey, M. (2003). Competing activation in bilingual language processing: Within-and between-language competition. Bilingualism: Language and cognition, 6(2), 97115.CrossRefGoogle Scholar
Martinez-Horta, S., Sampedro, F., Horta-Barba, A., Perez-Perez, J., Pagonabarraga, J., Gomez-Anson, B., & Kulisevsky, J. (2020). Structural brain correlates of dementia in Huntington's disease. NeuroImage: Clinical, 28, 102415.CrossRefGoogle ScholarPubMed
Miraglia, F., Vecchio, F., & Rossini, P. M. (2017). Searching for signs of aging and dementia in EEG through network analysis. Behavioural brain research, 317, 292300.CrossRefGoogle ScholarPubMed
Nilsson, J., Berggren, R., Garzón, B., Lebedev, A. V., & Lövdén, M. (2021). Second language learning in older adults: effects on brain structure and predictors of learning success. Frontiers in Aging Neuroscience, 13, 666851.CrossRefGoogle ScholarPubMed
Perani, D., & Abutalebi, J. (2015). Bilingualism, dementia, cognitive and neural reserve. Current opinion in neurology, 28(6), 618625.CrossRefGoogle ScholarPubMed
Pereira Soares, S. M., Kubota, M., Rossi, E., & Rothman, J. (2021). Determinants of bilingualism predict dynamic changes in resting state EEG oscillations. Brain and Language, 223, 105030.CrossRefGoogle ScholarPubMed
Perneczky, R., Kempermann, G., Korczyn, A. D., Matthews, F. E., Ikram, M. A., Scarmeas, N., Chetelat, G., Stern, Y., & Ewers, M. (2019). Translational research on reserve against neurodegenerative disease: consensus report of the International Conference on Cognitive Reserve in the Dementias and the Alzheimer's Association Reserve, Resilience and Protective Factors Professional Interest Area working groups. BMC medicine, 17(1), 47. https://doi.org/10.1186/s12916-019-1283-zCrossRefGoogle ScholarPubMed
Persson, J., Nyberg, L., Lind, J., Larsson, A., Nilsson, L. G., Ingvar, M., & Buckner, R. L. (2006). Structure–function correlates of cognitive decline in aging. Cerebral cortex, 16(7), 907915.CrossRefGoogle ScholarPubMed
Petrosini, L., De Bartolo, P., Foti, F., Gelfo, F., Cutuli, D., Leggio, M. G., & Mandolesi, L. (2009). On whether the environmental enrichment may provide cognitive and brain reserves. Brain research reviews, 61(2), 221239.CrossRefGoogle ScholarPubMed
Pliatsikas, C. (2019). Multilingualism and brain plasticity. The handbook of the neuroscience of multilingualism, 230251.CrossRefGoogle Scholar
Pliatsikas, C. (2020). Understanding structural plasticity in the bilingual brain: The Dynamic Restructuring Model. Bilingualism: Language and Cognition, 23(2), 459471.CrossRefGoogle Scholar
Pliatsikas, C., & Luk, G. (2016). Executive control in bilinguals: A concise review on fMRI studies. Bilingualism: Language and Cognition, 19(4), 699705.CrossRefGoogle Scholar
Polich, J. (1997). EEG and ERP assessment of normal aging. Electroencephalography and Clinical Neurophysiology/Evoked Potentials Section, 104(3), 244256.CrossRefGoogle ScholarPubMed
Prat, C. S., Yamasaki, B. L., & Peterson, E. R. (2019). Individual differences in resting-state brain rhythms uniquely predict second language learning rate and willingness to communicate in adults. Journal of Cognitive Neuroscience, 31(1), 7894.CrossRefGoogle ScholarPubMed
Rothman, J., Alonso, J. G., & Puig-Mayenco, E. (2019). Third language acquisition and linguistic transfer (Vol. 163). Cambridge University Press.CrossRefGoogle Scholar
Rothman, J., Bayram, F., DeLuca, V., Di Pisa, G., Dunabeitia, J. A., Gharibi, K., Hao, J., Kolb, N., Kubota, M., Kupisch, T., Laméris, T., Luque, A., van Osch, B., Pereira Soares, S. M., Prystauka, Y., & Wulff, S. (2023). Monolingual comparative normativity in bilingualism research is out of “control”: Arguments and alternatives. Applied Psycholinguistics, 44(3), 316329.CrossRefGoogle Scholar
Rowe, J. W., & Kahn, R. L. (1997). Successful aging. The gerontologist, 37(4), 433440.CrossRefGoogle ScholarPubMed
Salthouse, T. (2000). A theory of cognitive aging. Elsevier.Google Scholar
Salthouse, T. (2004). What and when of cognitive aging. Current directions in psychological science, 13(4), 140144.CrossRefGoogle Scholar
Salthouse, T. (2019). Trajectories of normal cognitive aging. Psychology and aging, 34(1), 17.CrossRefGoogle ScholarPubMed
Schlegel, A. A., Rudelson, J. J., & Tse, P. U. (2012). White matter structure changes as adults learn a second language. Journal of cognitive neuroscience, 24(8), 16641670.CrossRefGoogle Scholar
Schulz, R., & Heckhausen, J. (1996). A life span model of successful aging. American psychologist, 51(7), 702.CrossRefGoogle ScholarPubMed
Spivey, M. J., & Marian, V. (1999). Cross Talk between Native and Second Languages: Partial Activation of an Irrelevant Lexicon. Psychological Science, 10(3), 281284.CrossRefGoogle Scholar
Stern, Y. (2002). What is cognitive reserve? Theory and research application of the reserve concept. Journal of the international neuropsychological society, 8(3), 448460.CrossRefGoogle ScholarPubMed
Stern, Y. (2009). Cognitive reserve. Neuropsychologia, 47(10), 20152028.CrossRefGoogle ScholarPubMed
Stern, Y., Arenaza-Urquijo, E. M., Bartrés-Faz, D., Belleville, S., Cantilon, M., Chetelat, G., Ewers, M., Franzmeier, N., Kempermann, G., Kremen, W. S., Okonkwo, O., Scarmeas, N., Soldan, A., Udeh-Momoh, C., Valenzuela, M., Vemuri, P., Vuoksimaa, E., & the Reserve, Resilience and Protective Factors PIA Empirical Definitions and Conceptual Frameworks Workgroup (2020). Whitepaper: Defining and investigating cognitive reserve, brain reserve, and brain maintenance. Alzheimer's & Dementia: the journal of the Alzheimer's Association, 16(9), 13051311. https://doi.org/10.1016/j.jalz.2018.07.219CrossRefGoogle ScholarPubMed
Teixeira, C. V. L., Gobbi, L. T. B., Corazza, D. I., Stella, F., Costa, J. L. R., & Gobbi, S. (2012). Non-pharmacological interventions on cognitive functions in older people with mild cognitive impairment (MCI). Archives of gerontology and geriatrics, 54(1), 175180.CrossRefGoogle ScholarPubMed
Titone, D., & Tiv, M. (2022). Rethinking multilingual experience through a Systems Framework of Bilingualism. Bilingualism: Language and Cognition, 116. doi:10.1017/S1366728921001127Google Scholar
Tucker-Drob, E. M. (2019). Cognitive aging and dementia: a life-span perspective. Annual review of developmental psychology, 1, 177196.CrossRefGoogle ScholarPubMed
Villeneuve, S. (2019). Lifespan Cognitive Reserve – A Secret to Coping With Neurodegenerative Pathology. JAMA neurology, 76(10), 11451146.CrossRefGoogle ScholarPubMed
Voits, T., Pliatsikas, C., Robson, H., & Rothman, J. (2020). Beyond Alzheimer's disease: Can bilingualism be a more generalized protective factor in neurodegeneration?. Neuropsychologia, 147, 107593.CrossRefGoogle ScholarPubMed
Voits, T., DeLuca, V., & Abutalebi, J. (2022a). The nuance of bilingualism as a reserve contributor: Conveying research to the broader neuroscience community. Frontiers in Psychology, 13, 909266.CrossRefGoogle Scholar
Voits, T., Robson, H., Rothman, J., & Pliatsikas, C. (2022b). The effects of bilingualism on hippocampal volume in ageing bilinguals. Brain Structure and Function, 227(3), 979994.CrossRefGoogle ScholarPubMed
Voits, T., Rothman, J., Calabria, M., Robson, H., Aguirre, N., Cattaneo, G., Costumero, V., Hernández, M., Juncadella Puig, M., Marín-Marín, L., Suades, A., Costa, A. & Pliatsikas, C. (2023) Hippocampal adaptations in Mild Cognitive Impairment patients are modulated by bilingual language experiences. Bilingualism: Language and Cognition, 111. DOI: 10.1017/S1366728923000354Google Scholar
Wang, L. Y., Pei, J., Zhan, Y. J., & Cai, Y. W. (2020). Overview of meta-analyses of five non-pharmacological interventions for Alzheimer's disease. Frontiers in aging neuroscience, 12, 594432.CrossRefGoogle ScholarPubMed
Wong, P. C., Ou, J., Pang, C. W., Zhang, L., Tse, C. S., Lam, L. C., & Antoniou, M. (2019). Language training leads to global cognitive improvement in older adults: A preliminary study. Journal of Speech, Language, and Hearing Research, 62(7), 24112424.CrossRefGoogle ScholarPubMed
Xu, H., Zhang, Y., & Wu, B. (2017). Association between migration and cognitive status among middle-aged and older adults: a systematic review. BMC geriatrics, 17(1), 115.CrossRefGoogle ScholarPubMed
Yaffe, K., Fiocco, A. J., Lindquist, K., Vittinghoff, E., Simonsick, E. M., Newman, A. B., Satterfield, S., Rosano, C., Rubin, S. M., Ayonayon, H. N., Harris, T. B., & Study, Health ABC (2009). Predictors of maintaining cognitive function in older adults: the Health ABC study. Neurology, 72(23), 20292035. https://doi.org/10.1212/WNL.0b013e3181a92c36CrossRefGoogle ScholarPubMed