Introduction
Traumatic brain injury (TBI) is a leading cause of childhood death and acquired disability worldwide (Dewan, Mummareddy, Wellons, & Bonfield, Reference Dewan, Mummareddy, Wellons and Bonfield2016). Childhood TBI has been linked to a range of debilitating neurobehavioral sequelae, including an increased risk for developing novel psychiatric disorders (Emery et al., Reference Emery, Barlow, Brooks, Max, Villavicencio-Requis, Gnanakumar and Yeates2016; Li & Liu, Reference Li and Liu2013). Attention-deficit/hyperactivity disorder (ADHD), defined by developmentally inappropriate and functionally impairing symptoms of inattention and/or hyperactivity/impulsivity (American Psychiatric Association, 2013), is the most frequent novel psychiatric disorder after childhood TBI with a prevalence of approximately 20% (Max et al., Reference Max, Schachar, Levin, Ewing-Cobbs, Chapman, Dennis and Landis2005a, Reference Max, Schachar, Levin, Ewing-Cobbs, Chapman, Dennis and Landis2005b, Reference Max, Wilde, Bigler, MacLeod, Vasquez, Schmidt and Levin2012; Narad et al., Reference Narad, Kennelly, Zhang, Wade, Yeates, Taylor and Kurowski2018). New-onset ADHD symptomatology occurring after TBI is referred to as secondary ADHD (s-ADHD) (Narad et al., Reference Narad, Kennelly, Zhang, Wade, Yeates, Taylor and Kurowski2018). Despite evidence that children with s-ADHD show significantly more functional difficulties than those without s-ADHD, risk factors for elevated s-ADHD symptomatology are not well understood (Gerring et al., Reference Gerring, Brady, Chen, Vasa, Grados, Bandeen-Roche and Denckla1998; Narad et al., Reference Narad, Kennelly, Zhang, Wade, Yeates, Taylor and Kurowski2018).
Prior childhood TBI research suggests that the substantial heterogeneity in s-ADHD symptom severity is at least partly explained by acute TBI severity. In a prospective cohort of 81 children with complicated-mild to severe TBI, Narad et al. (Reference Narad, Kennelly, Zhang, Wade, Yeates, Taylor and Kurowski2018) found that children of all TBI severity levels had almost twice the risk for s-ADHD than age-matched orthopaedically injured children. The strongest associations were observed in children with severe TBI, who demonstrated a fourfold increased risk for developing s-ADHD (Narad et al., Reference Narad, Kennelly, Zhang, Wade, Yeates, Taylor and Kurowski2018). Similarly, a recent meta-analysis found that in children with severe TBI, the odds for ADHD were significantly higher than in children with other injuries (Asarnow, Newman, Weiss, & Su, Reference Asarnow, Newman, Weiss and Su2021).
In addition to the role of acute TBI severity, evidence links higher s-ADHD symptomatology to non-injury-related risk factors, including poorer pre-injury child adaptive functioning (Max et al., Reference Max, Schachar, Levin, Ewing-Cobbs, Chapman, Dennis and Landis2005a, Reference Max, Schachar, Levin, Ewing-Cobbs, Chapman, Dennis and Landis2005b), lower family socio-economic status (SES) (Gerring et al., Reference Gerring, Brady, Chen, Vasa, Grados, Bandeen-Roche and Denckla1998; Max et al., Reference Max, Schachar, Levin, Ewing-Cobbs, Chapman, Dennis and Landis2005a, Reference Max, Schachar, Levin, Ewing-Cobbs, Chapman, Dennis and Landis2005b) and pre- and post-injury family dysfunction (Max et al., Reference Max, Arndt, Castillo, Bokura, Robin, Lindgren and Mattheis1998; Narad et al., Reference Narad, Kennelly, Zhang, Wade, Yeates, Taylor and Kurowski2018). Interestingly, Max et al. (Reference Max, Arndt, Castillo, Bokura, Robin, Lindgren and Mattheis1998) found that when the effects of acute TBI severity, family psychiatric history, SES and pre-injury family functioning were modelled simultaneously, only poorer family functioning independently predicted higher ADHD symptomatology. While these findings suggest that pre-injury child and family environmental factors may interact with injury characteristics to heighten risk for s-ADHD symptomatology after childhood TBI (Gerring & Wade, Reference Gerring and Wade2012), the neurostructural brain correlates of these post-injury symptoms are largely unknown.
Based on the influential triple-network (TN) model of ADHD (Cai, Chen, Szegletes, Supekar, & Menon, Reference Cai, Chen, Szegletes, Supekar and Menon2018; Castellanos & Proal, Reference Castellanos and Proal2012; Menon, Reference Menon2011), one possibility is that s-ADHD symptomatology is associated with injury to large-scale, higher-order cognitive networks. According to the TN model, ADHD stems from aberrant structural and functional connectivity among three large-scale brain networks that function in concert to support top-down mental processes (Cai, Ryali, Chen, Li, & Menon, Reference Cai, Ryali, Chen, Li and Menon2014): the central executive network (CEN), the default mode network (DMN) and the salience network (SN). The CEN, which is anchored in the dorsolateral prefrontal cortex and the posterior parietal cortex, plays a central role in mediating aspects of top-down cognitive control, including working memory, selective attention, set-shifting and inhibition (Owen, McMillan, Laird, & Bullmore, Reference Owen, McMillan, Laird and Bullmore2005; Wager & Smith, Reference Wager and Smith2003). The DMN, which is anchored in the posterior cingulate cortex and the medial prefrontal cortex, is anti-correlated with the CEN and plays an indirect yet important role in higher-order cognitive processes. For instance, higher-order cognition relies on the availability of neuronal resources, which is accomplished by diminishing activation of the DMN during top-down mental processing (Baum et al., Reference Baum, Ciric, Roalf, Betzel, Moore, Shinohara and Quarmley2017; Gusnard, Akbudak, Shulman, & Raichle, Reference Gusnard, Akbudak, Shulman and Raichle2001; Satterthwaite et al., Reference Satterthwaite, Wolf, Erus, Ruparel, Elliott, Gennatas and Bilker2013). The TN model of higher-order cognition also posits a central role for the SN, which is anchored in the anterior insula and the anterior cingulate cortex and is responsible for modulating the activation of the CEN and deactivation of the DMN during tasks requiring top-down cognitive processes (Cai et al., Reference Cai, Chen, Ryali, Kochalka, Li and Menon2016; Sridharan, Levitin, & Menon, Reference Sridharan, Levitin and Menon2008).
The TN model of ADHD is supported by extensive meta-analytic evidence showing abnormal activation of the SN, CEN and DMN in participants with ADHD relative to neurotypical controls (Cortese et al., Reference Cortese, Kelly, Chabernaud, Proal, Di Martino, Milham and Castellanos2012). In one study, Cai et al. (Reference Cai, Chen, Szegletes, Supekar and Menon2018) found that childhood ADHD is associated with significantly lower time-varying engagement of the SN with the CEN and DMN relative to typically developing (TD) children. These intermittently weaker cross-network interactions between the SN, CEN and DMN were also shown to correlate with ADHD symptom severity in two independent child ADHD cohorts. Consistent with these findings, analyses of structural MRI using voxel-based morphometry in child and adolescent samples have consistently linked ADHD to grey matter structural alterations in hub regions of the CEN, SN and DMN (Francx et al., Reference Francx, Llera, Mennes, Zwiers, Faraone, Oosterlaan and Franke2016; Su et al., Reference Su, Chen, Dai, Lin, Qian, Zhou and Xiang2021). These findings suggest that ADHD may stem from aberrancies in structure and function of higher-order cognitive networks that are also highly susceptible to disruption in childhood TBI. However, no study has employed high-resolution structural brain MRI to establish whether elevated s-ADHD symptomatology after childhood TBI may be associated with neurostructural alterations within higher-order cognitive circuitry.
Several lines of behavioural and neuroimaging evidence suggest that childhood TBI is associated with abnormalities of large-scale, higher-order cognitive systems. At the group level, children with TBI demonstrate widespread impairments in top-down cognitive control, including poorer performance on tasks of cognitive flexibility, inhibition and working memory (Robinson et al., Reference Robinson, Fountain-Zaragoza, Dennis, Taylor, Bigler, Rubin and Yeates2014). Consistent with these behavioural findings, moderate-severe childhood TBI is associated with aberrant functional connectivity within the DMN and CEN (Risen, Barber, Mostofsky, & Suskauer, Reference Risen, Barber, Mostofsky and Suskauer2015; Stephens et al., Reference Stephens, Salorio, Barber, Risen, Mostofsky and Suskauer2018), as well as chronic grey matter structural alterations within the CEN, SN and DMN (Dennis et al., Reference Dennis, Simic, Bigler, Abildskov, Agostino, Taylor and Stancin2013). While these findings suggest that higher-order cognitive circuitry may be vulnerable in childhood TBI, large prospective studies are needed to evaluate whether regional brain morphometry within these large-scale cognitive networks has prognostic value for predicting s-ADHD symptom severity in children with TBI.
The current, prospective investigation aimed to (i) assess the effect of childhood TBI on sub-acute brain morphometry of the DMN, SN and CEN, and ADHD symptom severity, compared to a TD comparison group; and (ii) evaluate the independent prognostic value of DMN, SN and CEN morphometry for prospectively predicting s-ADHD symptom severity after adjusting for other established risk factors for s-ADHD, including acute TBI severity, SES, family function and pre-injury child adaptive functioning.
We expected significant group differences in DMN, SN and CEN morphometry, such that the severe TBI group would show diminished DMN, SN and CEN volumes compared to TD controls and children with milder head injuries. Based on prior research (Narad et al., Reference Narad, Kennelly, Zhang, Wade, Yeates, Taylor and Kurowski2018), we hypothesised that the TBI group would display significantly higher ADHD symptomatology and significantly higher rates of borderline-clinical scores (age-adjusted T > 65) than the TD group. Finally, we expected that, after adjusting for other well-established risk factors, altered morphometry of the DMN, CEN and SN would prospectively predict higher s-ADHD symptomatology at 12-months post-injury.
Methods
Participants and procedure
Children with mild-severe TBI were prospectively recruited into a larger longitudinal study (Anderson et al., Reference Anderson, Beauchamp, Yeates, Crossley, Ryan, Hearps and Catroppa2017), and represented consecutive admissions to the emergency department and intensive care unit at a state-wide paediatric level I trauma centre in Victoria, Australia. Age and sex-matched TD children were recruited from local community schools representing a range of socio-economic backgrounds. For the TBI group, we applied the following inclusion criteria: (i) 5–16 years of age at recruitment; and (ii) medically confirmed TBI, including availability of medical records to reliably determine TBI severity [i.e. Glasgow Coma Score (GCS), neurological findings]. Exclusion criteria were as follows: (i) suspected non-accidental injury or previous TBI; (ii) pre-injury history of congenital, neurological or neurodevelopmental diagnosis including ADHD, autism spectrum disorder and specific learning disorder, which were assessed using a parent interview-form administered upon initial study enrolment; and (iii) non-English speaking background. The human data reported in this study were obtained in compliance with the hospital Human Research Ethics committee. Parent consent and child assent were obtained prior to data collection.
In total, 112 TBI participants were enrolled in the study and were categorised as follows: (i) mild TBI (n = 57): GCS 13–15 on hospital admission, loss of consciousness (LOC) <1 h, negative brain CT/clinical MRI; (ii) complicated-mild TBI (n = 14): GCS 13–15 on admission, LOC <1 h, positive brain CT/clinical MRI finding; (iii) moderate TBI (n = 26): GCS 9–12 on hospital presentation, LOC 1–24 h; (iv) severe TBI (n = 15): GCS 3–8 on admission, LOC >24 h. The TD group (n = 43) were aged 5–16 years at recruitment and were group-matched to the TBI group on sex and SES. SES was assessed using the Australian Socioeconomic Index 2006 (McMillan, Beavis, & Jones, Reference McMillan, Beavis and Jones2009), which transforms the Australian and New Zealand Standard Classification of Occupations (ANZSCO) codes into a continuous measure of occupational status ranging from 0 (labourers) through to 100 (medical practitioners).
As reported in Table 1, groups did not significantly differ on age, sex or SES. Since group differences for SES neared statistical significance (p = 0.050), we covaried for SES in all subsequent analyses. With respect to injury-related characteristics (Table 2), falls/blows were most frequent in children with mild, complicated-mild and moderate TBI. Motor vehicle crashes and falls/blows were equally common in children with severe TBI. Children with moderate and severe TBI were more likely to receive surgical intervention.
Table 1. Baseline and demographic characteristics of enrolled sample
WASI-II, Wechsler Abbreviated Scale of Intelligence – Second Edition (WASI-II).
Table 2. Sample injury-related characteristics
GCS, Glasgow Coma Score.
Note: Statistically significant Bonferroni-corrected post-hoc analyses comparing amild TBI v. moderate TBI, bcomplicated-mild TBI v. moderate TBI, cmild TBI v. severe TBI, dcomplicated-mild TBI v. severe TBI, emoderate TBI v. severe TBI.
Pre-injury functioning
The primary caregiver retrospectively evaluated the child's pre-injury functioning using the Child Behaviour Check List (CBCL-6–18) (Achenbach & Rescorla, Reference Achenbach and Rescorla2001) and the Adaptive Behaviour Assessment System-II (ABAS-II) (Harrison & Oakland, Reference Harrison and Oakland2003). The ABAS-II is a well-validated parent-rated measure of conceptual, practical and social adaptive skills, ratings of which are used to derive the Global Adaptive Composite (GAC; M = 100, s.d. = 15) reported in Table 1. No significant group differences were identified when the pre-injury adaptive function of the TBI groups was compared to adaptive function ratings of the TD group collected at time of recruitment (Table 1). Similarly, the TBI groups did not significantly differ from the TDC group on pre-injury externalizing symptoms or pre-injury internalizing symptoms on the CBCL-6–18 (Table 1).
ADHD symptom severity at 12-months post-injury
CBCL-6–18 (Achenbach & Rescorla, Reference Achenbach and Rescorla2001) is a valid and reliable parent-rated questionnaire designed to assess child emotional and behavioural problems. Age-adjusted T scores for the DSM-oriented ADHD Problems scale and the Attention Problems scale (M = 50; s.d. = 10) were used to assess ADHD symptom severity. The ADHD Problems subscale consists of seven items aligned with DSM criteria for ADHD and shares five items with the Attention Problems scale (10 items), which is designed to more comprehensively assess symptoms of inattention associated with ADHD. T scores of 65 and above were used to denote borderline-clinical range symptomatology.
Family functioning at 6-months post-injury
The McMaster Family Assessment Device (FAD) – Global Functioning Scale (Epstein, Baldwin, & Bishop, Reference Epstein, Baldwin and Bishop1983) is a well-validated parent-report questionnaire, with higher scores indicative of worse family functioning.
High-resolution structural MRI
Image acquisition and pre-processing
Children were examined using high-resolution structural brain MRI acquired at 6 weeks post-injury (M = 42; s.d. = 29 days post-injury). As reported previously (Ryan et al., Reference Ryan, Catroppa, Hughes, Painter, Hearps, Beauchamp and Anderson2021), MR images were acquired on a 3 Tesla Siemens Trio scanner (Siemens Medical Systems, Erlangen, Germany) using a 32-Channel matrix head coil. In accordance with the protocol recommended by the National Institute of Neurological Disorders and Stroke Common Data Elements group, the MRI sequences included T1- and T2-weighted, axial T2-weighted fluid attenuated inversion recovery, axial susceptibility weighted and axial diffusion-weighted sequences. Quality control involved ranking the quality of T1-weighted images taking into account ringing, motion and susceptibility.
Of the 155 participants who underwent the research MR protocol, seven TBI participants and nine TD children were excluded due to motion artefact, dental artefact and/or incomplete data due to non-compliance. In addition, another two children with severe TBI had pronounced localised regions of encephalomalacia. In both cases, parenchymal distortion prohibited automated image analysis because of an absence of defining boundaries for image parcellation.
Morphometric analysis
Useable data for 137 participants were available for analysis. Cortical reconstruction and volumetric segmentation were completed using FreeSurfer Version 5.3 (http://surfer.nmr.mgh.harvard.edu.au). Details of the procedures are provided in previous publications (Fischl et al., Reference Fischl, Salat, Van Der Kouwe, Makris, Ségonne, Quinn and Dale2004; Jovicich et al., Reference Jovicich, Czanner, Han, Salat, van der Kouwe, Quinn and Blacker2009). Briefly, the processing includes the removal of non-brain tissue using a hybrid watershed/surface deformation procedure, automated Talairach transformation, segmentation of the subcortical WM and deep GM volumetric structures (Fischl et al., Reference Fischl, Salat, Busa, Albert, Dieterich, Haselgrove and Klaveness2002), intensity normalisation (Sled, Zijdenbos, & Evans, Reference Sled, Zijdenbos and Evans1998), tessellation of the GM–WM boundary, automated topology correction (Ségonne, Pacheco, & Fischl, Reference Ségonne, Pacheco and Fischl2007) and surface deformation following intensity gradients to optimally place the GM/WM and GM/CSF borders at the location where the greatest shift in intensity defines the transition to the other tissue class (Fischl & Dale, Reference Fischl and Dale2000). The resulting cortical models were registered to a spherical atlas, utilizing individual cortical folding patterns to match cortical geometry across subjects (Fischl, Sereno, Tootell, & Dale, Reference Fischl, Sereno, Tootell and Dale1999).
The cerebral cortex was parcellated into regions based on gyral and sulcal structure (Desikan et al., Reference Desikan, Ségonne, Fischl, Quinn, Dickerson, Blacker and Hyman2006). Results for each subject were visually inspected to ensure accuracy of registration, skull stripping, segmentation and cortical surface reconstruction. Manual editing, where necessary, was performed to optimise accuracy. The surface inaccuracies involving skull stripping or frank exclusion of brain parenchyma were edited either by (1) adding control points to aid FreeSurfer in the identification of white matter (since it uses the WM/GM boundary as a starting place for reconstructing the pial surface) (three cases) or (2) by fixing the skull strip by removing remaining dura (four cases).
Regions of interest (ROIs) defined in FreeSurfer variables (Desikan et al., Reference Desikan, Ségonne, Fischl, Quinn, Dickerson, Blacker and Hyman2006) were obtained by extracting volumes for each ROI bilaterally. Using the methodology outlined in previous childhood TBI research (Dennis et al., Reference Dennis, Simic, Bigler, Abildskov, Agostino, Taylor and Stancin2013; Hoskinson et al., Reference Hoskinson, Bigler, Abildskov, Dennis, Taylor, Rubin and Yeates2019), composite measures of DMN, CEN and SN morphometry were derived by summing together the bilateral ROIs within each of the respective neural networks of interest – DMN, CEN and SN (Dennis et al., Reference Dennis, Simic, Bigler, Abildskov, Agostino, Taylor and Stancin2013; Hoskinson et al., Reference Hoskinson, Bigler, Abildskov, Dennis, Taylor, Rubin and Yeates2019). Replicating the methodology from prior childhood TBI research (Dennis et al., Reference Dennis, Simic, Bigler, Abildskov, Agostino, Taylor and Stancin2013), the DMN composite was derived by summing the volumes of the bilateral ventromedial prefrontal cortex, posterior cingulate cortex, inferior parietal lobule and hippocampal formation. The CEN composite includes the dorsolateral prefrontal cortex, posterior parietal cortex, caudate nucleus and thalamus, whereas the SN composite includes the ventrolateral prefrontal cortex, insula, anterior cingulate cortex and amygdala. This process yielded three network-based morphometry variables (i.e. brain morphometry values for the DMN, CEN and SN, respectively) for use in subsequent analyses.
Statistical analysis
SPSS Version 25.00 (IBM Corporation) was used for screening and analysis of all study data. Statistical assumptions were met for each analysis, unless otherwise stated. The variance inflation factor (VIF) was used to assess for multi-collinearity. One-way analysis of covariance was used to assess for group differences in ADHD symptom severity after adjustment for SES, participant sex and age. Significant omnibus results were followed by Bonferroni-corrected post hoc pairwise comparisons. Network-based morphometry was examined using multivariate analysis of covariance (MANCOVA). In these analyses, group membership was entered as the between-subjects factor and network-based morphometry (DMN v. CEN v. SN) was entered as the within-subjects factor.
Multivariable regression analyses were used to assess prospective relationships between network-based morphometry (DMN, SN, CEN) and ADHD symptom severity in children with TBI. In each multivariate model, measures of network-based morphometry were modelled simultaneously with adjustment for other established s-ADHD risk factors, including acute TBI severity indexed by the GCS, SES, post-injury family functioning and retrospective ratings of pre-injury child adaptive skills. Participant age, sex, pre-injury CBCL externalizing symptoms and estimated total intracranial volume (TIV) were also entered as covariates in all multivariate regression models. This approach enabled us to assess if measures of network-based brain morphometry are unique and therefore useful markers of s-ADHD symptom severity in children with TBI.
Results
Effect of childhood TBI on network-based brain morphometry
In total, 137 participants had useable MRI for FreeSurfer to produce volumetric data. A sensitivity analysis found no significant differences in the pre-injury, demographic or injury-related characteristics of those with and without useable MRI. Groups did not significantly differ on measures of estimated TIV or whole brain volume (Table 2). The time interval between day-of-injury and research MRI was not significantly associated with measures of global brain volume or network-based morphometry (all p ⩾ 0.25).
Group means and standard deviations for network-based morphometry are presented in Table 3. To complement these data, online Supplementary Figure S1 includes violin plots depicting network-based brain morphometry (i.e. DMN, CEN, SN volume) as a function of TBI severity group membership. As expected, the overall MANCOVA was statistically significant after adjusting for participant sex, age at MRI, TIV and SES [F (5,129) = 8.97, p < 0.001, η 2 = 0.218]. As shown in Table 3, significant overall group differences were documented for DMN, CEN and SN morphometry. Post-hoc pairwise comparisons (see superscripts in Table 3) indicated that, compared to the TD group and all other TBI severity groups (mild, complicated mild, moderate groups), children with severe TBI had diminished DMN, CEN and SN volumes.
Table 3. Group differences in DMN, SN and CEN morphometry and ADHD symptom severity
Note: Significant (p < 0.05) Bonferroni corrected post-hoc analyses comparing aTD v. TBI-severe, bTBI-mild v. TBI-severe, cTBI-complicated-mild v. TBI-severe, dTBI-moderate v. TBI-severe, eTD v. TBI-moderate.
Group differences for the individual ROIs associated with each large-scale neural network are displayed in Table 4. As expected, post-hoc pairwise comparisons revealed that, for all individual ROIs within the DMN, CEN and SN, the severe TBI group showed significantly diminished volumes relative to TD controls (all p < 0.05), and children with mild, complicated-mild and moderate TBI (all p < 0.05) (see Table 4).
Table 4. Group differences in regions of interest associated with the DMN, CEN and SN
Note: Significant (p < 0.05) Bonferroni post-hoc analyses comparing aTBI-mild v. mild complex, bTD v. TBI-severe, cTBI-mild v. TBI-severe, dTBI-mild complex v. TBI-severe, eTBI-moderate v. TBI-severe.
The impact of TBI on ADHD symptomatology
In total, 129 participants (43 TD, 42 mild TBI, 11 complicated mild TBI, 23 moderate TBI, 10 severe TBI) completed standardised parent-report measures of ADHD symptomatology at 12-months post-injury. A sensitivity analysis found no significant differences in the pre-injury, demographic or injury-related characteristics of those with and without 12-month ADHD symptom rating data (all p ⩾ 0.17).
TBI v. TD
As expected, the TBI group displayed significantly higher ADHD symptomatology than the TD group on the CBCL DSM-oriented ADHD Problems scale (p = 0.016; η 2 = 0.045) and the CBCL Attention Problems scale (p = 0.043; η 2 = 0.032). Similarly, we found that compared to the TD group, scores within the borderline-clinical range (T > 65) for the CBCL DSM-oriented ADHD Problems scale were significantly more common in the TBI group (TBI: 19% v. TD control: 2%, Fisher's exact p = 0.011). Although the TBI group also displayed higher rates of impairment than TD controls on the CBCL Attention Problems scale, the difference did not reach statistical significance (TBI: 14% v. TD control: 2%, Fisher's exact p = 0.059).
Effect of TBI severity group membership
Online Supplementary Figure S2 includes violin plots depicting s-ADHD symptom severity as a function of TBI severity group membership. As shown in Table 3, TBI severity group membership was significantly associated with scores on the CBCL DSM-oriented ADHD Problems scale (p = 0.04; η 2 = 0.08) and the CBCL Attention Problems scale (p = 0.01; η 2 = 0.10). Post-hoc tests showed that in comparison to TD children, children in the moderate TBI and severe TBI groups had significantly higher levels of inattention and DSM-oriented ADHD symptomology measured by the CBCL Attention Problems and ADHD Problem scales, respectively (see Table 3).
Prospective associations between network-based brain morphometry and s-ADHD symptom severity
Multivariable regression models were used to evaluate the prognostic value of network-based brain morphometry for prospectively predicting s-ADHD symptom severity, after adjusting for age, sex, TIV and other established risk factors, including acute TBI severity, SES, family function and premorbid adaptive function. All variables had a VIF of less than 2.5, indicating a lack of multicollinearity between predictors. Bivariate correlations between ADHD symptom severity, network-based brain morphometry and other risk factor covariates are presented in online Supplementary Table S1.
The final adjusted regression model predicting CBCL DSM-oriented ADHD Problems was significant [R 2 = 0.31, F (9, 75) = 4.42, p < 0.001]. As shown in Table 5, DMN morphometry independently predicted ADHD symptomatology (p = 0.015), such that diminished DMN volume was independently associated with higher ADHD symptomatology. Greater ADHD symptomatology was also independently associated with poorer family functioning (p = 0.016) and lower pre-injury adaptive functioning (p = 0.005). The remaining covariates were not independently related to outcome (all p > 0.10).
Table 5. Multivariable regression models predicting ADHD symptom severity from network-based morphometry
a Multivariable model adjusted for sex, estimated total intracranial volume, acute TBI severity, SES, pre-injury ABAS GAC, FAD general functioning.
The final adjusted regression model predicting CBCL Attention Problems was also significant [R 2 = 0.30, F (9,75) = 3.14, p = 0.003]. As shown in Table 5, DMN morphometry was an independent predictor of CBCL Attention Problems at 12-months post-injury (p = 0.033), such that diminished DMN volume was associated with higher attention problems. Family functioning was also an independent predictor of outcome (p = 0.025), such that worse family functioning was prospectively associated with more frequent attention problems. The remaining covariates were not independently related to outcome (all p > 0.10).
Moderation analyses using hierarchical regression models revealed no statistically significant interactions between brain network morphometry and history of surgical intervention on s-ADHD symptom severity in the TBI sample (DMN: p = 0.71; CEN: p = 0.47; SN: p = 0.39).
Sensitivity analyses
To determine if findings were driven by children with severe TBI, multivariate regression models were re-run after excluding children with severe TBI. In keeping with the findings of the primary analyses reported above, all results remained highly similar when children with severe TBI were excluded (see online Supplementary Table S2).
Discussion
Despite a well-established association of childhood TBI with elevated s-ADHD symptomatology, the neurostructural brain correlates of these post-injury symptoms remain largely unknown. To address this substantial gap in evidence, we aimed to assess the effect of childhood TBI on DMN, CEN and SN morphometry, and evaluate whether neurostructural alterations within these higher-order cognitive networks have independent prognostic value for predicting s-ADHD symptom severity. As expected, the severe TBI group showed altered network-based brain morphometry, including significantly diminished grey matter volume within the DMN, CEN and SN. In multivariable models adjusted for other well-established s-ADHD risk factors, altered DMN morphometry independently predicted higher s-ADHD symptomatology at 12-months post-injury, whilst SN and CEN morphometry were not significant independent predictors. Findings from our relatively large childhood TBI cohort without preinjury ADHD suggest that neurostructural alterations within higher-order cognitive circuitry may represent a prospective risk factor for elevated s-ADHD symptomatology at 12-months post-injury.
Compared to the TD group, rates of clinically elevated ADHD symptomatology were significantly greater in the TBI sample overall. Similarly, when symptoms were evaluated dimensionally, children with TBI had significantly higher ADHD symptomatology than their TD peers 12-months post-injury. Although the association of childhood TBI with elevated ADHD symptomatology is relatively well documented (Bellesi, Barker, Brown, & Valmaggia, Reference Bellesi, Barker, Brown and Valmaggia2019; Li & Liu, Reference Li and Liu2013), our findings are the first to report this relationship in a sample of Australian children with medically confirmed TBI and no pre-injury ADHD. Since elevated s-ADHD symptomatology appears evident at 12-months post-injury, our findings emphasise the value of routine follow-up and where clinically indicated, early preventive measures for those children exhibiting risk factors for s-ADHD symptomatology, e.g. brain structural abnormalities, lower pre-injury adaptive function and poorer post-injury family function.
Consistent with prior research (Asarnow et al., Reference Asarnow, Newman, Weiss and Su2021; Narad et al., Reference Narad, Kennelly, Zhang, Wade, Yeates, Taylor and Kurowski2018), we found some evidence of a dose–response association between acute TBI severity and s-ADHD symptomatology. While the mild TBI group did not significantly differ from the TD group, children with moderate and severe TBI showed significantly higher ADHD symptomatology than their age-and-sex matched peers. Despite some evidence of a dose–response relationship, the group means of all TBI severity groups fell within normative limits and were notable for their large standard deviations. These findings suggest that acute TBI severity does not fully account for the substantial individual heterogeneity in s-ADHD symptomatology (Asarnow et al., Reference Asarnow, Newman, Weiss and Su2021), particularly among children with more severe TBI. Consequently, the current findings reinforce the importance of theory-driven approaches to prediction of s-ADHD symptomology, including the need to identify neurostructural risk factors linking childhood TBI to elevated ADHD symptomatology.
Guided by the influential TN theory of ADHD (Menon, Reference Menon2011), we sought to assess the effect of childhood TBI on brain morphometry of higher-order cognitive networks proposed to play a key role in ADHD pathophysiology (Cai et al., Reference Cai, Chen, Szegletes, Supekar and Menon2018; Castellanos & Proal, Reference Castellanos and Proal2012). In line with previous reports of grey matter neurostructural alterations following childhood TBI (Dennis et al., Reference Dennis, Simic, Bigler, Abildskov, Agostino, Taylor and Stancin2013), children with severe TBI showed altered brain morphometry within large-scale cognitive networks, including significantly diminished grey matter volume within the DMN, SN and CEN. Interestingly, altered regional brain volumes within these large-scale neural networks was documented alongside relative preservation of global brain volumes (e.g. total white matter, TIV), which did not significantly differ between groups. Although these findings suggest that large-scale, higher-order cognitive networks may be selectively vulnerable to the sub-acute effects of severe childhood TBI, to our knowledge no study has evaluated whether DMN, CEN and SN morphometry have independent prognostic value for predicting s-ADHD symptom severity in children with TBI.
In modelling these theory-driven relationships between network-based brain morphometry and s-ADHD symptom severity, we adjusted for other well-established s-ADHD risk factors, including acute TBI severity, post-injury family function, family SES and estimates of pre-injury child adaptive skills. Of these covariates in the final adjusted models, we found that lower pre-injury adaptive function and poorer post-injury family function were independently associated with higher s-ADHD symptomatology. Interestingly, acute TBI severity did not independently contribute to s-ADHD symptomatology in the final adjusted model. This finding is consistent with prior research by Max and et al. (Reference Max, Arndt, Castillo, Bokura, Robin, Lindgren and Mattheis1998), who found that the effect of TBI severity on s-ADHD symptom severity was not statistically significant after adjusting for pre-injury and family environmental factors. Though the current findings are broadly consistent with prior research suggesting that pre-injury and family-based risk factors may interact with injury-related characteristics to heighten vulnerability to chronic neurobehavioral sequelae (Gerring & Wade, Reference Gerring and Wade2012), our primary aim was to evaluate if neurostructural alterations within higher-order cognitive circuitry represent an independent, prospective risk factor for s-ADHD symptomatology in children with TBI.
In partial support of predictions, altered DMN morphometry independently predicted higher s-ADHD symptomatology at 12-months post-injury, whilst SN and CEN morphometry did not. Although the mechanism underlying this relation remains to be established, the TN model of ADHD may offer a useful framework to interpret the current findings. For example, extensive evidence suggests that top-down cognitive processes rely on the coordinated activity of multiple large-scale brain networks that are fundamentally altered in ADHD (Cai et al., Reference Cai, Chen, Ryali, Kochalka, Li and Menon2016, Reference Cai, Chen, Szegletes, Supekar and Menon2018; Chen et al., Reference Chen, Michels, Supekar, Kochalka, Ryali and Menon2015; Sridharan et al., Reference Sridharan, Levitin and Menon2008; Supekar & Menon, Reference Supekar and Menon2012). Specifically, numerous reports show that top-down cognitive processes are dependent on the diminishing activation of the DMN in synchrony with activation of task-relevant networks (Baum et al., Reference Baum, Ciric, Roalf, Betzel, Moore, Shinohara and Quarmley2017; Gu et al., Reference Gu, Satterthwaite, Medaglia, Yang, Gur, Gur and Bassett2015; Satterthwaite et al., Reference Satterthwaite, Wolf, Erus, Ruparel, Elliott, Gennatas and Bilker2013), including the SN, which modulates de-activation of the DMN during top-down cognitive processing (Crockett, Hsu, Best, & Liu-Ambrose, Reference Crockett, Hsu, Best and Liu-Ambrose2017). Given that diminished DMN volume may represent a proxy for disruption to intra- and inter-network structural connectivity (Bigler, Reference Bigler2013; Spitz et al., Reference Spitz, Bigler, Abildskov, Maller, O'Sullivan and Ponsford2013), s-ADHD symptoms after childhood TBI may be at least partly related to structural disconnection of the DMN from task-relevant networks, which is likely to constrain functional connectivity (Johnston et al., Reference Johnston, Vaishnavi, Smyth, Zhang, He, Zempel and Raichle2008). Such constraints may contribute to failure of the DMN to deactivate in synchrony with activation of task-relevant, cognitive control networks (Dennis et al., Reference Dennis, Simic, Bigler, Abildskov, Agostino, Taylor and Stancin2013; Satterthwaite et al., Reference Satterthwaite, Wolf, Erus, Ruparel, Elliott, Gennatas and Bilker2013).
An alternative account suggests that the DMN plays a critical role in making memory-based predictions to support decision-making under established behavioural contexts (Vatansever, Menon, & Stamatakis, Reference Vatansever, Menon and Stamatakis2017). Based on this account, one might predict that structural damage to the DMN may contribute to difficulties in maintaining detailed task representations, manifesting as ADHD-like behaviours (Vatansever, Bozhilova, Asherson, & Smallwood, Reference Vatansever, Bozhilova, Asherson and Smallwood2019). Taken together with previous reports suggesting that higher-order cognitive networks including the DMN are fundamentally altered in children with ADHD (Cai et al., Reference Cai, Chen, Szegletes, Supekar and Menon2018), our finding that altered DMN morphometry is a prospective risk factor for s-ADHD symptomology in children with TBI is perhaps not surprising.
Although the DMN was robustly associated with ADHD symptom severity, the CEN and SN did not independently contribute to s-ADHD symptom burden in our TBI sample. The non-significant effect of the SN and CEN on s-ADHD symptom severity may be partly explained by the limited scope of our longitudinal follow-up over time post-injury. Namely, we assessed s-ADHD symptom severity at 12-months post-injury when the developmental consequences of TBI may not be fully realised in our relatively young sample of children for whom higher-order cognitive networks are still undergoing rapid structural and functional maturation (Sherman et al., Reference Sherman, Rudie, Pfeifer, Masten, McNealy and Dapretto2014). Given the protracted maturational timetable of the CEN and SN (Satterthwaite et al., Reference Satterthwaite, Wolf, Erus, Ruparel, Elliott, Gennatas and Bilker2013; Sherman et al., Reference Sherman, Rudie, Pfeifer, Masten, McNealy and Dapretto2014), it is possible that the behavioural consequences of damage to these neural networks does not become apparent until later during development, i.e. beyond 12-month post-injury. Accordingly, further longitudinal follow-up is required to evaluate whether the hypothesised pattern of relationships between the CEN, SN and s-ADHD symptom severity becomes evident beyond 12-months post-injury.
Implications
Our findings address the dearth of well-powered, theory-driven research to identify neurostructural brain correlates of elevated s-ADHD symptomatology in children with TBI. Specifically, our study provides the first evidence for a robust prospective association between altered DMN morphometry and s-ADHD symptomatology in children with TBI and no preinjury ADHD. These findings suggest that when used to complement routine screening for other established risk factors, high-resolution structural brain MRI has potential to unlock early prognostic biomarkers, which may aid early identification of high-risk children with TBI who could benefit from ongoing surveillance and/or clinically indicated interventions to address modifiable risk factors.
From a broader clinical perspective, our findings suggest that elevated s-ADHD symptomatology is linked to several independent, prospective risk factors, including worse premorbid function, poorer post-injury family function and neurostructural alterations in higher-order cognitive circuitry. These findings suggest that clinicians should exercise caution when prognosticating post-injury outcomes based on acute TBI severity alone and underscore the need to consider the potential interplay of multiple biopsychosocial factors contributing to a child's post-injury neuropsychiatric presentation. Encouragingly, the prospective association between post-injury family functioning and ADHD-symptom severity underscores the potential value of family-based interventions that address potentially modifiable risk factors for s-ADHD symptomatology (Kurowski et al., Reference Kurowski, Taylor, McNally, Kirkwood, Cassedy, Horn and Wade2020).
Limitations and future directions
The current study is limited by a sole reliance on standardised parent ratings of s-ADHD symptoms, which cannot be used to establish rates of formal DSM-ADHD diagnoses and may underestimate the frequency and severity of symptoms in other contexts (e.g. school environment). To address this caveat and strengthen the quality of evidence regarding the prevalence of s-ADHD and its correlates after childhood TBI, future research should incorporate structured clinical interviews and standardised teacher ratings of ADHD symptoms in larger samples of children with more severe TBI. Furthermore, while the current study is strengthened by the inclusion of a well-matched group of TD children, future research should incorporate an additional orthopaedic injury comparison group to establish whether the current pattern of findings is brain injury-specific.
Secondly, we cannot entirely rule out the possibility that s-ADHD symptoms in our TBI sample are at least partly explained by pre-injury psychiatric and/or developmental vulnerabilities, including symptoms of ADHD and disruptive behaviour, which may place children at elevated risk for TBI. Nevertheless, there are several factors that do not support this possibility. Firstly, retrospective ratings of pre-injury functioning showed that the TBI groups did not significantly differ from TD controls on measures of pre-injury externalizing symptoms, adaptive behaviour or internalizing symptoms. Viewed collectively with the finding that all results remained statistically significant after adjusting for pre-injury externalizing symptoms, our results suggest that s-ADHD symptoms in our sample are more likely explained by brain injury-related processes than neurodevelopmental vulnerabilities pre-dating the injury.
Moreover, because we relied on structural imaging data collected at a single, sub-acute time-point to evaluate prospective associations between network-based brain morphometry and s-ADHD symptom severity, causal relationships between these variables cannot be established, and the stability of the structural brain abnormalities in the long-term post-injury could not be assessed in this study. Additionally, since structural brain MRI was acquired during the acute/sub-acute recovery period when valid and reliable estimates of s-ADHD symptom severity could not be obtained concurrently with the structural MRI, we were unable to examine cross-sectional associations between sub-acute volumetric differences and concurrent s-ADHD symptom severity.
Finally, our imaging protocol used only structural imaging techniques and did not include any functional neuroimaging sequences (e.g. resting state connectivity) that may have provided additional information regarding the neural correlates of s-ADHD symptoms in our sample. To address this limitation, future research using functional MRI would help to elucidate whether s-ADHD symptom severity is related to aberrancies in time-varying engagement of the SN with the DMN and CEN in children with TBI.
Conclusions
In addressing the paucity of prospective research to identify neurostructural brain correlates of elevated s-ADHD symptomology after childhood TBI, we show that childhood TBI is associated with significantly higher s-ADHD symptomatology and selective neurostructural alterations within higher-order cognitive networks proposed to play a key role in ADHD pathophysiology. After adjusting for other well-established risk factors, we found that altered DMN morphometry was prospectively associated with higher s-ADHD symptomatology at 12-months post-injury. These findings suggest that neurostructural alterations within higher-order cognitive circuitry may represent a potential prognostic marker of s-ADHD symptomatology, which may aid early identification of high-risk children with TBI who could benefit from early surveillance and preventive measures to optimise long-term neuropsychiatric outcomes.
Supplementary material
The supplementary material for this article can be found at https://doi.org/10.1017/S0033291722002598.
Acknowledgements
The authors wish to acknowledge all children and families who generously offered their time to participate in the study.
Financial support
This work was supported by a grant from the Victorian Neurotrauma Initiative (CO6E1), Australia, and the Victorian Government Operational Infrastructure Support Program. The funding bodies did not play a role in the design of the study, collection, analysis and interpretation of the data, or writing of the manuscript.
Author contributions
NR conceptualised and designed the analysis for this paper, carried out the data analysis, drafted the initial manuscript, revised the manuscript and approved the final manuscript as submitted. SW and LC assisted with the data collection and data analysis, reviewed the manuscript and approved the final manuscript as submitted. SH co-supervised coding and analysis of MRI data, reviewed the manuscript and approved the final manuscript as submitted. CC, MH, MB and KOY critically reviewed the manuscript and approved the final manuscript as submitted. VA conceptualised and designed the study, supervised data collection, critically reviewed the manuscript and approved the final manuscript as submitted.
Conflict of interest
None.
Ethical standards
The authors assert that all procedures contributing to this work comply with the ethical standards of the relevant national and institutional committees on human experimentation and with the Helsinki Declaration of 1975, as revised in 2008.
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