Introduction
Essential tremor (ET) is the second most common movement disorder with an estimated prevalence between 0.4% and 3.9%.Reference Louis and Ferreira1 ET is classically associated with an action tremor of the upper limbs (ULs) and occasional involvement of the head, legs, and trunk.Reference Bhatia, Bain and Bajaj2 Additionally, a rest tremor and a variety of symptoms ranging from gait and balance impairments to alterations in cognition have also been reported.Reference Chandran and Pal3–Reference Prasad, Velayutham, Reddam, Stezin, Jhunjhunwala and Pal5
Epidemiological studies in ET have demonstrated a bimodal age at onset (AAO) with “early onset” that peaks in late 20s and “late onset” with a peak in 50s.Reference Louis and Ottman6, Reference Louis and Dogu7 The possibility of clinical or pathophysiological differences between these groups has been repeatedly hypothesized but seldom explored. With the exception of a bilateral UL tremor, the remainder of clinical features in ET are highly heterogeneous and show significant variability based on AAO. Hopfner et al.Reference Hopfner, Ahlf and Lorenz8 reported variability in rates of progression, frequencies of positive family history, and effect of alcohol on tremor, suggesting that early onset (EO) and late onset (LO) ET patients represent clinically distinct groups. However, similar postmortem cerebellar pathology in both groups refutes the possibility of pathological differences.Reference Kuo, Wang and Tate9
The lack of coherence between clinical findings and neuropathological reports compounds the requirement for better classification and characterization of patients on the basis of AAO. This study aims to utilize mathematical modeling to explore the distribution of the AAO of patients with ET and ascertain differences, if any, in the clinical features of groups.
Materials and Methods
Subject Recruitment and Clinical Evaluation
This study was conducted at the Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India. A chart review was conducted for patients with ET who were evaluated over a 5-year period at the neurology outpatient and movement disorder clinic. Some of the patients included in this study have been part of previous studies from our group.Reference Bhalsing, Kumar, Saini, Yadav, Gupta and Pal10, Reference Lenka, Bhalsing, Jhunjhunwala, Chandran and Pal11 The diagnosis of ET was based on the Consensus statement of the Movement Disorder Society on TremorReference Deuschl, Bain and Brin12 and confirmed by a trained movement disorder specialist. Demographic details such as gender, age at evaluation, AAO, presence of family history of tremor or parkinsonian illness, reduction of tremor after alcohol consumption, and chronology of body part involvement were recorded. Tremor of the ULs was assessed at rest, with arms outstretched, flexed at the elbow, and while performing the finger–nose test. Tremor of lower limbs (LLs) was assessed while lying in bed at the following positions – at rest, while the LL was lifted off the bed flexed 90° at the hip and knee, while the LL was elevated at roughly 45° with the knee extended, and while performing the knee–heel test. Head tremor (HT) was assessed with the patient seated and recorded as present or absent. Voice tremor (VT) was assessed during normal speech and during sustained phonation. Cerebellar signs were evaluated by the finger–nose test, knee–heel test, dysdiadochokinesia, and tandem gait. Patients also underwent a detailed neurological examination with special emphasis to rule out parkinsonism and dystonia. We also excluded the presence of thyrotoxicosis, chronic alcohol consumption, and the use of tremorogenic drugs.
Statistical Analysis
Statistical analysis was performed using R (version 3.4.3).13 Distribution of AAO was estimated using the following packages: diptest (v.0.75-7), mclust (v.5.4), and mixtools (v.1.1.0).Reference Maechler and Ringach14–Reference Fraley and Raftery16 Diptest was used to perform Hartigan’s dip test in order to ascertain the basic distribution of the AAO dataset, that is, unimodal or bimodal. Following this, mclust was applied in order to identify statistically significant clusters in the dataset. Mclust performs finite mixture modeling for model-based clustering, classification, and density estimation and uses the Bayesian information criterion (BIC) to avoid overfitting. Finally, mixtools was used to graphically represent the results of mclust.
Descriptive statistical analysis was performed for the demographic features of patients with ET. Continuous variables were analyzed using analysis of variance with post hoc Bonferroni correction, and the chi-square test was used for categorical variables.
To predict the presence of any significantly different variables with binary outcomes such as HT, cerebellar signs, etc., we performed multivariate binary logistic regression analysis. The covariates used for this analysis were AAO and a proxy for tremor severity (TSP). The TSP refers to a score ranging from 1 to 4 which indicates the number of sites with tremor involved in a single patient, with each site given a score of 1. The sites considered were head, voice, ULs, and LLs, and the number of sites was chosen as a proxy for TSP since more sites tend to get involved as the disease progresses. The results of multivariate binary logistic regression were expressed as odds ratio (OR), confidence intervals (CIs), and p value. Statistical significance was set at p < 0.05.
Results
Demographic Data
A total of 252 patients with ET were reviewed in this study. Hartigan’s dip test revealed a bimodal distribution of AAO of the cohort (p < 0.05). The Gaussian finite mixture model fitted by Expectation-Maximization (EM) algorithm underlying normal distributions with unequal variance favored a three-component model over a two-component model (BIC: −2343.103 vs. −2373.52). The components of the three-component model were (a) Component 1: patients with EO ET (AAO: 15.57 ± 4.28 years), (b) Component 2: patients with intermediate onset (IO) ET (AAO: 28.40 ± 3.60 years), and (c) Component 3: patients with LO ET (AAO: 51.79 ± 9.06 years). We defined three groups based on two standard deviations as EO: AAO ≤ 22, IO: 23 ≤ AAO ≤ 35, and LO: AAO ≥ 36 (Figure 1). In addition to a comparison of the three groups – EO, IO, and LO – we also combined the EO and IO groups (EO + IO) and compared it with the LO group to ascertain if inclusion of the IO group with the EO group would alter the results.
Comparison of EO, IO, and LO ET
Men outnumbered women in all the three groups, and there were no significant gender differences between the three groups (Table 1). The range of AAO was as follows: EO: 5–22 years, IO: 23–35 years, and LO: 36–73 years. Duration of illness was significantly different between the EO and LO, and IO and LO groups. There were no differences with regard to response of the tremor to alcohol or positive family history of ET.
F = female; M = male; NS = not significant.
Tremor Topography
Onset (Table 2): Tremor of bilateral ULs was the most common initial symptom across groups, and a significantly higher percentage was reported by the EO group in comparison with the LO group. A significantly higher percentage with LO reported HT as the symptom at onset in comparison with IO. Unilateral UL at onset was uniformly reported in all three groups.
B/L = bilateral; NS = not significant; U/L = unilateral.
At evaluation: Tremor localization at evaluation (Figure 2) revealed the uniform presence of UL tremor in all the three groups. The EO group had significantly higher prevalence of LL tremor in comparison with the LO group. The prevalence of HT significantly increased with age, that is, the IO group had a significantly higher percentage of HT in comparison with the EO group, and the LO group had a significantly higher percentage of HT in comparison with the IO group. VT was also significantly higher in the LO group in comparison with the EO group.
On examination, patients displayed a variety of combinations of tremor localization (Table 2). An isolated HT was observed in 8% LO patients, which was significantly higher in comparison with the EO group, p < 0.01. Bilateral UL tremor was the most common form of presentation and significantly higher in the EO group in comparison with the LO group. Bilateral UL tremor in combination with HT, with or without VT was significantly higher in the LO group in comparison with the EO group. Involvement of all four limbs was maximal in the EO group.
There were no significant differences observed based on the activation pattern of the UL tremor, that is, action or rest. An isolated action tremor was present in 71%, 72%, and 62% of patients with EO, IO, and LO of ET. Both action and rest tremors were observed in 29%, 26%, and 32% of patients with EO, IO, and LO of ET.
Cervical Dystonia
Mild cervical dystonia (CD) was observed in 13% (n = 34) of subjects with ET, and no significant variability in prevalence was observed across groups (Table 2). Coexistence of CD and HT observed in 28% (n = 32) subjects with a HT, and there were no significant differences in this prevalence across the groups.
Cerebellar Signs
The prevalence of cerebellar involvement in the form of impaired finger–nose test, knee–heel test, dysdiadochokinesia, or tandem walking was found to increase with the AAO. The LO group had a significantly higher prevalence of cerebellar signs in comparison with the EO group, (36% vs. 6%, p < 0.01). The prevalence of cerebellar signs in the IO group was also higher than the EO group (23% vs. 6%, p < 0.01).
None of the patients had features suggestive of dystonia or parkinsonism.
Comparison of Early Plus IO ET with LO ET
Men outnumbered women in both groups, and there were no significant gender differences between the two groups (Table 3). Duration of illness was significantly different between the EO + IO and LO groups. There were no differences with regard to response of the tremor to alcohol or positive family history of ET.
F = female; M = male; NS = not significant.
Tremor Topography
Onset (Table 4): The LO group had a higher prevalence of HT in comparison with EO + IO, and the EO + IO group had a higher prevalence of bilateral UL tremor at the onset of disease.
B/L = bilateral; NS = not significant; U/L = unilateral.
At evaluation: Tremor localization at evaluation (Figure 3) revealed the uniform presence of UL tremor in both groups. The EO + IO group had significantly higher prevalence of LL tremor in comparison with the LO group. The prevalence of HT and VT was significantly higher in the LO group in comparison with the EO + IO group.
On examination, patients displayed a variety of combinations of tremor localization (Table 4). An isolated HT was observed in 8% LO patients, which was significantly higher in comparison with the EO + IO group. Isolated bilateral UL tremor was significantly more prevalent in the EO + IO group. No significant differences were observed with other combinations of tremor localization.
There were no significant differences observed based on the activation pattern of the UL tremor, that is, action or rest. An isolated action tremor was present in 72% and 62% of patients with EO + IO and LO of ET. Both action and rest tremors were observed in 27% and 32% of patients with EO + IO and LO of ET.
Cervical Dystonia
A significantly higher prevalence of mild CD was observed in the LO group in comparison with EO + LO. There was no significant difference in the prevalence of coexistent CD and HT in the two groups.
Cerebellar Signs
The LO group had a significantly higher prevalence of cerebellar signs in comparison with the EO + IO group, (36% vs. 13%, p < 0.01).
Multivariate Binary Logistic Regression
Since the presence of HT and cerebellar signs was found to be significantly associated with an increasing AAO, we chose these two parameters to perform the regression analysis. AAO and TSP were significant predictors for the presence of HT, AAO (OR: 1.03; CI: 1.008–1.053; p < 0.01), and TSP (OR: 11.59; CI: 6.486–20.724; p < 0.01). Only AAO was found to be a significant predictor for cerebellar signs (OR: 1.033; CI: 1.015–1.053, p < 0.01).
Discussion
The AAO of ET has been reported to show a bimodal distribution with the possibility that EO and LO ET are clinically distinct groups. In the present study, mathematical modeling of the AAO of ET showed a trimodal distribution. We compared the phenotypic characteristics of 252 patients with ET, grouped as EO, IO, or LO based on the AAO.
Patients with LO of ET formed the largest group of our cohort. This finding is in concurrence with previous reports of the incidence and prevalence of ET increasing with age.Reference Benito-Leon, Bermejo-Pareja and Louis17–Reference Rajput, Offord, Beard and Kurland19 Men outnumbered women in all three groups. This observation differs from community-based studies of ET from India which reported no gender discrepancy.Reference Bharucha, Bharucha, Bharucha, Bhise and Schoenberg20, Reference Das, Banerjee, Roy, Raut, Chaudhuri and Hazra21 It is plausible that the present observation is influenced by the nature of our cohort, that is, all patients being recruited from a tertiary care center. The LO group had a significantly shorter duration of illness prior to presentation which might indicate an increased severity of illness. Contrary to reports from other studies, the EO group in our cohort did not have a higher prevalence of family history of ET.Reference Louis and Dogu7 However, the observed prevalence was in accordance with previous reports.Reference Louis and Dogu7, Reference Lou and Jankovic22 It is possible that this result is secondary to a recall bias or tremor in an elderly relative being attributed to old age rather than ET. Although several studies have reported better alcohol responsiveness in patients with an EO of ET, we did not find similar results in our cohort.Reference Hopfner, Ahlf and Lorenz8, Reference Lou and Jankovic22 This could be due to a reporting bias or the social stigma associated with alcohol consumption. Additionally, several patients in the EO group presented for evaluation at an age lower than the legal drinking age, that is, 21 years.
Tremor localization at the time of onset and evaluation revealed significant differences. As expected, UL tremor was the predominant symptom across all groups. Isolated bilateral UL tremor was significantly higher in the EO group. This finding could either be due to a difference in the pathophysiology or more likely be due to patients in this group being more observant about the presence of a tremor in the hands, albeit a minimal tremor. The presence of a tremor involving all four limbs was maximal in the EO group. The above results could be suggestive of a higher appendicular involvement in patients with an early AAO of ET. Tremor localization at the onset of illness was based on history provided by patients. Even though ET is described as a symmetrical tremor, patients may report the presence of a unilateral tremor at onset with progression to a bilateral tremor.
HT at the onset of illness was significantly higher in the LO group. This finding has been reported by several previous studies.Reference Lenka, Bhalsing, Jhunjhunwala, Chandran and Pal11, Reference Louis23 LouisReference Louis23 had suggested that the appearance of a HT in ET was secondary to an intrinsic biological factor, that is, age or aging rather than the disease duration. This concept is supported by the increasing trend of HT on examination which was observed in our cohort. This trend was found to be inversely proportional to the duration of illness, that is, IO and LO groups had shorter duration of illness and a higher prevalence HT in comparison with the EO group. The prevalence of a VT in ET ranges from 10% to 62%.Reference Sulica and Louis24 A trend similar to the HT was also observed for a VT. However, it is uncertain whether this tremor was secondary to the HT influencing the vocal air stream and imparting a tremulous quality to the voice or due to the underlying pathophysiology of ET. The HT observed in ET is often considered to be dystonic, and mild CD has been frequently observed in patients with ET.Reference Lenka, Bhalsing, Jhunjhunwala, Chandran and Pal11 We observed this in 13% of subjects in this cohort with a higher prevalence of CD in the LO group. Additionally, although 94% of subjects with CD had a HT, only 28% of subjects with HT had CD, and no significant variations in prevalence were observed between groups.
No differences were observed in the activation patterns of tremor across groups. An isolated action tremor or a combination of action and rest tremor was equally observed. The prevalence of rest tremor in ET ranges from 1.9% to 46.4% and has been reported to be associated with older age and longer disease duration.Reference Louis, Hernandez and Michalec25
The increasing trend of cerebellar signs observed with an increase in AAO is highly suggestive of a difference in the degree of cerebellar involvement with AAO. The presence of this observation despite a shorter duration of illness in the IO and LO groups in comparison with the EO group further supports this concept. An increase in the prevalence of cerebellar signs in older patients of ET has been previously reported.Reference Benito-Leon and Labiano-Fontcuberta26 The presence of cerebellar signs and CD in ET is of importance following the introduction of the category “ET plus syndrome.”Reference Bhatia, Bain and Bajaj2 The ET plus syndrome includes patients with ET who demonstrate neurological signs of uncertain significance such as mild cerebellar signs, dystonic posturing, rest tremor, etc. in addition to the classical tremor. Future studies classifying patients as ET and ET plus are necessary to study the underlying basis for these seemingly similar disorders.
Based on the pattern of tremor topography, it may be postulated that patients with LO of ET have significantly higher axial involvement, while the EO group has appendicular involvement. The significant variations in the prevalence of cerebellar signs may be indicative of differences in underlying disease pathophysiology. Although, the study by Kuo et al.Reference Kuo, Wang and Tate9 did not demonstrate any differences in cerebellar pathology, further studies are necessary to validate this finding. The significant predictive value of AAO for HT and cerebellar signs obtained from regression analysis lends support to the role of AAO in the development of these symptoms.
Hopfner et al.Reference Hopfner, Ahlf and Lorenz8 followed a similar methodology when evaluating the possibility of clinical groups in ET, and despite the modeling suggesting a trimodal distribution, they evaluated only the EO and LO groups. We chose to compare all three groups in order to ascertain if the IO had different characteristics which could be indirectly indicative of the differences in the pathophysiology as the AAO increases. The lack of a clear pattern of topography in the IO group may be suggestive of the IO group being a transition group or a third clinical group of ET, which may be found to have specific characteristics if explored in a larger cohort. Several significant differences observed when three groups were compared were lost when the EO and IO group were combined, supporting the possibility of differences between these three groups.
This study has several limitations owing to its retrospective nature. Details pertaining to AAO and symptom at onset were based on history provided by the patient, hence subject to recall bias. We did not apply TSP rating scales to patients in our cohort, due to which we were unable to quantify the disease severity in groups and correlate it with variables such as duration of illness and age at evaluation. Additionally, the treatment profile and response to medication were not evaluated.
Conclusions
ET shows phenotypic variability based on the AAO. Patients with an EO of tremor are more likely to develop an appendicular tremor. Whereas, the probability of developing an axial tremor and cerebellar signs increases as the AAO increases. Further studies focusing on ascertaining the clinical, radiological, or pathological characteristics of patients with ET based on their AAO are necessary to enable a better understanding of this disease.
Disclosure
None of the authors has any financial disclosure to make or any conflict of interest.
Author Roles
Conception and design of study: SP, VSB, PKP.
Acquisition of data: SP, KSB, KJ, AL.
Analysis/interpretation of data: SP, VSB, PKP.
Drafting the manuscript: SP, PKP.
Revising the manuscript critically: SP, PKP.