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Trajectory Pattern of Cognitive Decline in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy


Cerebral small vessel diseases (cSVDs) are common in the general population and represent a major source of stroke events and cognitive impairment during aging.1,2 However, despite their frequency, the natural history of cognitive decline in cSVD remains poorly understood. This is likely due to the limited duration of previous longitudinal studies and their focus on elderly individuals, in whom manifestations of vascular origin are extremely variable in severity and often intertwined with effects of cerebral aging and early neurodegenerative processes.3

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a monogenic form of cerebral small artery disease caused by stereotyped mutations of the NOTCH3 gene.4 It is a unique model of severe ischemic cSVD5,6 that starts long before the effects of aging on cognition.7 Previous studies have shown that CADASIL can be responsible for slower processing speed, impaired executive functions, attention, and memory performances and, at the advanced stage, dementia.5,8,9 All these manifestations were shown to closely match those detected in sporadic forms of cSVD.6 However, the exact kinetics of cognitive decline throughout the whole course of CADASIL has not yet been investigated.

In this study, we aimed to analyze the trajectory of various cognitive deficiencies in patients with CADASIL using a comprehensive battery of neuropsychological tests in parallel with assessments of motor disability, functional dependence, and quality of life.

Methods

Study Population

Between 2003 and 2017, a total of 366 patients were recruited at the French National Referral Centre for rare cerebrovascular diseases, as a large prospective cohort of patients with CADASIL.10,11 Inclusion criteria were of age 18 years or older, documentation of a cysteine-related mutation in the NOTCH3 gene, and willingness to be evaluated regularly.

Standard Protocol Approvals, Registrations, and Patient Consents

Informed consent was obtained from each subject or from a close relative if necessary. The study was approved by an independent ethics committee (CEEI-IRB-17/388).

Evaluation of Patients During the Follow-up

Patients were evaluated every 18 months (on average) during the follow-up using various scales for assessing different clinical and cognitive aspects of the disease.10,11 In this study, 16 scores, determined by consensus among neurologists (N.A., D.H., and H.C.) and neuropsychologists (A.J., S.R., C.M., and C.R.) of the referral center, were selected for the analysis of global cognitive efficiency, memory performances, executive functions, focal deficits with disability, dependence, and quality of life. Ranges of the 16 scores selected for analysis in this sample are given in Table 1.

Table 1

Total Number of Observations for Each Score and Number of Observations per Patient

Global cognitive efficiency was analyzed using total scores obtained from 2 measures: (1) the Mattis Dementia Rating Scale (MDRS)12,13 and (2) the Vascular Dementia Assessment Scale cognitive subscale (VADAS-Cog).14 The MDRS (from 0 to 144 [best score]) includes 5 subscales related to Attention, Initiation/Perseveration, Construction, Conceptualization, and Memory.15 The VADAS-Cog (from 0 [normal] to 90 [severe impairment]) is composed of 14 items related to memory and orientation, language, praxis abilities, attention, and executive functions.14,16

Memory performance was analyzed specifically using 3 different scores obtained from the Free and Cued Selective Reminding Test adapted from the Grober and Buschke procedure.17 In this study, we analyzed the capacity of retrieval or storage of information, implying correct encoding, using (1) the Total Free Recall score (without cues over the course of three 16 word recall trials varying from 0 to 48 [best score]); (2) the Index of Sensitivity to Cueing, a measure of retrieval/storage ability that decreases when information storage is compromised and cues are not useful; and (3) the Delayed Total Recall (from 0 to 16 [normal]) with both free and cued recalls.18

Executive performance, including attention and working memory performance, was analyzed using 7 different scores. Three were obtained from the VADAS-Cog: (1) the Digit Cancellation Test (from 0 [no impairment] to 10 [serious impairment]),14,19 (2) Symbol Digit Test (from 0 [no impairment] to 10 [serious impairment]), and (3) Backward Digit Span (from 0 [no impairment] to 5 [serious impairment]).14,20 The 4 other scores included (4) the Initiation/Perseveration component score from the MDRS (from 0 [worst] to 37 [best]) and 3 scores obtained from the Trail Making Test (TMT) evaluating cognitive speed and mental flexibility based on (5) the time in seconds of TMT part A, (6) the time in seconds of TMT part B, and (7) the Number of Errors in TMT part B.21,22

Disability was assessed using the modified Rankin scale (mRS). The values of 6 (death) were excluded because death was not considered in the other test scores. The severity of focal neurologic deficits accumulated over time was analyzed using the NIH Stroke Score (NIHSS).23 Daily living activities and functional independence were evaluated globally using the Barthel Index.24 Finally, quality of life was assessed using the Visual Analog Scale of the 3-level EuroQol (EQ VAS).25

Explanatory Variables

The following parameters obtained at baseline were initially considered as potential predictors of clinical worsening in CADASIL: age, sex, education, smoking, alcohol consumption, diabetes, hypertension, systolic blood pressure, diastolic blood pressure, homocysteine, previous stroke events, gait disturbances, balance problems, disability, and dementia. Education was determined according to the French Barbizet scale26 split in high level (at least the final high school diploma) and low level otherwise. Alcohol consumption was a qualitative variable with 3 categories: never, <2 glasses of wine per day for a man (1 glass or equivalent for a woman), and over these thresholds. Disability was split in moderate or severe disability (mRS ≥3) and no or mild disability otherwise. Dementia was assessed according to the Diagnostic and Statistical Manual of Mental Disorders, 4th Edition criteria.27 Neuroimaging data were not considered in the present analysis.

Statistical Analysis

We selected from the cohort individuals having at least 1 measure for each of the 16 scores obtained during the follow-up and who were 25 years or older at inclusion and 75 years or younger during the follow-up, an age range chosen because of the small number of observations outside these 2 extremes. In cases where a subtest could not be performed because alterations were too severe, the most altered performance measure for this subtest was applied to the patient and used in the statistical analysis. In this study, only raw total scores were analyzed. Data at baseline were summarized using descriptive statistics, with frequencies and percentages for qualitative data and means and SDs for quantitative variables.

Latent process mixed models28,,30 were used to overcome common limitations encountered during the analysis of clinical scores, particularly the frequent lack of normality in the distribution of scores, potential floor or ceiling effects, and curvilinearity.30,31 This method allowed modeling the trajectory of the 16 scores selected for analysis in a more efficient way than simpler linear mixed models.30,32 Age available throughout the follow-up was considered as the time variable for delineating the trajectories of test scores. For computation purposes, the time scale was age minus 25 years per 10 years, where 25 years corresponds to the age of the youngest patient observed at baseline. Thus, the intercept represents the cognitive level at age 25 years, and the change in cognitive level is measured for a decade.

Information on the different steps followed to build the model is given in eMethods (links.lww.com/WNL/C131). The final model was adjusted for the education level for the 12 cognitive scores.33,34 The interaction between education and time was systematically assessed using the likelihood ratio test. Because potential heterogeneity in clinical progression cannot be excluded in the study population, we also considered this possible factor in the trajectory modeling analysis.28 Without a priori, the latent process mixed models allow fitting simultaneously several models with different evolutions. Each individual is then assigned to the most probable evolution.

Finally, in cases where the evolution of a score was heterogeneous, a logistic regression model using a stepwise selection process was used to understand what distinguishes patients between groups. Multiple imputations were performed to take into account for missing data. Independent variables with p values <0.20 in the univariate setting and less than 10% missing data were introduced in the multivariate model.

Statistical tests were performed at a conventional 2-tailed type I error of 0.05. Data were analyzed using SAS software version 9.4 (SAS Institute Inc., Cary, NC) and R software version 3.6.1.35 Latent process mixed models and latent class mixed models were estimated using the package “lcmm” version 1.8.1.36

Data Availability

Data not provided in the article because of space limitations may be shared (anonymized) at the request of any qualified investigator for purposes of replicating procedures and results.

Discussion

The results of this study show that cognitive decline not only develops gradually over several decades but also heterogeneously and depends on the cognitive ability evaluated and test used in CADASIL. Modeled evolution curves of different test scores vary widely in global amplitude and according to age. Although the Backward Digit Span remained essentially stable, a linear deterioration of scores obtained using the Symbol Digit Numbers or Number of Errors of TMT B was detected from 25 to 75 years. Conversely, changes observed using the Digit Cancellation Task show the largest variation occurring at midlife, with little or no significant change observed at the youngest or oldest ages. The progression of the other measures related to executive functions, memory performance, or global cognitive efficiency shows little or no variation at the onset of the disease, followed by an increase in changes that accelerates with aging.

Analysis of modeled curves allowed us to predict the potential extent of score changes over 3 age reference groups. Between 25 and 41.7 years, the first score to worsen is the Symbol Digit Number score, which primarily measures the speed of information processing.37 In line, a trend toward an increase in TMT B Time by 30 seconds is also predicted over the same age interval in individuals with a low education level. The lack of significant results in highly educated patients might be related to the strong influence of education and practice effects on some aspects of cognitive processing speed.38 Using a simple computer interface, we previously highlighted an increased reaction time for visual stimuli in patients with CADASIL for whom global cognitive abilities were preserved.39 All these results converge on the hypothesis that cognitive processing can long exhibit an isolated and limited slowdown at the onset of the disease.

By contrast, between 41.7 and 58.3 years of age, the model predicts that Symbol Digit Number scores continue to deteriorate at the same rate but in combination with alterations of other cognitive skills. The large increase in time to completion of TMT A and B during this age interval is possibly related to the further increase of cognitive slowness.22 The largest changes are detected using the Digit Cancellation Test which evaluates both focused and selective attention.19 This is observed in parallel with a reduction in the Initiation/Perseveration subscore, which mainly reflects a reduction in mental flexibility. These results are consistent because attentional control plays a key role in cognitive flexibility, defined as the ability to switch between different mental operations and strategies and to simultaneously override habitual responses.38 The high effect of education on cognitive flexibility also explains the largest change in the Initiation/Perseveration subscore in our patients having the lowest education level.40 In the same age interval, alterations in memory performance become detectable. The Total Free Recall is reduced, while the Index of Sensitivity to Cueing is only slightly decreased, and Delayed Total Recall is globally maintained. This indicates that memory retrieval of information is primarily affected, while the encoding of information remains largely preserved. Alterations in attention and mental flexibility might also be involved at this level.41 Finally, at this stage, the decreases in VADAS-Cog and MDRS scores may simply result from all previous specific alterations leading to a global reduction in cognitive efficiency. This occurs when some motor disability and functional alterations are just appearing, but while most patients remain independent.

After the age of 57.3 years, the model shows a steep acceleration of cognitive decline and disability. All chronometric measures related to mental processing speed, attention, and executive dysfunction showed the greatest increase. Memory performances and global efficiency scores drop sharply. Significant changes in TMT B accuracy also occur at this stage, possibly reflecting severe frontal dysfunction.42,43 Surprisingly, no significant change in the Backward Digit Span score is predicted by the model. This test has been previously linked to working memory and planning ability, as well as visual image processing.44,45 Our results may indicate that the underlying cognitive processes are essentially preserved during disease progression, but a poor sensitivity of the test to moderate working memory changes cannot be excluded.

Four measures, the Initiation/Perseveration subscale, Index of Sensitivity to Cueing, Delayed Total Recall and Barthel Index, do not follow a homogeneous progression across the entire study sample. For these tests, a group of individuals present with an earlier or larger decline in performance compared with the others. Depending on the test, these groups are of variable size, ranging from 22 to 60 individuals, half of whom belonged to another group (data not shown). This separation into distinct groups is possibly related to some intrinsic properties of each corresponding measure. Thus, the difference detected between the heterogeneous course of the Initiation/Perseveration subscore of the MDRS compared with the homogeneous variation in the global MDRS score illustrates that some specific cognitive changes occurring early in a distinct group of patients might be masked by a more global measure. These results may also support that some individuals within the study population really have a different evolution profile and may worsen much more rapidly than the other participants on some specific clinical aspects.

The results of this study are important for designing future clinical trials in ischemic cSVD, and particularly in CADASIL. Because clinical trials can be performed over a limited time frame, most likely less than 2 or 3 years, the present results support the conclusion that outcome metrics for measuring cognitive or clinical changes should be carefully selected during such a limited period. Our study suggests that, during the first 2 decades overall after the age of 25 years, only measures highly sensitive to processing speed should be considered. At this stage, only white-matter lesions are usually detected on cerebral MRI in patients with CADASIL.5,46,47 Their location within the forceps minor or along the thalamofrontal tracts might be responsible for cognitive slowdown.48 In this study, only limited variations are detected using the Symbol Digit Test. Additional studies are thus needed to determine which tests should be used for capturing the limited changes in cognitive processing speed when white-matter lesions are just appearing or expand slowly. Later, over the next 2 decades, the choice of cognitive tests capable of capturing variations over 2–3 years seems easier. Our results suggest that measures sensitive to cognitive speed, attention, and executive dysfunction should be used. Chronometric measures showing the largest changes seem to be of particular interest. A combination of cognitive measures may also represent an alternative approach for capturing the larger spectrum of cognitive alterations. The VADAS-Cog Total score seems a promising approach.14 An average variation of 9 points is predicted by our model over 17 years. Conversely, the modeled variation of the MDRS score, which is limited to 4 points over the same age interval, does not seem to be of sufficient amplitude to be recommended as a unique outcome. Finally, at the latest stage of the disease, the same tools, including the MDRS, could be proposed because their largest modifications are detected after the fifth decade.

Our results also suggest that some predictors may help identify patients with the highest risk of cognitive or clinical changes, particularly when memory performance, executive dysfunction, or functional dependence are targeted. Patients with some initial manifestations of disability or gait alterations might be at the highest risk of rapid cognitive decline, as previously reported in a 3-year longitudinal study.11 In contrast to all other cognitive or clinical test measures, the EuroQol score decreases progressively and linearly from 25 years, which does not seem related to changes in disability or cognitive scores. The multidimensional nature of quality of life, which includes various psychological, social, cultural, and economic aspects in addition to health status, might explain this discrepancy.25,49

This study has a number of limitations. Our study sample does not represent the entire population of patients with CADASIL. Our cohort participants were selected from our National Referral Centre, which only includes volunteers who can travel. Moreover, only individuals who had at least 1 measure for each of the 16 scores during the follow-up were included in the analysis. Consequently, patients at the most severe clinical stage who could not be assessed repeatedly are most likely underrepresented. On the other hand, we think that our sample is conversely well representative of the individuals who might be included in future therapeutic trials. The exclusion of incomplete data from analysis represents another potential selection bias. However, our results did not differ after including all data collected and using multiple imputations for lacking results. Another potential limitation is that, as age was considered as the time scale, this study is unable to discriminate effects related to aging from those related to the disease itself as often reported in studies of long-term degenerative disorders. Unfortunately, age at clinical onset is also particularly difficult to determine in this condition which may start by attacks of migraine with aura which are inconsistent and unrelated to the clinical severity or by subtle cognitive impairment particularly difficult to identify.

The study also has multiple strengths. The amount of data is considerable, particularly for such a rare disease. The neuropsychological measures assessed through a large battery of tests were selected by consensus as those that best reflect the most salient cognitive features of the disease. Our data were also acquired in multiple individuals of different ages and at very different stages of the disease. Thus, their evaluation at multiple time points allows mimicking a continuous collection of information. Finally, latent process modeling used to delineate their trajectories is a robust method considering missing at random data.

Finally, we think that these long-term cognitive changes delineated in CADASIL may indicate that the tools used to assess cognitive decline in similar conditions must be chosen with extreme caution depending on the rate of progression of the underlying disease, the duration of the study, and the stage of disease progression.



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