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GBA Variants are associated with a distinct pattern of cognitive deficits in P arkinson's disease
Author(s) -
Mata Ignacio F.,
Leverenz James B.,
Weintraub Daniel,
Trojanowski John Q.,
ChenPlotkin Alice,
Deerlin Vivianna M.,
Ritz Beate,
Rausch Rebecca,
Factor Stewart A.,
WoodSiverio Cathy,
Quinn Joseph F.,
Chung Kathryn A.,
PetersonHiller Amie L.,
Goldman Jennifer G.,
Stebbins Glenn T.,
Bernard Bryan,
Espay Alberto J.,
Revilla Fredy J.,
Devoto Johnna,
Rosenthal Liana S.,
Dawson Ted M.,
Albert Marilyn S.,
Tsuang Debby,
Huston Haley,
Yearout Dora,
Hu ShuChing,
Cholerton Brenna A.,
Montine Thomas J.,
Edwards Karen L.,
Zabetian Cyrus P.
Publication year - 2016
Publication title -
movement disorders
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.352
H-Index - 198
eISSN - 1531-8257
pISSN - 0885-3185
DOI - 10.1002/mds.26359
Subject(s) - cognition , verbal fluency test , psychology , verbal learning , executive dysfunction , dementia , odds ratio , california verbal learning test , cognitive test , audiology , verbal memory , genetics , neuropsychology , medicine , disease , psychiatry , biology
Background Loss‐of‐function mutations in the GBA gene are associated with more severe cognitive impairment in PD, but the nature of these deficits is not well understood and whether common GBA polymorphisms influence cognitive performance in PD is not yet known. Methods We screened the GBA coding region for mutations and the E326K polymorphism in 1,369 PD patients enrolled at eight sites from the PD Cognitive Genetics Consortium. Participants underwent assessments of learning and memory (Hopkins Verbal Learning Test–Revised), working memory/executive function (Letter‐Number Sequencing Test and Trail Making Test A and B), language processing (semantic and phonemic verbal fluency), visuospatial abilities (Benton Judgment of Line Orientation), and global cognitive function (MoCA). We used linear regression to test for association between genotype and cognitive performance with adjustment for important covariates and accounted for multiple testing using Bonferroni's corrections. Results Mutation carriers (n = 60; 4.4%) and E326K carriers (n = 65; 4.7%) had a higher prevalence of dementia (mutations, odds ratio = 5.1; P = 9.7 × 10 −6 ; E326K, odds ratio = 6.4; P = 5.7 × 10 −7 ) and lower performance on Letter‐Number Sequencing (mutations, corrected P [ P c ] = 9.0 × 10 −4 ; E326K, P c = 0.036), Trail Making B‐A (mutations, P c = 0.018; E326K, P c = 0.018), and Benton Judgment of Line Orientation (mutations, P c = 0.0045; E326K, P c = 0.0013). Conclusions Both GBA mutations and E326K are associated with a distinct cognitive profile characterized by greater impairment in working memory/executive function and visuospatial abilities in PD patients. The discovery that E326K negatively impacts cognitive performance approximately doubles the proportion of PD patients we now recognize are at risk for more severe GBA ‐related cognitive deficits. © 2015 International Parkinson and Movement Disorder Society