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The COMT rs4680 polymorphism is associated with rate of cognitive decline in older adults with type 2 diabetes
Author(s) -
Manzali Sigalit,
Beeri Michal Schnaider,
RavonaSpringer Ramit,
Lin HungMo,
Liu Xiaoyu,
Heymann Anthony,
Greenbaum Lior
Publication year - 2020
Publication title -
alzheimer's and dementia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.713
H-Index - 118
eISSN - 1552-5279
pISSN - 1552-5260
DOI - 10.1002/alz.045227
Subject(s) - rs4680 , catechol o methyl transferase , cognitive decline , episodic memory , dementia , psychology , cognition , medicine , genotype , psychiatry , genetics , biology , disease , gene
Abstract Background The single nucleotide polymorphism (SNP) rs4680 (Val158Met) in the Catechol‐O‐Methyltransferase ( COMT ) gene affects dopamine level and has been consistently associated with cognitive functioning; the A allele, encoding Methionine, is linked to better cognition (and higher cortical dopamine levels) and lower risk of dementia than the G allele, encoding Valine. Type 2 diabetes (T2D) older adults have greater cognitive decline and higher dementia risk than non‐T2D persons but the role of COMT in this association has not been examined. Method Using data from the Israel Diabetes and Cognitive Decline (IDCD; N=964) study, we examined associations of COMT rs4680 with cognitive decline over a 48‐month period. Approximately every 18 months, participants completed a comprehensive neuropsychological battery of 15 tests transformed into z‐scores and summarized into four cognitive domains: episodic memory, attention/working memory, executive functions and language/semantic categorization. The average of the z‐scores of the four domains defined global cognition. Mixed regression models examined the associations of rs4680 with cognitive decline adjusting for age, sex, education and Jewish origin (Ashkenazi or Sephardi). Result Participants were on average 71.6 (SD 4.6) years old; 42% women; 13.2 (3.5) years of education. Compared to carriers of rs4680 GG genotype (N=249, 25.8%), carriers of the A allele (AA genotype [N = 216, 22.4% ]+ AG genotype [N = 499, 51.8% ]) had faster rates of decline in global cognition (estimate= ‐0.004; p=0.03), executive functions (estimate= ‐ 0.009 ; p= 0.01) and episodic memory (estimate= ‐0.007 ; p=0.04), but not in attention/working memory nor language. For language, there was a main effect with significantly and consistent better function among the GG genotype carriers over time (estimate= ‐0.50; p=0.001). Additionally adjusting for numerous cardiovascular and T2D‐related risk factors and T2D medications did not alter the results. Conclusion Our finding suggests that among T2D elderly, COMT SNP rs4680 affects cognitive decline over time. In contrast to the anticipated direction, A allele carriers had poorer cognitive outcomes. There is evidence indicating that the GG genotype protects against onset of T2D and hyperglycemia; our results suggest a more global protective effect of this genotype against T2D and its complications, including cognitive impairment.