COMT genotype and cognitive function
COMT genotype and cognitive function
Catechol-O-methyltransferase (COMT), an enzyme that catalyzes the degradation of dopamine, is necessary for cognitive function. Few studies have examined the prospective association between COMT (val(158)met) genotype and cognition in older adults.We assessed a biracial cohort of 2,858 elderly subjects without dementia who were followed for 8 years. The Modified Mini-Mental State Examination (3MS) and Digit Symbol Substitution Test (DSST) were administered at baseline and years 3, 5, and 8. COMT by race, gender, and APOE status interactions were examined.Stratified by race and adjusted for covariates, repeated-measures mixed-effects models showed no association between COMT genotype and baseline cognitive function in black or white subjects. In white subjects, COMT was associated with change in 3MS (Met/Met: -2.3 [0.60], Met/Val: -1.7 [0.40], and Val/Val: -1.2 [0.50]) and DSST (Met/Met: -5.60 [1.00], Met/Val: -4.80 [0.70], Val/Val: -4.00 [0.90]). In black subjects, COMT was associated with change in the DSST (Met/Met: -4.10 [2.1], Met/Val: -4.80 [0.90], Val/Val -2.60 [1.00]).These findings suggest that the Val allele has a protective impact on cognitive decline in late life.
- National Institute of Health Pakistan
- University of Pittsburgh United States
- University of California, San Francisco United States
- United States Department of Veterans Affairs United States
- University of Tennessee Health Science Center United States
Brain Chemistry, Genetic Markers, Aging, Genotype, Dopamine, DNA Mutational Analysis, Age Factors, Black People, Catechol O-Methyltransferase, Gene Expression Regulation, Enzymologic, Amino Acid Substitution, Gene Frequency, Cytoprotection, Dementia, Female, Genetic Predisposition to Disease, Amino Acid Sequence, Genetic Testing, Cognition Disorders, Aged
Brain Chemistry, Genetic Markers, Aging, Genotype, Dopamine, DNA Mutational Analysis, Age Factors, Black People, Catechol O-Methyltransferase, Gene Expression Regulation, Enzymologic, Amino Acid Substitution, Gene Frequency, Cytoprotection, Dementia, Female, Genetic Predisposition to Disease, Amino Acid Sequence, Genetic Testing, Cognition Disorders, Aged
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