期刊
PSYCHOLOGICAL MEDICINE
卷 53, 期 7, 页码 2852-2860出版社
CAMBRIDGE UNIV PRESS
DOI: 10.1017/S0033291721004827
关键词
APOE-e4; cognition; genome-wide association studies; healthy ageing; polygenic score
This study examines the relationship between polygenic predisposition to general cognition and the rate of cognitive decline during a 10-year follow-up period. The results show that an increase in polygenic scores for general cognition is associated with higher baseline verbal memory and semantic fluency scores. However, there is no association between polygenic predisposition and age-related cognitive decline.
Background As an accelerated cognitive decline frequently heralds onset of severe neuropathological disorders, understanding the source of individual differences in withstanding the onslaught of cognitive ageing may highlight how best cognitive abilities may be retained into advanced age. Methods Using a population representative sample of 5088 adults aged center dot 50 years from the English Longitudinal Study of Ageing, we investigated relationships of polygenic predisposition to general cognition with a rate of change in cognition during a 10-year follow-up period. Polygenic predisposition was measured with polygenic scores for general cognition (GC-PGS). Cognition was measured employing tests for verbal memory and semantic fluency. Results The average baseline memory score was 11.1 (s.d. = 2.9) and executive function score was 21.5 (s.d. = 5.8). An increase in GC-PGS by one standard deviation (1-s.d.) was associated with a higher baseline verbal memory by an average 0.27 points (95% CI 0.19-0.34, p < 0.001). Similarly, 1-s.d. increase in GC-PGS was associated with a higher semantic fluency score at baseline in the entire sample (beta = 0.45, 95% CI 0.27-0.64, p < 0.001). These associations were significant for women and men, and all age groups. Nonetheless, 1-s.d. increase in GC-PGS was not associated with decreases in verbal memory nor semantic fluency during follow-up in the entire sample, as well stratified models by sex and age. Conclusion Although common genetic variants associated with general cognition additively are associated with a stable surplus to cognition in adults, a polygenic predisposition to general cognition is not associated with age-related cognitive decline during a 10-year follow-up.
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