Apolipoprotein E genotype and lifetime cognitive decline

被引:25
作者
Kozauer, Nicholas A. [1 ]
Mielke, Michelle M. [2 ]
Chan, Gary Kwun Chuen [3 ]
Rebok, George W. [4 ]
Lyketsos, Constantine G. [5 ,6 ]
机构
[1] Johns Hopkins Sch Med, Div Geriatr & Neuropsychiat, Baltimore, MD 21205 USA
[2] Johns Hopkins Sch Med, Div Geriatr Psychiat & Neuropsychiatr, Dept Psychiat, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Biostat, Baltimore, MD USA
[4] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Mental Hlth, Baltimore, MD USA
[5] Johns Hopkins Univ Hosp, Div Geriatr & Neuropsychiat, Baltimore, MD 21287 USA
[6] Johns Hopkins Univ Hosp, Dept Psychiat, Johns Hopkins Bayview Med Ctr, Baltimore, MD 21287 USA
关键词
neuropsychology; genetics; Alzheimer's disease; cognition; aging;
D O I
10.1017/S104161020700587X
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Objective: The relationship of apolipoprotein E (APOE) genotype to lifetime cognitive decline was examined over 22 years in a large community-based population study. Method: The sample for the present study was derived from follow-up of a probability sample of the adult household residents of East Baltimore. From the Baltimore cohort of the Epidemiologic Catchment Area Study, genotype data were collected on 818 participants at the study's fourth wave between 2003 and 2004. Participants were administered the Mini-mental State Examination (MMSE) at all four study waves. Three tests of verbal learning - immediate recall, delayed recall, and word recognition - were completed at waves 3 and 4. The 659 participants for whom genetic data were available had also completed cognitive testing at all time points. Test scores and changes in these scores were examined by APOE genotype group (x/x or 4/x) in younger and older subcohorts defined by age at wave 4 (< or >= age 65). Results: Cross-sectional wave 4 scores on all four cognitive tasks were lower in APOE4 epsilon 4 carriers when compared to non-carriers. In longitudinal univariate models epsilon 4 carriers in the younger cohort demonstrated a greater annual rate of decline on a delayed recall task and MMSE. After adjusting for covariates only the decline in the delayed recall task was significant. Conclusion: We report an association between APOE genotype and decline in delayed recall and possibly MMSE over this extended time period limited to younger individuals. The lack of an association between APOE and decline in older individuals is likely to be the result of survival bias. Although a clear association exists between APOE genotype and cognitive decline or dementia in late life, these findings suggest that over the lifespan the relationship between APOE and cognitive decline is more complicated.
引用
收藏
页码:109 / 123
页数:15
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