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认知衰退终末期的新型功能、健康和遗传决定因素:库阿基尼·檀香山心脏项目/檀香山-亚洲老龄化研究。

Novel Functional, Health, and Genetic Determinants of Cognitive Terminal Decline: Kuakini Honolulu Heart Program/Honolulu-Asia Aging Study.

机构信息

Department of Human Development and Family Studies, College of Human Sciences, Iowa State University, Ames, Iowa, USA.

Institute of Gerontology, University of Georgia, Athens, Georgia, USA.

出版信息

J Gerontol A Biol Sci Med Sci. 2022 Aug 12;77(8):1525-1533. doi: 10.1093/gerona/glab327.

Abstract

To investigate interindividual differences in cognitive terminal decline and identify determinants including functional, health, and genetic risk and protective factors, data from the Honolulu Heart Program/Honolulu-Asia Aging Study, a prospective cohort study of Japanese American men, were analyzed. The sample was recruited in 1965-1968 (ages 45-68 years). Longitudinal performance of cognitive abilities and mortality status were assessed from Exam 4 (1991-1993) through June 2014. Latent class analysis revealed 2 groups: maintainers retained relatively high levels of cognitive functioning until death and decliners demonstrated significant cognitive waning several years prior to death. Maintainers were more likely to have greater education, diagnosed coronary heart disease, and presence of the apolipoprotein E (APOE) ε2 allele and FOXO3 G allele (SNP rs2802292). Decliners were more likely to be older and have prior stroke, Parkinson's disease, dementia, and greater depressive symptoms at Exam 4, and the APOE ε4 allele. Findings support terminal decline using distance to death as the basis for modeling change. Significant differences were observed between maintainers and decliners 15 years prior to death, a finding much earlier compared to the majority of previous investigations.

摘要

为了探究认知功能最终衰退的个体差异,并确定包括功能、健康和遗传风险及保护因素在内的决定因素,对 Honolulu Heart Program/Honolulu-Asia Aging Study 的数据进行了分析,该研究是一项针对日本裔美国男性的前瞻性队列研究。该样本于 1965-1968 年(45-68 岁)招募。从第四次检查(1991-1993 年)到 2014 年 6 月,通过纵向评估认知能力和死亡率状况。潜在类别分析显示存在 2 个群组:维持者保留了相对较高的认知功能水平直至死亡,而衰退者在死亡前数年认知功能明显下降。维持者更有可能接受过更高的教育、被诊断为冠心病、存在载脂蛋白 E(APOE)ε2 等位基因和 FOXO3 G 等位基因(SNP rs2802292)。衰退者更有可能年龄较大、在第四次检查时患有中风、帕金森病、痴呆和更严重的抑郁症状,且携带 APOE ε4 等位基因。研究结果支持使用距死亡的距离作为建模变化的基础来进行最终衰退的研究。在死亡前 15 年就观察到了维持者和衰退者之间的显著差异,这一发现比大多数先前的研究更早。

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