Powell Danielle S, Kuo Pei-Lun, Qureshi Riaz, Coburn Sally B, Knopman David S, Palta Priya, Gottesman Rebecca, Griswold Michael, Albert Marilyn, Deal Jennifer A, Gross Alden L
Department of Epidemiology, Johns Hopkins University, Baltimore, MD, United States.
Center on Aging and Health, Johns Hopkins University, Baltimore, MD, United States.
Front Neurol. 2021 Oct 20;12:735036. doi: 10.3389/fneur.2021.735036. eCollection 2021.
To investigate whether ε4 genotype-an established risk factor for dementia-is associated with earlier age at diagnosis in addition to increased risk overall and in secondary analysis by race and sex. We followed up 13,782 dementia-free individuals ( = 10,137 White, = 3,645 Black, baseline age 60-66 years) in the Atherosclerosis Risk in Communities study for up to 30 years. Dementia was operationalized using standardized algorithms incorporating longitudinal cognitive change, proxy report, and hospital or death certificate dementia codes. We used a mixture of generalized gamma distributions to simultaneously estimate time to dementia, time to dementia-free death, and the proportion of individuals with dementia, by ε4 status (≥1 vs. no alleles). Median age of dementia onset among ε4 carriers was 81.7 (Blacks) and 83.3 years (Whites) compared with 82.6 (Blacks) and 85.7 years (Whites) in non- ε4 carriers ( > 0.05 Blacks; < 0.01 Whites). Age of dementia diagnosis did not differ by sex in ε4 carriers, but among non-carriers, average age was earlier in males than females regardless of race. ε4 carriers had on average a higher proportion of diagnoses; results did not differ by race or sex. ε4 carrier status is associated with earlier age of dementia diagnosis with differences across race and sex. These findings clarify the causal role of in dementia etiology, which could help better identify at-risk subgroups and may help facilitate better research trial recruitment and design.
为了研究ε4基因型(一种已确定的痴呆风险因素)除了总体风险增加以及在按种族和性别进行的二次分析中风险增加外,是否还与更早的诊断年龄相关。我们在社区动脉粥样硬化风险研究中对13782名无痴呆个体(n = 10137名白人,n = 3645名黑人,基线年龄60 - 66岁)进行了长达30年的随访。痴呆通过纳入纵向认知变化、代理报告以及医院或死亡证明痴呆编码的标准化算法进行操作定义。我们使用混合广义伽马分布,按ε4状态(≥1个等位基因与无等位基因)同时估计痴呆发生时间、无痴呆死亡时间以及痴呆个体的比例。ε4携带者中痴呆发病的中位年龄在黑人中为81.7岁,在白人中为83.3岁,而非ε4携带者在黑人中为82.6岁,在白人中为85.7岁(黑人p>0.05;白人p<0.01)。在ε4携带者中,痴呆诊断年龄在性别上没有差异,但在非携带者中,无论种族如何,男性的平均诊断年龄都早于女性。ε4携带者的诊断比例平均较高;结果在种族或性别上没有差异。ε4携带者状态与更早的痴呆诊断年龄相关,且存在种族和性别差异。这些发现阐明了ε4在痴呆病因学中的因果作用,这有助于更好地识别高危亚组,并可能有助于促进更好的研究试验招募和设计。