McLester-Davis Lauren W Y, Norton Derek, Papale Ligia A, James Taryn T, Salazar Hector, Asthana Sanjay, Johnson Sterling C, Gooding Diane C, Roy Trevor R, Alisch Reid S, Hogan Kirk J, Drury Stacy S, Gleason Carey E, Zuelsdorff Megan
University of Wisconsin Native American Center for Health Professions, Department of Biochemistry, Department of Medicine.
University of Wisconsin Biostatistics and Medical Informatics.
bioRxiv. 2024 Oct 16:2024.10.14.618331. doi: 10.1101/2024.10.14.618331.
Accelerated biological aging is a plausible and modifiable determinant of dementia burden facing minoritized communities, but is not well-studied in these historically underrepresented populations. Our objective was to preliminarily characterize relationships between telomere length and cognitive health among American Indian/Alaska Native (AI/AN) and Black/African American (B/AA) middle-aged and older adults.
This study included data on telomere length and cognitive test performance from 187 participants, enrolled in one of two community-based cognitive aging cohorts and who identified their primary race as AI/AN or B/AA.
Nested multivariable regression models revealed preliminary evidence for associations between telomere length and cognitive performance, and these associations were partially independent of chronological age.
Small sample size limited estimate precision, however, findings suggest future work on telomere length and cognitive health in underrepresented populations at high risk for dementia is feasible and valuable as a foundation for social and behavioral intervention research.
加速生物衰老可能是少数族裔社区面临的痴呆症负担的一个合理且可改变的决定因素,但在这些历史上代表性不足的人群中尚未得到充分研究。我们的目的是初步描述美国印第安人/阿拉斯加原住民(AI/AN)和黑人/非裔美国人(B/AA)中老年成年人端粒长度与认知健康之间的关系。
本研究纳入了187名参与者的端粒长度和认知测试表现数据,这些参与者来自两个基于社区的认知衰老队列之一,并将自己的主要种族确定为AI/AN或B/AA。
嵌套多变量回归模型揭示了端粒长度与认知表现之间关联的初步证据,且这些关联部分独立于实际年龄。
样本量小限制了估计精度,然而,研究结果表明,未来针对痴呆症高风险的代表性不足人群开展端粒长度与认知健康的研究是可行且有价值的,可为社会和行为干预研究奠定基础。