HudsonAlpha Institute for Biotechnology, Huntsville, Alabama, USA.
Neuroscience Research Institute, University of California, Santa Barbara, California, and Department of Molecular Cellular and Developmental Biology University of California, Santa Barbara, California, USA.
Alzheimers Dement. 2023 Sep;19(9):3835-3847. doi: 10.1002/alz.13021. Epub 2023 Mar 23.
Genetic associations with Alzheimer's disease (AD) age at onset (AAO) could reveal genetic variants with therapeutic applications. We present a large Colombian kindred with autosomal dominant AD (ADAD) as a unique opportunity to discover AAO genetic associations.
A genetic association study was conducted to examine ADAD AAO in 340 individuals with the PSEN1 E280A mutation via TOPMed array imputation. Replication was assessed in two ADAD cohorts, one sporadic early-onset AD study and four late-onset AD studies.
13 variants had p<1×10 or p<1×10 with replication including three independent loci with candidate associations with clusterin including near CLU. Other suggestive associations were identified in or near HS3ST1, HSPG2, ACE, LRP1B, TSPAN10, and TSPAN14.
Variants with suggestive associations with AAO were associated with biological processes including clusterin, heparin sulfate, and amyloid processing. The detection of these effects in the presence of a strong mutation for ADAD reinforces their potentially impactful role.
与阿尔茨海默病(AD)发病年龄(AAO)相关的遗传关联可以揭示具有治疗应用的遗传变异。我们提出了一个具有常染色体显性遗传 AD(ADAD)的大型哥伦比亚家族,这是一个独特的机会,可以发现 AAO 的遗传关联。
通过 TOPMed 阵列导入进行了一项遗传关联研究,以检查 340 名 PSEN1 E280A 突变个体的 ADAD AAO。在两个 ADAD 队列中进行了复制评估,一个是散发性早发性 AD 研究,四个是晚发性 AD 研究。
有 13 个变体的 p 值小于 1×10 或 p 值小于 1×10,具有复制性,包括三个与载脂蛋白 E 相关的独立位点,包括附近的 CLU。在 HS3ST1、HSPG2、ACE、LRP1B、TSPAN10 和 TSPAN14 中或附近还发现了其他提示性关联。
与 AAO 具有提示性关联的变体与包括载脂蛋白 E、肝素硫酸和淀粉样蛋白处理在内的生物学过程有关。在 ADAD 存在强烈突变的情况下检测到这些影响,增强了它们潜在的影响作用。