Vanderbilt Memory and Alzheimer's Center, Vanderbilt University Medical Center, Nashville, TN, USA.
Vanderbilt Genetics Institute, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Brain. 2019 Sep 1;142(9):2581-2589. doi: 10.1093/brain/awz206.
Autopsy measures of Alzheimer's disease neuropathology have been leveraged as endophenotypes in previous genome-wide association studies (GWAS). However, despite evidence of sex differences in Alzheimer's disease risk, sex-stratified models have not been incorporated into previous GWAS analyses. We looked for sex-specific genetic associations with Alzheimer's disease endophenotypes from six brain bank data repositories. The pooled dataset included 2701 males and 3275 females, the majority of whom were diagnosed with Alzheimer's disease at autopsy (70%). Sex-stratified GWAS were performed within each dataset and then meta-analysed. Loci that reached genome-wide significance (P < 5 × 10-8) in stratified models were further assessed for sex interactions. Additional analyses were performed in independent datasets leveraging cognitive, neuroimaging and CSF endophenotypes, along with age-at-onset data. Outside of the APOE region, one locus on chromosome 7 (rs34331204) showed a sex-specific association with neurofibrillary tangles among males (P = 2.5 × 10-8) but not females (P = 0.85, sex-interaction P = 2.9 × 10-4). In follow-up analyses, rs34331204 was also associated with hippocampal volume, executive function, and age-at-onset only among males. These results implicate a novel locus that confers male-specific protection from tau pathology and highlight the value of assessing genetic associations in a sex-specific manner.
尸检测量的阿尔茨海默病神经病理学已被用作先前全基因组关联研究 (GWAS) 的内表型。然而,尽管有证据表明阿尔茨海默病风险存在性别差异,但以前的 GWAS 分析并未纳入性别分层模型。我们从六个脑库数据库中寻找与阿尔茨海默病内表型具有性别特异性的遗传关联。合并数据集包括 2701 名男性和 3275 名女性,其中大多数在尸检时被诊断为阿尔茨海默病 (70%)。在每个数据集内进行了性别分层 GWAS,然后进行了荟萃分析。在分层模型中达到全基因组显着性 (P < 5 × 10-8) 的基因座进一步评估了性别相互作用。利用认知、神经影像学和 CSF 内表型以及发病年龄数据,在独立数据集中进行了额外的分析。除了 APOE 区域之外,染色体 7 上的一个位点 (rs34331204) 显示与男性的神经纤维缠结存在性别特异性关联 (P = 2.5 × 10-8),而不是女性 (P = 0.85,性别相互作用 P = 2.9 × 10-4)。在后续分析中,rs34331204 仅与男性的海马体积、执行功能和发病年龄相关。这些结果表明存在一个新的基因座,它赋予男性特有的 tau 病理学保护,并强调以性别特异性方式评估遗传关联的价值。