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本文引用的文献

1
Sex-specific genetic predictors of Alzheimer's disease biomarkers.性别特异性阿尔茨海默病生物标志物的遗传预测因子。
Acta Neuropathol. 2018 Dec;136(6):857-872. doi: 10.1007/s00401-018-1881-4. Epub 2018 Jul 2.
2
Sex, amyloid, and APOE ε4 and risk of cognitive decline in preclinical Alzheimer's disease: Findings from three well-characterized cohorts.性别、淀粉样蛋白、载脂蛋白 E ε4 与临床前阿尔茨海默病认知衰退的风险:三个特征明确队列的研究结果。
Alzheimers Dement. 2018 Sep;14(9):1193-1203. doi: 10.1016/j.jalz.2018.04.010. Epub 2018 May 24.
3
Sex-Specific Association of Apolipoprotein E With Cerebrospinal Fluid Levels of Tau.载脂蛋白 E 性别特异性与脑脊液 Tau 水平的关联。
JAMA Neurol. 2018 Aug 1;75(8):989-998. doi: 10.1001/jamaneurol.2018.0821.
4
Apolipoprotein E Genotype and Sex Risk Factors for Alzheimer Disease: A Meta-analysis.载脂蛋白E基因型与阿尔茨海默病的性别风险因素:一项荟萃分析。
JAMA Neurol. 2017 Oct 1;74(10):1178-1189. doi: 10.1001/jamaneurol.2017.2188.
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Loss of dual leucine zipper kinase signaling is protective in animal models of neurodegenerative disease.双亮氨酸拉链激酶信号缺失在神经退行性疾病的动物模型中具有保护作用。
Sci Transl Med. 2017 Aug 16;9(403). doi: 10.1126/scitranslmed.aag0394.
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Downregulation of BZW2 inhibits osteosarcoma cell growth by inactivating the Akt/mTOR signaling pathway.BZW2 的下调通过使 Akt/mTOR 信号通路失活来抑制骨肉瘤细胞的生长。
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F-AV-1451 and CSF T-tau and P-tau as biomarkers in Alzheimer's disease.F-AV-1451 与脑脊液 T 蛋白和 P 蛋白作为阿尔茨海默病的生物标志物。
EMBO Mol Med. 2017 Sep;9(9):1212-1223. doi: 10.15252/emmm.201707809.
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A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease.一种常见的单倍型会降低髓系细胞中PU.1的表达,并延缓阿尔茨海默病的发病。
Nat Neurosci. 2017 Aug;20(8):1052-1061. doi: 10.1038/nn.4587. Epub 2017 Jun 19.
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Sex differences in Alzheimer's disease and other dementias.阿尔茨海默病及其他痴呆症中的性别差异。
Lancet Neurol. 2016 Apr;15(5):451-2. doi: 10.1016/S1474-4422(16)00067-3.
10
Sex differences in the association between AD biomarkers and cognitive decline.阿尔茨海默病生物标志物与认知衰退之间关联的性别差异。
Brain Imaging Behav. 2017 Feb;11(1):205-213. doi: 10.1007/s11682-016-9523-8.

性别差异对阿尔茨海默病病理的遗传预测因素的影响。

Sex differences in the genetic predictors of Alzheimer's pathology.

机构信息

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.

出版信息

Brain. 2019 Sep 1;142(9):2581-2589. doi: 10.1093/brain/awz206.

DOI:10.1093/brain/awz206
PMID:31497858
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6736148/
Abstract

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.

摘要

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。