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阿尔茨海默病及相关痴呆症的遗传学病因新见解。

New insights into the genetic etiology of Alzheimer's disease and related dementias.

机构信息

Université de Lille, INSERM, CHU Lille, Institut Pasteur Lille, U1167-RID-AGE, Facteurs de risque et déterminants moléculaires des maladies liées au vieillissement, Lille, France.

Complex Genetics of Alzheimer's Disease Group, VIB Center for Molecular Neurology, VIB, Antwerp, Belgium.

出版信息

Nat Genet. 2022 Apr;54(4):412-436. doi: 10.1038/s41588-022-01024-z. Epub 2022 Apr 4.

Abstract

Characterization of the genetic landscape of Alzheimer's disease (AD) and related dementias (ADD) provides a unique opportunity for a better understanding of the associated pathophysiological processes. We performed a two-stage genome-wide association study totaling 111,326 clinically diagnosed/'proxy' AD cases and 677,663 controls. We found 75 risk loci, of which 42 were new at the time of analysis. Pathway enrichment analyses confirmed the involvement of amyloid/tau pathways and highlighted microglia implication. Gene prioritization in the new loci identified 31 genes that were suggestive of new genetically associated processes, including the tumor necrosis factor alpha pathway through the linear ubiquitin chain assembly complex. We also built a new genetic risk score associated with the risk of future AD/dementia or progression from mild cognitive impairment to AD/dementia. The improvement in prediction led to a 1.6- to 1.9-fold increase in AD risk from the lowest to the highest decile, in addition to effects of age and the APOE ε4 allele.

摘要

阿尔茨海默病(AD)和相关痴呆症(ADD)的遗传特征为深入了解相关病理生理过程提供了独特的机会。我们进行了两阶段的全基因组关联研究,共纳入了 111326 例临床诊断的 AD 病例和 677663 名对照。我们发现了 75 个风险位点,其中 42 个在分析时是新的。途径富集分析证实了淀粉样蛋白/tau 途径的参与,并强调了小胶质细胞的作用。在新位点的基因优先级排序中确定了 31 个基因,这些基因表明存在新的遗传相关过程,包括通过线性泛素链组装复合物的肿瘤坏死因子 alpha 途径。我们还构建了一个与未来 AD/痴呆风险或从轻度认知障碍向 AD/痴呆进展相关的新遗传风险评分。除了年龄和 APOE ε4 等位基因的影响外,该评分还可将 AD 风险从最低到最高十分位数的预测提高 1.6 至 1.9 倍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1859/9005347/dc8d84e4dbf9/41588_2022_1024_Fig1_HTML.jpg

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