PLCG2 中的非同义突变可降低阿尔茨海默病、路易体痴呆和额颞叶痴呆的风险,并增加长寿的可能性。

A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity.

机构信息

Alzheimer Center Amsterdam, Department of Neurology, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam, The Netherlands.

Department of Clinical Genetics, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam, The Netherlands.

出版信息

Acta Neuropathol. 2019 Aug;138(2):237-250. doi: 10.1007/s00401-019-02026-8. Epub 2019 May 27.

Abstract

The genetic variant rs72824905-G (minor allele) in the PLCG2 gene was previously associated with a reduced Alzheimer's disease risk (AD). The role of PLCG2 in immune system signaling suggests it may also protect against other neurodegenerative diseases and possibly associates with longevity. We studied the effect of the rs72824905-G on seven neurodegenerative diseases and longevity, using 53,627 patients, 3,516 long-lived individuals and 149,290 study-matched controls. We replicated the association of rs72824905-G with reduced AD risk and we found an association with reduced risk of dementia with Lewy bodies (DLB) and frontotemporal dementia (FTD). We did not find evidence for an effect on Parkinson's disease (PD), amyotrophic lateral sclerosis (ALS) and multiple sclerosis (MS) risks, despite adequate sample sizes. Conversely, the rs72824905-G allele was associated with increased likelihood of longevity. By-proxy analyses in the UK Biobank supported the associations with both dementia and longevity. Concluding, rs72824905-G has a protective effect against multiple neurodegenerative diseases indicating shared aspects of disease etiology. Our findings merit studying the PLCγ2 pathway as drug-target.

摘要

PLCγ2 基因中的遗传变异 rs72824905-G(次要等位基因)先前与阿尔茨海默病(AD)风险降低相关。PLCγ2 在免疫系统信号传导中的作用表明,它也可能对其他神经退行性疾病具有保护作用,并可能与长寿相关。我们使用 53627 名患者、3516 名长寿个体和 149290 名研究匹配对照,研究了 rs72824905-G 对七种神经退行性疾病和长寿的影响。我们复制了 rs72824905-G 与降低 AD 风险的关联,并且发现与降低路易体痴呆(DLB)和额颞叶痴呆(FTD)的风险相关。尽管样本量足够,但我们没有发现 rs72824905-G 对帕金森病(PD)、肌萎缩侧索硬化症(ALS)和多发性硬化症(MS)风险的影响的证据。相反,rs72824905-G 等位基因与长寿的可能性增加相关。英国生物库中的代理分析支持了痴呆症和长寿的关联。总之,rs72824905-G 对多种神经退行性疾病具有保护作用,表明疾病病因具有共同的方面。我们的发现值得研究 PLCγ2 途径作为药物靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17c7/6660501/c51bfb1199a9/401_2019_2026_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索