GWAS 突出显示了神经元对多发性硬化症易感性的贡献。

Lu Zeng, Khan Atlas, Tsering Lama, Tanuja Chitnis, Howard Weiner, Gao Wang, Masashi Fujita, Frauke Zipp, Mariko Taga, Krzysztof Kiryluk, Philip L De Jager
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摘要

多发性硬化症(MS)是一种影响大脑和脊髓的慢性炎症和神经退行性疾病。基因研究发现了许多风险位点,这些位点被认为主要影响免疫细胞和小胶质细胞。在此,我们对 20,831 名多发性硬化症患者和 729,220 名对照组患者进行了多基因组关联研究,发现了主要组织相容性复合体之外的 236 个易感基因变异,其中包括四个新的基因位点。我们得出了多发性硬化症的多基因评分,该评分针对欧洲血统进行了优化,对非洲裔美国人和拉丁裔参与者也有参考价值。通过整合血液和脑组织的单细胞数据,我们确定了 76 个受多发性硬化症风险变异影响的基因。值得注意的是,虽然 T 细胞显示出最强的富集性,但抑制性神经元成为一种关键的细胞类型,突出了神经元和神经胶质细胞功能障碍在多发性硬化症易感性中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GWAS highlights the neuronal contribution to multiple sclerosis susceptibility.

Multiple Sclerosis (MS) is a chronic inflammatory and neurodegenerative disease affecting the brain and spinal cord. Genetic studies have identified many risk loci, that were thought to primarily impact immune cells and microglia. Here, we performed a multi-ancestry genome-wide association study with 20,831 MS and 729,220 control participants, identifying 236 susceptibility variants outside the Major Histocompatibility Complex, including four novel loci. We derived a polygenic score for MS and, optimized for European ancestry, it is informative for African-American and Latino participants. Integrating single-cell data from blood and brain tissue, we identified 76 genes affected by MS risk variants. Notably, while T cells showed the strongest enrichment, inhibitory neurons emerged as a key cell type, highlighting the importance of neuronal and glial dysfunction in MS susceptibility.

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