Zeng Lu, Atlas Khan, Lama Tsering, Chitnis Tanuja, Weiner Howard, Wang Gao, Fujita Masashi, Zipp Frauke, Taga Mariko, Kiryluk Krzysztof, De Jager Philip L
Center for Translational and Computational Neuroimmunology & Columbia Multiple Sclerosis Center, Department of Neurology, Columbia University Irving Medical Center, New York, NY, USA.
Division of Nephrology, Dept of Medicine, Vagelos College of Physicians & Surgeons, Columbia University, New York, NY, USA.
medRxiv. 2024 Dec 5:2024.12.04.24318500. doi: 10.1101/2024.12.04.24318500.
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.
多发性硬化症(MS)是一种影响大脑和脊髓的慢性炎症性神经退行性疾病。基因研究已经确定了许多风险位点,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20831名多发性硬化症患者和729220名对照参与者进行了多血统全基因组关联研究,在主要组织相容性复合体之外鉴定出236个易感性变异,包括4个新位点。我们得出了一个针对多发性硬化症的多基因评分,并且针对欧洲血统进行了优化,该评分对非裔美国人和拉丁裔参与者也具有参考价值。整合来自血液和脑组织的单细胞数据,我们鉴定出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细胞表现出最强的富集,但抑制性神经元成为关键细胞类型,突出了神经元和神经胶质功能障碍在多发性硬化症易感性中的重要性。