Suppr超能文献

利用全基因组关联研究鉴定缺血性中风与帕金森病之间的共享基因

Identification of Shared Genes Between Ischemic Stroke and Parkinson's Disease Using Genome-Wide Association Studies.

作者信息

Lang Wenjing, Wang Junjie, Ma Xiaofeng, Zhang Nong, Li He, Cui Pan, Hao Junwei

机构信息

Department of Neurology and Tianjin Neurological Institute, Tianjin Medical University General Hospital, Tianjin, China.

Key Laboratory of Post-Neuroinjury Neuro-Repair and Regeneration in Central Nervous System, Tianjin Neurological Institute, Tianjin Medical University General Hospital, Ministry of Education and Tianjin City, Tianjin, China.

出版信息

Front Neurol. 2019 Mar 28;10:297. doi: 10.3389/fneur.2019.00297. eCollection 2019.

Abstract

Ischemic stroke (IS) and Parkinson's disease (PD) are two neurological diseases that often strike individuals of advanced age. Although thought of as a disease of old age, PD can occur in younger patients. In many of these cases, genetic mutations underlie the disease. As with PD, stroke can also have a genetic component. Although many of the risk factors for IS are considered to be modifiable, a significant portion is not, suggesting that some of stroke risk factors may have a genetic origin. Large-scale genome-wide association studies (GWAS) have identified several IS and PD gene variants recently. Converging epidemiologic and pathological evidence suggests that IS and PD may be linked. However, it is still unclear whether these two conditions share a common mechanism. Here, we sought to determine the genetic mechanism underlying the possible association between IS and PD. We conducted a multi-step systemic analysis comprising (1) identification of IS and PD variants validated by known GWAS, (2) two separate gene-based tests using Versatile Gene-based Association Study 2 (VEGAS2) and PLINK, (3) a transcriptome-wide association study (TWAS), and (4) analyses of gene expression using an online tool in Gene Expression Omnibus. Our investigation revealed that IS and PD have in common five shared genes: , and , which pass gene-based tests. Functionally, these genes are expressed differentially in IS and PD patients compared to neurologically healthy control subjects. This genetic overlap may provide clues on how IS and PD are linked mechanistically. This new genetic insight into these two diseases may be very valuable for narrowing the focus of future studies on the genetic basis of IS and PD and for developing novel therapies.

摘要

缺血性中风(IS)和帕金森病(PD)是两种常侵袭老年人的神经疾病。尽管PD被认为是一种老年疾病,但也可能发生在年轻患者身上。在许多这类病例中,基因突变是该疾病的基础。与PD一样,中风也可能有遗传因素。尽管IS的许多风险因素被认为是可改变的,但有很大一部分并非如此,这表明中风的一些风险因素可能有遗传根源。大规模全基因组关联研究(GWAS)最近已经确定了几种IS和PD的基因变异。越来越多的流行病学和病理学证据表明,IS和PD可能有关联。然而,这两种疾病是否共享一种共同机制仍不清楚。在这里,我们试图确定IS和PD之间可能关联的遗传机制。我们进行了一个多步骤的系统分析,包括(1)识别经已知GWAS验证的IS和PD变异,(2)使用通用基因关联研究2(VEGAS2)和PLINK进行两项单独的基于基因的测试,(3)全转录组关联研究(TWAS),以及(4)使用基因表达综合数据库中的在线工具进行基因表达分析。我们的研究表明,IS和PD共有五个共享基因: 、 和 ,这些基因通过了基于基因的测试。在功能上,与神经健康的对照受试者相比,这些基因在IS和PD患者中的表达存在差异。这种遗传重叠可能为IS和PD在机制上的关联提供线索。这种对这两种疾病的新的遗传学见解对于缩小未来关于IS和PD遗传基础的研究重点以及开发新疗法可能非常有价值。

相似文献

引用本文的文献

本文引用的文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验