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从基因水平揭示隐源性卒中的发病机制:系统文献综述。

Unraveling Mechanisms of Cryptogenic Stroke at the Genetic Level: A Systematic Literature Review.

机构信息

Department of Neurology Hannover Medical School Hannover Germany.

Clinical Neuroscience Max Planck Institute for Multidisciplinary Sciences Göttingen Germany.

出版信息

J Am Heart Assoc. 2023 Aug;12(15):e029843. doi: 10.1161/JAHA.123.029843. Epub 2023 Jul 25.

Abstract

Background A substantial proportion of ischemic strokes remain cryptogenic, which has important implications for secondary prevention. Identifying genetic variants related to mechanisms of stroke causes may provide a chance to clarify the actual causes of cryptogenic strokes. Methods and Results In a 2-step process, 2 investigators independently and systematically screened studies that reported genetic variants in regard to stroke causes that were published between January 1991 and April 2021. Studies on monogenetic disorders, investigation of vascular risk factors as the primary end point, reviews, meta-analyses, and studies not written in English were excluded. We extracted information on study types, ancestries, corresponding single nucleotide polymorphisms, and sample and effect sizes. There were 937 studies screened, and 233 were eligible. We identified 35 single nucleotide polymorphisms and allele variants that were associated with an overlap between cryptogenic strokes and another defined cause. Conclusions Associations of single variants with an overlap between cryptogenic stroke and another defined cause were limited to a few polymorphisms. A limitation of all studies is a low granularity of clinical data, which is of major importance in a complex disease such as stroke. Deep phenotyping is in supposed contradiction with large sample sizes but needed for genome-wide analyses. Future studies should attempt to address this restriction to advance the promising approach of elucidating the cause of stroke at the genetic level. Especially in a highly heterogenous disease such as ischemic stroke, genetics are promising to establish a personalized approach in diagnostics and treatment in the sense of precision medicine.

摘要

背景 相当一部分缺血性中风仍然是病因不明的,这对二级预防有重要意义。确定与中风病因机制相关的遗传变异可能有机会阐明病因不明性中风的实际病因。

方法和结果 采用 2 步流程,2 位研究者独立、系统地筛选了 1991 年 1 月至 2021 年 4 月间发表的有关中风病因的遗传变异的研究报告。排除了单基因疾病研究、以血管危险因素为主要终点的研究、综述、荟萃分析以及非英文发表的研究。我们提取了研究类型、祖源、相应的单核苷酸多态性以及样本和效应大小的信息。共筛选出 937 项研究,其中 233 项符合条件。我们确定了 35 个单核苷酸多态性和等位基因变异,这些变异与病因不明性中风和另一个明确病因之间存在重叠。

结论 单变异与病因不明性中风和另一个明确病因之间的重叠相关,仅限于少数多态性。所有研究的一个局限性是临床数据的粒度低,这在中风等复杂疾病中非常重要。深度表型分析与大样本量相矛盾,但需要进行全基因组分析。未来的研究应尝试解决这一限制,以推进在遗传水平阐明中风病因的有前景的方法。特别是在缺血性中风等高度异质性疾病中,遗传学有望在诊断和治疗方面建立个性化方法,即精准医学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8305/10492995/f39db5ed8a1c/JAH3-12-e029843-g002.jpg

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