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颅内动脉瘤性蛛网膜下腔出血后并发症的遗传多态性和易感性研究综述

A Review of Genetic Polymorphisms and Susceptibilities to Complications after Aneurysmal Subarachnoid Hemorrhage.

机构信息

Research Unit, University Hospital of Gran Canaria Dr. Negrín, 35010 Gran Canaria, Spain.

Department of Specific Teaching Methodologies, University of Las Palmas de Gran Canaria, 35004 Gran Canaria, Spain.

出版信息

Int J Mol Sci. 2022 Dec 6;23(23):15427. doi: 10.3390/ijms232315427.

Abstract

Delayed cerebral ischemia (DCI) and vasospasm are two complications of subarachnoid hemorrhages (SAHs) which entail high risks of morbidity and mortality. However, it is unknown why only some patients who suffer SAHs will experience DCI and vasospasm. The purpose of this review is to describe the main genetic single nucleotide polymorphisms (SNPs) that have demonstrated a relationship with these complications. The SNP of the nitric oxide endothelial synthase (eNOS) has been related to the size and rupture of an aneurysm, as well as to DCI, vasospasm, and poor neurological outcome. The SNPs responsible for the asymmetric dimetilarginine and the high-mobility group box 1 have also been associated with DCI. An association between vasospasm and the SNPs of the eNOS, the haptoglobin, and the endothelin-1 receptor has been found. The SNPs of the angiotensin-converting enzyme have been related to DCI and poor neurological outcome. Studies on the SNPs of the Ryanodine Receptor yielded varying results regarding their association with vasospasm.

摘要

迟发性脑缺血(DCI)和血管痉挛是蛛网膜下腔出血(SAH)的两种并发症,它们具有很高的发病率和死亡率风险。然而,目前尚不清楚为什么只有部分患有 SAH 的患者会出现 DCI 和血管痉挛。本综述的目的是描述与这些并发症相关的主要遗传单核苷酸多态性(SNP)。一氧化氮内皮合酶(eNOS)的 SNP 与动脉瘤的大小和破裂,以及 DCI、血管痉挛和不良神经预后有关。不对称二甲基精氨酸和高迁移率族蛋白 1 的 SNP 也与 DCI 有关。发现血管痉挛与 eNOS、触珠蛋白和内皮素-1 受体的 SNP 之间存在关联。血管紧张素转换酶的 SNP 与 DCI 和不良神经预后有关。关于 Ryanodine Receptor 的 SNP 与血管痉挛的相关性研究结果不一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7614/9739720/c928046d6eb0/ijms-23-15427-g001.jpg

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