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中风的遗传力:家族史采集至关重要。

Heritability for stroke: Essential for taking family history.

作者信息

Pourasgari Masoumeh, Mohamadkhani Ashraf

机构信息

Cell and Molecular Biology Department, Faculty of Biological Sciences, Kharazmi University, Tehran, Iran.

Liver and Pancreatobiliary Diseases Research Center, Digestive Disease Research Institute, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Caspian J Intern Med. 2020 May;11(3):237-243. doi: 10.22088/cjim.11.3.237.

DOI:10.22088/cjim.11.3.237
PMID:32874429
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7442467/
Abstract

BACKGROUND

There are many well-established factors that influence the risk of stroke including blood pressure, diabetes, low socioeconomic status and smoking, however, the shared genetic resource in members of a family effect on stroke predisposition. Genome-wide association studies (GWAS) have demonstrated evidence of a shared genetic source in stroke risk. This review considered the influence of family history as one of the main risk factors in stroke according to the literature.

METHODS

Literature review was obtained by searching for the key words "stroke", "family history" and "stroke gene" in PubMed. An overview has been made on the topics: relevance of stroke family history, family history assessment tools and specific candidate genes for stroke.

RESULTS

Family history of stroke is an important risk factor for the development of cerebrovascular diseases in addition to stroke subtypes in relatives who have reached the questionnaire and pedigree. While variation in a small number of loci showed Mendelian inheritance of stroke phenotypes, the genetic variations in several stroke risk loci are shared with multiple related vascular traits.

CONCLUSION

This study highlighted the importance of family history in stroke phenotypes and current related genetics information. Increasing awareness of the importance of family history in stroke has the advantage of preventing exposure to stroke with health care.

摘要

背景

有许多已明确的因素会影响中风风险,包括血压、糖尿病、社会经济地位低下和吸烟等,然而,家族成员共享的遗传因素对中风易感性也有影响。全基因组关联研究(GWAS)已证明中风风险存在共享遗传来源的证据。根据文献,本综述将家族史视为中风的主要风险因素之一。

方法

通过在PubMed中搜索关键词“中风”“家族史”和“中风基因”获取文献综述。对以下主题进行了概述:中风家族史的相关性、家族史评估工具以及中风的特定候选基因。

结果

除了通过问卷调查和系谱确定的亲属中的中风亚型外,中风家族史是脑血管疾病发生的重要风险因素。虽然少数基因座的变异显示出中风表型的孟德尔遗传,但多个中风风险基因座的遗传变异与多种相关血管性状存在共性。

结论

本研究强调了家族史在中风表型及当前相关遗传学信息中的重要性。提高对家族史在中风中重要性的认识,有利于通过医疗保健预防中风。

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本文引用的文献

1
Prevalence of Stroke Risk Factors and Their Distribution Based on Stroke Subtypes in Gorgan: A Retrospective Hospital-Based Study-2015-2016.基于戈尔甘地区卒中亚型的卒中危险因素患病率及其分布:一项2015 - 2016年基于医院的回顾性研究
Neurol Res Int. 2018 Jul 26;2018:2709654. doi: 10.1155/2018/2709654. eCollection 2018.
2
Causes of premature death and their associated risk factors in the Golestan Cohort Study, Iran.伊朗戈勒斯坦队列研究中的过早死亡原因及其相关风险因素。
BMJ Open. 2018 Jul 18;8(7):e021479. doi: 10.1136/bmjopen-2018-021479.
3
Significant SNPs Related to Telomere Length and Hepatocellular Carcinoma Risk in Chronic Hepatitis B Carriers.慢性乙型肝炎携带者中与端粒长度及肝细胞癌风险相关的重要单核苷酸多态性
Asian Pac J Cancer Prev. 2018 Mar 27;19(3):585-590. doi: 10.22034/APJCP.2018.19.3.585.
4
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.多祖裔全基因组关联研究 52 万受试者,确定 32 个与中风和中风亚型相关的位点。
Nat Genet. 2018 Apr;50(4):524-537. doi: 10.1038/s41588-018-0058-3. Epub 2018 Mar 12.
5
Prevalence of Fabry Disease in Young Patients with Stroke in Argentina.阿根廷年轻中风患者中法布里病的患病率。
J Stroke Cerebrovasc Dis. 2018 Mar;27(3):575-582. doi: 10.1016/j.jstrokecerebrovasdis.2017.09.045. Epub 2017 Nov 11.
6
Family History and Stroke Risk in China: Evidence from a Large Cohort Study.中国的家族病史与中风风险:来自一项大型队列研究的证据。
J Stroke. 2017 May;19(2):188-195. doi: 10.5853/jos.2016.01270. Epub 2017 May 31.
7
Genetics of stroke in a UK African ancestry case-control study: South London Ethnicity and Stroke Study.英国非洲裔病例对照研究中的中风遗传学:南伦敦种族与中风研究
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8
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Ann Indian Acad Neurol. 2017 Jan-Mar;20(1):5-12. doi: 10.4103/0972-2327.199910.
9
Assessing family history of chronic disease in primary care: Prevalence, documentation, and appropriate screening.在初级保健中评估慢性病家族史:患病率、记录情况及适当筛查
Can Fam Physician. 2017 Jan;63(1):e58-e67.
10
Difference in the Location and Risk Factors of Cerebral Microbleeds According to Ischemic Stroke Subtypes.根据缺血性卒中亚型分析脑微出血的位置及危险因素差异
J Stroke. 2016 Sep;18(3):297-303. doi: 10.5853/jos.2016.00360. Epub 2016 Sep 30.