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动脉僵硬度的遗传决定因素。

Genetic determinants of arterial stiffness.

作者信息

Logan Jeongok G, Engler Mary B, Kim Hyungsuk

机构信息

School of Nursing, University of Virginia, 225 Jeanette Lancaster Way, Charlottesville, VA, 22903-3388, USA,

出版信息

J Cardiovasc Transl Res. 2015 Feb;8(1):23-43. doi: 10.1007/s12265-014-9597-x. Epub 2014 Dec 4.

DOI:10.1007/s12265-014-9597-x
PMID:25472935
Abstract

Stiffness of large arteries (called arteriosclerosis) is an independent predictor of cardiovascular morbidity and mortality. Although previous studies have shown that arterial stiffness is moderately heritable, genetic factors contributing to arterial stiffness are largely unknown. In this paper, we reviewed the available literature on genetic variants that are potentially related to arterial stiffness. Most variants have shown mixed depictions of their association with arterial stiffness across multiple studies. Various methods to measure arterial stiffness at different arterial sites can contribute to these inconsistent results. In addition, studies in patient populations with hypertension or atherosclerosis may overestimate the impact of genetic variants on arterial stiffness. Future studies are recommended to standardize current measures of arterial stiffness in different age groups. Studies conducted in normal healthy subjects may also provide better opportunities to find novel genetic variants of arterial stiffness.

摘要

大动脉僵硬度(称为动脉硬化)是心血管疾病发病率和死亡率的独立预测指标。尽管先前的研究表明动脉僵硬度具有中度遗传性,但导致动脉僵硬度的遗传因素在很大程度上尚不清楚。在本文中,我们回顾了关于可能与动脉僵硬度相关的基因变异的现有文献。大多数变异在多项研究中对其与动脉僵硬度的关联呈现出混合的描述。在不同动脉部位测量动脉僵硬度的各种方法可能导致这些不一致的结果。此外,在高血压或动脉粥样硬化患者群体中的研究可能高估了基因变异对动脉僵硬度的影响。建议未来的研究对不同年龄组的当前动脉僵硬度测量方法进行标准化。在正常健康受试者中进行的研究也可能为发现动脉僵硬度的新基因变异提供更好的机会。

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J Cardiovasc Transl Res. 2015 Feb;8(1):23-43. doi: 10.1007/s12265-014-9597-x. Epub 2014 Dec 4.
2
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Kardiologiia. 2016 Aug;56(8):19-27. doi: 10.18565/cardio.2016.8.19-27.
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BMC Genet. 2016 Jan 11;17:19. doi: 10.1186/s12863-015-0324-7.
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本文引用的文献

1
Influence of the AGTR1 A1166C genotype on the progression of arterial stiffness: A 16-year longitudinal study.血管紧张素Ⅱ受体 1(AGTR1)A1166C 基因型对动脉僵硬度进展的影响:一项 16 年的纵向研究。
Am J Hypertens. 2013 Dec;26(12):1421-7. doi: 10.1093/ajh/hpt141. Epub 2013 Aug 13.
2
Impaired endothelial function is not associated with arterial stiffness in adults with type 1 diabetes.1 型糖尿病患者的内皮功能障碍与动脉僵硬度无关。
Diabetes Metab. 2013 Sep;39(4):355-62. doi: 10.1016/j.diabet.2013.03.006. Epub 2013 May 3.
3
Inflammation does not influence arterial stiffness and pulse-wave velocity in patients with coronary artery disease.
血压变异性的遗传结构:来自英国生物库的 9370 名参与者的全基因组关联研究。
J Clin Hypertens (Greenwich). 2022 Oct;24(10):1370-1380. doi: 10.1111/jch.14552. Epub 2022 Aug 8.
4
Arteriosclerosis: A Primer for "In Focus" Reviews on Arterial Stiffness.动脉硬化:关于动脉僵硬度“聚焦”综述的入门指南。
Arterioscler Thromb Vasc Biol. 2020 May;40(5):1025-1027. doi: 10.1161/ATVBAHA.120.314208. Epub 2020 Apr 22.
5
[Development of arteriosclerosis].[动脉硬化的发展]
Pathologe. 2019 Sep;40(5):559-572. doi: 10.1007/s00292-019-00656-z.
6
Genome-wide association study identifies loci for arterial stiffness index in 127,121 UK Biobank participants.全基因组关联研究鉴定出 127121 名英国生物库参与者的动脉僵硬指数相关位点。
Sci Rep. 2019 Jun 24;9(1):9143. doi: 10.1038/s41598-019-45703-0.
7
Early Vascular Ageing - A Concept in Development.早期血管衰老——一个正在发展的概念。
Eur Endocrinol. 2015 Apr;11(1):26-31. doi: 10.17925/EE.2015.11.01.26. Epub 2015 Apr 11.
8
Small dense low density lipoprotein-cholesterol and cholesterol ratios to predict arterial stiffness progression in normotensive subjects over a 5-year period.小而密的低密度脂蛋白胆固醇与胆固醇比值可预测 5 年内血压正常受试者的动脉僵硬度进展。
Lipids Health Dis. 2018 Feb 12;17(1):27. doi: 10.1186/s12944-018-0671-2.
炎症并不影响冠心病患者的动脉僵硬程度和脉搏波速度。
J Hum Hypertens. 2013 Oct;27(10):629-34. doi: 10.1038/jhh.2013.17. Epub 2013 Mar 28.
4
ATP2B1 and blood pressure: from associations to pathophysiology.ATP2B1 与血压:从关联到病理生理学。
Curr Opin Nephrol Hypertens. 2013 Mar;22(2):177-84. doi: 10.1097/MNH.0b013e32835da4ca.
5
Heart disease and stroke statistics--2013 update: a report from the American Heart Association.《2013年心脏病和中风统计数据更新:美国心脏协会报告》
Circulation. 2013 Jan 1;127(1):e6-e245. doi: 10.1161/CIR.0b013e31828124ad. Epub 2012 Dec 12.
6
Common variants in the ATP2B1 gene are associated with hypertension and arterial stiffness in Chinese population.ATP2B1 基因中的常见变异与中国人群的高血压和动脉僵硬有关。
Mol Biol Rep. 2013 Feb;40(2):1867-73. doi: 10.1007/s11033-012-2242-3. Epub 2012 Oct 19.
7
Adiponectin single nucleotide polymorphism is a genetic risk factor for stroke through high pulse wave pressure: a cohort study.脂联素单核苷酸多态性是通过高脉搏波压力导致中风的遗传风险因素:一项队列研究。
J Atheroscler Thromb. 2013;20(2):152-60. doi: 10.5551/jat.14696. Epub 2012 Oct 6.
8
Genetic pathways of vascular calcification.血管钙化的遗传途径。
Trends Cardiovasc Med. 2012 May;22(4):93-8. doi: 10.1016/j.tcm.2012.07.002.
9
Stiffness parameter β as a predictor of the 4-year all-cause mortality of chronic hemodialysis patients.僵硬度参数β作为慢性血液透析患者 4 年全因死亡率的预测指标。
Clin Exp Nephrol. 2013 Apr;17(2):268-74. doi: 10.1007/s10157-012-0674-7. Epub 2012 Aug 2.
10
Structure and function of the mammalian fibrillin gene family: implications for human connective tissue diseases.哺乳动物原纤维蛋白基因家族的结构与功能:对人类结缔组织疾病的影响。
Mol Genet Metab. 2012 Dec;107(4):635-47. doi: 10.1016/j.ymgme.2012.07.023. Epub 2012 Aug 3.