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原发性高血压患者血管紧张素II 1型受体(AT1R)基因多态性与血清血管紧张素II水平的相关性

Association of Angiotensin II Type 1 Receptor (AT1R) Gene Polymorphism with Angiotensin II Serum Levels in Patients with Essential Hypertension.

作者信息

Prasad M, Rajarajeswari D, Ramlingam K, Viswakumar R, Suneel B, Conjeevaram Jyothi, Aruna P, Fathima Nusrath, Vishwakarma Sandeep Kumar, Khan Aleem Ahmed

机构信息

Department of Biochemistry, Narayana Medical College and Hospital, Chinthareddy Palem, Nellore, Andhra Pradesh 524003 India.

Department of Community Medicine, Narayana Medical College, Nellore, Andhra Pradesh 524003 India.

出版信息

Indian J Clin Biochem. 2023 Jan;38(1):110-119. doi: 10.1007/s12291-022-01041-z. Epub 2022 Apr 30.

Abstract

Essential hypertension (EH) is a multifactorial, polygenic condition, and is one of the most important comorbidities that contributes to stroke, myocardial infarction, cardiac failure, and renal failure. The continuous increasing rate of morbidity and mortality associated with EH presents an unmet need of population-based studies to explore pathophysiology as well as newer strategies for better diagnosis, prognosis and treatment. This study aimed to determine genotype and allele frequencies of A1166C polymorphism of AT1R gene in Indian patients with EH and correlated with serum levels of Angiotensin II. A total of 200 patients with EH and 200 age- and gender-matched control individuals were included in this study from the General Medicine Department Outpatient at Narayana Medical College and Hospital, Nellore, Andhra Pradesh, India. Patients with systolic blood pressure (SBP) ≥ 140 mmHg and/or diastolic blood pressure (DBP) ≥ 90 mmHg were considered as hypertensive. The findings of this study revealed significantly increased risk of C/A heterozygote and allele C in both men and women. Moreover, both men and women patients with EH showed higher serum levels of Angiotensin II with C/A as well as AA genotypes. These findings indicate a significant association of 1166 C/A polymorphism of the AT1R gene with increased risk of hypertension in Indian population.

摘要

原发性高血压(EH)是一种多因素、多基因疾病,是导致中风、心肌梗死、心力衰竭和肾衰竭的最重要合并症之一。与EH相关的发病率和死亡率持续上升,这表明基于人群的研究在探索病理生理学以及更好的诊断、预后和治疗新策略方面存在未满足的需求。本研究旨在确定印度EH患者中AT1R基因A1166C多态性的基因型和等位基因频率,并与血管紧张素II的血清水平相关联。本研究纳入了印度安得拉邦内洛尔市纳拉亚纳医学院和医院普通内科门诊的200例EH患者以及200例年龄和性别匹配的对照个体。收缩压(SBP)≥140 mmHg和/或舒张压(DBP)≥90 mmHg的患者被视为高血压患者。本研究结果显示,男性和女性中C/A杂合子和等位基因C的风险显著增加。此外,EH男性和女性患者中,C/A以及AA基因型的血管紧张素II血清水平均较高。这些发现表明,AT1R基因的1166 C/A多态性与印度人群中高血压风险增加显著相关。

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