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

IF 1.5 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Indian Journal of Clinical Biochemistry Pub Date : 2023-01-01 Epub Date: 2022-04-30 DOI:10.1007/s12291-022-01041-z
M Prasad, D Rajarajeswari, K Ramlingam, R Viswakumar, B Suneel, Jyothi Conjeevaram, P Aruna, Nusrath Fathima, Sandeep Kumar Vishwakarma, Aleem Ahmed Khan
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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.

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本质性高血压患者血管紧张素 II 1 型受体 (AT1R) 基因多态性与血管紧张素 II 血清水平的关系。
继发性高血压(EH)是一种多因素、多基因疾病,是导致中风、心肌梗塞、心力衰竭和肾功能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,这就需要开展以人群为基础的研究,以探索病理生理学以及更新的诊断、预后和治疗策略。本研究旨在确定印度 EH 患者 AT1R 基因 A1166C 多态性的基因型和等位基因频率,以及与血清血管紧张素 II 水平的相关性。本研究共纳入了 200 名 EH 患者和 200 名年龄与性别匹配的对照组患者,这些患者均来自印度安得拉邦内洛尔市纳拉亚那医学院和医院的全科门诊部。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。研究结果显示,C/A 杂合子和等位基因 C 在男性和女性中的风险都明显增加。此外,男性和女性 EH 患者血清中血管紧张素 II 水平较高的基因型均为 C/A 和 AA。这些研究结果表明,在印度人群中,AT1R 基因的 1166 C/A 多态性与高血压风险的增加有重要关联。
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来源期刊
Indian Journal of Clinical Biochemistry
Indian Journal of Clinical Biochemistry BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
4.50
自引率
4.80%
发文量
74
期刊介绍: The primary mission of the journal is to promote improvement in the health and well-being of community through the development and practice of clinical biochemistry and dissemination of knowledge and recent advances in this discipline among professionals, diagnostics industry, government and non-government organizations. Indian Journal of Clinical Biochemistry (IJCB) publishes peer reviewed articles that contribute to the existing knowledge in all fields of Clinical biochemistry, either experimental or theoretical, particularly deal with the applications of biochemistry, molecular biology, genetics, biotechnology, and immunology to the diagnosis, treatment, monitoring and prevention of human diseases. The articles published also include those covering the analytical and molecular diagnostic techniques, instrumentation, data processing, quality assurance and accreditation aspects of the clinical investigations in which chemistry has played a major role, or laboratory animal studies with biochemical and clinical relevance.
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