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Genetic association study of prolylcarboxypeptidase polymorphisms with susceptibility to essential hypertension in the Yi minority of China: A case-control study based on an isolated population

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机构: [1]Cell Biology and Genetics Department, Kunming Medical University,China [2]School of Medicine, Yunnan University, China [3]The First Affiliated Hospital of Kunming Medical University, Kunming Medical University, China
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关键词: Essential hypertension PRCP polymorphisms Yi minority isolated population

摘要:
Objective: Prolylcarboxypeptidase (PRCP) is a negative regulator of the pressor actions of the renin-angiotensin-aldosterone system. It is also involved in the kallikrein-kinin system. This gene has an important role in blood pressure (BP) regulation. Methods: A case-control study was performed for 615 Yi participants (303 cases and 312 controls) from a remote mountainous area in Yunnan Province of China. For the PRCP gene, 11 tag single-nucleotide polymorphisms were genotyped using the polymerase chain reaction-restriction fragment length polymorphism method. Results: The PRCP gene rs12290550 was associated with the occurrence of essential hypertension (EH) and BP traits. Logistic regression analysis indicated that the rs12290550 T allele was significantly linked to the risk of EH (odds ratio (OR) = 1.85, 95% confidence interval (CI) 1.44-2.39, p = 0.2 x 10(-5)). Under Bonferroni correction, the H7 TAGCACTAACA haplotype containing the risk allele rs12290550 T increased the risk of EH (OR = 4.53, 95% CI 2.29-8.93, p = 0.2x10(-5)). Conclusions: The findings of this study demonstrate the strong association of the PRCP gene with EH. rs12290550 may be a useful genetic predictor of EH in the Yi minority.

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出版当年[2020]版:
大类 | 4 区 医学
小类 | 4 区 外周血管病
最新[2023]版:
大类 | 4 区 医学
小类 | 4 区 外周血管病
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出版当年[2019]版:
Q4 PERIPHERAL VASCULAR DISEASE
最新[2023]版:
Q3 PERIPHERAL VASCULAR DISEASE

影响因子: 最新[2023版] 最新五年平均 出版当年[2019版] 出版当年五年平均 出版前一年[2018版] 出版后一年[2020版]

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第一作者机构: [1]Cell Biology and Genetics Department, Kunming Medical University,China [2]School of Medicine, Yunnan University, China [*1]Cell Biology and Genetics Department, Kunming Medical University, #1168 N. West Chunrong Road, Kunming, Yunnan Province 650500, China.
通讯作者:
通讯机构: [1]Cell Biology and Genetics Department, Kunming Medical University,China [2]School of Medicine, Yunnan University, China [*1]Cell Biology and Genetics Department, Kunming Medical University, #1168 N. West Chunrong Road, Kunming, Yunnan Province 650500, China. [*2]School of Medicine, Yunnan University, #2 N. Cuihu Road, Kunming, Yunnan Province 650091, China.
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