The APLNR gene polymorphism rs7119375 is associated with an increased risk of development of essential hypertension in the Chinese population A meta-analysis

被引:3
|
作者
Yoshikawa, Masahiro [1 ]
Asaba, Kensuke [2 ]
Nakayama, Tomohiro [1 ]
机构
[1] Nihon Univ, Sch Med, Dept Pathol & Microbiol, Div Lab Med, Tokyo, Japan
[2] Univ Tokyo Hosp, Dept Computat Diagnost Radiol & Prevent Med, Tokyo, Japan
关键词
apelin; hypertension; single nucleotide polymorphism; BLOOD-PRESSURE; APELIN; SYSTEM; SYNTHASE; RECEPTOR; COLITIS;
D O I
10.1097/MD.0000000000022418
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hypertension (HT) has recently been defined as a systolic blood pressure (BP) of >= 130 mm Hg and/or a diastolic BP of >= 80 mm Hg. It is important to further understand the pathophysiology of essential HT as its proportion is larger among most of the diagnosed HT cases. The apelin and apelin receptor (APLNR) are known to play roles in regulating BP, but the putative associations of single nucleotide polymorphisms in the APLNR gene with the risk of development of essential HT have not yet been fully investigated. Herein, we conducted a meta-analysis to investigate the relationship between single nucleotide polymorphisms in the APLNR gene and the risk of essential HT. We conducted a search in the PubMed and Web of Science databases for eligible studies. The pooled odds ratios (ORs) with their 95% confidence intervals (CI) were calculated using random-effects models when heterogeneity was expected across the studies. Otherwise, fixed-effect models were used. Regarding the SNP rs7119375, 5 studies were analyzed, which included a total of 3567 essential HT patients and 3256 healthy controls. Four of the 5 studies were from China and 1 was from Mexico. The meta-analysis showed the existence of a significant association between the AA genotype of rs7119375 and the risk of developing essential HT in the Chinese population, as determined using additive and recessive models (OR, 2.11; 95% CI, 1.12-3.96; I-2 = 86% for AA vs GG. OR, 1.53; 95% CI, 1.21-1.94; I-2 = 28% for AA vs AG. OR, 1.88; 95% CI, 1.13-3.12; I-2 = 79% for AA vs AG + GG). Our study showed, for the first time, the existence of an association between rs7119375 and the risk of development of essential HT in the Chinese population, although the sample size was small and there was considerable population heterogeneity. The apelin/APLNR system could be a novel therapeutic target for the treatment of essential HT, and more studies are warranted to further investigate the association.
引用
收藏
页数:10
相关论文
共 50 条
  • [31] Association between the A46G polymorphism (rs1042713) in the β2-adrenergic receptor gene and essential hypertension susceptibility in the Chinese population A PRISMA-compliant meta-analysis
    Yan, Liyuan
    Wang, Haipeng
    Liu, Pengfei
    Wang, Minghan
    Chen, Jingjing
    Zhao, Xin
    MEDICINE, 2020, 99 (46) : E23164
  • [32] Association of lncRNA H19 rs217727 polymorphism and cancer risk in the Chinese population: a meta-analysis
    Lu, Yanjun
    Tan, Lu
    Shen, Na
    Peng, Jing
    Wang, Chunyu
    Zhu, Yaowu
    Wang, Xiong
    ONCOTARGET, 2016, 7 (37) : 59580 - 59588
  • [33] Angiotensin II type 1 receptor gene A1166C polymorphism and essential hypertension in Chinese: a meta-analysis
    Wang, Jia-Li
    Xue, Li
    Hao, Pan-Pan
    Xu, Feng
    Chen, Yu-Guo
    Zhang, Yun
    JOURNAL OF THE RENIN-ANGIOTENSIN-ALDOSTERONE SYSTEM, 2010, 11 (02) : 127 - 135
  • [34] Meta-Analysis of the Association Between the rs228570 Vitamin D Receptor Gene Polymorphism and Arterial Hypertension Risk
    Nunes, Ivone F. O. C.
    Cavalcante, Ana A. C. M.
    Alencar, Marcus V. O. B.
    Carvalho, Marcos D. F.
    Sarmento, Jose L. R.
    Teixeira, Nayra S. C. C. A.
    Paiva, Adriana A.
    Carvalho, Lidia R.
    Nascimento, Leopoldo F. M.
    Cruz, Maria S. P.
    Rogero, Marcelo M.
    Lima, Andreia C. B.
    Carvalho, Cecilia M. R. G.
    ADVANCES IN NUTRITION, 2020, 11 (05) : 1211 - 1220
  • [35] rs61764370 polymorphism of Kras and risk of cancer in Caucasian population: A meta-analysis
    Zhang, Shi-Yan
    Shi, Jing
    JOURNAL OF CANCER RESEARCH AND THERAPEUTICS, 2016, 12 (02) : 699 - 704
  • [36] Rs1625579 polymorphism in the MIR137 gene is associated with the risk of schizophrenia: updated meta-analysis
    Liu, Yong-ping
    Meng, Jing-hua
    Wu, Xue
    Xu, Feng-Ling
    Xia, Xi
    Zhang, Xi-cen
    Liu, Yi
    Yao, Jun
    Wang, Bao-jie
    NEUROSCIENCE LETTERS, 2019, 713
  • [37] Polymorphism rs1801516 (G > A) in the ATM gene is not associated with overall cancer risk: an updated meta-analysis
    Li, Yueting
    Shi, Pengxu
    Jiang, Daqing
    JOURNAL OF INTERNATIONAL MEDICAL RESEARCH, 2020, 48 (07)
  • [38] Association of A-20C polymorphism in the angiotensinogen gene with essential hypertension: a meta-analysis
    Zeng, R.
    Wang, Q. P.
    Fang, M. X.
    Zhuang, J.
    Fan, R. X.
    GENETICS AND MOLECULAR RESEARCH, 2015, 14 (04) : 12984 - 12992
  • [39] Apolipoprotein E Gene Polymorphism in a Chinese Population with Vascular Dementia: A Meta-Analysis
    Liu, Bo
    Shen, Yuefei
    Cen, Luan
    Tang, Yulan
    DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, 2012, 33 (2-3) : 96 - 103
  • [40] The SNP rs1883832 in CD40 Gene and Risk of Atherosclerosis in Chinese Population: A Meta-Analysis
    Yun, Yan
    Ma, Chi
    Ma, XiaoChun
    PLOS ONE, 2014, 9 (05):