Genetic associations with mountain sickness in Han and Tibetan residents at the Qinghai-Tibetan Plateau

被引:24
作者
Buroker, Norman E. [1 ]
Ning, Xue-Han [1 ,2 ]
Zhou, Zhao-Nian [4 ]
Li, Kui [3 ]
Cen, Wei-Jun [3 ]
Wu, Xiu-Feng [4 ]
Ge, Ming [5 ]
Fan, Lu-Ping [2 ]
Zhu, Wei-Zhong [4 ]
Portman, Michael A. [1 ,2 ]
Chen, Shi-Han [1 ]
机构
[1] Univ Washington, Dept Pediat, Seattle, WA 98195 USA
[2] Seattle Childrens Hosp, Div Cardiol, Seattle, WA USA
[3] Lhasa People Hosp, Tibet, Peoples R China
[4] Chinese Acad Sci, Shanghai Inst Biol Sci, Lab Hypoxia Physiol, Beijing 100864, Peoples R China
[5] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
关键词
Acute mountain sickness; Chronic mountain sickness; Renin-angiotensin and G protein; coupled-receptor systems; LDL cholesterol; Physiological parameters; Genetic polymorphism; ANGIOTENSIN-CONVERTING-ENZYME; II TYPE-1 RECEPTOR; HIGH-ALTITUDE; ESSENTIAL-HYPERTENSION; NO ASSOCIATION; ADAPTATION; POLYMORPHISM; ACE; HYPOXIA; HEART;
D O I
10.1016/j.cca.2010.05.043
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Acute (AMS) and chronic (CMS) mountain sicknesses are illnesses that occur among humans visiting or inhabiting high-altitude environments, respectively. Some individuals are genetically less fit than others when stressed by an extreme high-altitude environment. Seven blood physiological parameters and five genetic polymorphisrns were studied in Han patients with AMS and Tibetan patients with CMS. Methods: We compared 98 AMS patients with 60 Han controls as well as 50 CMS patients with 36 Tibetan controls. The genetic loci studied are ACE I/D (rs4340), ACT M235T (rs699), AGTR1 A1166C (rs5186), GNB3 A (-350)G (rs2071057) and APOB A/C (rs693). Results: All physiological parameters (RBC, HCT, Hb, SaO(2), HR, and BPs/d) studied significantly changed in the CMS patients while SaO(2) and HR changed in the AMS Han patients compared to their controls. The ACED and ACT 235 M alleles were found to be significantly associated with AMS and CMS, respectively, while a significantly high incidence of the G-protein (GNB3) (-350)A allele was found in the AMS patients. ACE (I/D) was significantly associated with HR in CMS patients while the ACT M235T was significantly associated with SaO(2) and BPs/d in AMS patients. APOB A/C was significantly associated with BPs/d in AMS and HR in CMS patients. Conclusion: AMS and CMS share very similar genetic results for the ACE I/D and ACT M235T polymorphisms indicating that these mutations have an effect on both illnesses. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1466 / 1473
页数:8
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