Luo Yongjun, Chen Yu, Zhang Yao, Zhou Qiquan, Gao Yuqi
Department of High Altitude Diseases, College of High Altitude Military Medicine, Third Military Medical University, Chongqing, China.
Wilderness Environ Med. 2012 Sep;23(3):270-4. doi: 10.1016/j.wem.2012.03.007. Epub 2012 Jul 13.
High altitude pulmonary edema (HAPE) is a potentially deadly disease associated with exposure to altitudes greater than 3000 m. Individuals who have previously experienced HAPE are at a significantly higher risk of recurrence, suggesting an underlying genetic component to HAPE pathogenesis. In a previous nuclear genomic study of individual variation in susceptibility to HAPE, the endothelial nitric oxide synthase (eNOS) gene G894T polymorphism was identified as being associated with HAPE. However, another study found no association. Because of the low incidence of HAPE, sample sizes in current reports have been relatively limited. In this study, the association between the eNOS G894T polymorphism and HAPE was assessed through a meta-analysis of published data.
The literature was searched in PubMed, Web of Science, and Embase for papers published before July 15, 2011. A fixed-effects model and a random-effects model were applied (Revman 5.0) on the basis of heterogeneity, and study quality was assessed in duplicate.
Five studies with 360 HAPE patients and 469 control subjects were analyzed. There were no significant differences between carriers of the eNOS 894G and 894T polymorphism alleles in terms of the risk of developing HAPE.
The eNOS 894G and 894T polymorphism alleles are not associated with HAPE incidence.
高原肺水肿(HAPE)是一种与暴露于海拔超过3000米相关的潜在致命疾病。既往曾患HAPE的个体复发风险显著更高,提示HAPE发病机制存在潜在的遗传因素。在先前一项关于个体对HAPE易感性差异的核基因组研究中,内皮型一氧化氮合酶(eNOS)基因G894T多态性被确定与HAPE相关。然而,另一项研究未发现关联。由于HAPE发病率较低,当前报告中的样本量相对有限。在本研究中,通过对已发表数据进行荟萃分析评估eNOS G894T多态性与HAPE之间的关联。
在PubMed、Web of Science和Embase中检索截至2011年7月15日发表的文献。根据异质性应用固定效应模型和随机效应模型(Revman 5.0),并由两人重复评估研究质量。
分析了五项研究,共360例HAPE患者和469例对照受试者。eNOS 894G和894T多态性等位基因携带者在发生HAPE的风险方面无显著差异。
eNOS 894G和894T多态性等位基因与HAPE发病率无关。