Department of Pediatrics, University of Washington, Seattle, WA 98195, USA.
Blood Cells Mol Dis. 2012 Aug 15;49(2):67-73. doi: 10.1016/j.bcmd.2012.04.004. Epub 2012 May 15.
High altitude sickness (HAS) occurs among humans visiting or inhabiting high altitude environments. Genetic differences in the EPAS1 and EGLN1 genes have been found between lowland (Han) and highland (Tibetan) Chinese. Three SNPs within EPAS1 and EGLN1 were evaluated in Han and Tibetan patients with acute mountain sickness (AMS) and chronic mountain sickness (CMS). We compared 85 patients with AMS to 79 Han unaffected with mountain sickness (MS) as well as 45 CMS patients to 34 unaffected Tibetan subjects. The three SNPs studied were EPAS1 [ch2: 46441523 (hg18], EGLN1 (rs480902) and (rs516651). Direct sequencing was used to identify individual genotypes for the three SNPs. Age was found to be significantly associated with the EPAS1 SNP in the CMS patients while heart rate (HR) and oxygen saturation level of hemoglobin (SaO(2)) were found to be significantly associated with the EGLN1 (rs480902) SNP in the Han patients with AMS. The individuals with CMS were found to diverge significantly for the EPAS1 SNP compared to their Tibetan control group as measured by genetic distance (0.123) indicating positive selection of the EPAS-G allele with age and illness. The EGLN1 (rs480902) SNP had a significant correlation with hematocrit (HCT), HR and SaO(2) in AMS patients. AMS and CMS were found to be significantly associated with the EPAS1 and EGLN1 SNPs compared to their Han and Tibetan control groups, respectively, indicating these nucleotide alterations have a physiological effect for the development of high altitude sickness.
高原病(HAS)发生在访问或居住在高海拔环境中的人群中。已经在低地(汉族)和高地(藏族)中国人的 EPAS1 和 EGLN1 基因中发现了遗传差异。在汉族和藏族的急性高原病(AMS)和慢性高原病(CMS)患者中评估了 EPAS1 和 EGLN1 中的三个 SNP。我们将 85 例 AMS 患者与 79 例未患高山病(MS)的汉族患者以及 45 例 CMS 患者与 34 例未患高山病的藏族受试者进行了比较。研究的三个 SNP 是 EPAS1 [ch2:46441523(hg18]、EGLN1(rs480902)和(rs516651)。直接测序用于确定三个 SNP 的个体基因型。发现 CMS 患者的年龄与 EPAS1 SNP 显著相关,而 AMS 汉族患者的心率(HR)和血红蛋白氧饱和度(SaO2)与 EGLN1(rs480902)SNP 显著相关。与藏族对照组相比,CMS 患者的 EPAS1 SNP 明显不同,遗传距离(0.123)表明 EPAS-G 等位基因与年龄和疾病呈正选择。EGLN1(rs480902)SNP 与 AMS 患者的红细胞压积(HCT)、HR 和 SaO2 有显著相关性。与汉族和藏族对照组相比,AMS 和 CMS 与 EPAS1 和 EGLN1 SNP 显著相关,表明这些核苷酸改变对高原病的发生有生理影响。