Cole Amy M, Petousi Nayia, Cavalleri Gianpiero L, Robbins Peter A
1 Department of Molecular and Cellular Therapeutics, The Royal College of Surgeons in Ireland , Dublin, Ireland .
High Alt Med Biol. 2014 Dec;15(4):497-9. doi: 10.1089/ham.2014.1036.
Chronic mountain sickness (CMS) is a serious illness that affects life-long high-altitude residents. A recent study analyzed whole genome sequence data from residents of Cerro de Pasco (Peru) in an effort to identify the genetic basis of CMS and reported SENP1 (rs7963934) and ANP32D (rs72644851) to show signatures consistent with natural selection and protective against CMS (Zhou et al. 2013 ). We set out to replicate these observations in two Andean cohorts from Cerro de Pasco, consisting of 84 CMS cases and 91 healthy controls in total. We report evidence of association for rs7963934 (SENP1) in the combined cohorts (meta-analysis p=8.8x10(-4) OR 2.91, CI 1.56-5.5, I=0). The direction of effect was the same as in the original publication. We did not observe any significant correlation between rs72644851 (ANP32D) and the CMS phenotype, within or across cohorts (meta-analysis p=0.204, OR 1.37, CI 0.84-2.241, I=0). Our results provide independent evidence in support of a role for SENP1 in CMS in individuals of Quechua ancestry and suggest the SENP1 and ANP32D signatures of selection are in tight linkage disequilibrium (LD).
慢性高山病(CMS)是一种影响长期居住在高海拔地区居民的严重疾病。最近一项研究分析了秘鲁塞罗德帕斯科居民的全基因组序列数据,以确定CMS的遗传基础,并报告称SENP1(rs7963934)和ANP32D(rs72644851)显示出与自然选择一致且对CMS有保护作用的特征(周等人,2013年)。我们着手在来自塞罗德帕斯科的两个安第斯队列中重复这些观察结果,这两个队列总共包括84例CMS病例和91名健康对照。我们报告了在合并队列中rs7963934(SENP1)的关联证据(荟萃分析p = 8.8×10⁻⁴,比值比2.91,置信区间1.56 - 5.5,I = 0)。效应方向与原始出版物相同。在队列内部或队列之间,我们未观察到rs72644851(ANP32D)与CMS表型之间存在任何显著相关性(荟萃分析p = 0.204,比值比1.37,置信区间0.84 - 2.241,I = 0)。我们的结果提供了独立证据,支持SENP1在克丘亚族个体的CMS中发挥作用,并表明SENP1和ANP32D的选择特征处于紧密连锁不平衡(LD)状态。