Literature DB >> 25225945

Genetic variation in SENP1 and ANP32D as predictors of chronic mountain sickness.

Amy M Cole1, Nayia Petousi, Gianpiero L Cavalleri, Peter A Robbins.   

Abstract

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).

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Year:  2014        PMID: 25225945      PMCID: PMC4273201          DOI: 10.1089/ham.2014.1036

Source DB:  PubMed          Journal:  High Alt Med Biol        ISSN: 1527-0297            Impact factor:   1.981


  14 in total

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3.  Whole-genome sequencing uncovers the genetic basis of chronic mountain sickness in Andean highlanders.

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  14 in total

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Review 7.  High-Altitude Erythrocytosis: Mechanisms of Adaptive and Maladaptive Responses.

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