SNPs, linkage disequilibrium, and chronic mountain sickness in Tibetan Chinese

• Published in: Hypoxia Vol. 5; pp. 67 - 74
• Main Authors: Buroker, Norman E, Ning, Xue-Han, Zhou, Zhao-Nian, Li, Kui, Cen, Wei-Jun, Wu, Xiu-Feng, Zhu, Wei-Zhong, Scott, C Ronald, Chen, Shi-Han
• Format: Journal Article
• Language: English
• Published: New Zealand Taylor & Francis Ltd 01.01.2017; Dove Medical Press
• Subjects: Aging; Arthritis; Binding sites; Disease; Genes; Genomes; Hospitals; Hypoxia; Medical prognosis; Original Research; Polymorphism; Studies; Vascular endothelial growth factor; Tibetan Plateau; Tibet; United States > US; China; HIF; RAS; VEGF; Qinghai-Tibetan Plateau; miRNA; pathways; HAS
• ISSN: 2324-1128; 2324-1128
• DOI: 10.2147/HP.S117967

Chronic mountain sickness (CMS) is estimated at 1.2% in Tibetans living at the Qinghai-Tibetan Plateau. Eighteen single-nucleotide polymorphisms (SNPs) from nine nuclear genes that have an association with CMS in Tibetans have been analyzed by using pairwise linkage disequilibrium (LD). The SNPs included are the angiotensin-converting enzyme (rs4340), the angiotensinogen (rs699), and the angiotensin II type 1 receptor ( ) (rs5186) from the renin-angiotensin system. A low-density lipoprotein apolipoprotein B (rs693) SNP was also included. From the hypoxia-inducible factor oxygen signaling pathway, the endothetal Per-Arnt-Sim domain protein 1 (EPAS1) and the egl nine homolog 1 (ENGL1) (rs480902) SNPs were included in the study. SNPs from the vascular endothelial growth factor (VEGF) signaling pathway included are the v-akt murine thymoma viral oncogene homolog 3 (rs4590656 and rs2291409), the endothelial cell nitric oxide synthase 3 (rs1007311 and rs1799983), and the ( ) (rs699947, rs34357231, rs79469752, rs13207351, rs28357093, rs1570360, rs2010963, and rs3025039). An increase in LD occurred in 40 pairwise comparisons, whereas a decrease in LD was found in 55 pairwise comparisons between the controls and CMS patients. These changes were found to occur within and between signaling pathways, which suggests that there is an interaction between SNP alleles from different areas of the genome that affect CMS.