Genetic associations with mountain sickness in Han and Tibetan residents at the Qinghai-Tibetan Plateau

Clin Chim Acta. 2010 Oct 9;411(19-20):1466-73. doi: 10.1016/j.cca.2010.05.043. Epub 2010 Jun 4.

Abstract

Background: Acute (AMS) and chronic (CMS) mountain sicknesses are illnesses that occur among humans visiting or inhabiting high-altitude environments, respectively. Some individuals are genetically less fit than others when stressed by an extreme high-altitude environment. Seven blood physiological parameters and five genetic polymorphisms were studied in Han patients with AMS and Tibetan patients with CMS.

Methods: We compared 98 AMS patients with 60 Han controls as well as 50 CMS patients with 36 Tibetan controls. The genetic loci studied are ACE I/D (rs4340), AGT M235T (rs699), AGTR1 A1166C (rs5186), GNB3 A(-350)G (rs2071057) and APOB A/G (rs693).

Results: All physiological parameters (RBC, HCT, Hb, SaO(2), HR, and BPs/d) studied significantly changed in the CMS patients while SaO(2) and HR changed in the AMS Han patients compared to their controls. The ACE D and AGT 235M alleles were found to be significantly associated with AMS and CMS, respectively, while a significantly high incidence of the G-protein (GNB3) (-350)A allele was found in the AMS patients. ACE (I/D) was significantly associated with HR in CMS patients while the AGT M235T was significantly associated with SaO(2) and BPs/d in AMS patients. APOB A/G was significantly associated with BPs/d in AMS and HR in CMS patients.

Conclusion: AMS and CMS share very similar genetic results for the ACE I/D and AGT M235T polymorphisms indicating that these mutations have an effect on both illnesses.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Acute Disease
  • Altitude
  • Altitude Sickness / blood
  • Altitude Sickness / epidemiology
  • Altitude Sickness / genetics*
  • Angiotensinogen / genetics
  • China
  • Chronic Disease
  • Genome-Wide Association Study*
  • Geography
  • Hematologic Tests
  • Humans
  • Peptidyl-Dipeptidase A / genetics
  • Polymorphism, Genetic*
  • Tibet

Substances

  • AGT protein, human
  • Angiotensinogen
  • ACE protein, human
  • Peptidyl-Dipeptidase A