The heterozygote advantage of the Chuvash polycythemia VHLR200W mutation may be protection against anemia

Haematologica. 2011 Sep;96(9):1371-4. doi: 10.3324/haematol.2011.045609. Epub 2011 May 23.

Abstract

The germ-line loss-of-function VHL(R200W) mutation is common in Chuvashia, Russia and occurs in other parts of the world. VHL(R200W) homozygotes have elevated hypoxia inducible factor (HIF)-1 and HIF-2 levels, increased hemoglobin concentration, propensity to thrombosis and early mortality. Because the mutation persists from an ancient origin, we hypothesized that there is a heterozygote advantage. Thirty-four VHL(R200W) heterozygotes and 44 controls over 35 years of age from Chuvashia, Russia were studied. Anemia was defined as hemoglobin less than 130 g/L in men and less than 120 g/L in women. Mild anemia was present in 15% of VHL(R200W) heterozygotes and 34% of controls without a mutated VHL allele. By multivariate logistic regression, the odds of anemia were reduced an estimated 5.6-fold in the VHL(R200W) heterozygotes compared to controls (95% confidence interval 1.4-22.7; P=0.017). In conclusion, heterozygosity for VHL(R200W) may provide protection from anemia; such protection could explain the persistence of this mutation.

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Anemia / epidemiology
  • Anemia / genetics*
  • Female
  • Gene Expression Regulation
  • Heterozygote*
  • Humans
  • Hypoxia-Inducible Factor 1 / metabolism
  • Male
  • Middle Aged
  • Mutation / genetics*
  • Polycythemia / genetics*
  • Polycythemia / metabolism
  • Prevalence
  • Von Hippel-Lindau Tumor Suppressor Protein / genetics*

Substances

  • Hypoxia-Inducible Factor 1
  • Von Hippel-Lindau Tumor Suppressor Protein
  • VHL protein, human