Hematological effects of atypical and Cameroon beta-globin gene haplotypes in adult sickle cell anemia

Am J Hematol. 1998 Oct;59(2):121-6. doi: 10.1002/(sici)1096-8652(199810)59:2<121::aid-ajh4>3.0.co;2-#.

Abstract

To examine the effects of unusual or atypical beta-globin gene cluster haplotypes on the hematological features and Hb F levels of sickle cell anemia, we studied African Americans who had an atypical or Cameroon haplotype chromosome in association with a typical haplotype. We identified over 20 atypical haplotypes. The distribution of 5' sub-haplotypes of the atypical chromosomes mirrored the distribution of common haplotypes in African Americans with sickle cell anemia. Neither 5' nor 3' subhaplotypes of the atypical chromosomes affected Hb F levels, packed cell volume, or mean corpuscular volume in individuals with a Benin chromosome. That the 5' subhaplotype is unaffected might be a consequence of the small numbers of Senegal 5' subhaplotypes in our sample, the need for linkage of both 5' and 3' subhaplotypes of any haplotype for an effect on Hb F to be present, or the likelihood that a normal beta-globin gene contributed the 5' subhaplotypes of some atypical haplotypes.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Anemia, Sickle Cell / genetics*
  • Anemia, Sickle Cell / physiopathology*
  • Black People / genetics
  • Blood Cell Count
  • Fetal Hemoglobin / analysis
  • Globins / genetics*
  • Haplotypes / genetics
  • Haplotypes / physiology
  • Humans
  • Multigene Family / genetics
  • Multigene Family / physiology
  • United States

Substances

  • Globins
  • Fetal Hemoglobin