Haptoglobin phenotypes and iron status in children living in a malaria endemic area of Kenyan coast

Acta Trop. 2013 May;126(2):127-31. doi: 10.1016/j.actatropica.2013.02.004. Epub 2013 Feb 13.

Abstract

Malaria infection may be affected by host genetic factors as well as nutritional status. Iron status and the phenotype of haptoglobin, a heme-binding acute phase reactant may be determinants of malaria parasitemia. A combination of cross sectional studies and longitudinal follow-up were used to describe the association between iron status, C-reactive protein, malaria infections and host genetic factors including; haptoglobin (Hp) phenotypes, in children below 9 years in a malaria endemic area in Coastal Kenya. The prevalence of 0.45 and 0.41, respectively for Hp 1-1 and Hp 2-1 phenotypes was significantly higher than 0.14 for Hp 2-2 phenotype (n=162). Children with Hp 2-2 phenotype showed significantly higher iron storage compared to those with Hp 1-1 and Hp 2-1 phenotypes when children with malaria parasites and high C-reactive protein (>9mg/L) were excluded from the analysis. There were no significant differences in malaria parasite densities among Hp phenotypes but children with Hp 2-2 had lower number of clinical malaria episodes (P=0.045). Taken together, this study shows that the presence of malaria may complicate the interpretation of iron status in children based on their Hp-phenotypes. Further studies will be required to address possible interactions among the various genetic factors and iron status in a malaria endemic setting.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers / metabolism
  • C-Reactive Protein / metabolism
  • Child
  • Child, Preschool
  • Cohort Studies
  • Cross-Sectional Studies
  • Endemic Diseases*
  • Female
  • Follow-Up Studies
  • Haptoglobins / genetics
  • Haptoglobins / metabolism*
  • Humans
  • Infant
  • Iron / metabolism*
  • Kenya / epidemiology
  • Longitudinal Studies
  • Malaria / epidemiology*
  • Malaria / parasitology
  • Male
  • Nutritional Status
  • Parasitemia
  • Phenotype
  • Plasmodium / physiology
  • Polymorphism, Genetic / genetics*
  • Prevalence

Substances

  • Biomarkers
  • Haptoglobins
  • C-Reactive Protein
  • Iron