Abstract

BackgroundHaptoglobin (Hp) is an acute phase protein that takes part in systemic regulation of haem during Plasmodium falciparum infections. Numerous genotypes of haptoglobin have been reported in malaria endemic populations. In this study, the relationship between haptoglobin genotypes and incidence of uncomplicated malaria in a cohort of children living in a malaria-endemic area of Uganda was determined.MethodsThis is an extension of a longitudinal study comprising of 423 children aged between six months and nine years, who were actively followed up for one year. Malaria episodes occurring in the cohort children were detected and the affected children treated with national policy drug regimen. Haptoglobin genotypes were determined by an allele-specific PCR method and their frequencies were calculated. A multivariate negative binomial regression model was used to estimate the impact of haptoglobin genotypes on incidence of uncomplicated malaria in the children’s cohort. In all statistical tests, a P–value of < 0.05 was considered as significant.ResultsThe prevalence of the Hp 1–1, Hp 2–1 and Hp 2–2 genotypes in the children’s cohort was 41%, 36.2% and 22.9%, respectively. The overall frequency for the Hp 1 allele was 59%, while Hp 2 allele occurred at a frequency of 41%. After adjustment of incidence rates for age, insecticide treated bed net (ITN) use and malaria history, the incidence of uncomplicated malaria for children carrying the Hp 2–2 genotype and those with the Hp 2–1 genotype was statistically similar (P = 0.41). Also, no difference in the incidence of uncomplicated malaria was observed between children carrying the Hp 1–1 genotype and those having the Hp 2–1 genotype (P = 0.84) or between Hp 2–2 Vs Hp 1–1 genotypes (P = 0.50).ConclusionsThis study showed that the Hp 1–1 and Hp 2–1 genotypes each occur in nearly 4 in 10 children and the Hp 2–2 genotype occurs in 2 of every 10 children. No association with incidence of uncomplicated malaria was found. Additional studies of influence of haptoglobin genotypes on P. falciparum malaria severity are needed to understand the role of these genotypes in malarial protection.

Highlights

  • Haptoglobin (Hp) is an acute phase protein that takes part in systemic regulation of haem during Plasmodium falciparum infections

  • Full list of author information is available at the end of the article

  • Haptoglobin (Hp) determines the course of Plasmodium infections by binding the free haem produced from intravascular lysis of the Red blood cell (RBC)

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Summary

Introduction

Haptoglobin (Hp) is an acute phase protein that takes part in systemic regulation of haem during Plasmodium falciparum infections. Haptoglobin (Hp) determines the course of Plasmodium infections by binding the free haem produced from intravascular lysis of the RBCs. Hp is secreted by the liver following acute infection and binds to free haem forming a stable haptoglobin- haemoglobin (Hp-Hb) complex [6]. Hp is secreted by the liver following acute infection and binds to free haem forming a stable haptoglobin- haemoglobin (Hp-Hb) complex [6] This complex is removed from circulation by binding to a cell-surface receptor (CD 163) expressed by monocytes or macrophages, internalized and destroyed within the spleen [7]. This is needed in the control of free radical induced oxidative damage and inflammation that may follow P. falciparum infections [8]

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