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Plasmodium falciparum malaria in children at a tertiary teaching hospital: ABO blood group is a risk factor
John Teye Kuadzi1, George Ankra-Badu, Mark Michael Addae
1Department of Medical Laboratory Sciences, School of Allied Health Sciences, Korle-Bu, Accra, Ghana.
Insights
Children with non-O blood groups may be more susceptible to severe Plasmodium falciparum malaria. This study investigated the link between ABO blood types and severe malaria in children, finding non-O groups potentially at higher risk.
Area of Science:
- Immunology and Infectious Diseases
- Genetics and Human Variation
Background:
- ABO blood group antigens are cell surface glycans influencing cell interactions.
- Adhesion mechanisms are critical in Plasmodium falciparum malaria severity.
- Glycosylation's role in malaria pathophysiology warrants investigation.
Purpose of the Study:
- To determine the association between ABO blood group phenotypes and the severity of Plasmodium falciparum malaria in children.
Main Methods:
- 121 children were assessed for ABO blood groups using agglutination.
- Haemoglobin levels were measured using a Sysmex KX-21N analyzer.
- Malaria parasite enumeration and Plasmodium falciparum identification were performed.
Main Results:
- 24.3% of children presented with severe falciparum malaria.
- No statistically significant association was found between ABO phenotypes and malaria infection (p > 0.05).
- Blood group A showed a trend towards more severe malaria compared to blood group O (OR=0.79).
Conclusions:
- Non-O blood group children may be more susceptible to severe P. falciparum malaria than blood group O.
- Despite observed trends, a significant association between ABO blood groups and falciparum malaria severity was not established in this cohort.
Background:
ABO blood group antigens are formed by terminal glycosylation of glycoproteins and glycolipid chains present on cell surfaces. Glycosylation modulates all kinds of cell-to-cell interactions and this may be relevant in malaria pathophysiology, in which adhesion has been increasingly implicated in disease severity. This study was done to determine the association between ABO phenotypes and the severity of P. falciparum malaria in children.
Methods:
One hundred and twenty one children were assessed at the Department of Child Health, KBTH from May to August 2008. ABO blood groups were determined by agglutination. The haemoglobin measurement was done with the haematology analyzer, Sysmex KX-21N. Malaria parasites were enumerated and the presence of malaria pigment noted. Identification of P. falciparum was done. Statistical tests used were odds ratio and chi square at a significance level of p<0.05.
Results:
24.3% of the 121 children had severe falciparum malaria, and their mean haemoglobin was 4.49 g/dl (SD ± 1.69). No significant association was found between the ABO phenotypes and malaria infection (p > 0.05). Blood group A was associated with more severe malaria as compared to the blood group O individuals (Odds ratio = 0.79, p > 0.05); blood group AB (Odds ratio = 0.14, p > 0.05) and also there was a significant difference in severity of malaria between blood group O and blood group B (Odds ratio = 1.28, p > 0.05).
Conclusion:
Non-O blood group children are more prone to severe malaria caused by P. falciparum malaria than the group O, despite the lack of significant association between ABO blood groups and falciparum malaria.
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