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Nutritional status of young children with inherited blood disorders in western Kenya
Insights
In Kenyan children, alpha-thalassemia is linked to anemia but not vitamin A or iron deficiency. Other inherited blood disorders showed no association with nutritional status or growth.
Area of Science:
- Hematology
- Nutritional Science
- Pediatrics
Background:
- Inherited blood disorders are prevalent in malaria-endemic regions.
- Nutritional deficiencies are common in young children in western Kenya.
- Understanding the interplay between blood disorders and nutrition is crucial for public health.
Purpose of the Study:
- To investigate the association between inherited blood disorders and nutritional indicators in young Kenyan children.
- To determine if conditions like alpha-thalassemia, G6PD deficiency, haptoglobin 2-2, and HbS are linked to anemia, vitamin A deficiency, or iron deficiency.
Main Methods:
- Cross-sectional population-based survey of 882 children aged 6-35 months in western Kenya.
- Analysis of hemoglobin, ferritin, and retinol binding protein (RBP) levels.
- Multivariable regression analysis to assess associations, adjusting for potential confounders.
Main Results:
- 71.7% of children were anemic, 19.1% had low ferritin (iron deficiency), and 30.9% had low RBP (vitamin A deficiency).
- Homozygous alpha(+)-thalassemia was significantly associated with anemia (aOR=1.8, P=0.004).
- No significant associations were found between alpha(+)-thalassemia, G6PD deficiency, haptoglobin 2-2, HbS, and iron deficiency, vitamin A deficiency, or poor growth.
Conclusions:
- Alpha-thalassemia is a significant risk factor for anemia in young Kenyan children.
- Common inherited blood disorders in this population are not associated with iron or vitamin A deficiency or impaired growth.
- Public health strategies should address anemia in the context of alpha-thalassemia prevalence.
Abstract:
To determine the association between a range of inherited blood disorders and indicators of poor nutrition, we analyzed data from a population-based, cross-sectional survey of 882 children 6-35 months of age in western Kenya. Of children with valid measurements, 71.7% were anemic (hemoglobin < 11 g/dL), 19.1% had ferritin levels < 12 μg/L, and 30.9% had retinol binding protein (RBP) levels < 0.7 μmol/L. Unadjusted analyses showed that compared with normal children, homozygous α(+)-thalassemia individuals had a higher prevalence of anemia (82.3% versus 66.8%, P = 0.001), but a lower prevalence of low RBP (20.5% versus 31.4%, P = 0.024). In multivariable analysis, homozygous α(+)-thalassemia remained associated with anemia (adjusted odds ratio [aOR] = 1.8, P = 0.004) but not with low RBP (aOR = 0.6, P = 0.065). Among young Kenyan children, α(+)-thalassemia is associated with anemia, whereas G6PD deficiency, haptoglobin 2-2, and HbS are not; none of these blood disorders are associated with iron deficiency, vitamin A deficiency, or poor growth.
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