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Hepatic Vitamin A Concentrations and Association with Infectious Causes of Child Death
Priya M Gupta1, Zachary J Madewell2, Bryan M Gannon3
1Hubert Department of Global Health, Rollins School of Public Health, Emory University, Atlanta, GA.
Insights
Postmortem analysis revealed vitamin A deficiency (VAD) and excess in children under five. VAD in boys was linked to increased infectious mortality, suggesting targeted vitamin A supplementation strategies.
Area of Science:
- Nutritional epidemiology
- Pediatric mortality
- Micronutrient status assessment
Background:
- Vitamin A deficiency (VAD) is a global health concern, particularly in young children.
- Accurate assessment of vitamin A status postmortem is crucial for understanding mortality.
- Previous studies have not fully elucidated the link between postmortem vitamin A levels and causes of death.
Purpose of the Study:
- To determine postmortem vitamin A concentrations in children under five.
- To investigate the association between vitamin A deficiency and infectious causes of death.
Main Methods:
- Cross-sectional study of 405 stillbirths and children under five in Kenya and South Africa.
- Analysis of liver biopsies using ultra-performance liquid chromatography to quantify total liver vitamin A (TLVA).
- Categorization of TLVA into deficiency, adequate, high, and hypervitaminosis A levels; causes of death determined by expert review.
Main Results:
- Prevalence of VAD was 34.2%, adequate status 51.1%, high VA 6.0%, and hypervitaminosis A 8.7%.
- VAD was more prevalent in neonates, low birthweight, underweight, and stunted children.
- No significant overall association between VAD and infectious causes of death, but VA-deficient boys showed increased risk (OR 3.4).
Conclusions:
- Postmortem assessment identified both vitamin A deficiency and excess in young children.
- Vitamin A deficiency in boys is associated with a higher risk of infectious mortality.
- Findings support a shift towards targeted vitamin A supplementation strategies in specific regions.
Objectives:
To assess postmortem vitamin A (VA) concentrations in children under 5 years of age and evaluate the association between VA deficiency (VAD) and infectious causes of death (CoD).
Study Design:
In this cross-sectional study from the Child Health and Mortality Prevention Surveillance (CHAMPS) Network, liver biopsies collected within 72 hours of death were analyzed from 405 stillbirths and children under 5 years in Kenya and South Africa. Total liver VA (TLVA) concentrations were quantified using ultra-performance liquid chromatography, and cutoffs of ≤0.1 μmol/g, >0.1 to <0.7 μmol/g, ≥0.7 to <1.0 μmol/g, and ≥1.0 μmol/g were used to define VAD, adequate VA status, high VA, and hypervitaminosis A, respectively. CoD were determined by expert panel review.
Results:
Among 366 liver samples with viable extraction, pooled prevalences of VAD, adequacy, high VA, and hypervitaminosis were 34.2%, 51.1%, 6.0%, and 8.7%, respectively. VAD was more common among neonates compared with stillbirths, infants, or children, and among those with low birthweight (LBW), underweight, or stunting (P < .05). When adjusting for site, age, and sex, there was no significant association of VAD with increased infectious CoD (OR 1.9, 95% confidence interval [CI] 0.9, 3.8, P = .073). In stratified analyses, VA deficient boys, but not girls, had an increased risk of infectious CoD (OR 3.4, 95% CI 1.3, 10.3, P = .013).
Conclusions:
Definitive postmortem assessment of VA status identified both VAD and VA excess among children under 5 years of age in Kenya and South Africa. VAD in boys was associated with increased risk of infectious mortality. Our findings may inform a transition from universal VA supplementation (VAS) to targeted strategies in certain countries.
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