Vitamin A deficiency impairs immune function against parasitic pathogens, which may be linked to schistosomiasis morbidity in children. Adjusting measures of vitamin A status to account for inflammation is necessary to estimate vitamin A status during periods of infection. A secondary analysis of a treatment-reinfection study of children and adolescents with Schistosoma japonicum infection from the Philippines was performed in the present study. Measurements included S. japonicum infection intensity via Kato-Katz (eggs per gram of stool [EPG]), retinol-binding protein (RBP), C-reactive protein (CRP), and alpha-1-acid glycoprotein (AGP). The Thurnham Correction Factor (TCF) inflammation-adjustment method was applied to RBP using measures of CRP and AGP. A sample of n = 40 participants aged 8 to 18 years was randomly selected on the basis of S. japonicum EPG distribution. After applying the TCF method, 14 participants (35.9%) were vitamin A-deficient (RBP <0.7 µ mol/L). Using multivariate regression models adjusting for sex, vitamin A deficiency was associated with higher S. japonicum EPG at baseline ( P = 0.02). Baseline vitamin A status was not associated with S. japonicum infection intensity (EPG) at subsequent visits over 18 months. This association between vitamin A deficiency and increased schistosomiasis egg burden agrees with findings from animal studies and enhances understanding of nutritional modulation of infection, specific to schistosomiasis.
No takes yet. Share an insight, caveat, or question.
Colt et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: