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Departments of * Epidemiology,
Laboratory Medicine, ** Medicine, and
Biostatistics, University of Washington, Seattle, WA; 
Coast Provincial General Hospital, Mombasa, Kenya; and the 
Department of Medical Microbiology, University of Nairobi, Nairobi, Kenya
2 To whom correspondence should be addressed at the Department of Medicine, Massachusetts General Hospital, Boston, MA. E-mail: jbaeten{at}u.washington.edu.
The ratio of retinol-binding protein (RBP) to transthyretin (TTR) has been proposed as an indirect method with which to assess vitamin A status in the context of inflammation. Few studies have been conducted among adults, and none examined the effect of HIV-1 infection. Our goal was to assess the RBP:TTR ratio among adults, including the effects of HIV-1 and the acute phase response. We used data from a cross-sectional study of 600 Kenyan women, of whom 400 had HIV-1. The effect of vitamin A supplementation among the HIV-1infected participants was subsequently assessed in a randomized trial. Among HIV-1uninfected women without an acute phase response, a RBP:TTR cut-off value of 0.25 had
80% sensitivity and specificity to detect vitamin A deficiency (retinol <0.70 µmol/L). No RBP:TTR cut-off value demonstrated both high sensitivity and specificity among HIV-1 infected women without evidence of inflammation. HIV-1 infection and advanced HIV-1 disease were associated with higher RBP:TTR ratios. The effect of HIV-1 was independent of the acute phase response, which also increased the RBP:TTR ratio. Serum retinol increased with vitamin A supplementation among those with a low RBP:TTR ratio, although the effect was small and was not present among those with concurrent inflammation. Thus, the RBP:TTR ratio has modest ability to predict vitamin A deficiency among healthy adults, but HIV-1 infection alters the ratio, even in the absence of the acute phase response. Our results raise questions about the utility of this measurement given the high prevalence of HIV-1 infection in areas where vitamin A deficiency is common.
KEY WORDS: vitamin A status retinol-binding protein transthyretin HIV inflammation