Adjusting retinol-binding protein concentrations for inflammation: Biomarkers Reflecting Inflammation and Nutritional Determinants of Anemia (BRINDA) project

• Type of Material: Article
• Authors: Leila M. Larson, Emory University; Sorrel M.L. Namaste, Strengthening Partnerships, Results, and Innovations in Nutrition Globally; Anne Williams, Emory University; Reina Engle-Stone, University of California Davis; O. Addo, Emory University; Parminder Suchdev, Emory University; James P. Wirth, GroundWork; Victor Temple, University of Papua New Guinea; Mary Serdula, CDC; Christine A. Northrop-Clewes, Independent Public Health Nutrition Consultant
• Language: English
• Date: 2017-07-01
• Publisher: American Society for Nutrition
• Publication Version: Final Published Version
• Copyright Statement: © 2017 American Society for Nutrition. Published by Elsevier Inc.
• License: Creative Commons Attribution 3.0 Unported
• Final Published Version (URL): http://ajcn.nutrition.org/content/106/Supplement_1/390S.full
• Title of Journal or Parent Work: American Journal of Clinical Nutrition
• ISSN: 0002-9165
• Volume: 106
• Issue: 1
• Start Page: 390S
• End Page: 401S
• Grant/Funding Information: Supported by the Bill & Meinda Gates Foundation, CDC, Global Alliance for Improved Nutrition, and Eunice Kennedy Shriver National Institute of Child Health and Human Development.
• Keywords: MALARIA; INFECTION; nutritional assessment; Science & Technology; Nutrition & Dietetics; retinol-binding protein; vitamin A deficiency; METAANALYSIS; FERRITIN; Life Sciences & Biomedicine; ACUTE-PHASE RESPONSE; anemia; CHILDREN; PREVALENCE; METABOLISM; IRON; meta-analysis; inflammation; VITAMIN-A-DEFICIENCY

Abstract

Background: The accurate estimation of the prevalence of vitamin A deficiency (VAD) is important in planning and implementing interventions. Retinol-binding protein (RBP) is often used in population surveys to measure vitamin A status, but its interpretation is challenging in settings where inflammation is common because RBP concentrations decrease during the acute-phase response.Objectives: We aimed to assess the relation between RBP concentrations and inflammation and malaria in preschool children (PSC) (age range: 6-59 mo) and women of reproductive age (WRA) (age range: 15-49 y) and to investigate adjustment algorithms to account for these effects.Design: Cross-sectional data from 8 surveys for PSC (n = 8803) and 4 surveys for WRA (n = 4191) from the Biomarkers Reflecting Inflammation and Nutritional Determinants of Anemia (BRINDA) project were analyzed individually and combined with the use of a meta-analysis. Several approaches were explored to adjust RBP concentrations in PSC in inflammation and malaria settings as follows: 1) the exclusion of subjects with C-reactive protein (CRP) concentrations > 5 mg/L or α-1-acid glycoprotein (AGP) concentrations > 1 g/L, 2) the application of arithmetic correction factors, and 3) the use of a regression correction approach. The impact of adjustment on the estimated prevalence of VAD (defined as < 0.7 μmol/L) was examined in PSC.Results: The relation between estimated VAD and CRP and AGP deciles followed a linear pattern in PSC. In women, the correlations between RBP and CRP and AGP were too weak to justify adjustments for inflammation. Depending on the approach used to adjust for inflammation (CRP+AGP), the estimated prevalence of VAD decreased by a median of 11-18 percentage points in PSC compared with unadjusted values. There was no added effect of adjusting for malaria on the estimated VAD after adjusting for CRP and AGP.Conclusions: The use of regression correction (derived from internal data), which accounts for the severity of inflammation, to estimate the prevalence of VAD in PSC in regions with inflammation and malaria is supported by the analysis of the BRINDA data. These findings contribute to the evidence on adjusting for inflammation when estimating VAD with the use of RBP.