Abstract

Deficiencies of vitamin A, iron, and iodine are major public health concerns in many low- and middle-income countries, but information on their status in populations is often lacking due to high costs and logistical challenges associated with assessing micronutrient status. Accurate, user-friendly, and low-cost analytical tools are needed to allow large-scale population surveys on micronutrient status. We present the expansion of a 7-plex protein microarray tool for the simultaneous measurement of up to seven biomarkers with relevance to the assessment of the key micronutrients iron, iodine, and vitamin A, and inflammation and malaria biomarkers: α-1-acid glycoprotein, C-reactive protein, ferritin, retinol binding protein 4, soluble transferrin receptor, thyroglobulin, and histidine-rich protein II. Assay performance was assessed using international reference standards and then verified by comparing the multiplexed and conventional immunoassay results on a training panel of plasma samples collected from US adults. These data were used to assign nominal concentrations to the calibrators of the assay to further improve performance which was then assessed by interrogating plasma samples from a cohort of pregnant women from Niger. The correlation between assays for each biomarker measured from this cohort was typically good, with the exception of thyroglobulin, and the sensitivity ranged from 74% to 93%, and specificity from 81% to 98%. The 7-Plex micronutrient assay has the potential for use as an affordable tool for population surveillance of vitamin A, iron, and iodine deficiencies as well as falciparum malarial parasitemia infectivity and inflammation. The assay is easy-to-use, requires minimal sample volume, and is scalable, rapid, and accurate—needing only a low-cost reader and basic equipment present in most reference laboratory settings and so may be employed by low and middle income countries for micronutrient surveillance to inform on status in key populations. Micronutrient deficiencies including iron, iodine, and vitamin A affect a significant portion of the world’s population. Efforts to assess the prevalence of these deficiencies in vulnerable populations are challenging, partly due to measurement tools that are inadequate for assessing multiple micronutrients in large-scale population surveys. We have developed a 7-plex immunoassay for the simultaneous measurement of seven biomarkers relevant to assessing iodine, iron, and vitamin A status, inflammation and Plasmodium falciparum parasitemia by measuring levels of thyroglobulin, ferritin, soluble transferrin receptor, retinol binding protein 4, α-1-acid glycoprotein, C-reactive protein, and histidine-rich protein II. This 7-plex immunoassay technique has potential as a rapid and effective tool for use in large-scale surveys and assessments of nutrition intervention programs in low- and middle-income countries.

Highlights

  • Micronutrient (MN) deficiencies, among young children and women of reproductive age, have long been recognized as a significant public health burden in low- and middleincome countries (LMICs); despite the implementation of health surveillance systems since the 1980’s, relatively limited literature has been published on micronutrient surveys in low-income countries [1,2,3]

  • We have developed a 7-plex immunoassay for the simultaneous measurement of seven biomarkers relevant to assessing iodine, iron, and vitamin A status, inflammation and Plasmodium falciparum parasitemia by measuring levels of thyroglobulin, ferritin, soluble transferrin receptor, retinol binding protein 4, α-1-acid glycoprotein, C-reactive protein, and histidine-rich protein II

  • This study expands upon our previous work that described a multiplexed tool for the simultaneous assessment of vitamin A (VA), iron deficiency (ID), and acute phase proteins (APP) by improving assay components and adding further biochemical indicators of iodine deficiency and recent or current malarial infection with Plasmodium falciparum [5]

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Summary

Introduction

Micronutrient (MN) deficiencies, among young children and women of reproductive age, have long been recognized as a significant public health burden in low- and middleincome countries (LMICs); despite the implementation of health surveillance systems since the 1980’s, relatively limited literature has been published on micronutrient surveys in low-income countries [1,2,3]. The Biomarkers Reflecting Inflammation and Nutritional Determinants of Anemia (BRINDA) project have released a series of reports describing the outputs of various analyses by which to adjust for total body iron, ferritin, RBP and sTfR levels when in conjunction with elevated APPs and malarial infection in preschool children and/or women of childbearing age [32,33,34,35]. For more effective population-based assessments of MN status, there is a need for tools that permit nutrition programs and researchers to collect, process, and accurately analyze MN status data in country, ideally for biomarkers of multiple micronutrients simultaneously Practical considerations, such as easy sample collection and processing, cold chain during transportation, and simplified testing in the laboratory are of heightened importance. The NiMaNu panel presented an excellent opportunity by which to compare the performance of the 7-plex assay with other current tools used to measure micronutrient status and inflammation

Materials and methods
Statistical methods
Findings
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