Clinical and Biochemical Markers of Risk in Uncomplicated Severe Acute Malnutrition | Marqueurs cliniques et biochimiques de disque de mortalité chez les enfants atteints de malnutrition aiguë sévère sans complication
2021
Dailey-Chwalibóg, Trenton | Freemark, Michael | Muehlbauer, Michael | Roberfroid, Dominique | Kemokai, Issa | Mostak, Md. Rayhan | Alim, Md. Abdul | Khan, Murad Md. Shamsher Tabris | Khan, Md. Abul Hashem | Bawo, Luke | Dunbar, Nelson | Taylor, Curtis | Fouillet, Hélène | Huneau, Jean-François | Kolsteren, Patrick | Guesdon, Benjamin | Physiologie de la Nutrition et du Comportement Alimentaire (PNCA (UMR 0914)) ; AgroParisTech-Université Paris-Saclay-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE) | Action contre la Faim (ACF) | Universiteit Gent = Ghent University = Université de Gand (UGENT) | Duke University Medical Center | Belgian Health Care Knowledge Centre (KCE) | Université de Namur [Namur] (UNamur) | Palli Karma-Sahayak Foundation (PKSF) | National Nutrition Service (NNS) | Ministry of Health, Monrovia, Liberia | Pacific Institute for Research and Evaluation, University of Liberia (UL-PIRE) | The data presented in this article are part of the OptiDiag study, which is funded by Action Contre la Faim France with financial support from the European Commission's Civil Protection and Humanitarian Aid Operations Enhanced Response Capacity (grant ECHO/ERC/BUD/2015/91002) and the Humanitarian Innovation Fund, a program managed by Enhanced Learning and Research for Humanitarian Assistance. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the article.
International audience
Show more [+] Less [-]English. Use of mid–upper arm circumference (MUAC) as a single screening tool for severe acute malnutrition (SAM) assumes that children with a low weight-for-height z score (WHZ) and normal MUAC have lower risks of morbidity and mortality. However, the pathophysiology and functional severity associated with different anthropometric phenotypes of SAM have never been well characterized. We compared clinical characteristics, biochemical features, and health and nutrition histories of nonedematous children with SAM who had (1) low WHZ only, (2) both low WHZ and low MUAC, or (3) low MUAC only. In Bangladesh, Burkina Faso, and Liberia, we conducted a multicentric cohort study in uncomplicated, nonedematous children with SAM and low MUAC only (n = 161), low WHZ only (n = 138), or a combination of low MUAC and low WHZ (n = 152). Alongside routine anthropometric measurements, we collected a wide range of critical indicators of clinical and nutritional status and viability; these included serum leptin, an adipocytokine negatively associated with mortality risk in SAM. Median leptin levels at diagnosis were lower in children with low WHZ only (215.8 pg/mL; P < .001) and in those with combined WHZ and MUAC deficits (180.1 pg/mL; P < .001) than in children with low MUAC only (331.50 pg/mL). The same pattern emerged on a wide range of clinical indicators, including signs of severe wasting, dehydration, serum ferritin levels, and caretaker-reported health deterioration, and was replicated across study sites. Illustrative of the likely heterogeneous functional severity of the different anthropometric phenotypes of SAM, our results confirm the need to retain low WHZ as an independent diagnostic criterion.
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