Child Stunting is Associated with Low Circulating Essential Amino Acids

Richard D Semba, Michelle Shardell, Fayrouz A Sakr Ashour, Ruin Moaddel, Indi Trehan, Kenneth M Maleta, M Isabel Ordiz, Klaus Kraemer, Mohammed A Khadeer, Luigi Ferrucci, Mark J Manary, Richard D Semba, Michelle Shardell, Fayrouz A Sakr Ashour, Ruin Moaddel, Indi Trehan, Kenneth M Maleta, M Isabel Ordiz, Klaus Kraemer, Mohammed A Khadeer, Luigi Ferrucci, Mark J Manary

Abstract

Background: Stunting affects about one-quarter of children under five worldwide. The pathogenesis of stunting is poorly understood. Nutritional interventions have had only modest effects in reducing stunting. We hypothesized that insufficiency in essential amino acids may be limiting the linear growth of children.

Methods: We used a targeted metabolomics approach to measure serum amino acids, glycerophospholipids, sphingolipids, and other metabolites using liquid chromatography-tandem mass spectrometry in 313 children, aged 12-59months, from rural Malawi. Children underwent anthropometry.

Findings: Sixty-two percent of the children were stunted. Children with stunting had lower serum concentrations of all nine essential amino acids (tryptophan, isoleucine, leucine, valine, methionine, threonine, histidine, phenylalanine, lysine) compared with nonstunted children (p<0.01). In addition, stunted children had significantly lower serum concentrations of conditionally essential amino acids (arginine, glycine, glutamine), non-essential amino acids (asparagine, glutamate, serine), and six different sphingolipids compared with nonstunted children. Stunting was also associated with alterations in serum glycerophospholipid concentrations.

Interpretation: Our findings support the idea that children with a high risk of stunting may not be receiving an adequate dietary intake of essential amino acids and choline, an essential nutrient for the synthesis of sphingolipids and glycerophospholipids.

Keywords: Amino acids; Children; Glycerophospholipids; Malnutrition; Sphingolipids; Stunting.

Conflict of interest statement

The authors declare no competing financial interests.

Copyright © 2016 The Authors. Published by Elsevier B.V. All rights reserved.

Figures

Fig. 1
Fig. 1
Heat map showing the relationship of the fifty most significant serum metabolites by HAZ, adjusted by age and gender. HAZ divided into deciles. Metabolites are ordered by p-values, with the lowest p-values on the left side. Standard three-letter abbreviations used for amino acids. Abbreviations for lipid nomenclature are described in the methods section. Other abbreviation: carnitine (C0).
Fig. 2
Fig. 2
Volcano plot showing the relationship of partial Spearman correlations, adjusted for age and gender, between HAZ and serum metabolites using Bonferroni-adjusted p-values. Horizontal line indicates p-value cut-off for Bonferroni-adjusted p-value of 0.05/5 (p 

Fig. 3

Scatterplots and fitted regression curves…

Fig. 3

Scatterplots and fitted regression curves using natural cubic splines for the 20 serum…

Fig. 3
Scatterplots and fitted regression curves using natural cubic splines for the 20 serum metabolites with the most significant correlations. Abbreviations for lipid nomenclature are described in the methods section. Standard three-letter abbreviations used for amino acids.
Fig. 3
Fig. 3
Scatterplots and fitted regression curves using natural cubic splines for the 20 serum metabolites with the most significant correlations. Abbreviations for lipid nomenclature are described in the methods section. Standard three-letter abbreviations used for amino acids.

References

    1. Ashorn P., Alho L., Ashorn U., et al. Supplementation of maternal diets during pregnancy and for 6 months postpartum and infant diets thereafter with small-quantity lipid-based nutrient supplements does not promote child growth by 18 months of age in rural Malawi: a randomized controlled trial. J. Nutr. 2015;145:1345–1353.
    1. Baron J., Sävendahl L., De Luca F., et al. Short and tall stature: a new paradigm emerges. Nat. Rev. Endocrinol. 2015;11:735–746.
    1. Beyersdorf N., Müller N. Sphingomyelin breakdown in T cells: role in activation, effector functions and immunoregulation. Biol. Chem. 2015;396:749–758.
    1. Bhutta Z.A., Das J.K., Rizvi A., et al. Evidence-based interventions for improvement of maternal and child nutrition: what can be done and at what cost? Lancet. 2013;382:452–477.
    1. Black R.E., Victora C.G., Walker S.P., et al. Maternal and child undernutrition and overweight in low-income and middle-income countries. Lancet. 2013;382:427–451.
    1. Breier M., Wahl S., Prehn C., et al. Targeted metabolomics identifies reliable and stable metabolites in human serum and plasma samples. PLoS One. 2014;9
    1. Cole L.K., Vance J.E., Vance D.E. Phosphatidylcholine biosynthesis and lipoprotein metabolism. Biochim. Biophys. Acta. 2012;1821:754–761.
    1. de Onis M., Dewey K.G., Borghi E., et al. The World Health Organization's global target for reducing childhood stunting by 2025: rationale and proposed actions. Matern. Child Nutr. 2013;9(Suppl. 2):6–26.
    1. de Onis M., Onyango A., Borghi E., et al. Worldwide implementation of the WHO Child Growth Standards. Public Health Nutr. 2012;15:1603–1610.
    1. Efeyan A., Comb W.C., Sabatini D.M. Nutrient-sensing mechanisms and pathways. Nature. 2015;517:302–310.
    1. Fagone P., Jackowski S. Phosphatidylcholine and the CDP-choline cycle. Biochim. Biophys. Acta. 2013;1831:523–532.
    1. Food and Nutrition Board, Institute of Medicine . National Academy of Sciences. Washington, D.C., Food and Nutrition Board, Institute of Medicine. National Academic Press; 1998. Dietary Reference Intakes: Thiamin, Riboflavin, Niacin, Vitamin B-6, Vitamin B-12, Panthothenic acid, Biotin, and Choline; pp. 390–422.
    1. Garza C. Commentary: Please sir, I want some more (and something else) Int. J. Epidemiol. 2015;44:1876–1878.
    1. Grantham-McGregor S., Cheung Y.B., Cueto S., et al. Developmental potential in the first 5 years for children in developing countries. Lancet. 2007;369:60–70.
    1. Johansson M.E., Ambort D., Pelaseyed T., et al. Composition and functional role of the mucus layers in the intestine. Cell. Mol. Life Sci. 2011;68:3635–3641.
    1. Kampman-van de Hoek E., Jansman A.J., van den Borne J.J., et al. Dietary amino acid deficiency reduces the utilization of amino acids for growth in growing pigs after a period of poor health. J. Nutr. 2016;146:51–58.
    1. Kim M.S., Wu K.Y., Auyeung V., et al. Leucine restriction inhibits chondrocyte proliferation and differentiation through mechanisms both dependent and independent of mTOR signaling. Am. J. Physiol. Endocrinol. Metab. 2009;296:E1374–E1382.
    1. Kular J., Tickner J.C., Pavlos N.J., et al. Choline kinase β mutant mice exhibit reduced phosphocholine, elevated osteoclast activity, and low bone mass. J. Biol. Chem. 2015;290:1729–1742.
    1. Laplante M., Sabatini D. mTOR signaling in growth control and disease. Cell. 2012;149:274–293.
    1. Lebrun-Julien F., Bachmann L., Norrmén C., et al. Balanced mTORC1 activity in oligodendrocytes is required for accurate CNS myelination. J. Neurosci. 2014;34:8432–8448.
    1. Li Z., Wu G., Sher R.B., et al. Choline kinase beta is required for normal endochondral bone formation. Biochim. Biophys. Acta. 2014;1840:2112–2122.
    1. Mayneris-Perxaches J., Lima A.A.M., Guerrant R.L., et al. Urinary N-methylnicotinamide and β-aminoisobutyric acid predict catch-up growth in undernourished Brazilian children. Sci. Rep. 2016;6:19780.
    1. Mayo-Wilson E., Junior J.A., Imdad A., et al. Zinc supplementation for preventing mortality, morbidity, and growth failure in children aged 6 months to 12 years of age. Cochrane Database Syst. Rev. 2014;5
    1. Murray C.J. Shifting to sustainable development goals–implications for global health. N. Engl. J. Med. 2015;373:1390–1393.
    1. Nuss E.T., Tanumihardjo S.A. Quality protein maize for Africa: closing the protein inadequacy gap in vulnerable populations. Adv. Nutr. 2011;2:217–224.
    1. Pillai R.R., Kurpad A.V. Amino acid requirements in children and the elderly population. Br. J. Nutr. 2012;108:S44–S49.
    1. Ramakrishnan U., Nguyen P., Martorell R. Effects of micronutrients on growth of children under 5 yrs. of age: meta-analyses of single and multiple nutrient interventions. Am. J. Clin. Nutr. 2009;89:191–203.
    1. Reinehr T., Wolters B., Knop C., et al. Changes in the serum metabolite profile in obese children with weight loss. Eur. J. Nutr. 2015;54:173–181.
    1. Saxton R.A., Knockenhauer K.E., Wolfson R.L., et al. Structural basis for leucine sensing by the Sestrin2-mTORC1 pathway. Science. 2016;351:53–58.
    1. Schmerler D., Neugebauer S., Ludewig K., et al. Targeted metabolomics for discrimination of systemic inflammatory disorders in critically ill patients. J. Lipid Res. 2012;53:1369–1375.
    1. Semba R.D. In: Nutrition and Health in Developing Countries. second ed. Semba R.D., Bloem M.W., editors. Humana Press; Totowa, NJ: 2008. Nutrition and development: a historical perspective; pp. 1–31.
    1. Slotte J.P. Biological functions of sphingomyelins. Prog. Lipid Res. 2013;52:424–437.
    1. Stammers A.L., Lowe N.M., Medina M.W., et al. The relationship between zinc intake and growth in children aged 1–8 years: a systematic review and meta-analysis. Eur. J. Clin. Nutr. 2015;69:147–153.
    1. UNICEF/World Health Organization/World Bank Group . United Nations Children's Fund, World Health Organization, and World Bank Group. 2015. Levels and Trends in Child Malnutrition: Key Findings of the 2015 Edition. ([ ] Accessed January 7, 2016)
    1. van der Merwe L.F., Moore S.E., Fulford A.J., Halliday K.E., Drammeh S., Young S., Prentice A.M. Long-chain PUFA supplementation in rural African infants: a randomized controlled trial of effects on gut integrity, growth, and cognitive development. Am. J. Clin. Nutr. 2013;97:45–57.
    1. Wu G. Amino acids: metabolism, functions, and nutrition. Amino Acids. 2009;37:1–17.
    1. Ye J., Palm W., Peng M., et al. GCN2 sustains mTORC1 suppression upon amino acid deprivation by inducing Sestrin2. Genes Dev. 2015;29:2331–2336.
    1. Zeisel S.H., da Costa K.A. Choline: an essential nutrient for public health. Nutr. Rev. 2009;67:615–623.

Source: PubMed

3
Suscribir