» Articles » PMID: 27211567

Child Stunting is Associated with Low Circulating Essential Amino Acids

Overview
Journal EBioMedicine
Date 2016 May 24
PMID 27211567
Citations 125
Authors
Affiliations
Soon will be listed here.
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.

Citing Articles

Leaf Extract Improves Cognitive Function in Rat Offspring Born to Protein-Deficient Mothers.

Kambuno N, Putra A, Louisa M, Wuyung P, Timan I, Silaen O Biomedicines. 2025; 13(2).

PMID: 40002759 PMC: 11852579. DOI: 10.3390/biomedicines13020346.


Food security and its impact on growth among Sri Lankan children under five during the economic crisis in 2022.

Vipulaguna D, de Silva H, Ranasinghe J, Sathiadas G, Sampath G, Dalpatadu A BMC Nutr. 2025; 11(1):1.

PMID: 39773767 PMC: 11707926. DOI: 10.1186/s40795-024-00979-y.


toxicity study in Sprague-Dawley rats receiving different doses of extract.

Kambuno N, Louisa M, Wuyung P, Silaen O, Supali T Open Vet J. 2024; 14(9):2294-2309.

PMID: 39553766 PMC: 11563609. DOI: 10.5455/OVJ.2024.v14.i9.18.


Unveiling the Nutritional Quality of Terrestrial Animal Source Foods by Species and Characteristics of Livestock Systems.

Rueda Garcia A, Fracassi P, Scherf B, Hamon M, Iannotti L Nutrients. 2024; 16(19).

PMID: 39408313 PMC: 11478523. DOI: 10.3390/nu16193346.


Nutritional status and extended metabolic screening in Egyptian children with uncomplicated type 1 diabetes.

Sakhr H, Hassan M, Ahmed A, Rashwan N, Abdel-Aziz R, Gouda A Sci Rep. 2024; 14(1):21055.

PMID: 39251658 PMC: 11383858. DOI: 10.1038/s41598-024-70660-8.


References
1.
Zeisel S, da Costa K . Choline: an essential nutrient for public health. Nutr Rev. 2009; 67(11):615-23. PMC: 2782876. DOI: 10.1111/j.1753-4887.2009.00246.x. View

2.
Kim M, Wu K, Auyeung V, Chen Q, Gruppuso P, Phornphutkul C . Leucine restriction inhibits chondrocyte proliferation and differentiation through mechanisms both dependent and independent of mTOR signaling. Am J Physiol Endocrinol Metab. 2009; 296(6):E1374-82. PMC: 2692404. DOI: 10.1152/ajpendo.91018.2008. View

3.
Nuss E, Tanumihardjo S . Quality protein maize for Africa: closing the protein inadequacy gap in vulnerable populations. Adv Nutr. 2012; 2(3):217-24. PMC: 3090170. DOI: 10.3945/an.110.000182. View

4.
Cole L, Vance J, Vance D . Phosphatidylcholine biosynthesis and lipoprotein metabolism. Biochim Biophys Acta. 2011; 1821(5):754-61. DOI: 10.1016/j.bbalip.2011.09.009. View

5.
Laplante M, Sabatini D . mTOR signaling in growth control and disease. Cell. 2012; 149(2):274-93. PMC: 3331679. DOI: 10.1016/j.cell.2012.03.017. View