DOI: https://doi.org/10.22263/2312-4156.2023.2.47
E.A. Hayeuskaya1, N.M. Tsikhan1, A.A. Glazev2, S.D. Klisa2
Fecal aminoacid profile in infants depending on their age and sex characteristics, type of feedingand allergic anamnesis
1Grodno State Medical University, Grodno, Republic of Belarus
2Grodno State University named after Yanka Kupala, Grodno, Republic of Belarus
Vestnik VGMU. 2023;22(2):47-53.
Abstract.
Objectives. To study the content of fecal amino acids in infants depending on their age and sex characteristics, as well as type of feeding and family allergic anamnesis.
Material and methods. 31 children aged from 1 month to 1 year were selected for participation in the study. The mothers of these children were instructed in detail about the procedure of collecting stool samples from their infants. Qualitative and quantitative determination of free amino acids and their derivatives was carried out by high performance liquid chromatography using the HP-Agilent 1100 liquid chromatograph (Agilent Technologies, USA).
Results. Concentrations of β-aminobutyric acid, 3-methylhistidine, β-alanine and ornithine in children of the second half of their life were higher than in those in the first 6 months of life. In children of the first half of life, the concentrations of β-aminobutyric acid and 3-methylhistidine were below the threshold level of determination, after 6 months the content of these amino acids increased. Boys had a higher concentration of ethanolamine and ornithine in the stool than girls. Children on artificial feeding had significantly lower taurine numbers. In children at risk for allergic diseases, the concentration of tryptophan was lower than in children with an unburdened history of allergies.
Conclusions. With age, the concentration of 3-methylhistidine, β-alanine, β-aminobutyric acid and ornithine increases in the stool. In boys, the concentration of ethanolamine and ornithine is higher than in girls. Artificially fed infants have lower fecal taurine concentrations than breastfed ones. The level of tryptophan in children at risk for allergies was lower than in the group of children with an unburdened allergic anamnesis.
Keywords: microbiota, children, fecal markers, amino acids, allergy, nutrition.
References
1. Tsabouri S, Priftis KN, Chaliasos N, Siamopoulou A. Modulation of Gut Microbiota Downregulates the Development of Food Allergy in Infancy. Allergol Immunopathol (Madr). 2014 Jan-Feb;42(1):69-77. doi: http://dx.doi.org/10.1016/j.aller.2013.03.010
2. Bunyavanich S, Shen N, Grishin A, Wood R, Burks W, Dawson P, et al. Early-life gut microbiome composition and milk allergy resolution. J Allergy Clin Immunol. 2016 Oct;138(4):1122-30. doi: http://dx.doi.org/10.1016/j.jaci.2016.03.041
3. David LA, Maurice CF, Carmody RN, Gootenberg DB, Button JE, Wolfe BE, et al. Diet rapidly and reproducibly alters the human gut microbiome. Nature. 2014 Jan;505(7484):559-63. doi: http://dx.doi.org/10.1038/nature12820
4. Bao R, Hesser LA, He Z, Zhou X, Nadeau KC, Nagler CR. Fecalmicrobiome and metabolome differ in healthy and food allergic twin. J Clin Invest. 2021 Jan;131(2):e141935. doi: http://dx.doi.org/10.1172/JCI141935
5. Roduit C, Frei R, Ferstl R, Loeliger S, Westermann P, Rhyner C, Schiavi E, Barcik W, et al. High levels of butyrate and propionate in early life are associated with protection against atopy. Allergy. 2019 Apr;74(4):799-809. doi: http://dx.doi.org/10.1111/all.13660
6. Gorina AS, Kulinskiy VI, Kolesnichenko LS, Mikhnovich VI. Changes in tryptophan and its metabolites in children with early childhood autism. Sibir Nauch Med Zhurn. 2010;30(5):19-24. (In Russ.)
7. Chiu C-Y, Cheng M-L, Chiang M-H, Kuo Y-L, Tsai M-H, Chiu C-C, Lin G. Gut microbial derived butyrate is inversely associated with IgE responses to allergens in childhood asthmа. Pediatr Allergy Immunol. 2019 Nov;30(7):689-697. doi: http://dx.doi.org/10.1111/pai.13096
8. Jagt JZ, Struys EA, Ayada I, Bakkali A, Jansen EEW, Claesen J, et al. Fecal amino acid analysis in newly diagnosed pediatric inflammatory bowel disease. Inflamm Bowel Dis. 2022 May;28(5):755-63. doi: http://dx.doi.org/10.1093/ibd/izab256
9. Sasaki K, Sasaki D, Okai N, Tanaka K, Nomoto R, Fukuda I, et al. Taurine does not affect the composition, diversity, or metabolism of human colonic microbiota simulated in a single-batch fermentation system. PLoS One. 2017 Jul;12(7):e0180991. doi: http://dx.doi.org/10.1371/journal.pone.0180991
10. Kornienko EA, Mitrofanova NI, Larchenkova LV. Lactase deficiency in young children. Vopr Sovrem Pediatrii. 2006;5(4):82-6. (In Russ.)
11. Su X, Gao Y, Yang R. Gut microbiota-derived tryptophan metabolites maintain gut and systemic homeostasis. Cells. 2022 Jul;11(15):2296. doi: http://dx.doi.org/10.3390/cells11152296
12. Wu GD, Chen J, Hoffmann C, Bittinger K, Chen Y-Y, Keilbaugh SA, et al. Linking long-term dietary patterns with gut microbial enterotypes. Science. 2011 Oct;334(6052):105-8. doi: http://dx.doi.org/10.1126/science.1208344
Information about authors:
E.A. Hayeuskaya – lecturer of the Chair of Childhood Diseases No.1, Grodno State Medical University, https://orcid.org/0000-0002-5197-9592
e-mail: Этот адрес электронной почты защищён от спам-ботов. У вас должен быть включен JavaScript для просмотра. – Evgenia A. Hayeuskaya;
N.M. Tsikhan – Candidate of Medical Sciences, associate professor, head of the Chair of Childhood Diseases No.1, Grodno State Medical University, https://orcid.org/0000-0002-7803-5460
A.A. Glazev– head of the research laboratory of biochemistry of biologically active substances, Grodno State University named after Yanka Kupala;
S.D. Klisa – junior research officer of the research laboratory of biochemistry of biologically active substances, Grodno State University named after Yanka Kupala.