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Serum levels of the novel adipokine isthmin-1 are associated with obesity in pubertal boys

OBJECTIVES: To evaluate whether there is an association between the serum levels of the novel insulin-like adipokine isthmin-1 (ISM1) and obesity-related phenotypes in a population of Spanish children and to investigate the plausible molecular alterations behind the alteration of the serum levels of...

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Autores principales: Ruiz-Ojeda, Francisco Javier, Anguita-Ruiz, Augusto, Rico, Maria C., Leis, Rosaura, Bueno, Gloria, Moreno, Luis A., Gil-Campos, Mercedes, Gil, Ángel, Aguilera, Concepción M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2023
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423122/
https://www.ncbi.nlm.nih.gov/pubmed/36595188
http://dx.doi.org/10.1007/s12519-022-00665-8
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author Ruiz-Ojeda, Francisco Javier
Anguita-Ruiz, Augusto
Rico, Maria C.
Leis, Rosaura
Bueno, Gloria
Moreno, Luis A.
Gil-Campos, Mercedes
Gil, Ángel
Aguilera, Concepción M.
author_facet Ruiz-Ojeda, Francisco Javier
Anguita-Ruiz, Augusto
Rico, Maria C.
Leis, Rosaura
Bueno, Gloria
Moreno, Luis A.
Gil-Campos, Mercedes
Gil, Ángel
Aguilera, Concepción M.
author_sort Ruiz-Ojeda, Francisco Javier
collection PubMed
description OBJECTIVES: To evaluate whether there is an association between the serum levels of the novel insulin-like adipokine isthmin-1 (ISM1) and obesity-related phenotypes in a population of Spanish children and to investigate the plausible molecular alterations behind the alteration of the serum levels of this protein in children with obesity. METHODS: The study population is a sub-cohort of the PUBMEP research project, consisting of a cross-sectional population of 119 pubertal children with overweight (17 boys, 19 girls), obesity (20 boys, 25 girls), and normal weight (17 boys, 21 girls). All subjects were classified into experimental groups according to their sex, obesity, and insulin resistance (IR) status. They were counted anthropometry, glucose and lipid metabolism, inflammation and cardiovascular biomarkers as well as isthmin-1 (ISM1) serum levels. This population was intended as a discovery population to elucidate the relationship between obesity and ISM1 levels in children. Furthermore, the study population had blood whole-genome DNA methylation examined, allowing deepening into the obesity–ISM1 molecular relationship. RESULTS: Higher serum ISM1 levels were observed in boys with obesity than in normal weight (P = 0.004) and overweight (P = 0.007) boys. ISM1 serum levels were positively associated with body mass index (BMI) Z-score (P = 0.005) and fat mass (P = 0.058) and negatively associated with myeloperoxidase (MPO) (P = 0.043) in boys. Although we did not find associations between ISM1 serum levels and metabolic outcomes in girls, which may indicate a putative sexual dimorphism, fat mass was positively associated in all children, including boys and girls (P = 0.011). DNA methylation levels in two-enhancer-related CpG sites of ISM1 (cg03304641 and cg14269097) were associated with serum levels of ISM1 in children. CONCLUSIONS: ISM1 is associated with obesity in boys at the pubertal stage, elucidating how this protein might be of special relevance as a new biomarker of obesity in children. Further studies including a longitudinal design during puberty are needed. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12519-022-00665-8.
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spelling pubmed-104231222023-08-14 Serum levels of the novel adipokine isthmin-1 are associated with obesity in pubertal boys Ruiz-Ojeda, Francisco Javier Anguita-Ruiz, Augusto Rico, Maria C. Leis, Rosaura Bueno, Gloria Moreno, Luis A. Gil-Campos, Mercedes Gil, Ángel Aguilera, Concepción M. World J Pediatr Original Article OBJECTIVES: To evaluate whether there is an association between the serum levels of the novel insulin-like adipokine isthmin-1 (ISM1) and obesity-related phenotypes in a population of Spanish children and to investigate the plausible molecular alterations behind the alteration of the serum levels of this protein in children with obesity. METHODS: The study population is a sub-cohort of the PUBMEP research project, consisting of a cross-sectional population of 119 pubertal children with overweight (17 boys, 19 girls), obesity (20 boys, 25 girls), and normal weight (17 boys, 21 girls). All subjects were classified into experimental groups according to their sex, obesity, and insulin resistance (IR) status. They were counted anthropometry, glucose and lipid metabolism, inflammation and cardiovascular biomarkers as well as isthmin-1 (ISM1) serum levels. This population was intended as a discovery population to elucidate the relationship between obesity and ISM1 levels in children. Furthermore, the study population had blood whole-genome DNA methylation examined, allowing deepening into the obesity–ISM1 molecular relationship. RESULTS: Higher serum ISM1 levels were observed in boys with obesity than in normal weight (P = 0.004) and overweight (P = 0.007) boys. ISM1 serum levels were positively associated with body mass index (BMI) Z-score (P = 0.005) and fat mass (P = 0.058) and negatively associated with myeloperoxidase (MPO) (P = 0.043) in boys. Although we did not find associations between ISM1 serum levels and metabolic outcomes in girls, which may indicate a putative sexual dimorphism, fat mass was positively associated in all children, including boys and girls (P = 0.011). DNA methylation levels in two-enhancer-related CpG sites of ISM1 (cg03304641 and cg14269097) were associated with serum levels of ISM1 in children. CONCLUSIONS: ISM1 is associated with obesity in boys at the pubertal stage, elucidating how this protein might be of special relevance as a new biomarker of obesity in children. Further studies including a longitudinal design during puberty are needed. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12519-022-00665-8. Springer Nature Singapore 2023-01-03 2023 /pmc/articles/PMC10423122/ /pubmed/36595188 http://dx.doi.org/10.1007/s12519-022-00665-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Ruiz-Ojeda, Francisco Javier
Anguita-Ruiz, Augusto
Rico, Maria C.
Leis, Rosaura
Bueno, Gloria
Moreno, Luis A.
Gil-Campos, Mercedes
Gil, Ángel
Aguilera, Concepción M.
Serum levels of the novel adipokine isthmin-1 are associated with obesity in pubertal boys
title Serum levels of the novel adipokine isthmin-1 are associated with obesity in pubertal boys
title_full Serum levels of the novel adipokine isthmin-1 are associated with obesity in pubertal boys
title_fullStr Serum levels of the novel adipokine isthmin-1 are associated with obesity in pubertal boys
title_full_unstemmed Serum levels of the novel adipokine isthmin-1 are associated with obesity in pubertal boys
title_short Serum levels of the novel adipokine isthmin-1 are associated with obesity in pubertal boys
title_sort serum levels of the novel adipokine isthmin-1 are associated with obesity in pubertal boys
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423122/
https://www.ncbi.nlm.nih.gov/pubmed/36595188
http://dx.doi.org/10.1007/s12519-022-00665-8
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