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Leptin, acylcarnitine metabolites and development of adiposity in the Rhea mother–child cohort in Crete, Greece
OBJECTIVE: This study aims to investigate relations of serum leptin at age 4 with development of adiposity and linear growth during 3 years of follow‐up among 75 Greek children and to identify serum metabolites associated with leptin at age 4 and to characterize their associations with adiposity gai...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5192536/ https://www.ncbi.nlm.nih.gov/pubmed/28090353 http://dx.doi.org/10.1002/osp4.65 |
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author | Perng, W. Oken, E. Roumeliotaki, T. Sood, D. Siskos, A. P. Chalkiadaki, G. Dermitzaki, E. Vafeiadi, M. Kyrtopoulos, S. Kogevinas, M. Keun, H. C. Chatzi, L. |
author_facet | Perng, W. Oken, E. Roumeliotaki, T. Sood, D. Siskos, A. P. Chalkiadaki, G. Dermitzaki, E. Vafeiadi, M. Kyrtopoulos, S. Kogevinas, M. Keun, H. C. Chatzi, L. |
author_sort | Perng, W. |
collection | PubMed |
description | OBJECTIVE: This study aims to investigate relations of serum leptin at age 4 with development of adiposity and linear growth during 3 years of follow‐up among 75 Greek children and to identify serum metabolites associated with leptin at age 4 and to characterize their associations with adiposity gain and linear growth. METHODS: Linear regression models that accounted for maternal age, education and gestational weight gain and child's age and sex were used to examine associations of leptin and leptin‐associated metabolites measured at age 4 with indicators of adiposity and linear growth at age 7. RESULTS: Each 1‐unit increment in natural log‐(ln)‐transformed leptin corresponded with 0.33 (95% CI: 0.10, 0.55) units greater body mass index‐for‐age z‐score gain during follow‐up. Likewise, higher levels of the leptin‐associated metabolites methylmalonyl‐carnitine and glutaconyl‐carnitine corresponded with 0.14 (95% CI: 0.01, 0.27) and 0.07 (95% CI: −0.01, 0.16) units higher body mass index‐for‐age z‐score gain, respectively. These relationships did not differ by sex or baseline weight status and were independent of linear growth. CONCLUSIONS: These findings suggest that leptin, methylmalonyl‐carnitine and possibly glutaconyl‐carnitine are associated with weight gain during early childhood. Future studies are warranted to confirm these findings in other populations. |
format | Online Article Text |
id | pubmed-5192536 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-51925362017-01-12 Leptin, acylcarnitine metabolites and development of adiposity in the Rhea mother–child cohort in Crete, Greece Perng, W. Oken, E. Roumeliotaki, T. Sood, D. Siskos, A. P. Chalkiadaki, G. Dermitzaki, E. Vafeiadi, M. Kyrtopoulos, S. Kogevinas, M. Keun, H. C. Chatzi, L. Obes Sci Pract Short Communications OBJECTIVE: This study aims to investigate relations of serum leptin at age 4 with development of adiposity and linear growth during 3 years of follow‐up among 75 Greek children and to identify serum metabolites associated with leptin at age 4 and to characterize their associations with adiposity gain and linear growth. METHODS: Linear regression models that accounted for maternal age, education and gestational weight gain and child's age and sex were used to examine associations of leptin and leptin‐associated metabolites measured at age 4 with indicators of adiposity and linear growth at age 7. RESULTS: Each 1‐unit increment in natural log‐(ln)‐transformed leptin corresponded with 0.33 (95% CI: 0.10, 0.55) units greater body mass index‐for‐age z‐score gain during follow‐up. Likewise, higher levels of the leptin‐associated metabolites methylmalonyl‐carnitine and glutaconyl‐carnitine corresponded with 0.14 (95% CI: 0.01, 0.27) and 0.07 (95% CI: −0.01, 0.16) units higher body mass index‐for‐age z‐score gain, respectively. These relationships did not differ by sex or baseline weight status and were independent of linear growth. CONCLUSIONS: These findings suggest that leptin, methylmalonyl‐carnitine and possibly glutaconyl‐carnitine are associated with weight gain during early childhood. Future studies are warranted to confirm these findings in other populations. John Wiley and Sons Inc. 2016-10-21 /pmc/articles/PMC5192536/ /pubmed/28090353 http://dx.doi.org/10.1002/osp4.65 Text en © 2016 The Authors. Obesity Science & Practice published by John Wiley & Sons Ltd, World Obesity and The Obesity Society. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Short Communications Perng, W. Oken, E. Roumeliotaki, T. Sood, D. Siskos, A. P. Chalkiadaki, G. Dermitzaki, E. Vafeiadi, M. Kyrtopoulos, S. Kogevinas, M. Keun, H. C. Chatzi, L. Leptin, acylcarnitine metabolites and development of adiposity in the Rhea mother–child cohort in Crete, Greece |
title | Leptin, acylcarnitine metabolites and development of adiposity in the Rhea mother–child cohort in Crete, Greece |
title_full | Leptin, acylcarnitine metabolites and development of adiposity in the Rhea mother–child cohort in Crete, Greece |
title_fullStr | Leptin, acylcarnitine metabolites and development of adiposity in the Rhea mother–child cohort in Crete, Greece |
title_full_unstemmed | Leptin, acylcarnitine metabolites and development of adiposity in the Rhea mother–child cohort in Crete, Greece |
title_short | Leptin, acylcarnitine metabolites and development of adiposity in the Rhea mother–child cohort in Crete, Greece |
title_sort | leptin, acylcarnitine metabolites and development of adiposity in the rhea mother–child cohort in crete, greece |
topic | Short Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5192536/ https://www.ncbi.nlm.nih.gov/pubmed/28090353 http://dx.doi.org/10.1002/osp4.65 |
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