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Serum Metrnl levels are decreased in subjects with overweight or obesity and are independently associated with adverse lipid profile

BACKGROUND: Meteorin-like (Metrnl), a novel adipokine, is highly expressed in adipose tissue and has a beneficial effect on energy metabolism. However, data on circulating Metrnl levels in obesity are scarce and inconsistent. This study aimed to evaluate the serum levels of Metrnl in adults with obe...

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Autores principales: Ding, Xiaoyu, Chang, Xiaona, Wang, Jiaxuan, Bian, Nannan, An, Yu, Wang, Guang, Liu, Jia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9483104/
https://www.ncbi.nlm.nih.gov/pubmed/36133314
http://dx.doi.org/10.3389/fendo.2022.938341
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author Ding, Xiaoyu
Chang, Xiaona
Wang, Jiaxuan
Bian, Nannan
An, Yu
Wang, Guang
Liu, Jia
author_facet Ding, Xiaoyu
Chang, Xiaona
Wang, Jiaxuan
Bian, Nannan
An, Yu
Wang, Guang
Liu, Jia
author_sort Ding, Xiaoyu
collection PubMed
description BACKGROUND: Meteorin-like (Metrnl), a novel adipokine, is highly expressed in adipose tissue and has a beneficial effect on energy metabolism. However, data on circulating Metrnl levels in obesity are scarce and inconsistent. This study aimed to evaluate the serum levels of Metrnl in adults with obesity and its association with glucose and lipid metabolism. METHODS: 182 subjects were included in the cross-sectional study. The participants were divided into three groups according to BMI: normal (n = 95), overweight (n = 46), and obesity (n = 41). Serum Metrnl concentrations were measured by enzyme-linked immunosorbent assay. RESULTS: Serum Metrnl levels in overweight or obese subjects were significantly lower than in the normal group. Circulating Metrnl levels were negatively correlated with TG, TC, LDL-C, and sdLDL and positively correlated with HDL-C before and after adjusting for age, sex, BMI, diabetes, HOMA-IR, and eGFR (all P < 0.05). Furthermore, logistic regression analysis indicated that compared with the highest tertile, the lowest tertile of Metrnl levels were significantly associated with the presence of hyper-TG, hyper-TC, and Hyper-LDL after full adjustment (all P for trend < 0.05). CONCLUSIONS: Serum Metrnl levels were reduced in individuals with overweight or obesity and were independently associated with adverse lipid profile, suggesting that modifying circulating Metrnl levels may serve as a potential therapeutic target for atherogenic dyslipidemia.
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spelling pubmed-94831042022-09-20 Serum Metrnl levels are decreased in subjects with overweight or obesity and are independently associated with adverse lipid profile Ding, Xiaoyu Chang, Xiaona Wang, Jiaxuan Bian, Nannan An, Yu Wang, Guang Liu, Jia Front Endocrinol (Lausanne) Endocrinology BACKGROUND: Meteorin-like (Metrnl), a novel adipokine, is highly expressed in adipose tissue and has a beneficial effect on energy metabolism. However, data on circulating Metrnl levels in obesity are scarce and inconsistent. This study aimed to evaluate the serum levels of Metrnl in adults with obesity and its association with glucose and lipid metabolism. METHODS: 182 subjects were included in the cross-sectional study. The participants were divided into three groups according to BMI: normal (n = 95), overweight (n = 46), and obesity (n = 41). Serum Metrnl concentrations were measured by enzyme-linked immunosorbent assay. RESULTS: Serum Metrnl levels in overweight or obese subjects were significantly lower than in the normal group. Circulating Metrnl levels were negatively correlated with TG, TC, LDL-C, and sdLDL and positively correlated with HDL-C before and after adjusting for age, sex, BMI, diabetes, HOMA-IR, and eGFR (all P < 0.05). Furthermore, logistic regression analysis indicated that compared with the highest tertile, the lowest tertile of Metrnl levels were significantly associated with the presence of hyper-TG, hyper-TC, and Hyper-LDL after full adjustment (all P for trend < 0.05). CONCLUSIONS: Serum Metrnl levels were reduced in individuals with overweight or obesity and were independently associated with adverse lipid profile, suggesting that modifying circulating Metrnl levels may serve as a potential therapeutic target for atherogenic dyslipidemia. Frontiers Media S.A. 2022-09-05 /pmc/articles/PMC9483104/ /pubmed/36133314 http://dx.doi.org/10.3389/fendo.2022.938341 Text en Copyright © 2022 Ding, Chang, Wang, Bian, An, Wang and Liu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Ding, Xiaoyu
Chang, Xiaona
Wang, Jiaxuan
Bian, Nannan
An, Yu
Wang, Guang
Liu, Jia
Serum Metrnl levels are decreased in subjects with overweight or obesity and are independently associated with adverse lipid profile
title Serum Metrnl levels are decreased in subjects with overweight or obesity and are independently associated with adverse lipid profile
title_full Serum Metrnl levels are decreased in subjects with overweight or obesity and are independently associated with adverse lipid profile
title_fullStr Serum Metrnl levels are decreased in subjects with overweight or obesity and are independently associated with adverse lipid profile
title_full_unstemmed Serum Metrnl levels are decreased in subjects with overweight or obesity and are independently associated with adverse lipid profile
title_short Serum Metrnl levels are decreased in subjects with overweight or obesity and are independently associated with adverse lipid profile
title_sort serum metrnl levels are decreased in subjects with overweight or obesity and are independently associated with adverse lipid profile
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9483104/
https://www.ncbi.nlm.nih.gov/pubmed/36133314
http://dx.doi.org/10.3389/fendo.2022.938341
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