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Prediabetes is associated with loss of appendicular skeletal muscle mass and sarcopenia

BACKGROUND: Decreasing mass and metabolism in skeletal muscle are associated with increasing insulin resistance (IR) and type 2 diabetes mellitus (T2DM). The causal relation between sarcopenia and abnormal glucose metabolism may be bidirectional. This investigation is aimed to explore the detailed c...

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Autores principales: Li, Shuying, Mao, Jiangfeng, Zhou, Weihong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014813/
https://www.ncbi.nlm.nih.gov/pubmed/36937340
http://dx.doi.org/10.3389/fnut.2023.1109824
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author Li, Shuying
Mao, Jiangfeng
Zhou, Weihong
author_facet Li, Shuying
Mao, Jiangfeng
Zhou, Weihong
author_sort Li, Shuying
collection PubMed
description BACKGROUND: Decreasing mass and metabolism in skeletal muscle are associated with increasing insulin resistance (IR) and type 2 diabetes mellitus (T2DM). The causal relation between sarcopenia and abnormal glucose metabolism may be bidirectional. This investigation is aimed to explore the detailed correlation between pre-diabetes and sarcopenia in United States (US) adults. METHODS: A total of 22,482 adults aged ≥20 years in the National Health and Nutrition Examination Survey (NHANES) were included. Generalized linear models were conducted to examine associations between diabetes status, serum glucose, glycohemoglobin (HbA1c), and sarcopenia. Generalized additive models and smooth fitting curves were used to examine the non-linear relationship between HbA1c and ASM(BMI). Sarcopenia was defined as ASM(BMI) (appendicular skeletal muscle mass/body mass index) < 0.789 for males, and <0.512 for females based on the cut-off values of the Foundation for the National Institutes of Health (FNIH) Sarcopenia Project. RESULTS: After fully adjusting for multiple covariates, sarcopenia was directly correlated with pre-diabetes [OR (95%CI) = 1.230 (1.057, 1.431), p = 0.008] and T2DM [OR (95%CI) = 2.106 (1.625, 2.729), p < 0.001]. In non-T2DM population, HbA1c was negatively correlated with ASM(BMI) [β (95%CI) = −0.009 (−0.013, −0.005), p < 0.001]. The correlations only persisted in males. Furthermore, in male non-T2DM population, the association of HbA1c and ASM(BMI) presents an inverted U-shape curve with an inflection point of HbA1c 5.2%. CONCLUSION: Pre-diabetes is associated with increased risk of sarcopenia. HbA1c is an independent risk factor for loss of appendicular skeletal muscle mass and sarcopenia when HbA1c greater than 5.2% in the male non-T2DM population.
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spelling pubmed-100148132023-03-16 Prediabetes is associated with loss of appendicular skeletal muscle mass and sarcopenia Li, Shuying Mao, Jiangfeng Zhou, Weihong Front Nutr Nutrition BACKGROUND: Decreasing mass and metabolism in skeletal muscle are associated with increasing insulin resistance (IR) and type 2 diabetes mellitus (T2DM). The causal relation between sarcopenia and abnormal glucose metabolism may be bidirectional. This investigation is aimed to explore the detailed correlation between pre-diabetes and sarcopenia in United States (US) adults. METHODS: A total of 22,482 adults aged ≥20 years in the National Health and Nutrition Examination Survey (NHANES) were included. Generalized linear models were conducted to examine associations between diabetes status, serum glucose, glycohemoglobin (HbA1c), and sarcopenia. Generalized additive models and smooth fitting curves were used to examine the non-linear relationship between HbA1c and ASM(BMI). Sarcopenia was defined as ASM(BMI) (appendicular skeletal muscle mass/body mass index) < 0.789 for males, and <0.512 for females based on the cut-off values of the Foundation for the National Institutes of Health (FNIH) Sarcopenia Project. RESULTS: After fully adjusting for multiple covariates, sarcopenia was directly correlated with pre-diabetes [OR (95%CI) = 1.230 (1.057, 1.431), p = 0.008] and T2DM [OR (95%CI) = 2.106 (1.625, 2.729), p < 0.001]. In non-T2DM population, HbA1c was negatively correlated with ASM(BMI) [β (95%CI) = −0.009 (−0.013, −0.005), p < 0.001]. The correlations only persisted in males. Furthermore, in male non-T2DM population, the association of HbA1c and ASM(BMI) presents an inverted U-shape curve with an inflection point of HbA1c 5.2%. CONCLUSION: Pre-diabetes is associated with increased risk of sarcopenia. HbA1c is an independent risk factor for loss of appendicular skeletal muscle mass and sarcopenia when HbA1c greater than 5.2% in the male non-T2DM population. Frontiers Media S.A. 2023-03-01 /pmc/articles/PMC10014813/ /pubmed/36937340 http://dx.doi.org/10.3389/fnut.2023.1109824 Text en Copyright © 2023 Li, Mao and Zhou. 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 Nutrition
Li, Shuying
Mao, Jiangfeng
Zhou, Weihong
Prediabetes is associated with loss of appendicular skeletal muscle mass and sarcopenia
title Prediabetes is associated with loss of appendicular skeletal muscle mass and sarcopenia
title_full Prediabetes is associated with loss of appendicular skeletal muscle mass and sarcopenia
title_fullStr Prediabetes is associated with loss of appendicular skeletal muscle mass and sarcopenia
title_full_unstemmed Prediabetes is associated with loss of appendicular skeletal muscle mass and sarcopenia
title_short Prediabetes is associated with loss of appendicular skeletal muscle mass and sarcopenia
title_sort prediabetes is associated with loss of appendicular skeletal muscle mass and sarcopenia
topic Nutrition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014813/
https://www.ncbi.nlm.nih.gov/pubmed/36937340
http://dx.doi.org/10.3389/fnut.2023.1109824
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