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GDF-15 Is Associated with Poor Physical Function in Prefrail Older Adults with Diabetes

INTRODUCTION: Growth differentiation factor 15 (GDF-15) has been shown to be a metabolic and appetite regulator in diabetes mellitus (DM) and obesity. We aimed to investigate (i) the association between GDF-15 and DM with and without poor physical function independent of inflammation and (ii) the pr...

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Autores principales: Merchant, Reshma Aziz, Chan, Yiong Huak, Duque, Gustavo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10162869/
https://www.ncbi.nlm.nih.gov/pubmed/37152099
http://dx.doi.org/10.1155/2023/2519128
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author Merchant, Reshma Aziz
Chan, Yiong Huak
Duque, Gustavo
author_facet Merchant, Reshma Aziz
Chan, Yiong Huak
Duque, Gustavo
author_sort Merchant, Reshma Aziz
collection PubMed
description INTRODUCTION: Growth differentiation factor 15 (GDF-15) has been shown to be a metabolic and appetite regulator in diabetes mellitus (DM) and obesity. We aimed to investigate (i) the association between GDF-15 and DM with and without poor physical function independent of inflammation and (ii) the prediction model for poor physical function in prefrail older adults. METHODS: A cross-sectional study of 108-prefrail participants ≥60 years recruited for multidomain interventions. Data was collected for demographics, cognition, function, frailty, nutrition, handgrip strength (HGS), short physical performance battery (SPPB), and gait speed. Serum concentrations of GDF-15, IL-6, and TNF-α were measured. GDF-15 was classified into tertiles (T1, T2, and T3), and its association was studied with DM and physical function (DM poor physical function, DM no poor physical function, no DM poor physical function, and no DM no poor physical function). RESULTS: Compared with T1, participants in T3 were significantly older, had a lower education level, had almost three times higher prevalence of DM, slower gait speed, longer chair-stand time, and lower SPPB scores. On multivariate analysis, the odds of having both DM and poor physical performance compared to having no DM and no poor physical performance were significantly higher in GDF-15 T3 vs. GDF-15 T1 (aOR 9.7, 95% CI 1.4-67.7; p = 0.021), and the odds of having DM no poor physical function compared to having no DM and no poor physical performance were significantly higher in GDF-15 T2 (aOR 12.7, 95% CI 1.1-143.7; p = 0.040) independent of BMI, IL-6, TNF-α, nutrition, physical function, education, age, and gender. CONCLUSION: The association of GDF-15 with DM-associated poor physical function is independent of inflammation in prefrail older adults. Its causal-association link needs to be determined in longitudinal studies.
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spelling pubmed-101628692023-05-06 GDF-15 Is Associated with Poor Physical Function in Prefrail Older Adults with Diabetes Merchant, Reshma Aziz Chan, Yiong Huak Duque, Gustavo J Diabetes Res Research Article INTRODUCTION: Growth differentiation factor 15 (GDF-15) has been shown to be a metabolic and appetite regulator in diabetes mellitus (DM) and obesity. We aimed to investigate (i) the association between GDF-15 and DM with and without poor physical function independent of inflammation and (ii) the prediction model for poor physical function in prefrail older adults. METHODS: A cross-sectional study of 108-prefrail participants ≥60 years recruited for multidomain interventions. Data was collected for demographics, cognition, function, frailty, nutrition, handgrip strength (HGS), short physical performance battery (SPPB), and gait speed. Serum concentrations of GDF-15, IL-6, and TNF-α were measured. GDF-15 was classified into tertiles (T1, T2, and T3), and its association was studied with DM and physical function (DM poor physical function, DM no poor physical function, no DM poor physical function, and no DM no poor physical function). RESULTS: Compared with T1, participants in T3 were significantly older, had a lower education level, had almost three times higher prevalence of DM, slower gait speed, longer chair-stand time, and lower SPPB scores. On multivariate analysis, the odds of having both DM and poor physical performance compared to having no DM and no poor physical performance were significantly higher in GDF-15 T3 vs. GDF-15 T1 (aOR 9.7, 95% CI 1.4-67.7; p = 0.021), and the odds of having DM no poor physical function compared to having no DM and no poor physical performance were significantly higher in GDF-15 T2 (aOR 12.7, 95% CI 1.1-143.7; p = 0.040) independent of BMI, IL-6, TNF-α, nutrition, physical function, education, age, and gender. CONCLUSION: The association of GDF-15 with DM-associated poor physical function is independent of inflammation in prefrail older adults. Its causal-association link needs to be determined in longitudinal studies. Hindawi 2023-04-28 /pmc/articles/PMC10162869/ /pubmed/37152099 http://dx.doi.org/10.1155/2023/2519128 Text en Copyright © 2023 Reshma Aziz Merchant et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Merchant, Reshma Aziz
Chan, Yiong Huak
Duque, Gustavo
GDF-15 Is Associated with Poor Physical Function in Prefrail Older Adults with Diabetes
title GDF-15 Is Associated with Poor Physical Function in Prefrail Older Adults with Diabetes
title_full GDF-15 Is Associated with Poor Physical Function in Prefrail Older Adults with Diabetes
title_fullStr GDF-15 Is Associated with Poor Physical Function in Prefrail Older Adults with Diabetes
title_full_unstemmed GDF-15 Is Associated with Poor Physical Function in Prefrail Older Adults with Diabetes
title_short GDF-15 Is Associated with Poor Physical Function in Prefrail Older Adults with Diabetes
title_sort gdf-15 is associated with poor physical function in prefrail older adults with diabetes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10162869/
https://www.ncbi.nlm.nih.gov/pubmed/37152099
http://dx.doi.org/10.1155/2023/2519128
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