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Sex-specific modulation of circulating growth differentiation factor-15 in patients with type 2 diabetes and/or obesity

OBJECTIVE: Growth differentiation factor-15 (GDF15), a key metabolic regulator, is associated with obesity and diabetes in which sex-specific differences have been reported. Thus, we assessed whether GDF15 could be dependent on sex in diabetes and/or obesity groups. METHODS: We measured serum GDF15...

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Autores principales: Asrih, Mohamed, Sinturel, Flore, Dubos, Richard, Guessous, Idris, Pataky, Zoltan, Dibner, Charna, Jornayvaz, François R, Gariani, Karim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9346339/
https://www.ncbi.nlm.nih.gov/pubmed/35700236
http://dx.doi.org/10.1530/EC-22-0054
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author Asrih, Mohamed
Sinturel, Flore
Dubos, Richard
Guessous, Idris
Pataky, Zoltan
Dibner, Charna
Jornayvaz, François R
Gariani, Karim
author_facet Asrih, Mohamed
Sinturel, Flore
Dubos, Richard
Guessous, Idris
Pataky, Zoltan
Dibner, Charna
Jornayvaz, François R
Gariani, Karim
author_sort Asrih, Mohamed
collection PubMed
description OBJECTIVE: Growth differentiation factor-15 (GDF15), a key metabolic regulator, is associated with obesity and diabetes in which sex-specific differences have been reported. Thus, we assessed whether GDF15 could be dependent on sex in diabetes and/or obesity groups. METHODS: We measured serum GDF15 levels by ELISA in eight lean women and men (n = 16), eight women and eight men having obesity (n = 16), eight women and eight men with type 2 diabetes (T2D, n = 16), and seven women and nine men with both diabetes and obesity (n = 16). Estimation of the difference in the means of each group was performed by two-way ANOVA. The interdependence of the different variates was addressed by multivariate analysis. Correlations between GDF15 levels and HOMA-IR, HbA1c, triglycerides, HDL, and LDL were explored by linear regression. RESULTS: Being a woman and having obesity alone or in combination with diabetes decreased GDF15 serum levels (β = −0.47, CI = −0.95, 0.00, P = 0.052; β = −0.45, CI = −0.94, 0.05, P= 0.075). Diabetes independently of metformin treatment and obesity were not predictive of low GDF15 levels (β = 0.10, CI = −0.36, 0.57, P = 0.7). Correlation analysis showed that HOMA-IR (r = 0.45, P = 0.008) and triglycerides (r = 0.41, P = 0.017) were positively correlated and HDL (r = −0.48, P = 0.005) was negatively correlated with GDF15 levels in men. CONCLUSIONS/INTERPRETATION: GDF15 level was significantly different between men and women, as well as between the groups. Sex and group interaction revealed that being a woman and having obesity alone or in combination with diabetes decreased GDF15 levels.
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spelling pubmed-93463392022-08-03 Sex-specific modulation of circulating growth differentiation factor-15 in patients with type 2 diabetes and/or obesity Asrih, Mohamed Sinturel, Flore Dubos, Richard Guessous, Idris Pataky, Zoltan Dibner, Charna Jornayvaz, François R Gariani, Karim Endocr Connect Research OBJECTIVE: Growth differentiation factor-15 (GDF15), a key metabolic regulator, is associated with obesity and diabetes in which sex-specific differences have been reported. Thus, we assessed whether GDF15 could be dependent on sex in diabetes and/or obesity groups. METHODS: We measured serum GDF15 levels by ELISA in eight lean women and men (n = 16), eight women and eight men having obesity (n = 16), eight women and eight men with type 2 diabetes (T2D, n = 16), and seven women and nine men with both diabetes and obesity (n = 16). Estimation of the difference in the means of each group was performed by two-way ANOVA. The interdependence of the different variates was addressed by multivariate analysis. Correlations between GDF15 levels and HOMA-IR, HbA1c, triglycerides, HDL, and LDL were explored by linear regression. RESULTS: Being a woman and having obesity alone or in combination with diabetes decreased GDF15 serum levels (β = −0.47, CI = −0.95, 0.00, P = 0.052; β = −0.45, CI = −0.94, 0.05, P= 0.075). Diabetes independently of metformin treatment and obesity were not predictive of low GDF15 levels (β = 0.10, CI = −0.36, 0.57, P = 0.7). Correlation analysis showed that HOMA-IR (r = 0.45, P = 0.008) and triglycerides (r = 0.41, P = 0.017) were positively correlated and HDL (r = −0.48, P = 0.005) was negatively correlated with GDF15 levels in men. CONCLUSIONS/INTERPRETATION: GDF15 level was significantly different between men and women, as well as between the groups. Sex and group interaction revealed that being a woman and having obesity alone or in combination with diabetes decreased GDF15 levels. Bioscientifica Ltd 2022-06-13 /pmc/articles/PMC9346339/ /pubmed/35700236 http://dx.doi.org/10.1530/EC-22-0054 Text en © The authors https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. (https://creativecommons.org/licenses/by-nc/4.0/)
spellingShingle Research
Asrih, Mohamed
Sinturel, Flore
Dubos, Richard
Guessous, Idris
Pataky, Zoltan
Dibner, Charna
Jornayvaz, François R
Gariani, Karim
Sex-specific modulation of circulating growth differentiation factor-15 in patients with type 2 diabetes and/or obesity
title Sex-specific modulation of circulating growth differentiation factor-15 in patients with type 2 diabetes and/or obesity
title_full Sex-specific modulation of circulating growth differentiation factor-15 in patients with type 2 diabetes and/or obesity
title_fullStr Sex-specific modulation of circulating growth differentiation factor-15 in patients with type 2 diabetes and/or obesity
title_full_unstemmed Sex-specific modulation of circulating growth differentiation factor-15 in patients with type 2 diabetes and/or obesity
title_short Sex-specific modulation of circulating growth differentiation factor-15 in patients with type 2 diabetes and/or obesity
title_sort sex-specific modulation of circulating growth differentiation factor-15 in patients with type 2 diabetes and/or obesity
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9346339/
https://www.ncbi.nlm.nih.gov/pubmed/35700236
http://dx.doi.org/10.1530/EC-22-0054
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