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Contribution of markers of adiposopathy and adipose cell size in predicting insulin resistance in women of varying age and adiposity
Adipose tissue (AT) dysfunctions, such as adipocyte hypertrophy, macrophage infiltration and secretory adiposopathy (low plasma adiponectin/leptin, A/L, ratio), associate with metabolic disorders. However, no study has compared the relative contribution of these markers to cardiometabolic risk in wo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9037496/ https://www.ncbi.nlm.nih.gov/pubmed/35436409 http://dx.doi.org/10.1080/21623945.2022.2059902 |
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author | Tremblay, Eve-Julie Tchernof, André Pelletier, Mélissa Chabot, Nicolas Joanisse, Denis R. Mauriège, Pascale |
author_facet | Tremblay, Eve-Julie Tchernof, André Pelletier, Mélissa Chabot, Nicolas Joanisse, Denis R. Mauriège, Pascale |
author_sort | Tremblay, Eve-Julie |
collection | PubMed |
description | Adipose tissue (AT) dysfunctions, such as adipocyte hypertrophy, macrophage infiltration and secretory adiposopathy (low plasma adiponectin/leptin, A/L, ratio), associate with metabolic disorders. However, no study has compared the relative contribution of these markers to cardiometabolic risk in women of varying age and adiposity. Body composition, regional AT distribution, lipid-lipoprotein profile, glucose homeostasis and plasma A and L levels were determined in 67 women (age: 40-62 years; BMI: 17-41 kg/m(2)). Expression of macrophage infiltration marker CD68 and adipocyte size were measured from subcutaneous abdominal (SCABD) and omental (OME) fat. AT dysfunction markers correlated with most lipid-lipoprotein levels. The A/L ratio was negatively associated with fasting insulinemia and HOMA-IR, while SCABD or OME adipocyte size and SCABD CD68 expression were positively related to these variables. Combination of tertiles of largest adipocyte size and lowest A/L ratio showed the highest HOMA-IR. Multiple regression analyses including these markers and TAG levels revealed that the A/L ratio was the only predictor of fasting insulinemia and HOMA-IR. The contribution of the A/L ratio was superseded by adipose cell size in the model where the latter replaced TAGs. Finally, leptinemia was a better predictor of IR than adipocyte size and the A/L ratio in our participants sample. |
format | Online Article Text |
id | pubmed-9037496 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-90374962022-04-26 Contribution of markers of adiposopathy and adipose cell size in predicting insulin resistance in women of varying age and adiposity Tremblay, Eve-Julie Tchernof, André Pelletier, Mélissa Chabot, Nicolas Joanisse, Denis R. Mauriège, Pascale Adipocyte Research Paper Adipose tissue (AT) dysfunctions, such as adipocyte hypertrophy, macrophage infiltration and secretory adiposopathy (low plasma adiponectin/leptin, A/L, ratio), associate with metabolic disorders. However, no study has compared the relative contribution of these markers to cardiometabolic risk in women of varying age and adiposity. Body composition, regional AT distribution, lipid-lipoprotein profile, glucose homeostasis and plasma A and L levels were determined in 67 women (age: 40-62 years; BMI: 17-41 kg/m(2)). Expression of macrophage infiltration marker CD68 and adipocyte size were measured from subcutaneous abdominal (SCABD) and omental (OME) fat. AT dysfunction markers correlated with most lipid-lipoprotein levels. The A/L ratio was negatively associated with fasting insulinemia and HOMA-IR, while SCABD or OME adipocyte size and SCABD CD68 expression were positively related to these variables. Combination of tertiles of largest adipocyte size and lowest A/L ratio showed the highest HOMA-IR. Multiple regression analyses including these markers and TAG levels revealed that the A/L ratio was the only predictor of fasting insulinemia and HOMA-IR. The contribution of the A/L ratio was superseded by adipose cell size in the model where the latter replaced TAGs. Finally, leptinemia was a better predictor of IR than adipocyte size and the A/L ratio in our participants sample. Taylor & Francis 2022-04-18 /pmc/articles/PMC9037496/ /pubmed/35436409 http://dx.doi.org/10.1080/21623945.2022.2059902 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Tremblay, Eve-Julie Tchernof, André Pelletier, Mélissa Chabot, Nicolas Joanisse, Denis R. Mauriège, Pascale Contribution of markers of adiposopathy and adipose cell size in predicting insulin resistance in women of varying age and adiposity |
title | Contribution of markers of adiposopathy and adipose cell size in predicting insulin resistance in women of varying age and adiposity |
title_full | Contribution of markers of adiposopathy and adipose cell size in predicting insulin resistance in women of varying age and adiposity |
title_fullStr | Contribution of markers of adiposopathy and adipose cell size in predicting insulin resistance in women of varying age and adiposity |
title_full_unstemmed | Contribution of markers of adiposopathy and adipose cell size in predicting insulin resistance in women of varying age and adiposity |
title_short | Contribution of markers of adiposopathy and adipose cell size in predicting insulin resistance in women of varying age and adiposity |
title_sort | contribution of markers of adiposopathy and adipose cell size in predicting insulin resistance in women of varying age and adiposity |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9037496/ https://www.ncbi.nlm.nih.gov/pubmed/35436409 http://dx.doi.org/10.1080/21623945.2022.2059902 |
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