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Role of adiponectin and free fatty acids on the association between abdominal visceral fat and insulin resistance

BACKGROUND: Experimental studies have shown that high free fatty acid (FFA) and low adiponectin (ADIPO) levels are involved in the mechanisms by which adiposity promotes insulin resistance (IR). However, no previous clinical studies have simultaneously analysed the relative contribution of FFA and A...

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Autores principales: Medina-Urrutia, Aida, Posadas-Romero, Carlos, Posadas-Sánchez, Rosalinda, Jorge-Galarza, Esteban, Villarreal-Molina, Teresa, González-Salazar, María del Carmen, Cardoso-Saldaña, Guillermo, Vargas-Alarcón, Gilberto, Torres-Tamayo, Margarita, Juárez-Rojas, Juan Gabriel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4332423/
https://www.ncbi.nlm.nih.gov/pubmed/25849597
http://dx.doi.org/10.1186/s12933-015-0184-5
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author Medina-Urrutia, Aida
Posadas-Romero, Carlos
Posadas-Sánchez, Rosalinda
Jorge-Galarza, Esteban
Villarreal-Molina, Teresa
González-Salazar, María del Carmen
Cardoso-Saldaña, Guillermo
Vargas-Alarcón, Gilberto
Torres-Tamayo, Margarita
Juárez-Rojas, Juan Gabriel
author_facet Medina-Urrutia, Aida
Posadas-Romero, Carlos
Posadas-Sánchez, Rosalinda
Jorge-Galarza, Esteban
Villarreal-Molina, Teresa
González-Salazar, María del Carmen
Cardoso-Saldaña, Guillermo
Vargas-Alarcón, Gilberto
Torres-Tamayo, Margarita
Juárez-Rojas, Juan Gabriel
author_sort Medina-Urrutia, Aida
collection PubMed
description BACKGROUND: Experimental studies have shown that high free fatty acid (FFA) and low adiponectin (ADIPO) levels are involved in the mechanisms by which adiposity promotes insulin resistance (IR). However, no previous clinical studies have simultaneously analysed the relative contribution of FFA and ADIPO levels on the relation of abdominal visceral fat (AVF) with insulin resistance. OBJECTIVE: To analyse the contribution of low ADIPO (adiponectin < =p25th: 8.67 μg/mL in women and 5.30 μg/mL in men), and high FFAs (FFAs > =p75th: 0.745 mEq/L in women and 0.60 mEq/L in men) to the association of high AVF (AVF > =p75th: 127 cm(2) in women; 152.7 cm(2) in men) with insulin resistance (HOMA-IR > =75th: 3.58 in women and 3.12 in men), in non-diabetic subjects. MATERIAL AND METHODS: A cross-sectional analysis was performed including 1217 control participants of the Genetics of Atherosclerotic Disease study (GEA). Clinical, tomographic and biochemical parameters were measured in all participants. Logistic regression models were used to assess the association of high AVF with IR stratifying according to gender, and to normal or low ADIPO and normal or high FFA serum levels. RESULTS: In comparison to referent group, in men low ADIPO unlike high FFA increased the risk of IR. Females with normal AVF and low ADIPO, or high AVF and normal ADIPO had aprox 3 folds risk of IR (OR [IC95%]: 3.7 [2.1-6.6], p < 0.001, and 3.4 [2.0-5.7], p < 0.001; respectively). The risk increased to 7.6 [4.2-13.8], p < 0.001 when high AVF and low ADIPO were present. Irrespective of AVF, the effect of low ADIPO on IR was higher than that seen for high FFA. Besides, our results suggest an additive effect of high AVF, high FFA and low ADIPO on the IR prevalence. CONCLUSIONS: The present study provides novel and important information about the combined effect of high AVF and low ADIPO on the risk of IR. Furthermore, our data suggest that the effect of low adiponectin levels on the high AVF-IR association is stronger than that observed for high FFA, suggesting that adiponectin could be used as biomarker to identify subjects at high risk for T2DM and CAD.
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spelling pubmed-43324232015-02-19 Role of adiponectin and free fatty acids on the association between abdominal visceral fat and insulin resistance Medina-Urrutia, Aida Posadas-Romero, Carlos Posadas-Sánchez, Rosalinda Jorge-Galarza, Esteban Villarreal-Molina, Teresa González-Salazar, María del Carmen Cardoso-Saldaña, Guillermo Vargas-Alarcón, Gilberto Torres-Tamayo, Margarita Juárez-Rojas, Juan Gabriel Cardiovasc Diabetol Original Investigation BACKGROUND: Experimental studies have shown that high free fatty acid (FFA) and low adiponectin (ADIPO) levels are involved in the mechanisms by which adiposity promotes insulin resistance (IR). However, no previous clinical studies have simultaneously analysed the relative contribution of FFA and ADIPO levels on the relation of abdominal visceral fat (AVF) with insulin resistance. OBJECTIVE: To analyse the contribution of low ADIPO (adiponectin < =p25th: 8.67 μg/mL in women and 5.30 μg/mL in men), and high FFAs (FFAs > =p75th: 0.745 mEq/L in women and 0.60 mEq/L in men) to the association of high AVF (AVF > =p75th: 127 cm(2) in women; 152.7 cm(2) in men) with insulin resistance (HOMA-IR > =75th: 3.58 in women and 3.12 in men), in non-diabetic subjects. MATERIAL AND METHODS: A cross-sectional analysis was performed including 1217 control participants of the Genetics of Atherosclerotic Disease study (GEA). Clinical, tomographic and biochemical parameters were measured in all participants. Logistic regression models were used to assess the association of high AVF with IR stratifying according to gender, and to normal or low ADIPO and normal or high FFA serum levels. RESULTS: In comparison to referent group, in men low ADIPO unlike high FFA increased the risk of IR. Females with normal AVF and low ADIPO, or high AVF and normal ADIPO had aprox 3 folds risk of IR (OR [IC95%]: 3.7 [2.1-6.6], p < 0.001, and 3.4 [2.0-5.7], p < 0.001; respectively). The risk increased to 7.6 [4.2-13.8], p < 0.001 when high AVF and low ADIPO were present. Irrespective of AVF, the effect of low ADIPO on IR was higher than that seen for high FFA. Besides, our results suggest an additive effect of high AVF, high FFA and low ADIPO on the IR prevalence. CONCLUSIONS: The present study provides novel and important information about the combined effect of high AVF and low ADIPO on the risk of IR. Furthermore, our data suggest that the effect of low adiponectin levels on the high AVF-IR association is stronger than that observed for high FFA, suggesting that adiponectin could be used as biomarker to identify subjects at high risk for T2DM and CAD. BioMed Central 2015-02-10 /pmc/articles/PMC4332423/ /pubmed/25849597 http://dx.doi.org/10.1186/s12933-015-0184-5 Text en © Medina-Urrutia et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Original Investigation
Medina-Urrutia, Aida
Posadas-Romero, Carlos
Posadas-Sánchez, Rosalinda
Jorge-Galarza, Esteban
Villarreal-Molina, Teresa
González-Salazar, María del Carmen
Cardoso-Saldaña, Guillermo
Vargas-Alarcón, Gilberto
Torres-Tamayo, Margarita
Juárez-Rojas, Juan Gabriel
Role of adiponectin and free fatty acids on the association between abdominal visceral fat and insulin resistance
title Role of adiponectin and free fatty acids on the association between abdominal visceral fat and insulin resistance
title_full Role of adiponectin and free fatty acids on the association between abdominal visceral fat and insulin resistance
title_fullStr Role of adiponectin and free fatty acids on the association between abdominal visceral fat and insulin resistance
title_full_unstemmed Role of adiponectin and free fatty acids on the association between abdominal visceral fat and insulin resistance
title_short Role of adiponectin and free fatty acids on the association between abdominal visceral fat and insulin resistance
title_sort role of adiponectin and free fatty acids on the association between abdominal visceral fat and insulin resistance
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4332423/
https://www.ncbi.nlm.nih.gov/pubmed/25849597
http://dx.doi.org/10.1186/s12933-015-0184-5
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