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Possible Role of Hyperinsulinemia and Insulin Resistance in Lower Vitamin D Levels in Overweight and Obese Patients

A cohort of 66 healthy overweight and obese patients, 53 women and 13 men were examined. Waist circumference and fasting 25(OH)D, insulin, glucose, lipid (cholesterol, HDL cholesterol, and triglyceride), C-reactive protein (CRP), and complement 3 (C(3)), and 4 (C(4)) serum concentrations were measur...

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Autores principales: De Pergola, Giovanni, Nitti, Alessandro, Bartolomeo, Nicola, Gesuita, Antonella, Giagulli, Vito Angelo, Triggiani, Vincenzo, Guastamacchia, Edoardo, Silvestris, Franco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3581124/
https://www.ncbi.nlm.nih.gov/pubmed/23509804
http://dx.doi.org/10.1155/2013/921348
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author De Pergola, Giovanni
Nitti, Alessandro
Bartolomeo, Nicola
Gesuita, Antonella
Giagulli, Vito Angelo
Triggiani, Vincenzo
Guastamacchia, Edoardo
Silvestris, Franco
author_facet De Pergola, Giovanni
Nitti, Alessandro
Bartolomeo, Nicola
Gesuita, Antonella
Giagulli, Vito Angelo
Triggiani, Vincenzo
Guastamacchia, Edoardo
Silvestris, Franco
author_sort De Pergola, Giovanni
collection PubMed
description A cohort of 66 healthy overweight and obese patients, 53 women and 13 men were examined. Waist circumference and fasting 25(OH)D, insulin, glucose, lipid (cholesterol, HDL cholesterol, and triglyceride), C-reactive protein (CRP), and complement 3 (C(3)), and 4 (C(4)) serum concentrations were measured. Insulin resistance was assessed by the homeostasis model assessment (HOMA(IR)). Results. 25(OH)D levels showed a significant negative correlation with BMI (P < 0.01), waist circumference (P < 0.05), fasting insulin (P < 0.01), HOMA(IR) (P < 0.01), triglycerides (P < 0.01), CRP (P < 0.01), C(3) (P < 0.05), and C(4) (P < 0.05). Multiple regression analyses were performed with 25(OH)D as the dependent variable and BMI (or waist circumferences), fasting insulin (or HOMA(IR)), triglycerides, and CRP (or C(3) or C(4)) as independent variables. Only insulin or HOMA(IR) maintained a significant independent association with 25(OH)D levels, whereas vitamin D did not maintain a significant independent association with CRP or C(3) or C(4) concentrations. Conclusions. The present study, performed in overweight and obese subjects, shows that 25(OH)D levels are negatively associated with inflammatory parameters such as CRP and C(3) and C(4) levels, but not independently of BMI, body fat distribution, insulin levels, or insulin resistance. Our results suggest that hyperinsulinemia and/or insulin resistance are directly responsible for decrease of 25(OH)D levels in obesity.
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spelling pubmed-35811242013-03-18 Possible Role of Hyperinsulinemia and Insulin Resistance in Lower Vitamin D Levels in Overweight and Obese Patients De Pergola, Giovanni Nitti, Alessandro Bartolomeo, Nicola Gesuita, Antonella Giagulli, Vito Angelo Triggiani, Vincenzo Guastamacchia, Edoardo Silvestris, Franco Biomed Res Int Research Article A cohort of 66 healthy overweight and obese patients, 53 women and 13 men were examined. Waist circumference and fasting 25(OH)D, insulin, glucose, lipid (cholesterol, HDL cholesterol, and triglyceride), C-reactive protein (CRP), and complement 3 (C(3)), and 4 (C(4)) serum concentrations were measured. Insulin resistance was assessed by the homeostasis model assessment (HOMA(IR)). Results. 25(OH)D levels showed a significant negative correlation with BMI (P < 0.01), waist circumference (P < 0.05), fasting insulin (P < 0.01), HOMA(IR) (P < 0.01), triglycerides (P < 0.01), CRP (P < 0.01), C(3) (P < 0.05), and C(4) (P < 0.05). Multiple regression analyses were performed with 25(OH)D as the dependent variable and BMI (or waist circumferences), fasting insulin (or HOMA(IR)), triglycerides, and CRP (or C(3) or C(4)) as independent variables. Only insulin or HOMA(IR) maintained a significant independent association with 25(OH)D levels, whereas vitamin D did not maintain a significant independent association with CRP or C(3) or C(4) concentrations. Conclusions. The present study, performed in overweight and obese subjects, shows that 25(OH)D levels are negatively associated with inflammatory parameters such as CRP and C(3) and C(4) levels, but not independently of BMI, body fat distribution, insulin levels, or insulin resistance. Our results suggest that hyperinsulinemia and/or insulin resistance are directly responsible for decrease of 25(OH)D levels in obesity. Hindawi Publishing Corporation 2013 2013-01-14 /pmc/articles/PMC3581124/ /pubmed/23509804 http://dx.doi.org/10.1155/2013/921348 Text en Copyright © 2013 Giovanni De Pergola et al. https://creativecommons.org/licenses/by/3.0/ 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
De Pergola, Giovanni
Nitti, Alessandro
Bartolomeo, Nicola
Gesuita, Antonella
Giagulli, Vito Angelo
Triggiani, Vincenzo
Guastamacchia, Edoardo
Silvestris, Franco
Possible Role of Hyperinsulinemia and Insulin Resistance in Lower Vitamin D Levels in Overweight and Obese Patients
title Possible Role of Hyperinsulinemia and Insulin Resistance in Lower Vitamin D Levels in Overweight and Obese Patients
title_full Possible Role of Hyperinsulinemia and Insulin Resistance in Lower Vitamin D Levels in Overweight and Obese Patients
title_fullStr Possible Role of Hyperinsulinemia and Insulin Resistance in Lower Vitamin D Levels in Overweight and Obese Patients
title_full_unstemmed Possible Role of Hyperinsulinemia and Insulin Resistance in Lower Vitamin D Levels in Overweight and Obese Patients
title_short Possible Role of Hyperinsulinemia and Insulin Resistance in Lower Vitamin D Levels in Overweight and Obese Patients
title_sort possible role of hyperinsulinemia and insulin resistance in lower vitamin d levels in overweight and obese patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3581124/
https://www.ncbi.nlm.nih.gov/pubmed/23509804
http://dx.doi.org/10.1155/2013/921348
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