Serum 25-Hydroxyvitamin D and Adipose Tissue Vitamin D Receptor Gene Expression: Relationship With Obesity and Type 2 Diabetes
Context:The relationship between 25-hydroxyvitamin D [25(OH)D] and obesity and type 2 diabetes is not completely understood. Vitamin D receptor (VDR) expression in adipose tissue (AT) is related to obesity and might be regulated by 1,25-dihydroxyvitamin D3 [1,25(OH)2D3].Objective:To analyze serum 25...
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Published in | The journal of clinical endocrinology and metabolism Vol. 100; no. 4; pp. E591 - E595 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Oxford University Press
01.04.2015
Copyright by The Endocrine Society |
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Abstract | Context:The relationship between 25-hydroxyvitamin D [25(OH)D] and obesity and type 2 diabetes is not completely understood. Vitamin D receptor (VDR) expression in adipose tissue (AT) is related to obesity and might be regulated by 1,25-dihydroxyvitamin D3 [1,25(OH)2D3].Objective:To analyze serum 25(OH)D and VDR gene expression in AT according to body mass index (BMI) and glycemic status and the effect of 1,25(OH)2D3 on AT according to BMI.Design and Patients:Two cohorts were studied: 1) 118 subjects classified according to their BMI (lean, overweight, obese, or morbidly obese [MO]) and their glycemic status (normoglycemic [NG] and prediabetic and diabetic [P&D]); and 2) 30 obese subjects (BMI > 30 kg/m2) classified as NG and P&D. VDR gene expression was analyzed during preadipocyte differentiation and in vitro stimulation with 1,25(OH)2D3 of AT explants from donors with different BMI values.Setting:University Hospital.Main Outcome Measures:Serum 25(OH)D, parathyroid hormone (PTH), and AT VDR gene expression.Results:25(OH)D levels were lower in P&D than NG subjects, significantly so in the lean and MO groups (P < .05). 25(OH)D levels correlated negatively with homeostasis model of assessment for insulin resistance (HOMA-IR) (r = −0.200; P = .032) and glucose (r = −0.295; P = .001), but not with BMI. VDR gene expression was higher in MO than in the other BMI groups (P < .05). 1,25(OH)2D3 increased VDR gene expression in AT from obese patients (P < .05) but not from lean subjects.Conclusions:25(OH)D levels are diminished in P&D compared to NG subjects, independently of BMI, and are closely related to glucose metabolism variables, suggesting that vitamin D deficiency is associated more with carbohydrate metabolism than with obesity. Moreover, AT has a different response to 1,25(OH)2D3 depending on the degree of obesity. |
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AbstractList | CONTEXT:The relationship between 25-hydroxyvitamin D [25(OH)D] and obesity and type 2 diabetes is not completely understood. Vitamin D receptor (VDR) expression in adipose tissue (AT) is related to obesity and might be regulated by 1,25-dihydroxyvitamin D3 [1,25(OH)2D3].
OBJECTIVE:To analyze serum 25(OH)D and VDR gene expression in AT according to body mass index (BMI) and glycemic status and the effect of 1,25(OH)2D3 on AT according to BMI.
DESIGN AND PATIENTS:Two cohorts were studied1) 118 subjects classified according to their BMI (lean, overweight, obese, or morbidly obese [MO]) and their glycemic status (normoglycemic [NG] and prediabetic and diabetic [P&D]); and 2) 30 obese subjects (BMI > 30 kg/m) classified as NG and P&D. VDR gene expression was analyzed during preadipocyte differentiation and in vitro stimulation with 1,25(OH)2D3 of AT explants from donors with different BMI values.
SETTING:University Hospital.
MAIN OUTCOME MEASURES:Serum 25(OH)D, parathyroid hormone (PTH), and AT VDR gene expression.
RESULTS:25(OH)D levels were lower in P&D than NG subjects, significantly so in the lean and MO groups (P < .05). 25(OH)D levels correlated negatively with homeostasis model of assessment for insulin resistance (HOMA-IR) (r = −0.200; P = .032) and glucose (r = −0.295; P = .001), but not with BMI. VDR gene expression was higher in MO than in the other BMI groups (P < .05). 1,25(OH)2D3 increased VDR gene expression in AT from obese patients (P < .05) but not from lean subjects.
CONCLUSIONS:25(OH)D levels are diminished in P&D compared to NG subjects, independently of BMI, and are closely related to glucose metabolism variables, suggesting that vitamin D deficiency is associated more with carbohydrate metabolism than with obesity. Moreover, AT has a different response to 1,25(OH)2D3 depending on the degree of obesity. The relationship between 25-hydroxyvitamin D [25(OH)D] and obesity and type 2 diabetes is not completely understood. Vitamin D receptor (VDR) expression in adipose tissue (AT) is related to obesity and might be regulated by 1,25-dihydroxyvitamin D3 [1,25(OH)2D3].CONTEXTThe relationship between 25-hydroxyvitamin D [25(OH)D] and obesity and type 2 diabetes is not completely understood. Vitamin D receptor (VDR) expression in adipose tissue (AT) is related to obesity and might be regulated by 1,25-dihydroxyvitamin D3 [1,25(OH)2D3].To analyze serum 25(OH)D and VDR gene expression in AT according to body mass index (BMI) and glycemic status and the effect of 1,25(OH)2D3 on AT according to BMI.OBJECTIVETo analyze serum 25(OH)D and VDR gene expression in AT according to body mass index (BMI) and glycemic status and the effect of 1,25(OH)2D3 on AT according to BMI.Two cohorts were studied: 1) 118 subjects classified according to their BMI (lean, overweight, obese, or morbidly obese [MO]) and their glycemic status (normoglycemic [NG] and prediabetic and diabetic [P&D]); and 2) 30 obese subjects (BMI > 30 kg/m(2)) classified as NG and P&D. VDR gene expression was analyzed during preadipocyte differentiation and in vitro stimulation with 1,25(OH)2D3 of AT explants from donors with different BMI values.DESIGN AND PATIENTSTwo cohorts were studied: 1) 118 subjects classified according to their BMI (lean, overweight, obese, or morbidly obese [MO]) and their glycemic status (normoglycemic [NG] and prediabetic and diabetic [P&D]); and 2) 30 obese subjects (BMI > 30 kg/m(2)) classified as NG and P&D. VDR gene expression was analyzed during preadipocyte differentiation and in vitro stimulation with 1,25(OH)2D3 of AT explants from donors with different BMI values.University Hospital.SETTINGUniversity Hospital.Serum 25(OH)D, parathyroid hormone (PTH), and AT VDR gene expression.MAIN OUTCOME MEASURESSerum 25(OH)D, parathyroid hormone (PTH), and AT VDR gene expression.25(OH)D levels were lower in P&D than NG subjects, significantly so in the lean and MO groups (P < .05). 25(OH)D levels correlated negatively with homeostasis model of assessment for insulin resistance (HOMA-IR) (r = -0.200; P = .032) and glucose (r = -0.295; P = .001), but not with BMI. VDR gene expression was higher in MO than in the other BMI groups (P < .05). 1,25(OH)2D3 increased VDR gene expression in AT from obese patients (P < .05) but not from lean subjects.RESULTS25(OH)D levels were lower in P&D than NG subjects, significantly so in the lean and MO groups (P < .05). 25(OH)D levels correlated negatively with homeostasis model of assessment for insulin resistance (HOMA-IR) (r = -0.200; P = .032) and glucose (r = -0.295; P = .001), but not with BMI. VDR gene expression was higher in MO than in the other BMI groups (P < .05). 1,25(OH)2D3 increased VDR gene expression in AT from obese patients (P < .05) but not from lean subjects.25(OH)D levels are diminished in P&D compared to NG subjects, independently of BMI, and are closely related to glucose metabolism variables, suggesting that vitamin D deficiency is associated more with carbohydrate metabolism than with obesity. Moreover, AT has a different response to 1,25(OH)2D3 depending on the degree of obesity.CONCLUSIONS25(OH)D levels are diminished in P&D compared to NG subjects, independently of BMI, and are closely related to glucose metabolism variables, suggesting that vitamin D deficiency is associated more with carbohydrate metabolism than with obesity. Moreover, AT has a different response to 1,25(OH)2D3 depending on the degree of obesity. Context:The relationship between 25-hydroxyvitamin D [25(OH)D] and obesity and type 2 diabetes is not completely understood. Vitamin D receptor (VDR) expression in adipose tissue (AT) is related to obesity and might be regulated by 1,25-dihydroxyvitamin D3 [1,25(OH)2D3].Objective:To analyze serum 25(OH)D and VDR gene expression in AT according to body mass index (BMI) and glycemic status and the effect of 1,25(OH)2D3 on AT according to BMI.Design and Patients:Two cohorts were studied: 1) 118 subjects classified according to their BMI (lean, overweight, obese, or morbidly obese [MO]) and their glycemic status (normoglycemic [NG] and prediabetic and diabetic [P&D]); and 2) 30 obese subjects (BMI > 30 kg/m2) classified as NG and P&D. VDR gene expression was analyzed during preadipocyte differentiation and in vitro stimulation with 1,25(OH)2D3 of AT explants from donors with different BMI values.Setting:University Hospital.Main Outcome Measures:Serum 25(OH)D, parathyroid hormone (PTH), and AT VDR gene expression.Results:25(OH)D levels were lower in P&D than NG subjects, significantly so in the lean and MO groups (P < .05). 25(OH)D levels correlated negatively with homeostasis model of assessment for insulin resistance (HOMA-IR) (r = −0.200; P = .032) and glucose (r = −0.295; P = .001), but not with BMI. VDR gene expression was higher in MO than in the other BMI groups (P < .05). 1,25(OH)2D3 increased VDR gene expression in AT from obese patients (P < .05) but not from lean subjects.Conclusions:25(OH)D levels are diminished in P&D compared to NG subjects, independently of BMI, and are closely related to glucose metabolism variables, suggesting that vitamin D deficiency is associated more with carbohydrate metabolism than with obesity. Moreover, AT has a different response to 1,25(OH)2D3 depending on the degree of obesity. The relationship between 25-hydroxyvitamin D [25(OH)D] and obesity and type 2 diabetes is not completely understood. Vitamin D receptor (VDR) expression in adipose tissue (AT) is related to obesity and might be regulated by 1,25-dihydroxyvitamin D3 [1,25(OH)2D3]. To analyze serum 25(OH)D and VDR gene expression in AT according to body mass index (BMI) and glycemic status and the effect of 1,25(OH)2D3 on AT according to BMI. Two cohorts were studied: 1) 118 subjects classified according to their BMI (lean, overweight, obese, or morbidly obese [MO]) and their glycemic status (normoglycemic [NG] and prediabetic and diabetic [P&D]); and 2) 30 obese subjects (BMI > 30 kg/m(2)) classified as NG and P&D. VDR gene expression was analyzed during preadipocyte differentiation and in vitro stimulation with 1,25(OH)2D3 of AT explants from donors with different BMI values. University Hospital. Serum 25(OH)D, parathyroid hormone (PTH), and AT VDR gene expression. 25(OH)D levels were lower in P&D than NG subjects, significantly so in the lean and MO groups (P < .05). 25(OH)D levels correlated negatively with homeostasis model of assessment for insulin resistance (HOMA-IR) (r = -0.200; P = .032) and glucose (r = -0.295; P = .001), but not with BMI. VDR gene expression was higher in MO than in the other BMI groups (P < .05). 1,25(OH)2D3 increased VDR gene expression in AT from obese patients (P < .05) but not from lean subjects. 25(OH)D levels are diminished in P&D compared to NG subjects, independently of BMI, and are closely related to glucose metabolism variables, suggesting that vitamin D deficiency is associated more with carbohydrate metabolism than with obesity. Moreover, AT has a different response to 1,25(OH)2D3 depending on the degree of obesity. |
Author | Clemente-Postigo, Mercedes Cardona, Fernando Muñoz-Garach, Araceli Garriga, Nuria Serrano, Marta Castellano-Castillo, Daniel Fernández-Real, Jose M. Tinahones, Francisco J. Bernal-López, M. Rosa Fernández-García, Diego Garrido-Sánchez, Lourdes Camargo, Antonio Moreno-Santos, Inmaculada Macías-González, Manuel |
AuthorAffiliation | Unidad de Gestión Clínica Endocrinología y Nutrición (M.C.-P., A.M.-G., L.G.-S., D.F.-G., D.C.-C., F.C., F.J.T., M.M.-G.), Instituto de Investigación Biomédica de Málaga (IBIMA), Complejo Hospitalario de Málaga (Virgen de la Victoria)/Universidad de Málaga, 29010 Málaga, Spain; Centro de Investigación Biomédica En Red, Pathophysiology of Obesity and Nutrition (CB06/03) (M.C.-P., L.G.-S., D.F.-G., A.C., J.M.F.-R., F.C., F.J.T., M.M.-G.), 28029, Madrid, Spain; Service of Diabetes, Endocrinology, and Nutrition (M.S., N.G., J.M.F.-R.), Institut dʼInvestigació Biomédica de Girona, 17007 Girona, Spain; Biomedical Research Laboratory (M.R.B.-L.), Internal Medicine Department, IBIMA, Regional University Hospital of Malaga (Carlos Haya Hospital), Universidad de Málaga, 29010 Málaga, Spain; Área del Corazón del Complejo Hospitalario de Málaga (Virgen de la Victoria) (I.M.-S.), IBIMA/Universidad de Malaga, Red de Investigación Cardiovascular, 29010 Málaga, Spain; and Lipid and Atherosclerosis Res |
AuthorAffiliation_xml | – name: Unidad de Gestión Clínica Endocrinología y Nutrición (M.C.-P., A.M.-G., L.G.-S., D.F.-G., D.C.-C., F.C., F.J.T., M.M.-G.), Instituto de Investigación Biomédica de Málaga (IBIMA), Complejo Hospitalario de Málaga (Virgen de la Victoria)/Universidad de Málaga, 29010 Málaga, Spain; Centro de Investigación Biomédica En Red, Pathophysiology of Obesity and Nutrition (CB06/03) (M.C.-P., L.G.-S., D.F.-G., A.C., J.M.F.-R., F.C., F.J.T., M.M.-G.), 28029, Madrid, Spain; Service of Diabetes, Endocrinology, and Nutrition (M.S., N.G., J.M.F.-R.), Institut dʼInvestigació Biomédica de Girona, 17007 Girona, Spain; Biomedical Research Laboratory (M.R.B.-L.), Internal Medicine Department, IBIMA, Regional University Hospital of Malaga (Carlos Haya Hospital), Universidad de Málaga, 29010 Málaga, Spain; Área del Corazón del Complejo Hospitalario de Málaga (Virgen de la Victoria) (I.M.-S.), IBIMA/Universidad de Malaga, Red de Investigación Cardiovascular, 29010 Málaga, Spain; and Lipid and Atherosclerosis Research Unit (IMIBIC) (A.C.), Reina Sofia University Hospital, University of Cordoba, 14004 Cordoba, Spain |
Author_xml | – sequence: 1 givenname: Mercedes surname: Clemente-Postigo fullname: Clemente-Postigo, Mercedes organization: 1Unidad de Gestión Clínica Endocrinología y Nutrición (M.C.-P., A.M.-G., L.G.-S., D.F.-G., D.C.-C., F.C., F.J.T., M.M.-G.), Instituto de Investigación Biomédica de Málaga (IBIMA), Complejo Hospitalario de Málaga (Virgen de la Victoria)/Universidad de Málaga, 29010 Málaga, Spain – sequence: 2 givenname: Araceli surname: Muñoz-Garach fullname: Muñoz-Garach, Araceli organization: 1Unidad de Gestión Clínica Endocrinología y Nutrición (M.C.-P., A.M.-G., L.G.-S., D.F.-G., D.C.-C., F.C., F.J.T., M.M.-G.), Instituto de Investigación Biomédica de Málaga (IBIMA), Complejo Hospitalario de Málaga (Virgen de la Victoria)/Universidad de Málaga, 29010 Málaga, Spain – sequence: 3 givenname: Marta surname: Serrano fullname: Serrano, Marta organization: 3Service of Diabetes, Endocrinology, and Nutrition (M.S., N.G., J.M.F.-R.), Institut d'Investigació Biomédica de Girona, 17007 Girona, Spain – sequence: 4 givenname: Lourdes surname: Garrido-Sánchez fullname: Garrido-Sánchez, Lourdes organization: 1Unidad de Gestión Clínica Endocrinología y Nutrición (M.C.-P., A.M.-G., L.G.-S., D.F.-G., D.C.-C., F.C., F.J.T., M.M.-G.), Instituto de Investigación Biomédica de Málaga (IBIMA), Complejo Hospitalario de Málaga (Virgen de la Victoria)/Universidad de Málaga, 29010 Málaga, Spain – sequence: 5 givenname: M. Rosa surname: Bernal-López fullname: Bernal-López, M. Rosa organization: 4Biomedical Research Laboratory (M.R.B.-L.), Internal Medicine Department, IBIMA, Regional University Hospital of Malaga (Carlos Haya Hospital), Universidad de Málaga, 29010 Málaga, Spain – sequence: 6 givenname: Diego surname: Fernández-García fullname: Fernández-García, Diego organization: 1Unidad de Gestión Clínica Endocrinología y Nutrición (M.C.-P., A.M.-G., L.G.-S., D.F.-G., D.C.-C., F.C., F.J.T., M.M.-G.), Instituto de Investigación Biomédica de Málaga (IBIMA), Complejo Hospitalario de Málaga (Virgen de la Victoria)/Universidad de Málaga, 29010 Málaga, Spain – sequence: 7 givenname: Inmaculada surname: Moreno-Santos fullname: Moreno-Santos, Inmaculada organization: 5Área del Corazón del Complejo Hospitalario de Málaga (Virgen de la Victoria) (I.M.-S.), IBIMA/Universidad de Malaga, Red de Investigación Cardiovascular, 29010 Málaga, Spain – sequence: 8 givenname: Nuria surname: Garriga fullname: Garriga, Nuria organization: 3Service of Diabetes, Endocrinology, and Nutrition (M.S., N.G., J.M.F.-R.), Institut d'Investigació Biomédica de Girona, 17007 Girona, Spain – sequence: 9 givenname: Daniel surname: Castellano-Castillo fullname: Castellano-Castillo, Daniel organization: 1Unidad de Gestión Clínica Endocrinología y Nutrición (M.C.-P., A.M.-G., L.G.-S., D.F.-G., D.C.-C., F.C., F.J.T., M.M.-G.), Instituto de Investigación Biomédica de Málaga (IBIMA), Complejo Hospitalario de Málaga (Virgen de la Victoria)/Universidad de Málaga, 29010 Málaga, Spain – sequence: 10 givenname: Antonio surname: Camargo fullname: Camargo, Antonio organization: 2Centro de Investigación Biomédica En Red, Pathophysiology of Obesity and Nutrition (CB06/03) (M.C.-P., L.G.-S., D.F.-G., A.C., J.M.F.-R., F.C., F.J.T., M.M.-G.), 28029, Madrid, Spain – sequence: 11 givenname: Jose M. surname: Fernández-Real fullname: Fernández-Real, Jose M. organization: 2Centro de Investigación Biomédica En Red, Pathophysiology of Obesity and Nutrition (CB06/03) (M.C.-P., L.G.-S., D.F.-G., A.C., J.M.F.-R., F.C., F.J.T., M.M.-G.), 28029, Madrid, Spain – sequence: 12 givenname: Fernando surname: Cardona fullname: Cardona, Fernando organization: 2Centro de Investigación Biomédica En Red, Pathophysiology of Obesity and Nutrition (CB06/03) (M.C.-P., L.G.-S., D.F.-G., A.C., J.M.F.-R., F.C., F.J.T., M.M.-G.), 28029, Madrid, Spain – sequence: 13 givenname: Francisco J. surname: Tinahones fullname: Tinahones, Francisco J. email: fjtinahones@hotmail.com organization: 1Unidad de Gestión Clínica Endocrinología y Nutrición (M.C.-P., A.M.-G., L.G.-S., D.F.-G., D.C.-C., F.C., F.J.T., M.M.-G.), Instituto de Investigación Biomédica de Málaga (IBIMA), Complejo Hospitalario de Málaga (Virgen de la Victoria)/Universidad de Málaga, 29010 Málaga, Spain – sequence: 14 givenname: Manuel surname: Macías-González fullname: Macías-González, Manuel email: mmacias.manuel@gmail.com organization: 1Unidad de Gestión Clínica Endocrinología y Nutrición (M.C.-P., A.M.-G., L.G.-S., D.F.-G., D.C.-C., F.C., F.J.T., M.M.-G.), Instituto de Investigación Biomédica de Málaga (IBIMA), Complejo Hospitalario de Málaga (Virgen de la Victoria)/Universidad de Málaga, 29010 Málaga, Spain |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/25706239$$D View this record in MEDLINE/PubMed |
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Copyright | Copyright © 2015 by the Endocrine Society 2015 Copyright © 2015 by The Endocrine Society Copyright © 2015 by the Endocrine Society |
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PublicationTitle | The journal of clinical endocrinology and metabolism |
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Snippet | Context:The relationship between 25-hydroxyvitamin D [25(OH)D] and obesity and type 2 diabetes is not completely understood. Vitamin D receptor (VDR)... CONTEXT:The relationship between 25-hydroxyvitamin D [25(OH)D] and obesity and type 2 diabetes is not completely understood. Vitamin D receptor (VDR)... The relationship between 25-hydroxyvitamin D [25(OH)D] and obesity and type 2 diabetes is not completely understood. Vitamin D receptor (VDR) expression in... |
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SubjectTerms | 25-Hydroxyvitamin D Adipose tissue Adipose Tissue - metabolism Adult Aged Body fat Body Mass Index Calcitriol Carbohydrate metabolism Cells, Cultured Cohort Studies Diabetes Diabetes mellitus (non-insulin dependent) Diabetes Mellitus, Type 2 - blood Diabetes Mellitus, Type 2 - genetics Explants Female Gene Expression Glucose metabolism Homeostasis Humans Insulin resistance Male Metabolism Middle Aged Obesity Obesity - blood Obesity - genetics Overweight - blood Overweight - genetics Parathyroid hormone Prediabetic State - blood Prediabetic State - genetics Receptors, Calcitriol - genetics Receptors, Calcitriol - metabolism Vitamin D Vitamin D - analogs & derivatives Vitamin D - blood Vitamin D Deficiency - blood Vitamin D Deficiency - genetics Vitamin D receptors Vitamin D3 Vitamin deficiency |
Title | Serum 25-Hydroxyvitamin D and Adipose Tissue Vitamin D Receptor Gene Expression: Relationship With Obesity and Type 2 Diabetes |
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