Enlarged adipocytes from subcutaneous vs. visceral adipose tissue differentially contribute to metabolic dysfunction and atherogenic risk of patients with obesity
Morphological characteristics and source of adipose tissue as well as adipokines may increase cardiometabolic risk. This study aimed to explore whether adipose tissue characteristics may impact metabolic and atherogenic risks. Subcutaneous Adipose Tissue (SAT), Visceral Adipose Tissue (VAT) and peri...
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Published in | Scientific reports Vol. 11; no. 1; pp. 1831 - 11 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
19.01.2021
Nature Publishing Group Nature Portfolio |
Subjects | |
Online Access | Get full text |
ISSN | 2045-2322 2045-2322 |
DOI | 10.1038/s41598-021-81289-2 |
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Abstract | Morphological characteristics and source of adipose tissue as well as adipokines may increase cardiometabolic risk. This study aimed to explore whether adipose tissue characteristics may impact metabolic and atherogenic risks. Subcutaneous Adipose Tissue (SAT), Visceral Adipose Tissue (VAT) and peripheral blood were obtained from obese patients submitted to bariatric surgery. Adipose tissue (morphometry), plasma adiponectin, TNF-α, resistin (multiplexing) and biochemical chemistry were analyzed; as well as endothelial dysfunction (Flow Mediated Dilation, FMD) and atherogenesis (Carotid Intima Media Thickness, CIMT). Subgroups divided by adipocyte size and source were compared; as well as correlation and multivariate analysis. Sixty patients 36.6% males, aged 44 years-old, BMI 46.7 kg/m
2
were included. SAT’s adipocytes showed a lower range of size expandability than VAT’s adipocytes. Independent from their source, larger adipocytes were associated with higher glucose, lower adiponectin and higher CIMT. Particularly, larger adipocytes from SAT were associated with higher blood pressure, lower insulin and HDL-cholesterol; and showed positive correlation with glucose, Hb
A1c
, systolic/diastolic values, and negatively correlated with insulin and adiponectin. VAT’s larger adipocytes particularly associated with lower resistin and lower FMD values. Gender and Diabetes Mellitus significantly impacted the relation of adipocyte size/source with the metabolic and atherogenic risk. Multivariable analysis suggested hypertension-resistin-Hb
A1c
interactions associated with SAT’s larger adipocytes; whereas potential insulin-adiponectin associations were observed for VAT’s larger adipocytes. Adipocyte morphology and source are differentially related with cardiometabolic and atherogenic risk in population with obesity, which are potentially affected by gender and Diabetes Mellitus. |
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AbstractList | Morphological characteristics and source of adipose tissue as well as adipokines may increase cardiometabolic risk. This study aimed to explore whether adipose tissue characteristics may impact metabolic and atherogenic risks. Subcutaneous Adipose Tissue (SAT), Visceral Adipose Tissue (VAT) and peripheral blood were obtained from obese patients submitted to bariatric surgery. Adipose tissue (morphometry), plasma adiponectin, TNF-α, resistin (multiplexing) and biochemical chemistry were analyzed; as well as endothelial dysfunction (Flow Mediated Dilation, FMD) and atherogenesis (Carotid Intima Media Thickness, CIMT). Subgroups divided by adipocyte size and source were compared; as well as correlation and multivariate analysis. Sixty patients 36.6% males, aged 44 years-old, BMI 46.7 kg/m
were included. SAT's adipocytes showed a lower range of size expandability than VAT's adipocytes. Independent from their source, larger adipocytes were associated with higher glucose, lower adiponectin and higher CIMT. Particularly, larger adipocytes from SAT were associated with higher blood pressure, lower insulin and HDL-cholesterol; and showed positive correlation with glucose, Hb
, systolic/diastolic values, and negatively correlated with insulin and adiponectin. VAT's larger adipocytes particularly associated with lower resistin and lower FMD values. Gender and Diabetes Mellitus significantly impacted the relation of adipocyte size/source with the metabolic and atherogenic risk. Multivariable analysis suggested hypertension-resistin-Hb
interactions associated with SAT's larger adipocytes; whereas potential insulin-adiponectin associations were observed for VAT's larger adipocytes. Adipocyte morphology and source are differentially related with cardiometabolic and atherogenic risk in population with obesity, which are potentially affected by gender and Diabetes Mellitus. Morphological characteristics and source of adipose tissue as well as adipokines may increase cardiometabolic risk. This study aimed to explore whether adipose tissue characteristics may impact metabolic and atherogenic risks. Subcutaneous Adipose Tissue (SAT), Visceral Adipose Tissue (VAT) and peripheral blood were obtained from obese patients submitted to bariatric surgery. Adipose tissue (morphometry), plasma adiponectin, TNF-α, resistin (multiplexing) and biochemical chemistry were analyzed; as well as endothelial dysfunction (Flow Mediated Dilation, FMD) and atherogenesis (Carotid Intima Media Thickness, CIMT). Subgroups divided by adipocyte size and source were compared; as well as correlation and multivariate analysis. Sixty patients 36.6% males, aged 44 years-old, BMI 46.7 kg/m2 were included. SAT’s adipocytes showed a lower range of size expandability than VAT’s adipocytes. Independent from their source, larger adipocytes were associated with higher glucose, lower adiponectin and higher CIMT. Particularly, larger adipocytes from SAT were associated with higher blood pressure, lower insulin and HDL-cholesterol; and showed positive correlation with glucose, HbA1c, systolic/diastolic values, and negatively correlated with insulin and adiponectin. VAT’s larger adipocytes particularly associated with lower resistin and lower FMD values. Gender and Diabetes Mellitus significantly impacted the relation of adipocyte size/source with the metabolic and atherogenic risk. Multivariable analysis suggested hypertension-resistin-HbA1c interactions associated with SAT’s larger adipocytes; whereas potential insulin-adiponectin associations were observed for VAT’s larger adipocytes. Adipocyte morphology and source are differentially related with cardiometabolic and atherogenic risk in population with obesity, which are potentially affected by gender and Diabetes Mellitus. Morphological characteristics and source of adipose tissue as well as adipokines may increase cardiometabolic risk. This study aimed to explore whether adipose tissue characteristics may impact metabolic and atherogenic risks. Subcutaneous Adipose Tissue (SAT), Visceral Adipose Tissue (VAT) and peripheral blood were obtained from obese patients submitted to bariatric surgery. Adipose tissue (morphometry), plasma adiponectin, TNF-α, resistin (multiplexing) and biochemical chemistry were analyzed; as well as endothelial dysfunction (Flow Mediated Dilation, FMD) and atherogenesis (Carotid Intima Media Thickness, CIMT). Subgroups divided by adipocyte size and source were compared; as well as correlation and multivariate analysis. Sixty patients 36.6% males, aged 44 years-old, BMI 46.7 kg/m 2 were included. SAT’s adipocytes showed a lower range of size expandability than VAT’s adipocytes. Independent from their source, larger adipocytes were associated with higher glucose, lower adiponectin and higher CIMT. Particularly, larger adipocytes from SAT were associated with higher blood pressure, lower insulin and HDL-cholesterol; and showed positive correlation with glucose, Hb A1c , systolic/diastolic values, and negatively correlated with insulin and adiponectin. VAT’s larger adipocytes particularly associated with lower resistin and lower FMD values. Gender and Diabetes Mellitus significantly impacted the relation of adipocyte size/source with the metabolic and atherogenic risk. Multivariable analysis suggested hypertension-resistin-Hb A1c interactions associated with SAT’s larger adipocytes; whereas potential insulin-adiponectin associations were observed for VAT’s larger adipocytes. Adipocyte morphology and source are differentially related with cardiometabolic and atherogenic risk in population with obesity, which are potentially affected by gender and Diabetes Mellitus. Morphological characteristics and source of adipose tissue as well as adipokines may increase cardiometabolic risk. This study aimed to explore whether adipose tissue characteristics may impact metabolic and atherogenic risks. Subcutaneous Adipose Tissue (SAT), Visceral Adipose Tissue (VAT) and peripheral blood were obtained from obese patients submitted to bariatric surgery. Adipose tissue (morphometry), plasma adiponectin, TNF-α, resistin (multiplexing) and biochemical chemistry were analyzed; as well as endothelial dysfunction (Flow Mediated Dilation, FMD) and atherogenesis (Carotid Intima Media Thickness, CIMT). Subgroups divided by adipocyte size and source were compared; as well as correlation and multivariate analysis. Sixty patients 36.6% males, aged 44 years-old, BMI 46.7 kg/m2 were included. SAT’s adipocytes showed a lower range of size expandability than VAT’s adipocytes. Independent from their source, larger adipocytes were associated with higher glucose, lower adiponectin and higher CIMT. Particularly, larger adipocytes from SAT were associated with higher blood pressure, lower insulin and HDL-cholesterol; and showed positive correlation with glucose, HbA1c, systolic/diastolic values, and negatively correlated with insulin and adiponectin. VAT’s larger adipocytes particularly associated with lower resistin and lower FMD values. Gender and Diabetes Mellitus significantly impacted the relation of adipocyte size/source with the metabolic and atherogenic risk. Multivariable analysis suggested hypertension-resistin-HbA1c interactions associated with SAT’s larger adipocytes; whereas potential insulin-adiponectin associations were observed for VAT’s larger adipocytes. Adipocyte morphology and source are differentially related with cardiometabolic and atherogenic risk in population with obesity, which are potentially affected by gender and Diabetes Mellitus. Morphological characteristics and source of adipose tissue as well as adipokines may increase cardiometabolic risk. This study aimed to explore whether adipose tissue characteristics may impact metabolic and atherogenic risks. Subcutaneous Adipose Tissue (SAT), Visceral Adipose Tissue (VAT) and peripheral blood were obtained from obese patients submitted to bariatric surgery. Adipose tissue (morphometry), plasma adiponectin, TNF-α, resistin (multiplexing) and biochemical chemistry were analyzed; as well as endothelial dysfunction (Flow Mediated Dilation, FMD) and atherogenesis (Carotid Intima Media Thickness, CIMT). Subgroups divided by adipocyte size and source were compared; as well as correlation and multivariate analysis. Sixty patients 36.6% males, aged 44 years-old, BMI 46.7 kg/m2 were included. SAT's adipocytes showed a lower range of size expandability than VAT's adipocytes. Independent from their source, larger adipocytes were associated with higher glucose, lower adiponectin and higher CIMT. Particularly, larger adipocytes from SAT were associated with higher blood pressure, lower insulin and HDL-cholesterol; and showed positive correlation with glucose, HbA1c, systolic/diastolic values, and negatively correlated with insulin and adiponectin. VAT's larger adipocytes particularly associated with lower resistin and lower FMD values. Gender and Diabetes Mellitus significantly impacted the relation of adipocyte size/source with the metabolic and atherogenic risk. Multivariable analysis suggested hypertension-resistin-HbA1c interactions associated with SAT's larger adipocytes; whereas potential insulin-adiponectin associations were observed for VAT's larger adipocytes. Adipocyte morphology and source are differentially related with cardiometabolic and atherogenic risk in population with obesity, which are potentially affected by gender and Diabetes Mellitus.Morphological characteristics and source of adipose tissue as well as adipokines may increase cardiometabolic risk. This study aimed to explore whether adipose tissue characteristics may impact metabolic and atherogenic risks. Subcutaneous Adipose Tissue (SAT), Visceral Adipose Tissue (VAT) and peripheral blood were obtained from obese patients submitted to bariatric surgery. Adipose tissue (morphometry), plasma adiponectin, TNF-α, resistin (multiplexing) and biochemical chemistry were analyzed; as well as endothelial dysfunction (Flow Mediated Dilation, FMD) and atherogenesis (Carotid Intima Media Thickness, CIMT). Subgroups divided by adipocyte size and source were compared; as well as correlation and multivariate analysis. Sixty patients 36.6% males, aged 44 years-old, BMI 46.7 kg/m2 were included. SAT's adipocytes showed a lower range of size expandability than VAT's adipocytes. Independent from their source, larger adipocytes were associated with higher glucose, lower adiponectin and higher CIMT. Particularly, larger adipocytes from SAT were associated with higher blood pressure, lower insulin and HDL-cholesterol; and showed positive correlation with glucose, HbA1c, systolic/diastolic values, and negatively correlated with insulin and adiponectin. VAT's larger adipocytes particularly associated with lower resistin and lower FMD values. Gender and Diabetes Mellitus significantly impacted the relation of adipocyte size/source with the metabolic and atherogenic risk. Multivariable analysis suggested hypertension-resistin-HbA1c interactions associated with SAT's larger adipocytes; whereas potential insulin-adiponectin associations were observed for VAT's larger adipocytes. Adipocyte morphology and source are differentially related with cardiometabolic and atherogenic risk in population with obesity, which are potentially affected by gender and Diabetes Mellitus. Abstract Morphological characteristics and source of adipose tissue as well as adipokines may increase cardiometabolic risk. This study aimed to explore whether adipose tissue characteristics may impact metabolic and atherogenic risks. Subcutaneous Adipose Tissue (SAT), Visceral Adipose Tissue (VAT) and peripheral blood were obtained from obese patients submitted to bariatric surgery. Adipose tissue (morphometry), plasma adiponectin, TNF-α, resistin (multiplexing) and biochemical chemistry were analyzed; as well as endothelial dysfunction (Flow Mediated Dilation, FMD) and atherogenesis (Carotid Intima Media Thickness, CIMT). Subgroups divided by adipocyte size and source were compared; as well as correlation and multivariate analysis. Sixty patients 36.6% males, aged 44 years-old, BMI 46.7 kg/m2 were included. SAT’s adipocytes showed a lower range of size expandability than VAT’s adipocytes. Independent from their source, larger adipocytes were associated with higher glucose, lower adiponectin and higher CIMT. Particularly, larger adipocytes from SAT were associated with higher blood pressure, lower insulin and HDL-cholesterol; and showed positive correlation with glucose, HbA1c, systolic/diastolic values, and negatively correlated with insulin and adiponectin. VAT’s larger adipocytes particularly associated with lower resistin and lower FMD values. Gender and Diabetes Mellitus significantly impacted the relation of adipocyte size/source with the metabolic and atherogenic risk. Multivariable analysis suggested hypertension-resistin-HbA1c interactions associated with SAT’s larger adipocytes; whereas potential insulin-adiponectin associations were observed for VAT’s larger adipocytes. Adipocyte morphology and source are differentially related with cardiometabolic and atherogenic risk in population with obesity, which are potentially affected by gender and Diabetes Mellitus. |
ArticleNumber | 1831 |
Author | Téllez-González, Mario Antonio Salamanca-García, Moisés Gaytán-Fuentes, Omar Felipe Orozco-Vázquez, Julita Mondragón-Terán, Paul Suárez-Cuenca, Juan Antonio De La Vega-Moreno, Karen Ruíz-Hernández, Atzín Suá Alcaráz-Estrada, Sofía Lizeth Banderas-Lares, Diana Zaineff Hernández-Patricio, Alejandro Pérez-Cabeza de Vaca, Rebeca De La Peña-Sosa, Gustavo Osorio-Valero, Mario Domínguez-Pérez, Gabriela Alexandra Ortíz-Fernández, Moisés Rodríguez-Arellano, Martha Eunice Zamora-Alemán, Carlos Ramiro Escamilla-Tilch, Mónica Montoya-Ramírez, Jesús Melchor-López, Alberto Maldonado-Arriaga, Brenda Toríz-Ortíz, Angélica Pineda-Juárez, Juan Antonio Gutiérrez-Buendía, Juan Ariel García, Silvia Vera-Gómez, Eduardo Martínez-Hernández, José Enrique |
Author_xml | – sequence: 1 givenname: Juan Antonio surname: Suárez-Cuenca fullname: Suárez-Cuenca, Juan Antonio email: suarej05@gmail.com organization: Laboratory of Experimental Metabolism and Clinical Research, Division of Research, Department of Clinical Research, Centro Médico Nacional “20 de Noviembre”, ISSSTE, Internal Medicine Department, H.G.Z. No. 58 “Manuel Ávila Camacho”, IMSS, and Hospital General “Xoco” SS CDMX – sequence: 2 givenname: Gustavo surname: De La Peña-Sosa fullname: De La Peña-Sosa, Gustavo organization: Laboratory of Experimental Metabolism and Clinical Research, Division of Research, Department of Clinical Research, Centro Médico Nacional “20 de Noviembre”, ISSSTE – sequence: 3 givenname: Karen surname: De La Vega-Moreno fullname: De La Vega-Moreno, Karen organization: Laboratory of Experimental Metabolism and Clinical Research, Division of Research, Department of Clinical Research, Centro Médico Nacional “20 de Noviembre”, ISSSTE – sequence: 4 givenname: Diana Zaineff surname: Banderas-Lares fullname: Banderas-Lares, Diana Zaineff organization: Laboratory of Experimental Metabolism and Clinical Research, Division of Research, Department of Clinical Research, Centro Médico Nacional “20 de Noviembre”, ISSSTE – sequence: 5 givenname: Moisés surname: Salamanca-García fullname: Salamanca-García, Moisés organization: Pathology Department, Centro Médico Nacional “20 de Noviembre”, ISSSTE – sequence: 6 givenname: José Enrique surname: Martínez-Hernández fullname: Martínez-Hernández, José Enrique organization: Laboratory of Experimental Metabolism and Clinical Research, Division of Research, Department of Clinical Research, Centro Médico Nacional “20 de Noviembre”, ISSSTE – sequence: 7 givenname: Eduardo surname: Vera-Gómez fullname: Vera-Gómez, Eduardo organization: Laboratory of Experimental Metabolism and Clinical Research, Division of Research, Department of Clinical Research, Centro Médico Nacional “20 de Noviembre”, ISSSTE – sequence: 8 givenname: Alejandro surname: Hernández-Patricio fullname: Hernández-Patricio, Alejandro organization: Laboratory of Experimental Metabolism and Clinical Research, Division of Research, Department of Clinical Research, Centro Médico Nacional “20 de Noviembre”, ISSSTE – sequence: 9 givenname: Carlos Ramiro surname: Zamora-Alemán fullname: Zamora-Alemán, Carlos Ramiro organization: Laboratory of Experimental Metabolism and Clinical Research, Division of Research, Department of Clinical Research, Centro Médico Nacional “20 de Noviembre”, ISSSTE – sequence: 10 givenname: Gabriela Alexandra surname: Domínguez-Pérez fullname: Domínguez-Pérez, Gabriela Alexandra organization: Laboratory of Experimental Metabolism and Clinical Research, Division of Research, Department of Clinical Research, Centro Médico Nacional “20 de Noviembre”, ISSSTE – sequence: 11 givenname: Atzín Suá surname: Ruíz-Hernández fullname: Ruíz-Hernández, Atzín Suá organization: Laboratory of Experimental Metabolism and Clinical Research, Division of Research, Department of Clinical Research, Centro Médico Nacional “20 de Noviembre”, ISSSTE – sequence: 12 givenname: Juan Ariel surname: Gutiérrez-Buendía fullname: Gutiérrez-Buendía, Juan Ariel organization: Laboratory of Experimental Metabolism and Clinical Research, Division of Research, Department of Clinical Research, Centro Médico Nacional “20 de Noviembre”, ISSSTE – sequence: 13 givenname: Alberto surname: Melchor-López fullname: Melchor-López, Alberto organization: Internal Medicine Department, H.G.Z. No. 8 “Gilberto Flores Izquierdo”, IMSS and Hospital General “Xoco” SS CDMX – sequence: 14 givenname: Moisés surname: Ortíz-Fernández fullname: Ortíz-Fernández, Moisés organization: Bariatric Surgery Department, Centro Médico Nacional “20 de Noviembre”, ISSSTE – sequence: 15 givenname: Jesús surname: Montoya-Ramírez fullname: Montoya-Ramírez, Jesús organization: Bariatric Surgery Department, Centro Médico Nacional “20 de Noviembre”, ISSSTE – sequence: 16 givenname: Omar Felipe surname: Gaytán-Fuentes fullname: Gaytán-Fuentes, Omar Felipe organization: Bariatric Surgery Department, Centro Médico Nacional “20 de Noviembre”, ISSSTE – sequence: 17 givenname: Angélica surname: Toríz-Ortíz fullname: Toríz-Ortíz, Angélica organization: Diagnostic Imaging Department, Centro Médico Nacional “20 de Noviembre”, ISSSTE – sequence: 18 givenname: Mario surname: Osorio-Valero fullname: Osorio-Valero, Mario organization: Diagnostic Imaging Department, Centro Médico Nacional “20 de Noviembre”, ISSSTE – sequence: 19 givenname: Julita surname: Orozco-Vázquez fullname: Orozco-Vázquez, Julita organization: Diagnostic Imaging Department, Centro Médico Nacional “20 de Noviembre”, ISSSTE – sequence: 20 givenname: Sofía Lizeth surname: Alcaráz-Estrada fullname: Alcaráz-Estrada, Sofía Lizeth organization: Laboratorio de Medicina Genómica, Centro Médico Nacional “20 de Noviembre”, ISSSTE – sequence: 21 givenname: Martha Eunice surname: Rodríguez-Arellano fullname: Rodríguez-Arellano, Martha Eunice organization: Laboratorio de Medicina Genómica, Hospital Regional “Lic, Adolfo López Mateos”, ISSSTE – sequence: 22 givenname: Brenda surname: Maldonado-Arriaga fullname: Maldonado-Arriaga, Brenda organization: Laboratory of Experimental Metabolism and Clinical Research, Division of Research, Department of Clinical Research, Centro Médico Nacional “20 de Noviembre”, ISSSTE – sequence: 23 givenname: Rebeca surname: Pérez-Cabeza de Vaca fullname: Pérez-Cabeza de Vaca, Rebeca organization: Coordination of Research and Tissue Engineering & Regenerative Medicine Research Group, Centro Médico Nacional “20 de Noviembre”, ISSSTE – sequence: 24 givenname: Mónica surname: Escamilla-Tilch fullname: Escamilla-Tilch, Mónica organization: Coordination of Research and Tissue Engineering & Regenerative Medicine Research Group, Centro Médico Nacional “20 de Noviembre”, ISSSTE – sequence: 25 givenname: Juan Antonio surname: Pineda-Juárez fullname: Pineda-Juárez, Juan Antonio organization: Coordination of Research and Tissue Engineering & Regenerative Medicine Research Group, Centro Médico Nacional “20 de Noviembre”, ISSSTE – sequence: 26 givenname: Mario Antonio surname: Téllez-González fullname: Téllez-González, Mario Antonio organization: Coordination of Research and Tissue Engineering & Regenerative Medicine Research Group, Centro Médico Nacional “20 de Noviembre”, ISSSTE – sequence: 27 givenname: Silvia surname: García fullname: García, Silvia organization: Laboratory of Experimental Metabolism and Clinical Research, Division of Research, Department of Clinical Research, Centro Médico Nacional “20 de Noviembre”, ISSSTE – sequence: 28 givenname: Paul surname: Mondragón-Terán fullname: Mondragón-Terán, Paul organization: Coordination of Research and Tissue Engineering & Regenerative Medicine Research Group, Centro Médico Nacional “20 de Noviembre”, ISSSTE |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33469087$$D View this record in MEDLINE/PubMed |
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ContentType | Journal Article |
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Title | Enlarged adipocytes from subcutaneous vs. visceral adipose tissue differentially contribute to metabolic dysfunction and atherogenic risk of patients with obesity |
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