Effect of Bariatric Weight Loss on the Adipose Lipolytic Transcriptome in Obese Humans

Background. Dysregulated lipolysis has been implicated in mechanisms of cardiometabolic disease and inflammation in obesity. Purpose. We sought to examine the effect of bariatric weight loss on adipose tissue lipolytic gene expression and their relationship to systemic metabolic parameters in obese...

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Main Authors: Shakun Karki, Melissa G. Farb, Samantha Myers, Caroline Apovian, Donald T. Hess, Noyan Gokce
Format: Article
Language:English
Published: Wiley 2015-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2015/106237
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author Shakun Karki
Melissa G. Farb
Samantha Myers
Caroline Apovian
Donald T. Hess
Noyan Gokce
author_facet Shakun Karki
Melissa G. Farb
Samantha Myers
Caroline Apovian
Donald T. Hess
Noyan Gokce
author_sort Shakun Karki
collection DOAJ
description Background. Dysregulated lipolysis has been implicated in mechanisms of cardiometabolic disease and inflammation in obesity. Purpose. We sought to examine the effect of bariatric weight loss on adipose tissue lipolytic gene expression and their relationship to systemic metabolic parameters in obese subjects. Methods/Results. We biopsied subcutaneous adipose tissue in 19 obese individuals (BMI 42 ± 5 kg/m2, 79% female) at baseline and after a mean period of 8 ± 5 months (range 3–15 months) following bariatric surgery. We performed adipose tissue mRNA expression of proteins involved in triglyceride hydrolysis and correlated their weight loss induced alterations with systemic parameters associated with cardiovascular disease risk. mRNA transcripts of adipose triglyceride lipase (ATGL), hormone-sensitive lipase (HSL), and lipid droplet proteins comparative gene identification 58 (CGI-58) and perilipin increased significantly after weight loss (p<0.05 for all). ATGL expression correlated inversely with plasma triglyceride (TG), hemoglobin A1C (HbA1C), and glucose, and HSL expression correlated negatively with glucose, while CGI-58 was inversely associated with HbA1C. Conclusion. We observed increased expression of adipose tissue lipolytic genes following bariatric weight loss which correlated inversely with systemic markers of lipid and glucose metabolism. Functional alterations in lipolysis in human adipose tissue may play a role in shaping cardiometabolic phenotypes in human obesity.
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spelling doaj-art-6b809f03332a418fa3df17d58842d5572025-02-03T01:27:45ZengWileyMediators of Inflammation0962-93511466-18612015-01-01201510.1155/2015/106237106237Effect of Bariatric Weight Loss on the Adipose Lipolytic Transcriptome in Obese HumansShakun Karki0Melissa G. Farb1Samantha Myers2Caroline Apovian3Donald T. Hess4Noyan Gokce5Evans Department of Medicine and Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, MA 02118, USAEvans Department of Medicine and Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, MA 02118, USAEvans Department of Medicine and Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, MA 02118, USAEvans Department of Medicine and Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, MA 02118, USADepartment of General Surgery, Boston University School of Medicine, Boston, MA 02118, USAEvans Department of Medicine and Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, MA 02118, USABackground. Dysregulated lipolysis has been implicated in mechanisms of cardiometabolic disease and inflammation in obesity. Purpose. We sought to examine the effect of bariatric weight loss on adipose tissue lipolytic gene expression and their relationship to systemic metabolic parameters in obese subjects. Methods/Results. We biopsied subcutaneous adipose tissue in 19 obese individuals (BMI 42 ± 5 kg/m2, 79% female) at baseline and after a mean period of 8 ± 5 months (range 3–15 months) following bariatric surgery. We performed adipose tissue mRNA expression of proteins involved in triglyceride hydrolysis and correlated their weight loss induced alterations with systemic parameters associated with cardiovascular disease risk. mRNA transcripts of adipose triglyceride lipase (ATGL), hormone-sensitive lipase (HSL), and lipid droplet proteins comparative gene identification 58 (CGI-58) and perilipin increased significantly after weight loss (p<0.05 for all). ATGL expression correlated inversely with plasma triglyceride (TG), hemoglobin A1C (HbA1C), and glucose, and HSL expression correlated negatively with glucose, while CGI-58 was inversely associated with HbA1C. Conclusion. We observed increased expression of adipose tissue lipolytic genes following bariatric weight loss which correlated inversely with systemic markers of lipid and glucose metabolism. Functional alterations in lipolysis in human adipose tissue may play a role in shaping cardiometabolic phenotypes in human obesity.http://dx.doi.org/10.1155/2015/106237
spellingShingle Shakun Karki
Melissa G. Farb
Samantha Myers
Caroline Apovian
Donald T. Hess
Noyan Gokce
Effect of Bariatric Weight Loss on the Adipose Lipolytic Transcriptome in Obese Humans
Mediators of Inflammation
title Effect of Bariatric Weight Loss on the Adipose Lipolytic Transcriptome in Obese Humans
title_full Effect of Bariatric Weight Loss on the Adipose Lipolytic Transcriptome in Obese Humans
title_fullStr Effect of Bariatric Weight Loss on the Adipose Lipolytic Transcriptome in Obese Humans
title_full_unstemmed Effect of Bariatric Weight Loss on the Adipose Lipolytic Transcriptome in Obese Humans
title_short Effect of Bariatric Weight Loss on the Adipose Lipolytic Transcriptome in Obese Humans
title_sort effect of bariatric weight loss on the adipose lipolytic transcriptome in obese humans
url http://dx.doi.org/10.1155/2015/106237
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