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PMID: 16731817 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Increased infiltration of macrophages in omental adipose tissue is associated with marked hepatic lesions in morbid human obesity.

Diabetes ·Vol. 55 ·No. 6 ·2006-06-00 ·Pages 1554-61

Cancello R, Tordjman J, Poitou C, Guilhem G, Bouillot JL, Hugol D, Coussieu C, Basdevant A, Bar Hen A, Bedossa P, Guerre-Millo M, Clément K

Abstract

In human obesity, white adipose tissue (WAT) is enriched in macrophages. How macrophage infiltration in WAT contributes to the complications of obesity is unknown. This study tested the hypothesis that recruitment of macrophages in omental WAT is associated with hepatic damage in obese patients. Paired biopsies of subcutaneous and omental WAT and a liver biopsy were collected during gastric surgery in 46 obese women and 9 obese men (BMI 47.9 +/- 0.93 kg/m(2)). The number of HAM56+ macrophages in WAT was quantified microscopically, and correlations with clinical and biological parameters and histological liver pathology were investigated. There were twice as many macrophages in omental as in subcutaneous WAT (P<0.0001). After adjustment for age, omental WAT macrophage infiltration was correlated to fasting glucose and insulin, quantitative insulin sensitivity check index, triglycerides, aspartate aminotransferase (AST), and gamma-glutamyltranspeptidase. We propose an easy equation to estimate the amount of macrophages in omental WAT. Increased macrophage accumulation specifically in omental WAT was associated with hepatic fibroinflammatory lesions (P=0.01). The best predictive model for the severity of hepatic damage includes adiponectinemia, AST, and omental WAT macrophages. These data suggest that the presence of macrophages in omental WAT participates in the cellular mechanisms favoring hepatic fibroinflammatory lesions in obese patients.

MeSH Terms
Adipocytes/metabolism,pathology Adipose Tissue, White/metabolism,pathology Adult Analysis of Variance Aspartate Aminotransferases/metabolism Blood Glucose/metabolism Cholesterol, HDL/metabolism Female Humans Immunohistochemistry Insulin/metabolism Linear Models Liver/metabolism,pathology Macrophages/metabolism,pathology Male Obesity, Morbid/metabolism,pathology Omentum/metabolism,pathology Subcutaneous Fat/metabolism,pathology Triglycerides/metabolism gamma-Glutamyltransferase/metabolism
Chemicals
Blood Glucose Cholesterol, HDL Insulin Triglycerides gamma-Glutamyltransferase Aspartate Aminotransferases
Authors & Affiliations
12 authors, click to expand affiliations / ORCID
Cancello Raffaella
INSERM, U755 Nutriomique, Service de Nutrition, Hôtel-Dieu, 1 Place du Parvis Notre-Dame, 75004 Paris, France.
Tordjman Joan
Poitou Christine
Guilhem Gaël
Bouillot Jean Luc
Hugol Danielle
Coussieu Christiane
Basdevant Arnaud
Bar Hen Avner
Bedossa Pierre
Guerre-Millo Michèle
Clément Karine
Article Info
Journal
Diabetes
Abbr.
Diabetes
ISSN
0012-1797
Published
2006-06-00
Pages
1554-61
Language
English
Region
United States
NLM ID
0372763
Subset
IM
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