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Adipose Tissue CTGF Expression is Associated with Adiposity and Insulin Resistance in Humans.

Citation
Yoshino, J., et al. “Adipose Tissue Ctgf Expression Is Associated With Adiposity And Insulin Resistance In Humans.”. Obesity (Silver Spring, Md.), pp. 957-962.
Center Washington University in St Louis
Author Jun Yoshino, Bruce W Patterson, Samuel Klein
Abstract

OBJECTIVE: Connective tissue growth factor (CTGF) is an important regulator of fibrogenesis in many organs. This study evaluated the interrelationship among adipose tissue CTGF expression, fat mass, and insulin resistance in humans.

METHODS: This study examined (1) CTGF gene expression in human subcutaneous preadipocytes before and after inducing adipogenesis; (2) relationships among abdominal subcutaneous adipose tissue CTGF gene expression, body fat mass, and indices of insulin sensitivity, including the hepatic insulin sensitivity index and the hyperinsulinemic-euglycemic clamp procedure in conjunction with stable isotope glucose tracer infusion, in 72 people who had marked differences in adiposity and insulin sensitivity; (3) localization of CTGF protein in subcutaneous adipose tissue; and (4) effect of progressive (5%, 11%, and 16%) weight loss on adipose tissue CTGF gene expression.

RESULTS: CTGF was highly expressed in preadipocytes, not adipocytes. Adipose tissue CTGF expression was strongly correlated with body fat mass and both skeletal muscle and liver insulin sensitivity, and CTGF-positive cells were predominantly found in areas of fibrosis. Progressive weight loss caused a stepwise decrease in adipose tissue CTGF expression.

CONCLUSIONS: It was concluded that increased CTGF expression is associated with adipose tissue expansion, adipose tissue fibrosis, and multi-organ insulin resistance in people with obesity.

Year of Publication
2019
Journal
Obesity (Silver Spring, Md.)
Volume
27
Issue
6
Number of Pages
957-962
Date Published
12/2019
ISSN Number
1930-739X
DOI
10.1002/oby.22463
Alternate Journal
Obesity (Silver Spring)
PMID
31004409
PMCID
PMC6533148
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