Adipose Dipeptidyl Peptidase-4 and Obesity

Author:

Sell Henrike1,Blüher Matthias2,Klöting Nora2,Schlich Raphaela1,Willems Miriam13,Ruppe Florian3,Knoefel Wolfram Trudo3,Dietrich Arne4,Fielding Barbara A.56,Arner Peter7,Frayn Keith N.5,Eckel Jürgen1

Affiliation:

1. Paul-Langerhans-Group Integrative Physiology, German Diabetes Center, Düsseldorf, Germany

2. Department of Medicine, University of Leipzig, Leipzig, Germany

3. Department of General, Visceral, and Pediatric Surgery, Heinrich-Heine-University and University Hospital Düsseldorf, Düsseldorf, Germany

4. Department of Surgery, University of Leipzig, Leipzig, Germany

5. Oxford Centre for Diabetes, Endocrinology & Metabolism, Churchill Hospital, Oxford, U.K.

6. Faculty of Health and Medical Sciences, University of Surrey, Guildford, U.K.

7. Department of Medicine, Karolinska Institutet, Karolinska University Hospital Huddinge, Stockholm, Sweden

Abstract

OBJECTIVE To study expression of the recently identified adipokine dipeptidyl peptidase-4 (DPP4) in subcutaneous adipose tissue (SAT) and visceral adipose tissue (VAT) of patients with various BMIs and insulin sensitivities, as well as to assess circulating DPP4 in relation to obesity and insulin sensitivity. RESEARCH DESIGN AND METHODS DPP4 expression was measured in SAT and VAT from 196 subjects with a wide range of BMIs and insulin sensitivities. DPP4 release was measured ex vivo in paired biopsies from SAT and VAT as well as in vivo from SAT of lean and obese patients. Circulating DPP4 was measured in insulin-sensitive and insulin-resistant BMI-matched obese patients. RESULTS DPP4 expression was positively correlated with BMI in both SAT and VAT, with VAT consistently displaying higher expression than SAT. Ex vivo release of DPP4 from adipose tissue explants was higher in VAT than in SAT in both lean and obese patients, with obese patients displaying higher DPP4 release than lean controls. Net release of DPP4 from adipose tissue was also demonstrated in vivo with greater release in obese subjects than in lean subjects and in women than in men. Insulin-sensitive obese patients had significantly lower circulating DPP4 than did obesity-matched insulin-resistant patients. In this experiment, DPP4 positively correlated with the amount of VAT, adipocyte size, and adipose tissue inflammation. CONCLUSIONS DPP4, a novel adipokine, has a higher release from VAT that is particularly pronounced in obese and insulin-resistant patients. Our data suggest that DPP4 may be a marker for visceral obesity, insulin resistance, and the metabolic syndrome.

Publisher

American Diabetes Association

Subject

Advanced and Specialized Nursing,Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference35 articles.

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