Changes in Circulating Cytokines and Adipokines After RYGB in Patients with and without Type 2 Diabetes

Objective This study aimed to compare cytokine and adipokine levels in patients with obesity with and without type 2 diabetes (T2D) at baseline and 6 months after Roux‐en‐Y gastric bypass (RYGB) with healthy controls. Methods A total of 34 patients (21 with T2D) with BMI of 30 to 45 kg/m2 were compa...

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Published in:Obesity (Silver Spring, Md.) Vol. 29; no. 3; pp. 535 - 542
Main Authors: Katsogiannos, Petros, Kamble, Prasad G., Pereira, Maria J., Sundbom, Magnus, Carlsson, Per‐Ola, Eriksson, Jan W., Espes, Daniel
Format: Journal Article
Language:English
Published: United States Blackwell Publishing Ltd 01-03-2021
John Wiley and Sons Inc
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Summary:Objective This study aimed to compare cytokine and adipokine levels in patients with obesity with and without type 2 diabetes (T2D) at baseline and 6 months after Roux‐en‐Y gastric bypass (RYGB) with healthy controls. Methods A total of 34 patients (21 with T2D) with BMI of 30 to 45 kg/m2 were compared with 25 healthy controls without obesity. Cytokines, adipokines, and peptides of relevance for inflammation and metabolism were analyzed in plasma. Results Significant decreases in weight and glycated hemoglobin A1c were observed. At baseline, interleukin‐6 (IL‐6), IFN‐β, IL‐18, leptin, and hepatocyte growth factor were higher in all patients with obesity compared with healthy controls. In patients without T2D, TNF‐α, IL‐1α, IL‐2, IL‐15, and visfatin were also increased, whereas bone morphogenic protein‐4 was decreased. Following RYGB, IL‐6 and hepatocyte growth factor were still increased in both groups compared with controls. In T2D patients, IFN‐β, IL‐27, IL‐1α, IL‐2, regenerating islet‐derived protein 3A, visfatin, and osteopontin were found to be increased. In patients without T2D, TNF‐α, IL‐1α, IL‐2, IL‐15, leptin, and visfatin remained increased. Conclusions The altered cytokine profile of patients with obesity persisted after RYGB despite large weight loss and improved metabolic status, thus reflecting an inherent inflammatory state.
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ISSN:1930-7381
1930-739X
1930-739X
DOI:10.1002/oby.23093