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Association between plasma proteomic dynamic changes and metabolic outcomes in patients undergoing bariatric surgery

International Journal of Obesity, 2025

Diaz-Canestro C., Yang W., Chen J., Cheung K., Han H., Wang C., Song E., Lee K., Xue J., Xu A.

Disease areaApplication areaSample typeProducts
Metabolic Diseases
Pathophysiology
Plasma
Olink Target 96

Olink Target 96

Abstract

Background
Bariatric surgery (BS) improves long-term glycemic control more effectively than medical treatment in patients with type 2 diabetes mellitus. The objective of this study was to explore the dynamic changes on inflammatory and metabolic-related circulating proteins in a large cohort of overweight patients and patients with class I to III obesity undergoing bariatric surgery (BS).

Subjects/methods
We performed quantitative proteomic analysis (399 inflammatory/metabolic proteins, Olink Proteomics) in plasma samples collected before (n = 114) and 1 month (n = 67), 3 months (n = 64), 6 months (n = 60), 12 months (n = 48) and 24 months (n = 18) after either Roux-en-Y gastric bypass (RYGB) or vertical sleeve gastrectomy (VSG).

Results
Circulating proteins primarily expressed in the liver markedly changed after BS including IGFBP-1/2 (upregulated at all time points post-surgery) and the peroxisomal enzyme HAOX1 (downregulated at all time points post-surgery). Regression analysis revealed a strong association between the changes in HAOX1 and improvements in liver enzymes. In addition, a soluble broad-spectrum pattern recognition receptor, scavenger receptor cysteine rich family member with 4 domains (SSC4D), exhibited the highest decrease among all proteins at 24 months post-surgery. Finally, we detected that inflammatory markers were transiently increased after RYGB compared to VSG as well as in patients with severe obesity compared to patients with overweight and patients with obesity at 1-month post-surgery.

Conclusions
This study identified novel inflammatory and metabolic proteins possibly implicated in the systemic metabolic response to BS.

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