Long-term changes in adipose tissue gene expression following bariatric surgery

J Intern Med. 2020 Aug;288(2):219-233. doi: 10.1111/joim.13066. Epub 2020 May 14.

Abstract

Objective: Patients undergoing bariatric surgery present long-term metabolic improvements and reduced type 2 diabetes risk, despite long-term weight regain. We hypothesized that part of these protective effects could be linked to altered gene expression in white adipose tissue (WAT).

Methods: Transcriptomic profiling by gene microarray was performed in abdominal subcutaneous WAT from women before (n = 50) and two (n = 49) and five (n = 38) years after Roux-en-Y gastric bypass (RYGB) surgery as well as in 28 age-matched nonoperated women.

Results: In the obese women, the average body weight decrease was 38 kg 2 years postsurgery followed by an 8 kg weight regain between 2 and 5 years. Most of the long-term changes in WAT gene expression occurred during the first 2 years. However, a subset of genes encoding proteins involved in inflammation displayed a continued decrease between baseline, 2 and 5 years, respectively; that is an expression pattern independent of body weight regain. Expression of 71 of these genes correlated with measurements of adipocyte morphology or serum adipokine levels.

Conclusion: The continuous improvement in WAT inflammatory gene expression, despite body weight relapse, may contribute to the sustained effects on adipose morphology after bariatric surgery.

Keywords: Roux-en-Y gastric bypass surgery; inflammation; inflammatory gene expression; subcutaneous white adipose tissue.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes
  • Adiponectin / blood
  • Adult
  • Body Mass Index
  • Case-Control Studies
  • Cell Count
  • Cell Size
  • Down-Regulation
  • Female
  • Follow-Up Studies
  • Gastric Bypass*
  • Gene Expression*
  • Gene Ontology
  • Humans
  • Leptin / blood
  • Middle Aged
  • Subcutaneous Fat, Abdominal / metabolism*
  • Tissue Array Analysis
  • Up-Regulation

Substances

  • Adiponectin
  • Leptin