Obesity

Adiposome Lipidomic Shifts Following Bariatric Surgery in Association With Weight Loss and Cardiometabolic Benefit

J Clin Endocrinol MetabPublished Prospective cohort study

Authors' conclusion

Bariatric surgery remodels adiposome lipids, and these shifts align with improvements in cardiometabolic risk markers.

Study context

Population
Obese individuals undergoing bariatric surgery; adipose tissue biopsies with adiposome isolation
Participants
23 individuals
Exposure
After vs before bariatric surgery
Outcome
Adiposome lipidome remodelling
Methodological detailsbefore-and-after, non-targeted lipidomic analysis using mass spectrometry
  • Before-and-after
  • Non-targeted lipidomic analysis using mass spectrometry

Main finding

As reported in the abstract

Lipid species identified across 19 classes

550

Species increased after surgery

124

Species decreased after surgery

66

Lipid species whose change correlated with body mass index (BMI) change (TG 18:1/20:4/22:6 positively; Sphingomyelins (SM) d40:1, SM d42:4, phosphatidylcholine 17:0/18:2 inversely)

36

Observational data: associations, not effects.

Further findings

Clinical and vascular changes after surgery

Significant reductions in BMI, visceral fat, HOMA-IR, inflammatory markers and systolic blood pressure, with marked improvements in vascular function
Improvements in nitric oxide, vascular reactivity and adiponectin tracked with rises in ultralong-chain ceramide/fatty acid-hydroxy fatty acids (FAHFAs)/phospholipids and declines in acylcarnitine/cholesterol esters/diacylglycerols/phosphatidic acids

Machine learning prediction of BMI from lipid features

Accuracy
>80%
R2
>0.90
Mean absolute error
<0.3
Top contributors: SM d40:1, SM d42:4 and fatty acid 17:1

Pathway enrichment

Changes linked to sphingolipid signaling and glycerophospholipid metabolism

Original publication

Adiposome Lipidomic Shifts Following Bariatric Surgery in Association With Weight Loss and Cardiometabolic Benefit. J Clin Endocrinol Metab. Published 24 October 2025. doi:10.1210/clinem/dgaf586

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