The metabolic phenotype of the patient influences the reduction in carotid intima-media thickness achieved following metabolic surgery

J Int Med Res. 2022 Nov;50(11):3000605221137475. doi: 10.1177/03000605221137475.

Abstract

Objectives: To determine whether metabolic phenotype is associated with the change in carotid intima-media thickness (CIMT) in patients undergoing bariatric /metabolic surgery (BMS).

Methods: We performed a case-control study of BMS candidates who had metabolically unhealthy obesity (MUO) or metabolically healthy obesity (MHO). We measured the change in CIMT during the 9 months following BMS. The plasma tumor necrosis factor-α, interleukin-1β, adiponectin, leptin, nitric oxide (NO), vascular endothelial growth factor A (VEGF-A), and malondialdehyde concentrations were determined, adipocyte area was measured histologically, and adipose tissue area was estimated using computed tomography.

Results: Fifty-six patients (mean age 44.5 years, mean body mass index 44.9 kg/m2, 53% women, and 53% had MUO) were studied. Nine months following BMS, the MUO phenotype was not associated with a significant reduction in CIMT, and that of the MHO group was larger. In addition, fewer participants achieved a 10% reduction in CIMT in the MUO group. A CIMT reduction was associated with lower VEGF-A and NO in the MUO group, while that in the MHO group was associated with a higher NO concentration.

Conclusion: The metabolic phenotype of patients may influence their change in CIMT following BMS, probably through circulating vasodilatory and pro-inflammatory molecules.

Keywords: Metabolic surgery; bariatric surgery; carotid intima-media thickness; metabolic phenotype; nitric oxide; obesity; vascular endothelial growth factor A.

MeSH terms

  • Bariatric Surgery*
  • Carotid Intima-Media Thickness
  • Case-Control Studies
  • Female
  • Humans
  • Male
  • Obesity / metabolism
  • Obesity, Metabolically Benign* / metabolism
  • Risk Factors
  • Vascular Endothelial Growth Factor A

Substances

  • Vascular Endothelial Growth Factor A