Lipids & metabolic liver disease

Contribution of intestinal triglyceride-rich lipoproteins to residual atherosclerotic cardiovascular disease risk in individuals with type 2 diabetes on statin therapy

DiabetologiaPublished Secondary analysis of a clinical study

Authors' conclusion

Abnormalities in the metabolism of intestinally derived ApoB-48-containing lipoproteins in individuals with type 2 diabetes on statins may help to explain the residual risk of CVD and may be suitable targets for interventions.

Study context

Population
Overweight/obese individuals with T2D on metformin and statin therapy, and matched controls on statins
Participants
11 vs 11
Comparison
T2D on statins vs matched controls on statins
  • T2Dn = 11
  • Controlsn = 11reference
Primary endpoint
Kinetics of ApoB-48 (chylomicrons, VLDL), ApoB-100 (VLDL, IDL, LDL) and VLDL TG in response to a standard fat-rich meal
Methodological detailsmechanistic kinetic study, case-control comparison, frequency-matched for age, BMI and sex, stable isotope tracers, standard fat-rich meal
  • Mechanistic kinetic study
  • Case-control comparison
  • Frequency-matched for age, BMI and sex
  • Stable isotope tracers
  • Standard fat-rich meal

Primary result

As reported in the abstract

ApoB-48 kinetics

Postprandial ApoB-48 share of total VLDL: T2D vs controls

44% vs 25%

Further findings

Fasting lipid profile

Did not differ significantly between groups

ApoB-100 and triglyceride (TG) kinetics

No between-group differences in VLDL ApoB-100 and TG kinetics, or LDL ApoB-100 production, pool size and clearance
Intermediate-density lipoprotein (IDL) ApoB-100 pool higher in T2D due to increased conversion from VLDL2

Original publication

Contribution of intestinal triglyceride-rich lipoproteins to residual atherosclerotic cardiovascular disease risk in individuals with type 2 diabetes on statin therapy. Diabetologia. Published 29 September 2023. doi:10.1007/s00125-023-06008-0

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