Epidemiology
C-peptide outperforms Lp(a) as a cardiometabolic risk predictor in type 2 diabetes, a nested case-control study of 253 participants (PLoS One 2022)
Original title: Association of C-peptide and lipoprotein(a) as two predictors with cardiometabolic biomarkers in patients with type 2 diabetes in KERCADR population-based study
In a nested case-control study of 253 participants with and without type 2 diabetes from the KERCADR population-based cohort, the authors compared C-peptide and Lp(a) as predictors of cardiometabolic biomarkers. The plasma Atherogenic Index of Plasma significantly decreased (P=0.002) in case males with the highest Lp(a) dichotomy, while the Castelli Risk Index II increased (P=0.008) in control males with high Lp(a); C-peptide showed stronger and more consistent associations with atherogenic indices and anthropometric measures across groups. The authors conclude that raised C-peptide is a more consistent predictor of cardiometabolic risk than raised Lp(a), though they still regard Lp(a) as a risk-independent biomarker for type 2 diabetes, and recommend reducing Lp(a) below 30 ng/mL alongside strict LDL cholesterol control to help prevent coronary artery disease, alongside community screening for Lp(a) in those with cardiometabolic risk factors.
Original abstract
We sought association between serum Lipoprotein(a) and C-Peptide levels as two predictors with cardiometabolic biomarkers in patients with type 2 diabetes mellitus. This nested case-control study was conducted on 253 participants with type 2 diabetes mellitus and control from the second phase of the KERCADR cohort study. The participants were randomly allocated into case and control groups. The quantitative levels of Lipoprotein(a) and C-Peptide were measured by ELISA. Atherogenic indices of plasma were measured. The plasma Atherogenic Index of Plasma significantly decreased (P = 0.002) in case-male participants, and plasma Castelli Risk Index II level significantly increased (P = 0.008) in control-male participants with the highest dichotomy of Lipoprotein(a). The plasma Atherogenic Index of Plasma level in case-female participants significantly increased (P = 0.023) with the highest dichotomy of C-Peptide. Serum C-Peptide level significantly increased (P = 0.010 and P = 0.002, respectively) in control-male participants with the highest dichotomies of Atherogenic Index of Plasma and Castelli Risk Index I. There was a significant association between the highest quartile of C-Peptide and higher anthropometric values in case participants; and higher atherogenic indices of plasma and anthropometric values in control participants. Raised serum C-peptide than raised Lipoprotein(a) can be a prior predictor for cardiometabolic disease risk in healthy participants and patients with type 2 diabetes mellitus with increased cardiometabolic biomarkers. Case and control males with general and visceral obesity and case and control females with visceral obesity are exposure to increased C-peptide, respectively. Lipoprotein(a) may be risk independent biomarker for type 2 diabetes mellitus. Reducing raised Lipoprotein(a) levels to less than 30ng/ml with strict control of low density lipoprotein cholesterol would be the best approach to prevent coronary artery disease consequences. It is suggested that a screening system be set up to measure the Lp(a) levels in the community for seemingly healthy people or individuals with one or more cardiometabolic biomarkers.
Summary written by lp-a.org from the published abstract; figures as published. Page updated 18 August 2026. Methods.