Type 2 & other diabetes

Risk of Incident Diabetes Related to Lipoprotein(a), LDL Cholesterol, and Their Changes With Alirocumab: Post Hoc Analyses of the ODYSSEY OUTCOMES Randomized Trial

Diabetes CarePublished Post hoc analysis of the ODYSSEY OUTCOMES randomised trial

Authors' conclusion

Baseline lipoprotein(a) was inversely associated with risk of NOD. Alirocumab-induced reductions of lipoprotein(a) and LDL-C were associated with increased and decreased risk of NOD, respectively, without net effect on NOD. Ongoing trials will determine the impact of larger and longer lipoprotein(a) reductions on NOD.

Study context

Population
Patients with recent acute coronary syndrome on optimized statin therapy, without diabetes at baseline782 NOD cases
Participants
8,107 patients
Comparison
Alirocumab vs placebo; baseline Lp(a), LDL-C, insulin/HOMA-IR and their changes on alirocumab as predictors of new-onset T2D
Primary endpoint
New-onset T2D (NOD)
Follow-up
Median 2.4 years
Methodological detailslogistic regression with splines
  • Logistic regression with splines

Primary result

As reported in the abstract

NOD predicted by baseline and on-alirocumab changes in lipoprotein(a) and LDL-C
OR for NOD
Odds ratio (95% CI)
25% lipoprotein(a) reduction on alirocumab
1.12(1.01–1.23)
50% lipoprotein(a) reduction on alirocumab
1.24(1.02–1.52)
25% LDL-C reduction on alirocumab
0.88(0.80–0.97)
50% LDL-C reduction on alirocumab
0.77(0.64–0.94)

Further findings

OutcomeOR (95% CI)
NOD risk, alirocumabvs placebo0.998 (0.860–1.158)

NOD risk, alirocumab vs placebo

Alirocumab reduced lipoprotein(a) and LDL-C without affecting insulin or NOD risk

Original publication

Risk of Incident Diabetes Related to Lipoprotein(a), LDL Cholesterol, and Their Changes With Alirocumab: Post Hoc Analyses of the ODYSSEY OUTCOMES Randomized Trial. Diabetes Care. Published 6 February 2025. doi:10.2337/dc24-2110

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