Abstract 4369532: Estimated absolute coronary heart disease risk reduction with Lp(a) lowering among adults with atherosclerotic cardiovascular disease

C Christy Avery (UNIV N CAROLINA, Chapel Hill, North Carolina, United States) K Katherine Conners (University of North Carolina at Chapel Hill, Carrboro, North Carolina, United States) J John Booth J Joshua Bundy (AMGEN, Thousand Oaks, California, United States) M Mary Cushman R Ron Hoogeveen (BAYLOR COLLEGE MEDICINE, Houston, Texas, United States) M Michael Tsai (University of Minnesota, Minneapolis, MN, USA.) J J. Antonio Lopez (AMGEN, Thousand Oaks, California, United States) L Leah Sadinski (AMGEN, Thousand Oaks, California, United States) E Eduard Sidelnikov (Amgen Europe GmbH, Rotkreuz, Switzerland) C Christie Ballantyne (BAYLOR COLLEGE MEDICINE, Houston, Texas, United States) C Carlos Rodriguez R Robert Rosenson P Paul Muntner (Perisphere real world evidence, Austin, Texas, United States)

Abstract

Background: Elevated lipoprotein(a) [Lp(a)] is a presumed causal risk factor for coronary heart disease (CHD). Estimating the absolute CHD risk reduction with potential Lp(a) lowering using real-world data may help characterize the anticipated patient-level benefits for new therapies directed to Lp(a). Aim: Model the magnitude of absolute reduction in recurrent CHD events that may be achieved by lowering Lp(a) concentration among adults with established atherosclerotic cardiovascular disease (ASCVD). Methods: The absolute risk of recurrent CHD was estimated using pooled data on participants with ASCVD at the time of Lp(a) measurement (nmol/L) from three observational studies: Atherosclerosis Risk in Communities Study, Reasons for Geographic and Racial Differences in Stroke, and UK Biobank. Recurrent CHD included non-fatal myocardial infarction, coronary revascularization, and fatal CHD. The absolute risk reduction over 10 years was extrapolated from Madsen et al. (2020) who estimated lowering Lp(a) by 105 nmol/L would be associated with a 20% recurrent CHD absolute risk reduction (i.e., equivalent risk reduction to a 1 mmol/L reduction in low-density lipoprotein cholesterol over 5 years). Results: Among 20,165 participants (mean age: 62 years, 31% female, mean follow-up: 10 years), 24% had Lp(a) ≥125 nmol/L (median level: 192 nmol/L) and 11% had Lp(a) ≥200 nmol/L median level: 254 nmol/L). Projecting a 60% or 95% reduction in Lp(a) among those with Lp(a) ≥125 nmol/L or ≥200 nmol/L indicates the absolute recurrent CHD risk reduction would increase across greater magnitudes of Lp(a) lowering. Lp(a) lowering of 150 nmol/L, 180 nmol/L and 240 nmol/L would result in a 26%, 32% and 84% greater reduction of recurrent CHD events per 1,000 person years, respectively, compared with the event reduction for Lp(a) lowering of 115 nmol/L ( Figure ). Conclusions: These modelled projections from observational data suggest greater lowering of Lp(a) concentration may result in larger absolute reduction in recurrent CHD risk among adults with established ASCVD.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (14)

C

Christy Avery

UNIV N CAROLINA, Chapel Hill, North Carolina, United States

K

Katherine Conners

University of North Carolina at Chapel Hill, Carrboro, North Carolina, United States

J

John Booth

J

Joshua Bundy

AMGEN, Thousand Oaks, California, United States

M

Mary Cushman

R

Ron Hoogeveen

BAYLOR COLLEGE MEDICINE, Houston, Texas, United States

M

Michael Tsai

University of Minnesota, Minneapolis, MN, USA.

J

J. Antonio Lopez

AMGEN, Thousand Oaks, California, United States

L

Leah Sadinski

AMGEN, Thousand Oaks, California, United States

E

Eduard Sidelnikov

Amgen Europe GmbH, Rotkreuz, Switzerland

C

Christie Ballantyne

BAYLOR COLLEGE MEDICINE, Houston, Texas, United States

C

Carlos Rodriguez

R

Robert Rosenson

P

Paul Muntner

Perisphere real world evidence, Austin, Texas, United States