Abstract 4339897: Lipid lowering effects of inclisiran in statin- or PCSK9i monoclonal antibody-intolerant patients

A Ashish Sarraju (Section of Preventive Cardiology and Rehabilitation, Department of Cardiovascular Medicine, Cleveland Clinic Foundation, Cleveland) A Astefanos Al-Dalakta (Cleveland Clinic, Cleveland, Ohio, United States) K Kathy Gambino (Cleveland Clinic, Cleveland, Ohio, United States) E Erik Van Iterson (Cleveland Clinic, Cleveland, Ohio, United States) R Ryan Tang (Cleveland Clinic, Cleveland, Ohio, United States) B Bianca Honnekeri (Cleveland Clinic Foundation, Cleveland, Ohio, United States) S Stanley Hazen (CLEVELAND CLINIC FOUNDATION, Cleveland, Ohio, United States) L Luke Laffin D Dennis Bruemmer (Cleveland Clinic Foundation, Cleveland, Ohio, United States) J Julie Huang (CLEVELAND CLINIC, Cleveland, Ohio, United States) A Abhayjit Singh (Cleveland Clinic, Cleveland, Ohio, United States) V Vikas Sunder (Cleveland Clinic, Cleveland, Ohio, United States) L Leslie Cho

Abstract

Introduction: Inclisiran is a small-interfering RNA therapy that lowered plasma LDL-C levels by ~50% at 90 days in placebo-controlled trials. The LDL-C lowering effects of inclisiran in patients with prior adverse effects (AEs) to statins or PCSK9 inhibiting (PCSK9i) monoclonal antibody therapies (mAbs), who may have limited therapeutic options and experience suboptimal LDL-C control, is not well-known. Research Question: What are the LDL-C lowering effects of inclisiran in patients who have a history of AEs to statins and/or PCSK9i mAbs? Methods: At a tertiary US preventive cardiology clinic, we retrospectively evaluated electronic health records of patients > 18 years of age who received > 1 dose of inclisiran between 1/1/2022 and 2/29/2024. LDL-C was measured at 3 and 9 months (mos). Median (IQR) values were reported for LDL-C reductions because data were not normally distributed. Results: Of 62 patients, 56 had available LDL-C data at 3 mos, 57 received a second dose, and 44 had available LDL-C data at 9 mos. The mean age was 67.3 y (SD 10.9), 60.3% were female, 44.4% were secondary prevention, 28.6% had at least possible FH by Dutch Lipid Clinic Network criteria ( > 3 points), 33.3% were receiving statins at baseline, and 41.3% were receiving ezetimibe at baseline. A total of 55/62 (89%) had a history of prior AEs from statins at baseline, and 17/62 (27.4%) had a history of prior PCSK9i-mAb AEs at baseline. The mean LDL-C at baseline was 137.2 mg/dL (SD 62.9). Median lipoprotein (a) was 27.5 mg/dL (IQR 10.5 to 86.5). At 3 mos, overall median reduction was 40.7% (IQR 15.7 to 51.7). A total of 11/56 (19.6%) patients had <10% LDL-C reduction. Median LDL-C reductions were 40.7% (IQR 9.3 to 50.7) in patients with statin AEs, and 23.6% (IQR 0.5 to 46.7) in patients with PCSK9i mAb AEs. Upon excluding patients with prior PCSK9i mAb AEs, the median 3-mo reduction was 46.4% (IQR 25.4 to 54.4). At 9 mos, the median overall LDL-C reduction was 33.2% (95% CI 10.9 to 46.4). Conclusion: In a retrospective cohort of patients mostly with a history of AEs from statins and/or PCSK9i mAbs, inclisiran use was associated with lower percent LDL-C reductions at 3 and 9 mos than reported in placebo-controlled trials, driven by attenuated LDL-C reductions in patients with prior PCSK9i mAb AEs. Exclusion of patients with prior PCSK9i mAb use with AEs led to similar overall LDL-C lowering as in trials. Further investigation is warranted.

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 (13)

A

Ashish Sarraju

Section of Preventive Cardiology and Rehabilitation, Department of Cardiovascular Medicine, Cleveland Clinic Foundation, Cleveland

A

Astefanos Al-Dalakta

Cleveland Clinic, Cleveland, Ohio, United States

K

Kathy Gambino

Cleveland Clinic, Cleveland, Ohio, United States

E

Erik Van Iterson

Cleveland Clinic, Cleveland, Ohio, United States

R

Ryan Tang

Cleveland Clinic, Cleveland, Ohio, United States

B

Bianca Honnekeri

Cleveland Clinic Foundation, Cleveland, Ohio, United States

S

Stanley Hazen

CLEVELAND CLINIC FOUNDATION, Cleveland, Ohio, United States

L

Luke Laffin

D

Dennis Bruemmer

Cleveland Clinic Foundation, Cleveland, Ohio, United States

J

Julie Huang

CLEVELAND CLINIC, Cleveland, Ohio, United States

A

Abhayjit Singh

Cleveland Clinic, Cleveland, Ohio, United States

V

Vikas Sunder

Cleveland Clinic, Cleveland, Ohio, United States

L

Leslie Cho