Intensive Lowering of LDL Cholesterol Levels With Evolocumab in Autoimmune or Inflammatory Diseases: An Analysis of the FOURIER Trial

A Andre Zimerman (TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women’s Hospital, Boston) A Ana Laura F. Kunzler (Hospital Moinhos de Vento, Moinhos de Vento College of Health Sciences, Porto Alegre, Brazil (A.Z., A.L.F.K.).) B Brittany N. Weber (Cardiovascular Imaging Program, Departments of Radiology and Medicine, Brigham and Women’s Hospital, Boston, MA (D.M.L., B.N.W., J.H., S.C., R.B., S.D., M.F.D.).) X Xinhui Ran (Thrombolysis in Myocardial Infarction Study Group, Division of Cardiovascular Medicine, Brigham and Women’s Hospital, Boston, MA (N.A.M., B.A.B., X.R., S.A.M., S.Z., R.P.G., M.S.S.).) S Sabina A. Murphy (TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women’s Hospital, Boston) H Huei Wang (Amgen, Thousand Oaks, CA) N Narimon Honarpour (Global Development (N.H.), Amgen, Thousand Oaks, CA.) A Anthony C. Keech (Department of Medicine, University of Sydney and Royal Prince Alfred Hospital, Australia (A.C.K.).) P Peter S. Sever (National Heart and Lung Institute, Imperial College London, United Kingdom (P.S.S.).) M Marc S. Sabatine (TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women’s Hospital, Boston) R Robert P. Giugliano

Abstract

BACKGROUND: Patients with an autoimmune or inflammatory disease (AIID) are at increased cardiovascular risk and may benefit more from statin therapy. In the FOURIER trial (Further Cardiovascular Outcomes Research with PCSK9 Inhibition in Subjects with Elevated Risk), the PCSK9 (proprotein convertase subtilisin/kexin type 9) inhibitor evolocumab lowered low-density lipoprotein cholesterol levels, but not hsCRP (high-sensitivity C-reactive protein) levels, and reduced the risk of cardiovascular events. METHODS: FOURIER was a randomized trial of evolocumab versus placebo in 27 564 patients with stable atherosclerosis who were taking statins. This analysis focused on the effect of evolocumab in patients with or without an AIID, defined as any autoimmune or chronic inflammatory condition. The primary end point was a composite of cardiovascular death, myocardial infarction, stroke, unstable angina, or coronary revascularization. RESULTS: At baseline, 889 patients (3.2%) had an AIID, most commonly rheumatoid arthritis (33.7%) or psoriasis (15.6%). Median (interquartile range) low-density lipoprotein cholesterol levels were 90.0 mg/dL (79.5–105.5) and 91.5 mg/dL (79.5–108.5) in patients with or without an AIID, respectively ( P =0.025), and the placebo-adjusted percent reduction with evolocumab was consistent (60.2% versus 59.0%; P =0.57). Baseline hsCRP was higher in patients with an AIID (median 2.1 versus 1.7 mg/L; P <0.001) and did not significantly change with evolocumab in either group. Compared with placebo, evolocumab reduced the rate of the primary end point by 14% in patients without an AIID (hazard ratio, 0.86 [95% CI, 0.80–0.93]) and by 42% in patients with an AIID (hazard ratio, 0.58 [95% CI, 0.38–0.89]; P interaction =0.066). Likewise, evolocumab reduced the key secondary end point of cardiovascular death, myocardial infarction, or stroke by 19% in patients without an AIID (hazard ratio, 0.81 [95% CI, 0.74–0.89]) and 58% in those with an AIID (hazard ratio, 0.42 [95% CI, 0.24–0.74]; P interaction =0.022). CONCLUSIONS: Intensive lowering of low-density lipoprotein cholesterol levels with evolocumab may lead to greater relative reduction in cardiovascular events in patients with an AIID. REGISTRATION: URL: https://www.clinicaltrials.gov ; Unique identifier: NCT01764633.

Article Details

Journal Circulation
Volume / Issue Vol. 151, Issue 20
Published May 20, 2025
Pages 1467-1476
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (11)

A

Andre Zimerman

TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women’s Hospital, Boston

A

Ana Laura F. Kunzler

Hospital Moinhos de Vento, Moinhos de Vento College of Health Sciences, Porto Alegre, Brazil (A.Z., A.L.F.K.).

B

Brittany N. Weber

Cardiovascular Imaging Program, Departments of Radiology and Medicine, Brigham and Women’s Hospital, Boston, MA (D.M.L., B.N.W., J.H., S.C., R.B., S.D., M.F.D.).

X

Xinhui Ran

Thrombolysis in Myocardial Infarction Study Group, Division of Cardiovascular Medicine, Brigham and Women’s Hospital, Boston, MA (N.A.M., B.A.B., X.R., S.A.M., S.Z., R.P.G., M.S.S.).

S

Sabina A. Murphy

TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women’s Hospital, Boston

H

Huei Wang

Amgen, Thousand Oaks, CA

N

Narimon Honarpour

Global Development (N.H.), Amgen, Thousand Oaks, CA.

A

Anthony C. Keech

Department of Medicine, University of Sydney and Royal Prince Alfred Hospital, Australia (A.C.K.).

P

Peter S. Sever

National Heart and Lung Institute, Imperial College London, United Kingdom (P.S.S.).

M

Marc S. Sabatine

TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women’s Hospital, Boston

R

Robert P. Giugliano