Efficacy and Safety of Very Low Achieved LDL Cholesterol in Patients With Previous Ischemic Stroke

V Victorien Monguillon (Brigham and Women’s Hospital and Harvard Medical School, Boston, MA (B.B., R.P.G., V.M.).) P Peter J. Kelly (Mater Misericordiae University Hospital, Dublin, Ireland (P.J.K.).) M Michelle L. O’Donoghue (TIMI (Thrombolysis in Myocardial Infarction Study) Group, Boston, MA (V.M., N.A.M., E.A.B., J.-G.P., J.F.K., S.A.M., R.P.G., M.S.S., M.L.O.).) J Jeong-Gun Park (Thrombolysis in Myocardial Infarction (TIMI) Study Group, Division of Cardiovascular Medicine, Brigham and Women’s Hospital, Boston) E Erin A. Bohula (Thrombolysis in Myocardial Infarction (TIMI) Study Group, Division of Cardiovascular Medicine, Brigham and Women’s Hospital, Boston) J Jeffrey L. Saver (Comprehensive Stroke Center and Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles) D Dan Atar (Department of Cardiology, Oslo University Hospital Ullevaal, Oslo) 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.).) H Huei Wang (Amgen, Thousand Oaks, CA) G Gabriel Paiva da Silva Lima (Amgen, Thousand Oaks, CA) 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 previous ischemic stroke are at high risk for recurrent stroke and other major adverse cardiovascular events. The benefits of achieving very low levels of low-density lipoprotein cholesterol (LDL-C) in such patients is unclear. METHODS: We analyzed patients with previous ischemic stroke enrolled in FOURIER (Further Cardiovascular Outcomes Research With PCSK9 Inhibition in Subjects With Elevated Risk), a randomized placebo-controlled trial studying evolocumab in patients with stable atherosclerotic cardiovascular disease (median follow-up, 2.2 years), and through the open-label extension (FOURIER-OLE) period (additional median follow-up, 5 years), to examine the relationship between achieved LDL-C and the long-term incidence of the primary end point (cardiovascular death, myocardial infarction, stroke, or hospitalization for unstable angina or coronary revascularization) and stroke-related end points. RESULTS: The analysis included 5291 patients with previous ischemic stroke (>4 weeks). Of these, 666 (12.6%), 1410 (26.6%), 586 (11.1%), 508 (9.6%), and 2121 (40.1%) patients achieved LDL-C values of <20, 20 to <40, 40 to <55, 55 to <70, and ≥70 mg/dL, respectively. The incidence of the primary end point, all stroke, and ischemic stroke each decreased in a monotonic fashion with lower achieved LDL-C levels on a continuous scale ( P trend <0.001, 0.002, and 0.002, respectively). Compared with patients with LDL-C ≥70 mg/dL, those who achieved levels <40 mg/dL had incidence rate ratios of 0.69 (95% CI, 0.57–0.84), 0.73 (95% CI, 0.53–0.99), and 0.75 (95% CI, 0.54–1.05) for the outcomes of the primary end point, all stroke, and ischemic stroke, respectively. Hemorrhagic strokes were infrequent and unrelated to achieved LDL-C ( P trend =0.85). CONCLUSIONS: In patients with previous ischemic stroke, it appeared that the lower the LDL-C, down to levels <40 mg/dL, the lower the risk of major adverse cardiovascular events, including recurrent stroke, without a clear increase in risk of hemorrhagic stroke. These findings support the concept that more intensive LDL-C lowering in patients with previous ischemic stroke may be warranted. REGISTRATION: URL: https://www.clinicaltrials.gov ; Unique identifier: NCT01764633/NCT01764633.

Article Details

Journal Circulation
Volume / Issue Vol. 153, Issue 2
Published January 13, 2026
Pages 86-93
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (13)

V

Victorien Monguillon

Brigham and Women’s Hospital and Harvard Medical School, Boston, MA (B.B., R.P.G., V.M.).

P

Peter J. Kelly

Mater Misericordiae University Hospital, Dublin, Ireland (P.J.K.).

M

Michelle L. O’Donoghue

TIMI (Thrombolysis in Myocardial Infarction Study) Group, Boston, MA (V.M., N.A.M., E.A.B., J.-G.P., J.F.K., S.A.M., R.P.G., M.S.S., M.L.O.).

J

Jeong-Gun Park

Thrombolysis in Myocardial Infarction (TIMI) Study Group, Division of Cardiovascular Medicine, Brigham and Women’s Hospital, Boston

E

Erin A. Bohula

Thrombolysis in Myocardial Infarction (TIMI) Study Group, Division of Cardiovascular Medicine, Brigham and Women’s Hospital, Boston

J

Jeffrey L. Saver

Comprehensive Stroke Center and Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles

D

Dan Atar

Department of Cardiology, Oslo University Hospital Ullevaal, Oslo

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.).

H

Huei Wang

Amgen, Thousand Oaks, CA

G

Gabriel Paiva da Silva Lima

Amgen, Thousand Oaks, CA

M

Marc S. Sabatine

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

R

Robert P. Giugliano