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Randomized Controlled Trial
. 2023 Aug;54(8):1993-2001.
doi: 10.1161/STROKEAHA.123.042621. Epub 2023 Jun 28.

More Than 50 Percent Reduction in LDL Cholesterol in Patients With Target LDL <70 mg/dL After a Stroke

Collaborators, Affiliations
Free article
Randomized Controlled Trial

More Than 50 Percent Reduction in LDL Cholesterol in Patients With Target LDL <70 mg/dL After a Stroke

Pierre Amarenco et al. Stroke. 2023 Aug.
Free article

Abstract

Background: Whether a strategy to target an LDL (low-density lipoprotein) cholesterol <70 mg/dL is more effective when LDL is reduced >50% from baseline rather than <50% from baseline has not been investigated.

Methods: The Treat Stroke to Target trial was conducted in France and South Korea in 61 sites between March 2010 and December 2018. Patients with ischemic stroke in the previous 3 months or transient ischemic attack within the previous 15 days and evidence of cerebrovascular or coronary artery atherosclerosis were randomly assigned to a target LDL cholesterol of <70 mg/dL or 100±10 mg/dL, using statin and/or ezetimibe as needed. We used the results of repeated LDL measurements (median, 5 [2-6] per patient) during 3.9 years (interquartile range, 2.1-6.8) of follow-up. The primary outcome was the composite of ischemic stroke, myocardial infarction, new symptoms requiring urgent coronary or carotid revascularization, and vascular death. Cox regression model including lipid-lowering therapy as a time-varying variable, after adjustment for randomization strategy, age, sex, index event (stroke or transient ischemic attack), and time since the index event.

Results: Among 2860 patients enrolled, patients in the lower target group who had >50% LDL cholesterol reduction from baseline during the trial had a higher baseline LDL cholesterol and a lower LDL cholesterol achieved as compared to patients who had <50% LDL cholesterol reduction (155±32 and 62 mg/dL versus 121±34 and 74 mg/dL, respectively, P<0.001 for both). In the <70 mg/dL target group, patients with >50% LDL reduction had a significant reduction in the primary outcome as compared to the higher target group (hazard ratio, 0.61 [95% CI, 0.43-0.88]; P=0.007) and patients with <50% LDL reduction from baseline had little reduction (hazard ratio, 0.96 [95% CI, 0.73-1.26]; P=0.75).

Conclusions: In this post hoc analysis of the TST trial, targeting an LDL cholesterol of <70 mg/dL reduced the risk of primary outcome compared with 100±10 mg/dL provided LDL cholesterol reduction from baseline was superior to 50%, thereby suggesting that the magnitude of LDL cholesterol reduction was as important to consider as the target level to achieve.

Registration: URL: https://www.

Clinicaltrials: gov; Unique identifier: NCT01252875. URL: https://clinicaltrialsregister.eu; Unique identifier: EUDRACT2009-A01280-57.

Keywords: atherosclerosis; cholesterol; lipoprotein; stroke.

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Conflict of interest statement

Disclosures Dr Amarenco reports receipt of research grant support from Pfizer, Sanofi, Bristol-Myers-Squibb (BMS), Merck, AstraZeneca, Boston Scientific, Althera Pharmaceutical, from the French government and consulting fees from Pfizer, BMS, AstraZeneca, Bayer, Janssen, Kowa, Amgen, Portola, Novartis, and lecture fees from Amgen, Pfizer, and Sanofi. Dr Kim reports the following relationships: Dong-A, Pfizer, Servier, Daiichi-Sankyo, and Shin-Poong. Dr Giroud reports the following relationships: Sanofi, Bayer, Boehringer-Ingelheim, Pfizer, AstraZeneca, BMS, Daiichi-Sankyo. Dr Lee reports the following relationships: Boehringer-Ingelheim, Bayer, Daiichi-Sankyo, Esai, and AstraZeneca. Dr Steg discloses the following relationships: Research grant from Bayer, Merck, Sanofi, and Servier; speaking or consulting fees from Amarin, Amgen, AstraZeneca, Bayer/Janssen, Boehringer-Ingelheim, BMS, Lilly, Merck, Novartis, Pfizer, Regeneron, Sanofi, Servier, Novo Nordisk, Idorsia, PhaseBio; and patent for use of alirocumab use to reduce cardiovascular risk (patent assigned to Sanofi). Dr Vicaut reports Consulting/speaking honoraria from Abbott, Amgen, BMS, Fresenius, GSK, Medtronic, Pfizer, Sanofi, Stallergenes, Novartis. Dr Bruckert reports having received grants from Pfizer and AstraZeneca, honorarium for Consulting/presentation from Amryt Pharma Holdings Ltd, Novartis, Merck, AstraZeneca, Amarin Pharma Inc, Silence Therapeutics, AMGEN, Genfit, Sanofi and Regeneron, Aegerion, Mylan, AKCEA, Danone, and Servier. The other authors report no conflicts.

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