Yield of Dual Therapy With Statin and Ezetimibe in the Treat Stroke to Target Trial.


Journal

Stroke
ISSN: 1524-4628
Titre abrégé: Stroke
Pays: United States
ID NLM: 0235266

Informations de publication

Date de publication:
11 2022
Historique:
pubmed: 27 9 2022
medline: 27 10 2022
entrez: 26 9 2022
Statut: ppublish

Résumé

In atherosclerotic stroke, lipid-lowering treatment with a target LDL (low-density lipoprotein) cholesterol of <70 compared with 100±10 mg/dL reduced the risk of subsequent cardiovascular events. This post hoc analysis explored the relative effects of the combination of statin and ezetimibe (dual therapy) and statin monotherapy in achieving the lower LDL cholesterol target and in reducing the risk of major vascular events, as compared with the higher target group. 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 or 100±10 mg/dL, using statin and/or ezetimibe as needed. 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. Among 2860 patients enrolled, patients who were on dual therapy during the trial in the lower target group had a higher baseline LDL cholesterol as compared to patients on statin monotherapy (141±38 versus 131±36, respectively, In the TST trial (Treat Stroke to Target), targeting an LDL cholesterol of < 70 mg/dL with a combination of statin and ezetimibe compared with 100±10 mg/dL consistently reduced the risk of subsequent stroke. URL: https://www. gov; Unique identifier: NCT01252875. URL: clinicaltrialsregister.eu; Unique identifier: EUDRACT2009-A01280-57.

Sections du résumé

BACKGROUND
In atherosclerotic stroke, lipid-lowering treatment with a target LDL (low-density lipoprotein) cholesterol of <70 compared with 100±10 mg/dL reduced the risk of subsequent cardiovascular events. This post hoc analysis explored the relative effects of the combination of statin and ezetimibe (dual therapy) and statin monotherapy in achieving the lower LDL cholesterol target and in reducing the risk of major vascular events, as compared with the higher target group.
METHODS
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 or 100±10 mg/dL, using statin and/or ezetimibe as needed. 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 who were on dual therapy during the trial in the lower target group had a higher baseline LDL cholesterol as compared to patients on statin monotherapy (141±38 versus 131±36, respectively,
CONCLUSIONS
In the TST trial (Treat Stroke to Target), targeting an LDL cholesterol of < 70 mg/dL with a combination of statin and ezetimibe compared with 100±10 mg/dL consistently reduced the risk of subsequent stroke.
REGISTRATION
URL: https://www.
CLINICALTRIALS
gov; Unique identifier: NCT01252875. URL: clinicaltrialsregister.eu; Unique identifier: EUDRACT2009-A01280-57.

Identifiants

pubmed: 36154103
doi: 10.1161/STROKEAHA.122.039728
doi:

Substances chimiques

Ezetimibe EOR26LQQ24
Hydroxymethylglutaryl-CoA Reductase Inhibitors 0
Cholesterol, LDL 0
Anticholesteremic Agents 0

Banques de données

ClinicalTrials.gov
['NCT01252875']
EudraCT
['2009-A01280-57']

Types de publication

Randomized Controlled Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3260-3267

Auteurs

Pierre Amarenco (P)

APHP, Department of Neurology and Stroke center, Bichat Hospital, INSERM LVTS-U1148, DHU FIRE, University of Paris, France (P.A., H.C., P.C.L., E.M.).
Population Health Research Institute, McMaster University, Hamilton, Ontario, Canada (P.A.).

Jong S Kim (JS)

Asan Medical Center, Seoul, South Korea (J.S.K.).

Julien Labreuche (J)

CHU Lille, Department of Biostatistics, France (J.L.).

Hugo Charles (H)

APHP, Department of Neurology and Stroke center, Bichat Hospital, INSERM LVTS-U1148, DHU FIRE, University of Paris, France (P.A., H.C., P.C.L., E.M.).

Maurice Giroud (M)

Department of Neurology, University Hospital of Dijon, Dijon Stroke Registry, EA 7460, University of Burgundy, UBFC, France (M.G.).

Byung-Chul Lee (BC)

Department of Neurology, Hallym University Sacred Heart Hospital, Anyang, Korea (B.-C.L.).

Philippa C Lavallée (PC)

APHP, Department of Neurology and Stroke center, Bichat Hospital, INSERM LVTS-U1148, DHU FIRE, University of Paris, France (P.A., H.C., P.C.L., E.M.).

Marie-Hélène Mahagne (MH)

Stroke Unit, Pasteur Hospital, Nice, France (M.-H.M.).

Elena Meseguer (E)

APHP, Department of Neurology and Stroke center, Bichat Hospital, INSERM LVTS-U1148, DHU FIRE, University of Paris, France (P.A., H.C., P.C.L., E.M.).

Norbert Nighoghossian (N)

Hospices Civils de Lyon, Department of Neurology and Stroke Center, Lyon University, France (N.N.).

Philippe Gabriel Steg (PG)

Université de Paris, INSERM LVTS-U1148, France (P.G.S.).
AP-HP, Hôpital Bichat, France (P.G.S.).

Éric Vicaut (É)

APHP, Department of Biostatistics, Université Paris-Diderot, Sorbonne-Paris Cité, Fernand Widal hospital, Paris, France (É.V.).

Eric Bruckert (E)

APHP, Department of Endocrinology, Pitié-Salpêtrière hospital, Sorbonne University, Paris, France (E.B.).

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Classifications MeSH