Low-density lipoprotein cholesterol reduction and statin intensity in myocardial infarction patients and major adverse outcomes: a Swedish nationwide cohort study.


Journal

European heart journal
ISSN: 1522-9645
Titre abrégé: Eur Heart J
Pays: England
ID NLM: 8006263

Informations de publication

Date de publication:
20 01 2021
Historique:
received: 16 07 2020
revised: 02 10 2020
accepted: 27 11 2020
pubmed: 29 12 2020
medline: 28 5 2021
entrez: 28 12 2020
Statut: ppublish

Résumé

Clinical trials have demonstrated that a reduction in low-density lipoprotein cholesterol (LDL-C) reduces cardiovascular (CV) events. This has, however, not yet been shown in a real-world setting. We aimed to investigate the association between LDL-C changes and statin intensity with prognosis after a myocardial infarction (MI). Patients admitted with MI were followed for mortality and major CV events. Changes in LDL-C between the MI and a 6- to 10-week follow-up visit were analysed. The associations between quartiles of LDL-C change and statin intensity with outcomes were assessed using adjusted Cox regression analyses. A total of 40 607 patients were followed for a median of 3.78 years. The median change in LDL-C was a 1.20 mmol/L reduction. Patients with larger LDL-C reduction (1.85 mmol/L, 75th percentile) compared with a smaller reduction (0.36 mmol/L, 25th percentile) had lower hazard ratios (HR) for all outcomes (95% confidence interval): composite of CV mortality, MI, and ischaemic stroke 0.77 (0.70-0.84); all-cause mortality 0.71 (0.63-0.80); CV mortality 0.68 (0.57-0.81); MI 0.81 (0.73-0.91); ischaemic stroke 0.76 (0.62-0.93); heart failure hospitalization 0.73 (0.63-0.85), and coronary artery revascularization 0.86 (0.79-0.94). Patients with ≥50% LDL-C reduction using high-intensity statins at discharge had a lower incidence of all outcomes compared with those using a lower intensity statin. Larger early LDL-C reduction and more intensive statin therapy after MI were associated with a reduced hazard of all CV outcomes and all-cause mortality. This supports clinical trial data suggesting that earlier lowering of LDL-C after an MI confers the greatest benefit.

Identifiants

pubmed: 33367526
pii: 6047259
doi: 10.1093/eurheartj/ehaa1011
pmc: PMC7954251
doi:

Substances chimiques

Hydroxymethylglutaryl-CoA Reductase Inhibitors 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

243-252

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of the European Society of Cardiology.

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Auteurs

Jessica Schubert (J)

Department of Medical Sciences, Uppsala University, Uppsala, Sweden.

Bertil Lindahl (B)

Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
Uppsala Clinical Research Center, Uppsala, Sweden.

Håkan Melhus (H)

Department of Medical Sciences, Uppsala University, Uppsala, Sweden.

Henrik Renlund (H)

Uppsala Clinical Research Center, Uppsala, Sweden.

Margrét Leosdottir (M)

Department of Cardiology, Skåne University Hospital, Malmö, Sweden.
Department of Clinical Sciences, Faculty of Medicine, Lund University, Malmö, Sweden.

Ali Yari (A)

Department of Clinical Sciences, Karolinska Institutet, Danderyd Hospital, Stockholm, Sweden.

Peter Ueda (P)

Clinical Epidemiology Division, Department of Medicine, Karolinska Institutet, Stockholm, Sweden.

Stefan James (S)

Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
Uppsala Clinical Research Center, Uppsala, Sweden.

Stephanie R Reading (SR)

Amgen, Inc, Thousand Oaks, CA, USA.

Paul J Dluzniewski (PJ)

Amgen, Inc, Thousand Oaks, CA, USA.

Andrew W Hamer (AW)

Amgen, Inc, Thousand Oaks, CA, USA.

Tomas Jernberg (T)

Department of Clinical Sciences, Karolinska Institutet, Danderyd Hospital, Stockholm, Sweden.

Emil Hagström (E)

Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
Uppsala Clinical Research Center, Uppsala, Sweden.

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Classifications MeSH