The effect of statin therapy on heart failure events: a collaborative meta-analysis of unpublished data from major randomized trials
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Author(s)
Type
Journal Article
Abstract
Aims The effect of statins on risk of heart failure (HF) hospitalization and HF death remains uncertain. We aimed to establish
whether statins reduce major HF events.
Methods
and results
We searched Medline, EMBASE, and the Cochrane Central Register of Controlled Trials for randomized controlled endpoint
statin trials from 1994 to 2014. Collaborating trialists provided unpublished data from adverse event reports. We included
primary- and secondary-prevention statin trials with .1000 participants followed for .1 year. Outcomes consisted of first
non-fatal HF hospitalization, HF death and a composite of first non-fatal HF hospitalization or HF death. HF events occurring
,30 days after within-trial myocardial infarction (MI) were excluded. We calculated risk ratios (RR) with fixed-effects metaanalyses.
In up to 17 trials with 132 538 participants conducted over 4.3 [weighted standard deviation (SD) 1.4] years, statin
therapy reduced LDL-cholesterol by 0.97 mmol/L (weighted SD 0.38 mmol/L). Statins reduced the numbers of patients
experiencing non-fatal HF hospitalization (1344/66 238 vs. 1498/66 330; RR 0.90, 95% confidence interval, CI 0.84–0.97) and
the composite HF outcome (1234/57 734 vs. 1344/57 836; RR 0.92, 95% CI 0.85–0.99) but not HF death (213/57 734 vs. 220/
57 836;RR 0.97, 95%CI 0.80–1.17).Theeffect of statinson first non-fatalHF hospitalizationwas similarwhether thiswaspreceded
by MI (RR 0.87, 95% CI 0.68–1.11) or not (RR 0.91, 95% CI 0.84–0.98).
Conclusion In primary- and secondary-prevention trials, statinsmodestly reduced the risksof non-fatalHF hospitalization and acompositeof nonfatal
HF hospitalization and HF death with no demonstrable difference in risk reduction between those who suffered an MI or not.
whether statins reduce major HF events.
Methods
and results
We searched Medline, EMBASE, and the Cochrane Central Register of Controlled Trials for randomized controlled endpoint
statin trials from 1994 to 2014. Collaborating trialists provided unpublished data from adverse event reports. We included
primary- and secondary-prevention statin trials with .1000 participants followed for .1 year. Outcomes consisted of first
non-fatal HF hospitalization, HF death and a composite of first non-fatal HF hospitalization or HF death. HF events occurring
,30 days after within-trial myocardial infarction (MI) were excluded. We calculated risk ratios (RR) with fixed-effects metaanalyses.
In up to 17 trials with 132 538 participants conducted over 4.3 [weighted standard deviation (SD) 1.4] years, statin
therapy reduced LDL-cholesterol by 0.97 mmol/L (weighted SD 0.38 mmol/L). Statins reduced the numbers of patients
experiencing non-fatal HF hospitalization (1344/66 238 vs. 1498/66 330; RR 0.90, 95% confidence interval, CI 0.84–0.97) and
the composite HF outcome (1234/57 734 vs. 1344/57 836; RR 0.92, 95% CI 0.85–0.99) but not HF death (213/57 734 vs. 220/
57 836;RR 0.97, 95%CI 0.80–1.17).Theeffect of statinson first non-fatalHF hospitalizationwas similarwhether thiswaspreceded
by MI (RR 0.87, 95% CI 0.68–1.11) or not (RR 0.91, 95% CI 0.84–0.98).
Conclusion In primary- and secondary-prevention trials, statinsmodestly reduced the risksof non-fatalHF hospitalization and acompositeof nonfatal
HF hospitalization and HF death with no demonstrable difference in risk reduction between those who suffered an MI or not.
Date Issued
2015-06-21
Date Acceptance
2015-02-26
Citation
European Heart Journal, 2015, 36 (24), pp.1536-1546
ISSN
1522-9645
Publisher
Oxford University Press (OUP)
Start Page
1536
End Page
1546
Journal / Book Title
European Heart Journal
Volume
36
Issue
24
Copyright Statement
© The Author 2015. Published by Oxford University Press on behalf of the European Society of Cardiology.
This is anOpenAccess article distributed under the terms of the CreativeCommonsAttribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse,
distribution, and reproduction in any medium, provided the original work is properly cited.
This is anOpenAccess article distributed under the terms of the CreativeCommonsAttribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse,
distribution, and reproduction in any medium, provided the original work is properly cited.
License URL
Sponsor
Imperial College Healthcare NHS Trust- BRC Funding
National Institute for Health Research
Grant Number
RDC02 79560
n/a
Subjects
Science & Technology
Life Sciences & Biomedicine
Cardiac & Cardiovascular Systems
Cardiovascular System & Cardiology
Statin
Heart failure
Randomized trial
Prevention
Meta-analysis
AVERAGE CHOLESTEROL LEVELS
PLACEBO-CONTROLLED TRIAL
ACUTE CORONARY SYNDROMES
HIGH-DOSE ATORVASTATIN
PRIMARY PREVENTION
MYOCARDIAL-INFARCTION
CARDIOVASCULAR-DISEASE
HYPERTENSIVE PATIENTS
VASCULAR EVENTS
LDL CHOLESTEROL
Publication Status
Published