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Efficacy and safety of more intensive lowering of LDL cholesterol: A meta-analysis of data from 170 000 participants in 26 randomised trials

  • Cholesterol Treatment Trialists’ (CTT) Collaboration
  • SHARP (Study of Heart and Renal Protection)
  • HPS (Heart Protection Study)
  • SEARCH (Study of Effectiveness of Additional Reductions in Cholesterol and Homocysteine)
  • FIELD (Fenofibrate Intervention and Event Lowering in Diabetes)
  • LIPID (Long-term Intervention with Pravastatin in Ischaemic Disease)
  • Phase Z
  • PROVE-IT (Pravastatin or Atorvastatin Evaluation and Infection Therapy)
  • AFCAPS/TEXCAPS (AirForce/Texas Coronary Atherosclerosis Prevention Study)
  • ALERT (Assessment of Lescol in Transplantation)
  • AURORA
  • ALLHAT (Antihypertensive Lipid Lowering Heart Attack Trial)
  • ALLIANCE (Aggressive Lipid-Lowering Initiation Abates New Cardiac Events)
  • ASCOT (Anglo-Scandinavian Cardiac Outcomes Trial)
  • Aspen
  • BIP (Bezafibrate Infarction Prevention Study)
  • CARDS (Collaborative Atorvastatin Diabetes Study)
  • 4D (Die Deutsche Diabetes Dialyse Study)
  • CARE (Cholesterol and Recurrent Events Study)
  • GISSI (Gruppo Italiano per Lo Studio della Sopravvivenza nell'Infarto Miocardico)-Heart Failure
  • GISSI-Prevention
  • HIT (Veteran Administration Low HDL Intervention Trial)
  • IDEAL (Incremental Decrease in Endpoints through Aggressive Lipid-Lowering)
  • JUPITER
  • LDS (Lipids in Diabetes Study)
  • LEADER (Lower Extremity Arterial Disease Event Reduction Trial)
  • LIPS (Lescol Intervention Prevention Study)
  • MEGA (Management of Elevated Cholesterol in the Primary Prevention Group of Adult Japanese)
  • Post-CABG (Post- Coronary Artery Bypass Graft Study)
  • PPP (Pravastatin Pooling Project)
  • PROSPER (Prospective Study of Pravastatin in the Elderly
  • WOSCOPS (West of Scotland Coronary Prevention Study)
  • 4S (Scandinavian Simvastatin Survival Study)
  • TNT (Testing New Targets)
  • WHI (Women's Health Initiative)
  • Bristol-Myers Squibb
  • Merck
  • Laboratoires Fournier
  • Bayer AG
  • Novartis
  • AstraZeneca
  • Pfizer

Research output: Contribution to journalArticlepeer-review

Abstract

Lowering of LDL cholesterol with standard statin regimens reduces the risk of occlusive vascular events in a wide range of individuals. We aimed to assess the safety and efficacy of more intensive lowering of LDL cholesterol with statin therapy. We undertook meta-analyses of individual participant data from randomised trials involving at least 1000 participants and at least 2 years' treatment duration of more versus less intensive statin regimens (five trials; 39 612 individuals; median follow-up 5·1 years) and of statin versus control (21 trials; 129 526 individuals; median follow-up 4·8 years). For each type of trial, we calculated not only the average risk reduction, but also the average risk reduction per 1·0 mmol/L LDL cholesterol reduction at 1 year after randomisation. In the trials of more versus less intensive statin therapy, the weighted mean further reduction in LDL cholesterol at 1 year was 0·51 mmol/L. Compared with less intensive regimens, more intensive regimens produced a highly significant 15 (95 CI 11-18; p<0·0001) further reduction in major vascular events, consisting of separately significant reductions in coronary death or non-fatal myocardial infarction of 13 (95 CI 7-19; p<0·0001), in coronary revascularisation of 19 (95 CI 15-24; p<0·0001), and in ischaemic stroke of 16 (95 CI 5-26; p=0·005). Per 1·0 mmol/L reduction in LDL cholesterol, these further reductions in risk were similar to the proportional reductions in the trials of statin versus control. When both types of trial were combined, similar proportional reductions in major vascular events per 1·0 mmol/L LDL cholesterol reduction were found in all types of patient studied (rate ratio [RR] 0·78, 95 CI 0·76-0·80; p<0·0001), including those with LDL cholesterol lower than 2 mmol/L on the less intensive or control regimen. Across all 26 trials, all-cause mortality was reduced by 10 per 1·0 mmol/L LDL reduction (RR 0·90, 95 CI 0·87-0·93; p<0·0001), largely reflecting significant reductions in deaths due to coronary heart disease (RR 0·80, 99 CI 0·74-0·87; p<0·0001) and other cardiac causes (RR 0·89, 99 CI 0·81-0·98; p=0·002), with no significant effect on deaths due to stroke (RR 0·96, 95 CI 0·84-1·09; p=0·5) or other vascular causes (RR 0·98, 99 CI 0·81-1·18; p=0·8). No significant effects were observed on deaths due to cancer or other non-vascular causes (RR 0·97, 95 CI 0·92-1·03; p=0·3) or on cancer incidence (RR 1·00, 95 CI 0·96- 1·04; p=0·9), even at low LDL cholesterol concentrations. Further reductions in LDL cholesterol safely produce definite further reductions in the incidence of heart attack, of revascularisation, and of ischaemic stroke, with each 1·0 mmol/L reduction reducing the annual rate of these major vascular events by just over a fifth. There was no evidence of any threshold within the cholesterol range studied, suggesting that reduction of LDL cholesterol by 2-3 mmol/L would reduce risk by about 40-50. UK Medical Research Council, British Heart Foundation, European Community Biomed Programme, Australian National Health and Medical Research Council, and National Heart Foundation.

Original languageEnglish
Pages (from-to)1670-1681
Number of pages12
JournalThe Lancet
Volume376
Issue number9753
DOIs
Publication statusPublished - 13 Nov 2010

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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