Efficacy and safety of LDL-lowering therapy among men and women: Meta-analysis of individual data from 174 000 participants in 27 randomised trials

  • Jordan Fulcher
  • , Rachel O'Connell
  • , Merryn Voysey
  • , Jonathan Emberson
  • , Lisa Blackwell
  • , B. Mihaylova
  • , J. Simes
  • , R. Collins
  • , Adrienne Kirby
  • , Helen Colhoun
  • , Eugene Braunwald
  • , John La Rosa
  • , T. R. Pedersen
  • , Andrew Tonkin
  • , Barry Davis
  • , Peter Sleight
  • , Maria Grazia Franzosi
  • , Colin Baigent
  • , Anthony Keech
  • , J. De Lemos
  • M. Blazing, S. Murphy, J. R. Downs, A. Gotto, M. Clearfield, H. Holdaas, D. Gordon, M. Koren, B. Dahlöf, N. Poulter, P. Sever, R. H. Knopp, B. Fellström, A. Jardine, R. Schmieder, F. Zannad, U. Goldbourt, E. Kaplinsky, D. J. Betteridge, P. N. Durrington, G. A. Hitman, J. Fuller, A. Neil, C. Wanner, V. Krane, F. Sacks, L. Moyé, M. Pfeffer, C. M. Hawkins, J. Kjekshus, H. Wedel, J. Wikstrand, P. Barter, L. Tavazzi, A. Maggioni, R. Marchioli, G. Tognoni, H. Bloomfield, S. Robins, J. Armitage, S. Parish, R. Peto, P. M. Ridker, R. Holman, T. Meade, S. MacMahon, I. C. Marschner, J. Shaw, P. W. Serruys, H. Nakamura, G. Knatterud, C. Furberg, R. Byington, P. Macfarlane, S. Cobbe, I. Ford, M. Murphy, G. J. Blauw, C. Packard, J. Shepherd, L. Wilhelmsen, C. Cannon, L. Bowman, M. Landray, J. Rossouw, J. Probstfield, S. Cobbe, M. Flather, J. Kastelein, C. Newman, C. Shear, J. Tobert, J. Varigos, H. White, S. Yusuf, E. H. Barnes, W. G. Herrington, L. E. Holland, C. Reith

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

1298 Citations (Scopus)

Abstract

Background: Whether statin therapy is as effective in women as in men is debated, especially for primary prevention. We undertook a meta-analysis of statin trials in the Cholesterol Treatment Trialists' (CTT) Collaboration database to compare the effects of statin therapy between women and men. Methods: We performed meta-analyses on data from 22 trials of statin therapy versus control (n=134 537) and five trials of more-intensive versus less-intensive statin therapy (n=39 612). Effects on major vascular events, major coronary events, stroke, coronary revascularisation and mortality were weighted per 1·0 mmol/L reduction in LDL cholesterol and effects in men and women compared with a Cox model that adjusted for non-sex differences. For subgroup analyses, we used 99% CIs to make allowance for the multiplicity of comparisons. Findings 46 675 (27%) of 174 149 randomly assigned participants were women. Allocation to a statin had similar absolute effects on 1 year lipid concentrations in both men and women (LDL cholesterol reduced by about 1·1 mmol/L in statin vs control trials and roughly 0·5 mmol/L for more-intensive vs less-intensive therapy). Women were generally at lower cardiovascular risk than were men in these trials. The proportional reductions per 1·0 mmol/L reduction in LDL cholesterol in major vascular events were similar overall for women (rate ratio [RR] 0·84, 99% CI 0·78-0·91) and men (RR 0·78, 99% CI 0·75-0·81, adjusted p value for heterogeneity by sex=0·33) and also for those women and men at less than 10% predicted 5 year absolute cardiovascular risk (adjusted heterogeneity p=0·11). Likewise, the proportional reductions in major coronary events, coronary revascularisation, and stroke did not differ significantly by sex. No adverse effect on rates of cancer incidence or non-cardiovascular mortality was noted for either sex. These net benefits translated into all-cause mortality reductions with statin therapy for both women (RR 0·91, 99% CI 0·84-0·99) and men (RR 0·90, 99% CI 0·86-0·95; adjusted heterogeneity p=0·43). Interpretation In men and women at an equivalent risk of cardiovascular disease, statin therapy is of similar effectiveness for the prevention of major vascular events.

Original languageEnglish
Pages (from-to)1397-1405
Number of pages9
JournalThe Lancet
Volume385
Issue number9976
DOIs
Publication statusPublished - 1 Jan 2015

Fingerprint

Dive into the research topics of 'Efficacy and safety of LDL-lowering therapy among men and women: Meta-analysis of individual data from 174 000 participants in 27 randomised trials'. Together they form a unique fingerprint.

Cite this