Literature DB >> 24602799

Long-term efficacy and safety of statin treatment beyond six years: a meta-analysis of randomized controlled trials with extended follow-up.

Han-lu Lv1, Dong-mei Jin2, Mo Liu3, Ying-mei Liu1, Jing-feng Wang1, Deng-feng Geng4.   

Abstract

Large-scale randomized controlled trials (RCTs) have well demonstrated the beneficial effects of cholesterol-lowering treatment with statins in patients at high risk of vascular disease. However, large statin RCTs were usually restricted to the typical 5-6 years. Moreover, non-cardiovascular events, especially the risk of cancer, probably failed to emerge within a restricted period of 6 years. The aim of this study was to evaluate the long-term efficacy and safety of statin treatment by performing a meta-analysis of statin RCTs with extended follow-up beyond 6 years. Six RCTs with post-trial follow-up were eligible for inclusion, involving 47,296 patients with total follow-up ranging from 6.7 to 14.7 years. During the post-trial period, all the surviving participants were advised to take a statin and the cholesterol level were almost identical between the original statin group and the original placebo group. Over the entire 6.7-14.7 years of follow-up, a significant reduction in the rates of all-cause mortality (relative risk 0.90, 95% confidence interval 0.85-0.96; P=0.0009), cardiovascular mortality (0.87, 0.81-0.93; P<0.0001) and major coronary events (0.79, 0.72-0.86; P<0.00001) was observed in favour of the original statin group. During 2-year post-trial period, further reduction in all-cause mortality (0.83, 0.74-0.93; P=0.001), cardiovascular mortality (0.81, 0.69-0.95; P=0.01) and major coronary events (0.77, 0.63-0.95; P=0.01) was observed among initially statin-treated patients. Over the entire follow-up period, statin treatment did not increase the incidence of cancers (0.99, 0.95-1.04; P=0.79), deaths from cancers (1.00, 0.93-1.07; P=0.98) and non-cardiovascular mortality (0.95, 0.90-1.00; P=0.07). In conclusion, statin treatment beyond 6 years is effective and safe in patients at high risk of vascular events. Moreover, earlier treatment with statin may not only preserve the initial benefit but also have further survival benefit for additional 2 years. Further studies are called for to explore the underlying mechanisms.
Copyright © 2014 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Atorvastatin (PubChem CID: 60823); Cancer; Cholesterol (PubChem CID: 5997); Fluvastatin (PubChem CID: 446155); Meta-analysis; Mortality; Pravastatin (PubChem CID: 54687); Safety; Simvastatin (PubChem CID: 54454); Statin

Mesh:

Substances:

Year:  2014        PMID: 24602799     DOI: 10.1016/j.phrs.2014.02.006

Source DB:  PubMed          Journal:  Pharmacol Res        ISSN: 1043-6618            Impact factor:   7.658


  9 in total

Review 1.  Impediments to clinical application of exercise interventions in the treatment of cardiometabolic disease.

Authors:  N John Bosomworth
Journal:  Can Fam Physician       Date:  2019-03       Impact factor: 3.275

2. 

Authors:  N John Bosomworth
Journal:  Can Fam Physician       Date:  2019-03       Impact factor: 3.275

3.  Statins and mortality: the untold story.

Authors:  Michael S Kostapanos; Moses S Elisaf
Journal:  Br J Clin Pharmacol       Date:  2017-03-17       Impact factor: 4.335

Review 4.  Is there sufficient enhancement of the reduction in CVD rates after a decade of statin therapy to justify continuation?

Authors:  Jonathan Soverow; Karol Watson
Journal:  Curr Atheroscler Rep       Date:  2014-08       Impact factor: 5.113

Review 5.  Statins: do they have a potential role in cancer prevention and modifying cancer-related outcomes?

Authors:  Stefanos Bonovas
Journal:  Drugs       Date:  2014-10       Impact factor: 9.546

6.  Reporting bias in the literature on the associations of health-related behaviors and statins with cardiovascular disease and all-cause mortality.

Authors:  Leandro Fórnias Machado de Rezende; Juan Pablo Rey-López; Thiago Hérick de Sá; Nicholas Chartres; Alice Fabbri; Lauren Powell; Emmanuel Stamatakis; Lisa Bero
Journal:  PLoS Biol       Date:  2018-06-18       Impact factor: 8.029

7.  Simvastatin as a neuroprotective treatment for Parkinson's disease (PD STAT): protocol for a double-blind, randomised, placebo-controlled futility study.

Authors:  Camille B Carroll; Douglas Webb; Kara Nicola Stevens; Jane Vickery; Vicky Eyre; Susan Ball; Richard Wyse; Mike Webber; Andy Foggo; John Zajicek; Alan Whone; Siobhan Creanor
Journal:  BMJ Open       Date:  2019-10-07       Impact factor: 2.692

8.  Randomised double-blind phase 3 clinical study testing impact of atorvastatin on prostate cancer progression after initiation of androgen deprivation therapy: study protocol.

Authors:  Aino Siltari; Jarno Riikonen; Juha Koskimäki; Tomi Pakarainen; Otto Ettala; Peter Boström; Heikki Seikkula; Andres Kotsar; Teuvo Tammela; Mika Helminen; Paavo V Raittinen; Terho Lehtimäki; Mikkel Fode; Peter Østergren; Michael Borre; Antti Rannikko; Timo Marttila; Arto Salonen; Hanna Ronkainen; Sven Löffeler; Teemu J Murtola
Journal:  BMJ Open       Date:  2022-04-29       Impact factor: 2.692

9.  Legacy effects of statins on cardiovascular and all-cause mortality: a meta-analysis.

Authors:  Agnish Nayak; Andrew Hayen; Lin Zhu; Kevin McGeechan; Paul Glasziou; Les Irwig; Jenny Doust; Gabriel Gregory; Katy Bell
Journal:  BMJ Open       Date:  2018-10-04       Impact factor: 2.692

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.