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PMID: 15325833 Published · ppublish English Clinical Trial Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Primary prevention of cardiovascular disease with atorvastatin in type 2 diabetes in the Collaborative Atorvastatin Diabetes Study (CARDS): multicentre randomised placebo-controlled trial.

Lancet (London, England) ·Vol. 364 ·No. 9435 ·2004-00-00 ·Pages 685-96

Colhoun HM, Betteridge DJ, Durrington PN, Hitman GA, Neil HA, Livingstone SJ, Thomason MJ, Mackness MI, Charlton-Menys V, Fuller JH, CARDS investigators

Abstract

Type 2 diabetes is associated with a substantially increased risk of cardiovascular disease, but the role of lipid-lowering therapy with statins for the primary prevention of cardiovascular disease in diabetes is inadequately defined. We aimed to assess the effectiveness of atorvastatin 10 mg daily for primary prevention of major cardiovascular events in patients with type 2 diabetes without high concentrations of LDL-cholesterol. 2838 patients aged 40-75 years in 132 centres in the UK and Ireland were randomised to placebo (n=1410) or atorvastatin 10 mg daily (n=1428). Study entrants had no documented previous history of cardiovascular disease, an LDL-cholesterol concentration of 4.14 mmol/L or lower, a fasting triglyceride amount of 6.78 mmol/L or less, and at least one of the following: retinopathy, albuminuria, current smoking, or hypertension. The primary endpoint was time to first occurrence of the following: acute coronary heart disease events, coronary revascularisation, or stroke. Analysis was by intention to treat. The trial was terminated 2 years earlier than expected because the prespecified early stopping rule for efficacy had been met. Median duration of follow-up was 3.9 years (IQR 3.0-4.7). 127 patients allocated placebo (2.46 per 100 person-years at risk) and 83 allocated atorvastatin (1.54 per 100 person-years at risk) had at least one major cardiovascular event (rate reduction 37% [95% CI -52 to -17], p=0.001). Treatment would be expected to prevent at least 37 major vascular events per 1000 such people treated for 4 years. Assessed separately, acute coronary heart disease events were reduced by 36% (-55 to -9), coronary revascularisations by 31% (-59 to 16), and rate of stroke by 48% (-69 to -11). Atorvastatin reduced the death rate by 27% (-48 to 1, p=0.059). No excess of adverse events was noted in the atorvastatin group. Atorvastatin 10 mg daily is safe and efficacious in reducing the risk of first cardiovascular disease events, including stroke, in patients with type 2 diabetes without high LDL-cholesterol. No justification is available for having a particular threshold level of LDL-cholesterol as the sole arbiter of which patients with type 2 diabetes should receive statins. The debate about whether all people with this disorder warrant statin treatment should now focus on whether any patients are at sufficiently low risk for this treatment to be withheld.

MeSH Terms
Adult Aged Anticholesteremic Agents/therapeutic use Atorvastatin Cardiovascular Diseases/prevention & control Cholesterol, LDL/blood Coronary Disease/etiology,prevention & control Diabetes Mellitus, Type 2/blood,complications Double-Blind Method Female Heptanoic Acids/therapeutic use Humans Hydroxymethylglutaryl-CoA Reductase Inhibitors/therapeutic use Male Middle Aged Pyrroles/therapeutic use Risk Factors Stroke/etiology,prevention & control
Chemicals
Anticholesteremic Agents Cholesterol, LDL Heptanoic Acids Hydroxymethylglutaryl-CoA Reductase Inhibitors Pyrroles Atorvastatin
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Colhoun Helen M
EURODIAB, Department of Epidemiology and Public Health, Royal Free and University College Medical School, London, UK. [email protected]
Betteridge D John
Durrington Paul N
Hitman Graham A
Neil H Andrew W
Livingstone Shona J
Thomason Margaret J
Mackness Michael I
Charlton-Menys Valentine
Fuller John H
CARDS investigators
Article Info
Journal
Lancet (London, England)
Abbr.
Lancet
ISSN
1474-547X
Published
2004-00-00
Pages
685-96
Language
English
Region
England
NLM ID
2985213R
Subset
IM
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