TY - JOUR
T1 - The prevention of progression of arterial disease and diabetes (POPADAD) trial
T2 - Factorial randomised placebo controlled trial of aspirin and antioxidants in patients with diabetes and asymptomatic peripheral arterial disease
AU - Prevention of Progression of Arterial Disease and Diabetes Study Group
AU - Diabetes Registry Group
AU - Royal College of Physicians Edinburgh
AU - Belch, Jill
AU - MacCuish, Angus
AU - Campbell, Iain
AU - Cobbe, Stuart
AU - Taylor, Roy
AU - Prescott, Robin
AU - Lee, Robert
AU - Bancroft, Jean
AU - MacEwan, Shirley
AU - Shepherd, James
AU - Macfarlane, Peter
AU - Morris, Andrew
AU - Jung, Roland
AU - Kelly, Christopher
AU - Connacher, Alan
AU - Peden, Norman
AU - Jamieson, Andrew
AU - Mathews, David
AU - Leese, Graeme
AU - McKnight, John
AU - O'Brien, Iain
AU - Semple, Colin
AU - Petrie, John
AU - Gordon, Derek
AU - Pringle, Stuart
AU - MacWalter, Ron
AU - Fox, Keith
AU - Johnston, Desmond G
AU - Murray, Gordon
AU - Stirling, Mairi
AU - Newton, Ray
AU - Kesson, Colin
AU - Benbow, Susan
AU - Chalmers, John
AU - Chalmers, Joycelin
AU - Doig, John
AU - Fraser, David
AU - Gray, Stuart
AU - Hawthorne, Victor
AU - Lewis, Susan
AU - McCullough, Derreck
AU - MacLeod, Margaret
AU - Matthews, David
AU - Newton, Ray
AU - Reith, Sheila
AU - Scott, Mary
AU - Siann, Tanya
AU - Smith, Alan
AU - Walker, James
PY - 2008/10/16
Y1 - 2008/10/16
N2 - Objective: To determine whether aspirin and antioxidant therapy, combined or alone, are more effective than placebo in reducing the development of cardiovascular events in patients with diabetes mellitus and asymptomatic peripheral arterial disease. Design: Multicentre, randomised, double blind, 2x2 factorial, placebo controlled trial. Setting: 16 hospital centres in Scotland, supported by 188 primary care groups. Participants: 1276 adults aged 40 or more with type 1 or type 2 diabetes and an ankle brachial pressure index of 0.99 or less but no symptomatic cardiovascular disease. Interventions: Daily, 100 mg aspirin tablet plus antioxidant capsule (n=320), aspirin tablet plus placebo capsule (n=318), placebo tablet plus antioxidant capsule (n=320), or placebo tablet plus placebo capsule (n=318). Main outcome measures: Two hierarchical composite primary end points of death from coronary heart disease or stroke, non-fatal myocardial infarction or stroke, or amputation above the ankle for critical limb ischaemia; and death from coronary heart disease or stroke. Results: No evidence was found of any interaction between aspirin and antioxidant. Overall, 116 of 638 primary events occurred in the aspirin groups compared with 117 of 638 in the no aspirin groups (18.2% v 18.3%): hazard ratio 0.98 (95% confidence interval 0.76 to 1.26). Forty three deaths from coronary heart disease or stroke occurred in the aspirin groups compared with 35 in the no aspirin groups (6.7% v 5.5%): 1.23 (0.79 to 1.93). Among the antioxidant groups 117 of 640 (18.3%) primary events occurred compared with 116 of 636 (18.2%) in the no antioxidant groups (1.03, 0.79 to 1.33). Forty two (6.6%) deaths from coronary heart disease or stroke occurred in the antioxidant groups compared with 36 (5.7%) in the no antioxidant groups (1.21, 0.78 to 1.89). Conclusion: This trial does not provide evidence to support the use of aspirin or antioxidants in primary prevention of cardiovascular events and mortality in the population with diabetes studied. Trial registration Current Controlled Trials ISRCTN53295293.
AB - Objective: To determine whether aspirin and antioxidant therapy, combined or alone, are more effective than placebo in reducing the development of cardiovascular events in patients with diabetes mellitus and asymptomatic peripheral arterial disease. Design: Multicentre, randomised, double blind, 2x2 factorial, placebo controlled trial. Setting: 16 hospital centres in Scotland, supported by 188 primary care groups. Participants: 1276 adults aged 40 or more with type 1 or type 2 diabetes and an ankle brachial pressure index of 0.99 or less but no symptomatic cardiovascular disease. Interventions: Daily, 100 mg aspirin tablet plus antioxidant capsule (n=320), aspirin tablet plus placebo capsule (n=318), placebo tablet plus antioxidant capsule (n=320), or placebo tablet plus placebo capsule (n=318). Main outcome measures: Two hierarchical composite primary end points of death from coronary heart disease or stroke, non-fatal myocardial infarction or stroke, or amputation above the ankle for critical limb ischaemia; and death from coronary heart disease or stroke. Results: No evidence was found of any interaction between aspirin and antioxidant. Overall, 116 of 638 primary events occurred in the aspirin groups compared with 117 of 638 in the no aspirin groups (18.2% v 18.3%): hazard ratio 0.98 (95% confidence interval 0.76 to 1.26). Forty three deaths from coronary heart disease or stroke occurred in the aspirin groups compared with 35 in the no aspirin groups (6.7% v 5.5%): 1.23 (0.79 to 1.93). Among the antioxidant groups 117 of 640 (18.3%) primary events occurred compared with 116 of 636 (18.2%) in the no antioxidant groups (1.03, 0.79 to 1.33). Forty two (6.6%) deaths from coronary heart disease or stroke occurred in the antioxidant groups compared with 36 (5.7%) in the no antioxidant groups (1.21, 0.78 to 1.89). Conclusion: This trial does not provide evidence to support the use of aspirin or antioxidants in primary prevention of cardiovascular events and mortality in the population with diabetes studied. Trial registration Current Controlled Trials ISRCTN53295293.
UR - http://www.scopus.com/inward/record.url?scp=55949127696&partnerID=8YFLogxK
U2 - 10.1136/bmj.a1840
DO - 10.1136/bmj.a1840
M3 - Article
AN - SCOPUS:55949127696
VL - 337
SP - 1030
EP - 1034
JO - BMJ (Clinical research ed.)
JF - BMJ (Clinical research ed.)
SN - 0959-8146
IS - 7677
M1 - a1840
ER -