1990
DOI: 10.1016/0140-6736(90)91121-p
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Retardation of angiographic progression of coronary artery disease by nifedipine

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Cited by 572 publications
(71 citation statements)
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“…46 The ability of CR nifedipine to inhibit MDMP generation provides additional evidence for the antiatherosclerotic action of this drug. 47,48 However, further studies are required to elucidate the mechanism by which hypoadiponectinaemia is improved by CR nifedipine. In conclusion, CR nifedipine directly or indirectly improved platelet activation markers, microparticles and adiponectin levels in hypertensive patients with diabetes.…”
Section: Discussionmentioning
confidence: 99%
“…46 The ability of CR nifedipine to inhibit MDMP generation provides additional evidence for the antiatherosclerotic action of this drug. 47,48 However, further studies are required to elucidate the mechanism by which hypoadiponectinaemia is improved by CR nifedipine. In conclusion, CR nifedipine directly or indirectly improved platelet activation markers, microparticles and adiponectin levels in hypertensive patients with diabetes.…”
Section: Discussionmentioning
confidence: 99%
“…Studies with angiographic endpoints [2][3][4]7,8] have shown that medical therapy can attenuate the rate of lesion development and/or reduce existing lesions. However, most angiographic studies have had too small a sample size to detect a reduction in morbidity or mortality associated with the measured changes in coronary artery diameter.…”
Section: Discussionmentioning
confidence: 99%
“…For the angiographic analyses the incidence of progression in the placebo treatment group was assumed to be 0.45 (45% of patients in the placebo treatment group demonstrating "progression"--however defined--over a 3-year period) [3,4,7,8,[34][35][36][37][38][39][40]. Thus, for a test with 80% power at a two-sided 5% significance level to detect a 30% reduction (to 0.315) in the quinapril treatment group, 203 patients are required per treatment group.…”
Section: Methodsmentioning
confidence: 99%
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“…Meta-analysis by Furberg et al showed that nifedipine is associated with dose related increase in mortality in patients with CAD, a study which included patients with acute coronary syndromes (ACS) (Furberg et al, 1995). However, the only trial included in the meta-analysis that involved patients with stable angina was the International Nifedipine trial on Antiatherosclerotic Therapy (INTACT), which showed that patients on nifedipine had retardation of atherosclerotic disease by angiogram, though clinical symptoms were not reported (Lichtlen et al, 1990). A Coronary Disease Trial Investigating Outcome with Nifedipine gastrointestinal therapeutic system (ACTION) study reported that, in patients with stable angina and hypertension, long-acting nifedipine was acceptably safe (no increased incidence of myocardial infarction, heart failure or death), but there was no evidence of improvement in mortality or other major cardiac endpoints and no reduction in refractory angina in already maximally medically treated patients (Poole-Wilson et al, 2004;Sierra & Coca, 2008).…”
Section: Clinical Applicationmentioning
confidence: 99%