Literature DB >> 15851624

Quantitative coronary angiogram analysis: nifedipine retard versus angiotensin-converting enzyme inhibitors (JMIC-B side arm study).

Eiji Shinoda1, Yoshiki Yui, Kazuhisa Kodama, Atsushi Hirayama, Hiroshi Nonogi, Kazuo Haze, Tetsuya Sumiyoshi, Saichi Hosoda, Chuichi Kawai.   

Abstract

This study was performed to compare the effects of nifedipine retard and angiotensin-converting enzyme (ACE) inhibitors on the progression of coronary atherosclerosis by means of quantitative coronary angiogram. Coronary angiogram was performed before the start of the study and during the 3-year treatment period. This study was conducted on the assumption that possible coronary vasodilation, which may be caused by nifedipine, was excluded by administration of sufficient isosorbide dinitrate. The changes from the baseline in the minimum lumen diameter of the coronary artery in all measured segments were negligible in the nifedipine group (+0.02+/-0.27 mm; P=0.543), whereas they were significantly reduced in the ACE inhibitor group (-0.12+/-0.27 mm; P<0.001), with a significant difference observed between the groups (P=0.002). The number of progressors in the nifedipine group was significantly lower than that in the ACE inhibitor group (P=0.019), and there was also a significant difference between the groups in the number of patients in whom > or =1 lesion developed after treatment (P=0.040). However, the changes of minimum lumen diameter stratified by baseline percent diameter stenosis demonstrated that progression of coronary atherosclerosis was suppressed in the nifedipine group for lesions with a percent diameter stenosis of < or =40 but was suppressed in both groups for those with a percent diameter stenosis of > or =41. This study suggests that nifedipine retard and ACE inhibitors may be effective in suppression of progression of coronary atherosclerosis, and that nifedipine in particular may be effective for mild to moderate stenosis.

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Year:  2005        PMID: 15851624     DOI: 10.1161/01.HYP.0000165677.71421.8c

Source DB:  PubMed          Journal:  Hypertension        ISSN: 0194-911X            Impact factor:   10.190


  4 in total

Review 1.  Modified-release nifedipine: a review of the use of modified-release formulations in the treatment of hypertension and angina pectoris.

Authors:  Katherine F Croom; Keri Wellington
Journal:  Drugs       Date:  2006       Impact factor: 11.431

Review 2.  Thiazolidinedione-independent activation of peroxisome proliferator-activated receptor γ is a potential target for diabetic macrovascular complications.

Authors:  Takeshi Matsumura; Kayo Taketa; Seiya Shimoda; Eiichi Araki
Journal:  J Diabetes Investig       Date:  2012-02-20       Impact factor: 4.232

3.  Estimated glomerular filtration rate reversal by blood pressure lowering in chronic kidney disease: Japan Multicenter Investigation for Cardiovascular DiseaseB CKD study.

Authors:  Yoshiki Yui; Kazuhisa Kodama; Atsushi Hirayama; Saichi Hosoda; Chuichi Kawai
Journal:  J Clin Hypertens (Greenwich)       Date:  2012-12-14       Impact factor: 3.738

Review 4.  Review of nifedipine GITS in the treatment of high risk patients with coronary artery disease and hypertension.

Authors:  Amber Lundy; Nahla Lutfi; Cherylyn Beckey
Journal:  Vasc Health Risk Manag       Date:  2009
  4 in total

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