Literature DB >> 9351739

Effectiveness of tranilast on restenosis after directional coronary atherectomy.

K Kosuga1, H Tamai, K Ueda, Y S Hsu, S Ono, S Tanaka, T Doi, W Myou-U, S Motohara, H Uehata.   

Abstract

Tranilast is an antiallergic drug used widely in Japan that also inhibits the migration and proliferation of vascular smooth muscle cells. This pilot study was undertaken to determine the effectiveness of tranilast on restenosis after successful directional coronary atherectomy. After the procedure, 40 patients (56 lesions, tranilast group) were treated with oral tranilast for 3 months, and 152 patients (188 lesions, control group) did not receive tranilast. Angiographic and clinical variables were compared between the two groups. The minimal lumen diameter was significantly larger in the tranilast group than in the control group at both 3-month (2.08 vs 1.75 mm, p = 0.004) and 6-month follow-up (2.04 vs 1.70 mm, p = 0.003). The diameter stenosis in the tranilast group was smaller than that in the control group both 3 months (28% vs 40%, p = 0.0007) and 6 months (30% vs 43%, p = 0.0001) after the procedure, with a lower restenosis rate (percent diameter stenosis > or =50) in the tranilast group at 3 months (11 % vs 26%, p = 0.03). The number of clinical events over the 12-month period after the procedure was significantly reduced by tranilast administration (p = 0.013). These findings suggest that the oral administration of tranilast strongly prevents restenosis after directional coronary atherectomy.

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Year:  1997        PMID: 9351739     DOI: 10.1016/s0002-8703(97)70055-3

Source DB:  PubMed          Journal:  Am Heart J        ISSN: 0002-8703            Impact factor:   4.749


  6 in total

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2.  Inhibitory mechanism of tranilast in human coronary artery smooth muscle cells proliferation, due to blockade of PDGF-BB-receptors.

Authors:  S Watanabe; A Matsuda; Y Suzuki; K Kondo; Y Ikeda; H Hashimoto; K Umemura
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Authors:  Hiroshi Nakada; Atsushi Yamashita; Masaomi Kuroki; Eiji Furukoji; Noriko Uchino; Taketoshi Asanuma; Yujiro Asada; Shozo Tamura
Journal:  Jpn J Radiol       Date:  2014-01-22       Impact factor: 2.374

4.  Transcriptional activation of p21 by Tranilast is mediated via transforming growth factor beta signal pathway.

Authors:  Min-Ji Charng; Chieh-Hsi Wu
Journal:  Br J Pharmacol       Date:  2006-01       Impact factor: 8.739

Review 5.  Medical applications of transforming growth factor-beta.

Authors:  Kathleen C Flanders; James K Burmester
Journal:  Clin Med Res       Date:  2003-01

6.  Evidence for a role of mast cells in the evolution to congestive heart failure.

Authors:  Masatake Hara; Koh Ono; Myung-Woo Hwang; Atsushi Iwasaki; Masaharu Okada; Kazuki Nakatani; Shigetake Sasayama; Akira Matsumori
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  6 in total

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