Cilostazol for treatment of cerebral infarction

被引:65
作者
Noma, Kensuke
Higashi, Yukihito
机构
[1] Hiroshima Univ, Dept Cardiovasc Regenerat & Med, Res Ctr Radiat Genome Med, RIRBM, Hiroshima, Japan
[2] Hiroshima Univ Hosp, Med Ctr Translat & Clin Res, Div Regenerat & Med, Hiroshima, Japan
关键词
Cilostazol; secondary stroke prevention; Asian populations; SMOOTH-MUSCLE-CELLS; ISCHEMIC-STROKE; GLOBAL BURDEN; PHOSPHODIESTERASE INHIBITOR; PLATELET-AGGREGATION; SECONDARY PREVENTION; SYSTEMATIC ANALYSIS; REGIONAL BURDEN; RAT MODEL; PHASE-I;
D O I
10.1080/14656566.2018.1515199
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Stroke not only causes critical disability and death but is also a cause of anxiety with the possibility of secondary cardiovascular events including secondary ischemic stroke. Indeed, patients with a history of previous stroke have a high rate of stroke recurrence, indicating the clinical importance of secondary stroke prevention.Area of covered: This review provides an overview of the pooled evidence for cilostazol's use in the management of secondary stroke prevention. Among the various antiplatelet agents that are available, aspirin is the most frequently used agent worldwide for the prevention of secondary stroke. Cilostazol, a selective phosphodiesterase (PDE) 3A inhibitor, is used worldwide for the treatment of patients with intermittent claudication. However, in Asia, cilostazol is recommended and used in practice for secondary stroke prevention.Expert opinion: The authors believe that cilostazol could be used for secondary stroke prevention not only in Asia but worldwide. However, further randomized trials on cilostazol are needed, especially in the US and Europe to better support its case.
引用
收藏
页码:1719 / 1726
页数:8
相关论文
共 63 条
[1]   Cilostazol reduces inflammatory burden and oxidative stress in hypertensive type 2 diabetes mellitus patients [J].
Agrawal, Neeraj K. ;
Maiti, Rituparna ;
Dash, D. ;
Pandey, B. L. .
PHARMACOLOGICAL RESEARCH, 2007, 56 (02) :118-123
[2]  
AKIYAMA H, 1985, ARZNEIMITTEL-FORSCH, V35-2, P1124
[3]   Cilostazol in patients with ischemic stroke [J].
Al-Qudah, Zaid A. ;
Hassan, Ameer E. ;
Qureshi, Adnan I. .
EXPERT OPINION ON PHARMACOTHERAPY, 2011, 12 (08) :1305-1315
[4]   Inhibition of the p53 tumor suppressor gene results in growth of human aortic vascular smooth muscle cells - Potential role of p53 in regulation of vascular smooth muscle cell growth [J].
Aoki, M ;
Morishita, R ;
Matsushita, H ;
Hayashi, S ;
Nakagami, H ;
Yamamoto, K ;
Moriguchi, A ;
Kaneda, Y ;
Higaki, J ;
Ogihara, T .
HYPERTENSION, 1999, 34 (02) :192-200
[5]  
Benjamin EJ, 2018, CIRCULATION, V137, pE67, DOI [10.1161/CIR.0000000000000558, 10.1161/CIR.0000000000000485, 10.1161/CIR.0000000000000530]
[6]   Characterization of White Matter Injury in a Rat Model of Chronic Cerebral Hypoperfusion [J].
Choi, Bo-Ryoung ;
Kim, Dong-Hee ;
Bin Back, Dong ;
Kang, Chung Hwan ;
Moon, Won-Jin ;
Han, Jung-Soo ;
Choi, Dong-Hee ;
Kwon, Kyoung Ja ;
Shin, Chan Young ;
Kim, Bo-Ram ;
Lee, Jongmin ;
Han, Seol-Heui ;
Kim, Hahn Young .
STROKE, 2016, 47 (02) :542-+
[7]   Recurrent stroke and cardiac risks after first ischemic stroke - The Northern Manhattan Study [J].
Dhamoon, MS ;
Sciacca, RR ;
Rundek, T ;
Sacco, RL ;
Elkind, MSV .
NEUROLOGY, 2006, 66 (05) :641-646
[8]   Cilostazol reduces blood brain barrier dysfunction, white matter lesion formation and motor deficits following chronic cerebral hypoperfusion [J].
Edrissi, Hamidreza ;
Schock, Sarah C. ;
Cadonic, Robert ;
Hakim, Antoine M. ;
Thompson, Charlie S. .
BRAIN RESEARCH, 2016, 1646 :494-503
[9]   Effect of the novel antiplatelet agent cilostazol on plasma lipoproteins in patients with intermittent claudication [J].
Elam, MB ;
Heckman, J ;
Crouse, JR ;
Hunninghake, DB ;
Herd, JA ;
Davidson, M ;
Gordon, IL ;
Bortey, EB ;
Forbes, WP .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1998, 18 (12) :1942-1947
[10]   Global Burden of Stroke [J].
Feigin, Valery L. ;
Norrving, Bo ;
Mensah, George A. .
CIRCULATION RESEARCH, 2017, 120 (03) :439-448