Abstract:Background: Although calcium channel blockers (CCB) are highly effective for suppression of vasospastic angina (VSA) attacks, their prognostic effects in VSA patients remain to be examined in a large number of patients.
Methods and Results:Databases for related papers were searched and then a meta-analysis regarding the effects of CCB on major adverse cardiovascular events (MACE) in Japanese VSA patients with the 4 previous studies was performed. A total of 1,997 patients with positive coronary spasm provocati… Show more
“…However, it is possible that the long-acting CCB benidipine-based treatment in the COPE trial would result in little difference in cardiac ischemic events between the β-blocker group and the other 2 groups, because benidipine is beneficial for preventing cardiac events caused by vasospastic angina. 13 Further studies are required to confirm the results of this study of the secondary prevention of patients with hypertension and coronary artery disease.…”
Section: Japanese Hypertensive Patientsmentioning
confidence: 82%
“…15 In addition, no apparent differences were observed in concomitant medication usage, such as antiplatelets, lipid-lowering drugs, ment effects than the others. 13 The Combination Therapy of Hypertension to Prevent Cardiovascular Events (COPE) trial is the first clinical trial to examine benidipine-combination therapy for the treatment of hypertension in Japan. 14, 15 The trial results demonstrated that both the percentages of subjects achieving the target blood pressure (BP) and the incidences of primary composite cardiovascular endpoints were similar among the benidipine-thiazide diuretic (thiazide), benidipineangiotensin-receptor blocker (ARB), and benidipine-β-blocker groups.…”
Section: Demographic and Baseline Patient Characteristics And Bp Contmentioning
“…However, it is possible that the long-acting CCB benidipine-based treatment in the COPE trial would result in little difference in cardiac ischemic events between the β-blocker group and the other 2 groups, because benidipine is beneficial for preventing cardiac events caused by vasospastic angina. 13 Further studies are required to confirm the results of this study of the secondary prevention of patients with hypertension and coronary artery disease.…”
Section: Japanese Hypertensive Patientsmentioning
confidence: 82%
“…15 In addition, no apparent differences were observed in concomitant medication usage, such as antiplatelets, lipid-lowering drugs, ment effects than the others. 13 The Combination Therapy of Hypertension to Prevent Cardiovascular Events (COPE) trial is the first clinical trial to examine benidipine-combination therapy for the treatment of hypertension in Japan. 14, 15 The trial results demonstrated that both the percentages of subjects achieving the target blood pressure (BP) and the incidences of primary composite cardiovascular endpoints were similar among the benidipine-thiazide diuretic (thiazide), benidipineangiotensin-receptor blocker (ARB), and benidipine-β-blocker groups.…”
Section: Demographic and Baseline Patient Characteristics And Bp Contmentioning
“…These agents have been shown to reduce symptomatic angina episodes, 56-62 suppress inducible coronary spasm, 60 and most importantly are an independent determinant of preventing MACE in vasospastic angina patients. 33, 63 Nitrates have been used since the first description of vasospastic angina and are effective in reducing anginal episodes, 57 although their efficacy in reducing MACE is not evident. 64, 65 Nicorandil is a potassium-channel opener with nitrate-like effects that is extensively used in Japan for the treatment of vasospastic angina.…”
Ischemic heart disease involves both "structural" and/or "functional" disorders of the coronary circulation. Structural atherosclerotic coronary artery disease (CAD) is well recognized, with established diagnostic and treatment strategies. In contrast, "functional CAD" has received limited attention and is seldom actively pursued in the investigation of ischemic heart disease. Vasospastic angina encompasses "functional CAD" attributable to coronary artery spasm and this "state of the art" consensus statement reviews contemporary aspects of this disorder. Patients with vasospastic angina typically present with angina at rest that promptly responds to short-acting nitrates and is associated with transient ischemic ECG changes. Although spontaneous episodes may be documented, provocative spasm testing may be required to confirm the diagnosis. It is important to diagnose vasospastic angina because it may be associated with major adverse events that can be prevented with the use of appropriate vasodilator therapy (eg, calcium-channel blockers) and the avoidance of aggravating stimuli (eg, smoking). Future studies are required to clarify the underlying pathophysiology, natural history and effective treatments for patients refractory to conventional therapy. (Circ J 2016; 80: 289 -298)
“…[35][36][37][38] From now on, it seems important to select drugs by considering the class effects of CCB on the inhibition of cardiovascular accidents. Study limitations: First, it should be remembered that the current study adopted a switchover design and did not carefully investigate potential differences between different drugs (Ltype CCBs, T-type CCB).…”
SummaryAlbuminuria and a high plasma aldosterone concentration (PAC) are prognosis factors predicting a poor outcome for cardiovascular disease. We examined here the effects of benidipine, a T/L-type calcium channel blocker (CCB), on albuminuria and PAC.Thirty-one patients with essential hypertension who received an L-type CCB and achieved the target blood pressure (BP) indicated by the Treatment Guidelines of the Japan Society of Hypertension (JSH2009) were investigated. The Ltype CCB under treatment was switched to benidipine at a dose in which equivalent BP reduction was expected. BP and estimated glomerular filtration rate at 6 months after switching to benidipine were not significantly different from those at baseline. The urinary-albumin-creatinine ratio (UACR) decreased significantly by 36.9% (P = 0.001). No significant change was observed in plasma renin activity (P = 0.063). The PAC of all patients decreased significantly by 11.8% (P = 0.002). When analyzed by daily doses of benidipine, the PAC appeared to have decreased in patients who received 4 mg per day of benidipine (n = 14), although statistical significance was not reached (P = 0.096). The PAC in patients who received 8 mg per day of benidipine (n =17) was significantly reduced by 13.2% (P = 0.017).In hypertensive patients whose BP is controlled by L-type CCB, switching to the T/L-type CCB benidipine maintained BP control and reduced UACR. In addition, the high dose of benidipine reduced the PAC independent of BP control. These results suggest the T/L-type CCB benidipine may contribute to cardio-renal protection in addition to lowering BP. (Int Heart J 2014; 55: 519-525)
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