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双重钙通道阻滞剂疗法治疗高血压

Dual calcium-channel blocker therapy in the treatment of hypertension.

作者信息

Saseen J J, Carter B L

机构信息

Department of Pharmacy Practice, School of Pharmacy, University of Colorado Health Sciences Center, Denver 80262, USA.

出版信息

Ann Pharmacother. 1996 Jul-Aug;30(7-8):802-10. doi: 10.1177/106002809603000719.

Abstract

OBJECTIVE

To review the in vitro receptor binding data of calcium-channel blockers (CCBs) and in vivo studies in humans regarding the use of dual calcium-channel blocker therapy, with a focus on the use of this therapy for hypertension.

DATA SOURCE

A MEDLINE search was conducted to identify literature pertaining to CCBs.

STUDY SELECTION

In vitro studies and investigations that evaluated CCB receptor binding and the interactions between subclasses of CCBs were chosen. All studies in humans and clinical trials that evaluated the use of dual CCB therapy in the treatment of cardiovascular diseases were selected for review. Also, case reports describing the use of dual CCB therapy were included in this article.

DATA EXTRACTION

The methodology, results, and conclusions of the selected data were evaluated. Data regarding the in vitro receptor binding kinetics of CCBs, as well as interactions, were reported. Because there is limited information on dual CCB therapy for hypertension, clinical studies using this treatment for ischemic heart disease were also reviewed. They were summarized and compared on the basis of the degree of disease control (e.g., blood pressure, exercise tolerance), adverse effects, and other clinical endpoints of pharmacologic therapy.

DATA SYNTHESIS

In vitro studies have identified binding sites for the dihydropyridine (nifedipine), diphenylalkylamine (verapamil), and benzothiazepine (diltiazem) subclasses of CCBs, and indicate that they are allosterically related to each other within the voltage-sensitive calcium-channel receptor. Dihydropyridine binding affinity is decreased with concomitant verapamil binding, but is enhanced by concomitant diltiazem binding. Dual CCB therapy has been shown to be efficacious in patients with ischemic heart disease. Although this therapy is limited by dose-related adverse effects, it appears to have an important role in patients with ischemia that is refractory to conventional therapy, or for those whose therapeutic options are limited by contraindications. Theoretically, many patients with hypertension may benefit similarly from dual CCB therapy. Because data evaluating this treatment option are sparse, recommendations regarding safety, efficacy, and the role of dual CCB therapy for hypertension would be premature.

CONCLUSIONS

Controlled data evaluating dual CCB therapy for the treatment of hypertension are lacking. This treatment modality may be beneficial in the future, but requires further investigation to determine safety and efficacy.

摘要

目的

回顾钙通道阻滞剂(CCB)的体外受体结合数据以及关于联合使用钙通道阻滞剂治疗的人体体内研究,重点关注该疗法在高血压治疗中的应用。

数据来源

进行了MEDLINE检索以识别与CCB相关的文献。

研究选择

选择了评估CCB受体结合以及CCB亚类之间相互作用的体外研究和调查。所有评估联合CCB疗法治疗心血管疾病的人体研究和临床试验均被选入进行综述。此外,本文还纳入了描述联合CCB疗法使用情况的病例报告。

数据提取

对所选数据的方法、结果和结论进行了评估。报告了有关CCB体外受体结合动力学以及相互作用的数据。由于关于联合CCB疗法治疗高血压的信息有限,因此也对使用该疗法治疗缺血性心脏病的临床研究进行了综述。根据疾病控制程度(如血压、运动耐量)、不良反应和药物治疗的其他临床终点对这些研究进行了总结和比较。

数据综合

体外研究已确定CCB的二氢吡啶类(硝苯地平)、二苯烷基胺类(维拉帕米)和苯并硫氮䓬类(地尔硫䓬)亚类的结合位点,并表明它们在电压敏感性钙通道受体内彼此呈变构相关。维拉帕米同时结合时,二氢吡啶的结合亲和力降低,但地尔硫䓬同时结合时则增强。联合CCB疗法已被证明对缺血性心脏病患者有效。尽管该疗法受到剂量相关不良反应的限制,但它似乎在对传统治疗难治的缺血患者或因禁忌症而治疗选择有限的患者中具有重要作用。从理论上讲,许多高血压患者可能同样会从联合CCB疗法中获益。由于评估该治疗方案的数据稀少,因此关于联合CCB疗法治疗高血压的安全性、有效性和作用的建议尚不成熟。

结论

缺乏评估联合CCB疗法治疗高血压的对照数据。这种治疗方式未来可能有益,但需要进一步研究以确定其安全性和有效性。

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