Colesevelam hydrochloride: evidence for its use in the treatment of hypercholesterolemia and type 2 diabetes mellitus with insights into mechanism of action.

Core Evidence Pub Date : 2012-01-01 Epub Date: 2012-07-12 DOI:10.2147/CE.S26725
Michael James Zema
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引用次数: 20

Abstract

Colesevelam hydrochloride is a molecularly engineered, second-generation bile acid sequestrant demonstrating enhanced specificity for bile acids which has been approved for use as adjunctive therapy to diet and exercise as monotherapy or in combination with a β-hydroxymethylglutaryl-coenzyme A reductase inhibitor for the reduction of elevated low-density lipoprotein cholesterol in patients with primary hypercholesterolemia. It is also the only lipid-lowering agent currently available in the United States which has been approved for use as adjunctive therapy in patients with type 2 diabetes mellitus whose glycemia remains inadequately controlled on therapy with metformin, sulfonylurea, or insulin. With the recent emphasis upon drug safety by the Food and Drug Administration and various consumer agencies, it is fitting that the role of nonsystemic lipid-lowering therapies such as bile acid sequestrants - with nearly 90 years of in-class, clinically safe experience - should be reexamined. This paper presents information on the major pharmacologic effects of colesevelam, including a discussion of recent data derived from both in vitro and in vivo rodent and human studies, which shed light on the putative mechanisms involved.

Abstract Image

Abstract Image

盐酸科尔西韦兰:用于治疗高胆固醇血症和2型糖尿病的证据及其作用机制。
Colesevelam hydrochloride是一种分子工程的第二代胆汁酸隔离剂,具有增强的胆汁酸特异性,已被批准用作饮食和运动的辅助疗法,作为单一疗法或与β-羟甲基戊二酰辅酶a还原酶抑制剂联合使用,用于降低原发性高胆固醇血症患者的低密度脂蛋白胆固醇升高。它也是目前在美国唯一可获得的降脂药物,已被批准用于使用二甲双胍,磺脲类或胰岛素治疗血糖控制不充分的2型糖尿病患者的辅助治疗。随着食品和药物管理局和各种消费者机构最近对药物安全性的强调,有必要重新审视具有近90年同类临床安全经验的胆汁酸隔离剂等非系统性降脂疗法的作用。本文介绍了colesevelam主要药理作用的信息,包括对来自体外和体内啮齿动物和人类研究的最新数据的讨论,这些数据揭示了所涉及的假定机制。
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来源期刊
Core Evidence
Core Evidence PHARMACOLOGY & PHARMACY-
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期刊介绍: Core Evidence evaluates the evidence underlying the potential place in therapy of drugs throughout their development lifecycle from preclinical to postlaunch. The focus of each review is to evaluate the case for a new drug or class in outcome terms in specific indications and patient groups The emerging evidence on new drugs is reviewed at key stages of development and evaluated against unmet needs
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