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肥胖对药物代谢动力学的影响及其对药物治疗的意义。

Effects of obesity on pharmacokinetics implications for drug therapy.

作者信息

Cheymol G

机构信息

Department of Pharmacology, Faculty of Medicine Saint-Antoine, Paris, France.

出版信息

Clin Pharmacokinet. 2000 Sep;39(3):215-31. doi: 10.2165/00003088-200039030-00004.

Abstract

Obesity is a worldwide problem, with major health, social and economic implications. The adaptation of drug dosages to obese patients is a subject of concern, particularly for drugs with a narrow therapeutic index. The main factors that affect the tissue distribution of drugs are body composition, regional blood flow and the affinity of the drug for plasma proteins and/or tissue components. Obese people have larger absolute lean body masses as well as fat masses than non-obese individuals of the same age, gender and height. However, the percentage of fat per kg of total bodyweight (TBW) is markedly increased, whereas that chrome P450 isoforms are altered, but no clear overview of drug hepatic metabolism in obesity is currently available. Pharmacokinetic studies provide differing data on renal function in obese patients. This review analyses recent publications on several classes of drugs: antibacterials, anticancer drugs, psychotropic drugs, anticonvulsants, general anaesthetics, opioid analgesics, neuromuscular blockers, beta-blockers and drugs commonly used in the management of obesity. Pharmacokinetic studies in obesity show that the behaviour of molecules with weak or moderate lipophilicity (e.g. lithium and vecuronium) is generally rather predictable, as these drugs are distributed mainly in lean tissues. The dosage of these drugs should be based on the ideal bodyweight (IBW). However, some of these drugs (e.g. antibacterials and some anticancer drugs) are partly distributed in adipose tissues, and their dosage is based on IBW plus a percentage of the patient's excess bodyweight. There is no systematic relationship between the degree of lipophilicity of markedly lipophilic drugs (e.g. remifentanil and some beta-blockers) and their distribution in obese individuals. The distribution of a drug between fat and lean tissues may influence its pharmacokinetics in obese patients. Thus, the loading dose should be adjusted to the TBW or IBW, according to data from studies carried out in obese individuals. Adjustment of the maintenance dosage depends on the observed modifications in clearance. Our present knowledge of the influence of obesity on drug pharmacokinetics is limited. Drugs with a small therapeutic index should be used prudently and the dosage adjusted with the help of drug plasma concentrations.

摘要

肥胖是一个全球性问题,具有重大的健康、社会和经济影响。调整药物剂量以适应肥胖患者是一个备受关注的问题,尤其是对于治疗指数较窄的药物。影响药物组织分布的主要因素包括身体组成、局部血流以及药物与血浆蛋白和/或组织成分的亲和力。与年龄、性别和身高相同的非肥胖个体相比,肥胖者的瘦体重和脂肪量的绝对值更大。然而,每千克总体重(TBW)中的脂肪百分比显著增加,而细胞色素P450同工酶发生改变,但目前尚无关于肥胖患者药物肝脏代谢的清晰概述。药代动力学研究提供了关于肥胖患者肾功能的不同数据。本综述分析了几类药物的近期出版物:抗菌药物、抗癌药物、精神药物、抗惊厥药物、全身麻醉剂、阿片类镇痛药、神经肌肉阻滞剂、β受体阻滞剂以及肥胖管理中常用的药物。肥胖的药代动力学研究表明,亲脂性弱或中等的分子(如锂和维库溴铵)的行为通常相当可预测,因为这些药物主要分布在瘦组织中。这些药物的剂量应基于理想体重(IBW)。然而,其中一些药物(如抗菌药物和一些抗癌药物)部分分布于脂肪组织中,其剂量基于IBW加上患者超重体重的一定百分比。亲脂性明显的药物(如瑞芬太尼和一些β受体阻滞剂)的亲脂性程度与其在肥胖个体中的分布之间没有系统的关系。药物在脂肪组织和瘦组织之间的分布可能会影响其在肥胖患者中的药代动力学。因此,根据在肥胖个体中进行的研究数据,负荷剂量应根据TBW或IBW进行调整。维持剂量的调整取决于观察到的清除率变化。我们目前对肥胖对药物药代动力学影响的了解有限。治疗指数小的药物应谨慎使用,并借助药物血浆浓度调整剂量。

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