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肝脏药物代谢与衰老

Hepatic drug metabolism and aging.

作者信息

Durnas C, Loi C M, Cusack B J

机构信息

Clinical Pharmacology and Gerontology Research Unit, Veterans Affairs Medical Center, Boise, Idaho.

出版信息

Clin Pharmacokinet. 1990 Nov;19(5):359-89. doi: 10.2165/00003088-199019050-00002.

DOI:10.2165/00003088-199019050-00002
PMID:2268986
Abstract

Although there is considerable variation in the effect of age on drug biotransformation, the metabolism of many drugs is impaired in the elderly. Age-related physiological changes, such as a reduction in liver mass, hepatic metabolising enzyme activity, liver blood flow and alterations in plasma drug binding may account for the decreased elimination of some metabolised drugs in the elderly. It is difficult, however, to separate an effect of aging from a background of marked variation in the rate of metabolism due to factors such as individual metabolic phenotype, environmental influences, concomitant disease states and drug intake. The prevailing data suggest that initial doses of metabolised drugs should be reduced in older patients and then modified according to the clinical response. In most studies the elderly appear as responsive as young individuals to the effects of compounds which induce or inhibit the activity of cytochrome P450 isozymes. Concurrent use of other agents, which induce or inhibit drug metabolism, mandates dose adjustment as in younger patients. Many questions remain unanswered. For instance, limitations of in vitro studies prevent any firm conclusion about changes in hepatic drug metabolising enzyme activity in the elderly. With aging, some pathways of drug metabolism may be selectively affected, but this has not been adequately scrutinised. The possibility that metabolism of stereoisomers may be altered in the elderly has not been adequately tested. The effect of aging on the distribution of polymorphic drug metabolism phenotypes is still not established, despite potential implications for disease susceptibility and survival advantage.

摘要

尽管年龄对药物生物转化的影响存在很大差异,但许多药物的代谢在老年人中会受损。与年龄相关的生理变化,如肝脏质量减少、肝脏代谢酶活性降低、肝血流量减少以及血浆药物结合的改变,可能是老年人中某些代谢药物消除减少的原因。然而,由于个体代谢表型、环境影响、伴随疾病状态和药物摄入等因素,很难将衰老的影响与代谢速率显著变化的背景区分开来。现有数据表明,老年患者应减少代谢药物的初始剂量,然后根据临床反应进行调整。在大多数研究中,老年人对诱导或抑制细胞色素P450同工酶活性的化合物的反应似乎与年轻人一样。与年轻患者一样,同时使用其他诱导或抑制药物代谢的药物需要调整剂量。许多问题仍未得到解答。例如,体外研究的局限性使得无法就老年人肝脏药物代谢酶活性的变化得出任何确凿结论。随着年龄增长,药物代谢的某些途径可能会受到选择性影响,但这尚未得到充分研究。老年人中立体异构体代谢可能改变的可能性尚未得到充分测试。尽管衰老对多态性药物代谢表型分布的影响对疾病易感性和生存优势有潜在影响,但仍未确定。

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