Crooks J, O'Malley K, Stevenson I H
Clin Pharmacokinet. 1976;1(4):280-96. doi: 10.2165/00003088-197601040-00003.
The elderly are generally considered to be different from young people in terms of drug response and this applies particularly to quantitative differences. While altered drug handling is a major potential source of difference in responsiveness to drugs, the relative contribution of pharmacokinetics and pharmacodynamics to this difference is not clear. In the present review we have examined the available data on pharmacokinetics in the elderly. In the past, data pertaining to animal models have been extrapolated to man and in the absence of human experimentation these assumptions have tended to hold sway. This is best exemplified by studies on drug absorption. The absorption of actively transported substance may in fact be diminished in the elderly. However, most drugs are absorbed by passive diffusion and the recently available evidence in man indicates that there is no age-dependent change. While definitive data on the effect of old age on drug metabolising ability in animals is available, no direct assessments have been made in man. Many of the studies carried out using drug plasma half-life and clearance assessments are complicated by changes in distribution. This is best illustrated by a definitive study with diazepam, in which marked prolongation of plasma half-life was accompained by an increase in apparent volume of distribution in the elderly. This latter change influences plasma drug clearance and, possibly, drug concentration at its site of action. Thus, the implications for drug effect of such changes in volume of distribution remain to be clarified. In theory, the rate of elimination of antipyrine should provide a good index of drug metabolising ability. Both plasma half-life and clearance values suggest a decreased in metabolism in the elderly. No other drug has been studied as intensively and the evidence for a diminished metabolism of other drug in the elderly is less definite. Thus, while it is likely that the metabolism of some drugs is imparied in old age, it is not possible at this time to generalise with regard to the effect of age on drug metabolising ability in man. It is also difficult to generalise about age-related changes in plasma protein binding of drugs. With some drugs, binding to plasma protein does not appear to be altered and for two drugs-warfarin and phenytoin, the findings of different investigators conflict. Diminution of glomerular filtration rate, renal plasma flow and associated tubular function with age have been well documented. Drug clearance comparisons between old and young have been carried out for only three renally excreted drugs-digoxin, propicillin and sulphamethizole. With digoxine and sulphamethizole, the evidence is that renal excretion is diminished in the elderly. With propicillin, changes in volume of distribution predominate, resulting in higher plasma levels in the elderly but similar percent recovery in urine...
一般认为老年人在药物反应方面与年轻人不同,这尤其适用于定量差异。虽然药物处置的改变是药物反应性差异的一个主要潜在来源,但药代动力学和药效学对这种差异的相对贡献尚不清楚。在本综述中,我们研究了老年人药代动力学的现有数据。过去,与动物模型相关的数据已被外推至人类,在缺乏人体实验的情况下,这些假设往往占主导地位。这在药物吸收研究中体现得最为明显。实际上,主动转运物质的吸收在老年人中可能会减少。然而,大多数药物是通过被动扩散吸收的,最近在人体获得的证据表明不存在年龄依赖性变化。虽然有关于老年对动物药物代谢能力影响的确切数据,但尚未在人体进行直接评估。许多使用药物血浆半衰期和清除率评估进行的研究因分布变化而变得复杂。地西泮的一项确定性研究对此进行了最好的说明,其中老年人血浆半衰期显著延长,同时表观分布容积增加。后一种变化会影响血浆药物清除率,并可能影响药物作用部位的药物浓度。因此,分布容积的这种变化对药物效应的影响仍有待阐明。理论上,安替比林的消除速率应能很好地反映药物代谢能力。血浆半衰期和清除率值均表明老年人的代谢有所下降。没有对其他药物进行过如此深入的研究,关于老年人其他药物代谢减少的证据不太明确。因此,虽然老年时某些药物的代谢可能受损,但目前还无法就年龄对人体药物代谢能力的影响进行概括。关于药物与血浆蛋白结合的年龄相关变化也很难进行概括。对于某些药物,与血浆蛋白的结合似乎没有改变,而对于华法林和苯妥英钠这两种药物,不同研究者的研究结果相互矛盾。随着年龄增长,肾小球滤过率、肾血浆流量及相关肾小管功能的降低已得到充分证明。仅对三种经肾排泄的药物——地高辛、丙匹西林和磺胺甲噻二唑进行了老年人与年轻人之间的药物清除率比较。对于地高辛和磺胺甲噻二唑,有证据表明老年人的肾排泄减少。对于丙匹西林,分布容积的变化占主导,导致老年人血浆水平升高,但尿中回收率相似……