Cusack Barry J
Gerontology and Pharmacology Research Unit, VA Medical Center, Boise, Idaho 83702, USA.
Am J Geriatr Pharmacother. 2004 Dec;2(4):274-302. doi: 10.1016/j.amjopharm.2004.12.005.
Physiologic changes and disease-related alterations in organ function occur with aging. These changes can affect drug pharmacokinetics in older persons.
This article reviews age-related changes in pharmacokinetics and their clinical relevance.
A PubMed search was conducted using the terms elderly and pharmacokinetics. Other reviews were also included for literature searching. The review includes literature in particular from 1990 through April 2004. Some articles from before 1990 were included to help illustrate principles of age-related pharmacokinetics.
There are minor changes in drug absorption with aging. The effect of aging on small-bowel transporter systems is not yet fully established. Bioavailability of highly extracted drugs often is increased with age. Transdermal absorption may be delayed, especially in the case of water-soluble compounds. Fat-soluble drugs may distribute more widely and water-soluble drugs less extensively in older persons. Hepatic drug metabolism shows wide interindividual variation, and in many cases, there is an age-related decline in elimination of metabolized drugs, particularly those eliminated by the cytochrome enzyme system. Any decrement in cytochrome enzyme metabolism appears nonselective. Synthetic conjugation metabolism is less affected by age. Pseudocapillarization of the sinusoidal endothelium in the liver, restricting oxygen diffusion, and the decline in liver size and liver blood flow may influence age-related changes in rate of hepatic metabolism. Frailty, physiological stress, and illness are important predictors of drug metabolism in older individuals. Inhibition of drug metabolism is not altered with aging, but induction is reduced in a minority of studies. Renal drug elimination typically declines with age, commensurate with the fall in creatinine clearance. Renal tubular organic acid transport may decline with age, while the function of the organic base transporter is preserved but may be less responsive to stimulation.
Changes in pharmacokinetics occur due to age-related physiologic perturbations. These changes contribute to altered dose requirements in older persons, particularly in the case of drugs eliminated by the kidney. Interindividual variation, disease, frailty, and stress may overshadow age-related changes.
随着年龄增长,器官功能会发生生理变化以及与疾病相关的改变。这些变化会影响老年人的药物药代动力学。
本文综述了药代动力学中与年龄相关的变化及其临床意义。
使用“老年人”和“药代动力学”等术语在PubMed上进行检索。还纳入了其他综述以进行文献检索。该综述特别包括1990年至2004年4月的文献。纳入了一些1990年之前的文章以帮助阐明与年龄相关的药代动力学原理。
随着年龄增长,药物吸收有轻微变化。衰老对小肠转运系统的影响尚未完全明确。高提取率药物的生物利用度通常会随着年龄增长而增加。经皮吸收可能会延迟,尤其是水溶性化合物的情况。在老年人中,脂溶性药物可能分布更广泛,而水溶性药物分布范围较小。肝脏药物代谢存在广泛的个体差异,在许多情况下,代谢药物的消除存在与年龄相关的下降,特别是那些由细胞色素酶系统消除的药物。细胞色素酶代谢的任何下降似乎都没有选择性。合成结合代谢受年龄影响较小。肝脏窦状内皮的假毛细血管化限制了氧气扩散,以及肝脏大小和肝血流量的下降可能会影响与年龄相关的肝脏代谢速率变化。虚弱、生理应激和疾病是老年个体药物代谢的重要预测因素。药物代谢的抑制作用不会随着年龄增长而改变,但在少数研究中诱导作用会降低。肾脏药物消除通常会随着年龄增长而下降,与肌酐清除率的下降相当。肾小管有机酸转运可能会随着年龄增长而下降,而有机碱转运体的功能得以保留,但对刺激的反应可能会减弱。
药代动力学的变化是由于与年龄相关的生理扰动引起的。这些变化导致老年人的剂量需求改变,特别是在经肾脏消除的药物情况下。个体差异、疾病、虚弱和应激可能会掩盖与年龄相关的变化。