Clinical Pharmacology Associates, Miami, Florida, USA.
Clin Drug Investig. 2005;25(2):107-14. doi: 10.2165/00044011-200525020-00003.
Bisphosphonates are commonly used to treat and prevent osteoporosis. These compounds have unusual pharmacokinetic characteristics because they bind strongly to bone, and a portion becomes buried under newly formed bone. Once incorporated into bone tissue, the subsequent release during bone remodeling is probably the rate-limiting step in the terminal elimination of bisphosphonates. Because of this unique property of bisphosphonates, pharmacokinetic studies with insufficient lengths of follow-up might entirely miss the true terminal elimination phase. A terminal half-life (t((1/2)gamma)) of approximately 11 years, similar to that of calcium and other minerals in bone, was reported from an 18-month study of alendronic acid in postmenopausal women with osteoporosis. We are not aware of any other published reports in which the elimination of a bisphosphonate has been followed for more than a few weeks post-dose. The purpose of the present study was to reanalyse the alendronic acid data to examine the effect of truncating the length of follow-up on the calculated t((1/2)gamma).
Twenty-one postmenopausal women with osteoporosis (mean age 66 years) received intravenous alendronic acid 30mg over 4 consecutive days (7.5 mg/day), and urinary excretion of alendronic acid was monitored over the following 18-24 months. Terminal elimination half-life was originally calculated by log-linear regression of the percentage retained versus time curve between days 240 and 540 and substituting the slope of the regression line into the equation, t((1/2)gamma) = -log 2/slope. These data were reanalysed based on the period up to 30 days.
Data were sufficient for analysis of pharmacokinetics in 11 patients. A mean t((1/2)gamma) of approximately 11 years was reported previously, based on analysis of data between days 240 and 540. Recalculating the 'terminal' half-life of alendronic acid using only data from the first 30 days resulted in an 'observed' half-life of only 11 days.
This analysis illustrates the importance of sufficient length of follow-up to accurately characterise the true terminal elimination half-life of bisphosphonates. The relatively short (expressed in units of days rather than years) terminal elimination half-lives reported for some bisphosphonates based on only 30 days of follow-up or less are likely to substantially underestimate the true terminal elimination half-lives.
双膦酸盐常用于治疗和预防骨质疏松症。这些化合物具有不同寻常的药代动力学特征,因为它们与骨骼结合紧密,一部分被埋在新形成的骨骼下。一旦被整合到骨组织中,在骨重塑过程中的随后释放可能是双膦酸盐终末消除的限速步骤。由于双膦酸盐具有这种独特的特性,因此随访时间不足的药代动力学研究可能完全错过真正的终末消除阶段。在一项对 21 名绝经后骨质疏松症妇女进行的为期 18 个月的阿仑膦酸研究中,报道了类似钙和其他矿物质在骨骼中的约 11 年的终端半衰期(t((1/2)gamma)。我们不知道有任何其他已发表的报告,其中双膦酸盐的消除已被跟踪超过几个星期。本研究的目的是重新分析阿仑膦酸数据,以检查缩短随访时间对计算的 t((1/2)gamma)的影响。
21 名绝经后骨质疏松症妇女(平均年龄 66 岁)连续 4 天接受静脉内阿仑膦酸 30mg(7.5mg/天),并在接下来的 18-24 个月内监测阿仑膦酸的尿排泄。最初通过在第 240 天和第 540 天之间的时间与时间曲线的保留百分比的对数线性回归计算终端消除半衰期,并将回归线的斜率代入方程,t((1/2)gamma)=-log2/斜率。根据前 30 天的数据对这些数据进行了重新分析。
11 名患者的数据足以进行药代动力学分析。根据第 240 天至 540 天的数据分析,先前报道了约 11 年的平均 t((1/2)gamma)。仅使用前 30 天的数据重新计算阿仑膦酸的“终末”半衰期,导致“观察到”半衰期仅为 11 天。
这项分析说明了足够的随访时间对于准确描述双膦酸盐的真实终末消除半衰期的重要性。根据仅 30 天或更少的随访报告的一些双膦酸盐的相对较短(以天而不是年为单位表示)的终端消除半衰期很可能大大低估了真实的终端消除半衰期。