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骨质疏松症女性治疗后的双膦酸盐延长释放。与骨转换的关系。

Prolonged bisphosphonate release after treatment in women with osteoporosis. Relationship with bone turnover.

机构信息

Department of Rheumatology, IDIBAPS, CIBERehd, Hospital Clínic, University of Barcelona, Spain.

出版信息

Bone. 2011 Oct;49(4):706-9. doi: 10.1016/j.bone.2011.06.027. Epub 2011 Jun 30.

Abstract

Bisphosphonates (BP), especially alendronate and risedronate, are the drugs most commonly used for osteoporosis treatment, being incorporated into the skeleton where they inhibit bone resorption and are thereafter slowly released during bone turnover. However, there are few data on the release of BP in patients who have received treatment with these drugs for osteoporosis. This information is essential for evaluating the possibility of BP cyclic therapy in these patients and for controlling their long-term presence in bone tissue. This study evaluated the urinary excretion of alendronate and risedronate in patients treated with these drugs for osteoporosis and analysed its relationship with bone turnover, time of previous drug exposure and time of treatment discontinuation. We included 43 women (aged 65±9.4 years) previously treated with alendronate (36) or risedronate (7) during a mean of 51±3 and 53±3 months, respectively, who had not been treated with other antiosteoporotic treatment and with a median time of discontinuation of 13.5 and 14 months, respectively. Both BP were detected in 24-hour urine by HPLC. In addition, bone formation (PINP) and resorption (NTx) markers were analysed. Both BP were also determined in a control group of women during treatment. Alendronate was detected in 41% of women previously treated with this drug whereas no patient previously treated with risedronate showed detectable urinary values. All control patients showed detectable values of both BP. In patients with detectable alendronate levels, the time of drug cessation was shorter than in patients with undetectable values (12 [6-19] versus 31 [7-72] months, p<0.001). Alendronate was not detected in any patient 19 months after treatment cessation. Alendronate levels were inversely related to time of treatment discontinuation (r=-0.403, p=0.01) and the latter was directly related to NTx (r=0.394, p=0.02). No relationship was observed with age, length of drug exposure, renal function or weight. In conclusion, contrary to risedronate, which was not detected in patients after cessation of treatment, alendronate was frequently detected in women previously treated with this agent up to 19 months after discontinuation of therapy. The relationship between alendronate levels and both bone resorption and time of treatment cessation further indicates a residual effect of this drug in bone, despite treatment discontinuation.

摘要

双膦酸盐(BP),特别是阿仑膦酸盐和利塞膦酸盐,是治疗骨质疏松症最常用的药物,它们被整合到骨骼中,抑制骨吸收,然后在骨转换过程中缓慢释放。然而,关于接受这些药物治疗骨质疏松症的患者中 BP 的释放数据很少。这些信息对于评估这些患者中 BP 循环治疗的可能性以及控制其在骨组织中的长期存在至关重要。本研究评估了接受这些药物治疗骨质疏松症的患者的阿仑膦酸盐和利塞膦酸盐的尿排泄情况,并分析了其与骨转换、先前药物暴露时间和治疗停药时间的关系。我们纳入了 43 名女性(年龄 65±9.4 岁),她们在平均 51±3 和 53±3 个月之前分别接受了阿仑膦酸盐(36 名)或利塞膦酸盐(7 名)治疗,并且没有接受过其他抗骨质疏松治疗,停药时间中位数分别为 13.5 和 14 个月。通过 HPLC 检测 24 小时尿液中的两种 BP。此外,还分析了骨形成(PINP)和骨吸收(NTx)标志物。在治疗期间还在一组女性对照中检测了两种 BP。在先前接受这种药物治疗的 41%的女性中检测到阿仑膦酸盐,而在先前接受利塞膦酸盐治疗的患者中没有检测到可检测的尿液值。所有对照患者均显示出两种 BP 的可检测值。在可检测到阿仑膦酸盐水平的患者中,停药时间短于不可检测值的患者(12 [6-19]与 31 [7-72]个月,p<0.001)。在停药 19 个月后,没有患者检测到阿仑膦酸盐。阿仑膦酸盐水平与停药时间呈负相关(r=-0.403,p=0.01),后者与 NTx 呈直接相关(r=0.394,p=0.02)。与年龄、药物暴露时间、肾功能或体重无关。总之,与停药后未检测到的利塞膦酸盐不同,阿仑膦酸盐在停药后 19 个月内仍频繁在先前接受该药物治疗的女性中检测到。阿仑膦酸盐水平与骨吸收和治疗停药时间之间的关系进一步表明,尽管停止治疗,但该药物仍在骨骼中产生残留效应。

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