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单次静脉注射唑来膦酸18个月后的骨转换情况。

Bone turnover 18 months after a single intravenous dose of zoledronic acid.

作者信息

Borba V Z C, Paz-Filho G, Kulak C A M, Seibel M J, Bilezikian J P

机构信息

Serviço de Endocrinologia e Metabologia da UFPR (SEMPR), Curitiba, Brazil.

出版信息

Int J Clin Pract. 2007 Jun;61(6):1058-62. doi: 10.1111/j.1742-1241.2007.01392.x.

Abstract

Zoledronic acid inhibits bone resorption for up to 12 months. It is not known whether the duration of this antiresorptive effect extends beyond this period of time. The aim of this study was to evaluate the changes in bone turnover at 12 months (T12) and 18 months (T18) after a single injection of 4 mg of zoledronic acid. It is a prospective, longitudinal study, with a follow-up for 18 months. We studied male and female patients (60.5 +/- 11.0 years old), with low bone mineral density (BMD) coming from the outpatient clinic in a metabolic bone unit of a tertiary care hospital. All patients received a single intravenous dose of 4 mg of zoledronic acid, bone turnover markers [serum carboxyterminal telopeptide of type I collagen (CTX-I), bone-specific alkaline phosphatase (BSAP)] and BMD [lumbar spine (LS) and total hip (TH)] were measured at baseline, and after 12 months (T12) and 18 months (T18). Median serum CTX-I and BSAP levels were suppressed at T12 in comparison with baseline values: 0.183 to 0.039 ng/ml for CTX-I (p = 0.0002) and 16.95 to 13.96 U/l for BSAP (p = 0.005). At T18, both CTX-I and BSAP continued to be suppressed below baseline at 0.108 ng/ml and 12.23 U/l (p = 0.009 and p = 0.02, vs. T0). Significant increases in BMD at T18 as compared with T12 were observed in patients (median increase 6.1% for LS and 2.0% for TH). Zoledronic acid inhibits bone turnover effectively for 12 months, with evidence for continued suppression and gains in BMD even after 18 months.

摘要

唑来膦酸抑制骨吸收长达12个月。目前尚不清楚这种抗吸收作用的持续时间是否会超过这段时间。本研究的目的是评估单次注射4mg唑来膦酸后12个月(T12)和18个月(T18)时骨转换的变化。这是一项前瞻性纵向研究,随访18个月。我们研究了来自三级护理医院代谢骨病科门诊的男性和女性患者(年龄60.5±11.0岁),他们的骨矿物质密度(BMD)较低。所有患者均接受单次静脉注射4mg唑来膦酸,在基线、12个月(T12)和18个月(T18)时测量骨转换标志物[血清I型胶原羧基末端肽(CTX-I)、骨特异性碱性磷酸酶(BSAP)]和BMD[腰椎(LS)和全髋(TH)]。与基线值相比,T12时血清CTX-I和BSAP水平的中位数受到抑制:CTX-I从0.183降至0.039ng/ml(p = 0.0002),BSAP从16.95降至13.96U/l(p = 0.005)。在T18时,CTX-I和BSAP均继续被抑制在基线以下,分别为0.108ng/ml和12.23U/l(与T0相比,p = 0.009和p = 0.02)。与T12相比,患者在T18时BMD显著增加(LS中位数增加6.1%,TH中位数增加2.0%)。唑来膦酸可有效抑制骨转换12个月,即使在18个月后仍有持续抑制和BMD增加的证据。

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