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使用特立帕肽治疗的骨质疏松症患者中高钙尿症的发生情况。

Occurrence of hypercalciuria in patients with osteoporosis treated with teriparatide.

作者信息

Miller Paul D, Bilezikian John P, Diaz-Curiel Manuel, Chen Peiqi, Marin Fernando, Krege John H, Wong Mayme, Marcus Robert

机构信息

FACP, Colorado Center for Bone Research, 3190 South Wadsworth, Suite 250, Lakewood, Colorado 80227, USA.

出版信息

J Clin Endocrinol Metab. 2007 Sep;92(9):3535-41. doi: 10.1210/jc.2006-2439. Epub 2007 Jul 3.

DOI:10.1210/jc.2006-2439
PMID:17609307
Abstract

CONTEXT

Teriparatide (TPTD) [recombinant human PTH(1-34)] given sc once daily transiently increases serum calcium concentrations at 4-6 h after dosing, but its effects on urinary calcium excretion are less well studied.

OBJECTIVE

Our objective was to evaluate urinary calcium excretion, a prespecified safety endpoint, for up to 12 months of TPTD treatment.

DESIGN

This study included two prospective, randomized, double-blind placebo-controlled clinical trials.

PARTICIPANTS

A total of 2074 participants with osteoporosis or low bone mass (study 1, 1637 postmenopausal women; study 2, 437 men) were included.

INTERVENTIONS

Participants were given calcium (1000 mg/d) and vitamin D (400-1200 IU/d) supplements, and were randomized to placebo, TPTD 20 mug/d, or TPTD 40 mug/d.

MAIN OUTCOME MEASURES

Urinary calcium excretion was measured in 24-h collections at baseline, 1, 6, and 12 months.

RESULTS

In each study, baseline urinary calcium excretion was similar among groups. All groups had significantly increased urinary calcium excretion, compared with baseline, at most post-baseline time points. Post-baseline urinary calcium excretion was increased in the TPTD 20 microg/d group by up to 32 mg/d compared with placebo at the same time point (P < 0.05) in study 1. A total of seven participants (0.3%), of which three and four were in the placebo and TPTD groups, respectively, discontinued study drug due to repeated hypercalciuria (>300 mg/d).

CONCLUSION

Urinary calcium excretion was increased with TPTD treatment for up to 12 months, compared with placebo and baseline values, but the magnitude of these changes is unlikely to be clinically relevant or warrant urinary calcium monitoring for most patients.

摘要

背景

特立帕肽(TPTD)[重组人甲状旁腺激素(1 - 34)]每日一次皮下注射给药后,在给药后4 - 6小时会使血清钙浓度短暂升高,但其对尿钙排泄的影响研究较少。

目的

我们的目的是评估长达12个月的TPTD治疗对尿钙排泄这一预先设定的安全性终点指标的影响。

设计

本研究包括两项前瞻性、随机、双盲、安慰剂对照的临床试验。

参与者

共纳入2074名患有骨质疏松症或骨量低的参与者(研究1为1637名绝经后女性;研究2为437名男性)。

干预措施

参与者补充钙(1000毫克/天)和维生素D(400 - 1200国际单位/天),并随机分为安慰剂组、20微克/天的TPTD组或40微克/天的TPTD组。

主要观察指标

在基线、1个月、6个月和12个月时,收集24小时尿液测量尿钙排泄量。

结果

在每项研究中,各治疗组的基线尿钙排泄量相似。与基线相比,在大多数基线后时间点,所有组的尿钙排泄量均显著增加。在研究1中,与安慰剂组相比,20微克/天的TPTD组在同一时间点的基线后尿钙排泄量增加了高达32毫克/天(P < 0.05)。共有7名参与者(0.3%)因反复高钙尿症(>300毫克/天)停止研究药物治疗,其中安慰剂组3名,TPTD组4名。

结论

与安慰剂和基线值相比,TPTD治疗长达12个月会使尿钙排泄量增加,但这些变化的幅度在临床上可能无关紧要,大多数患者无需进行尿钙监测。

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