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在患有确诊骨质疏松症的绝经后女性中,使用特立帕肽(重组人甲状旁腺激素1-34)期间,内源性完整甲状旁腺激素受到抑制。

Endogenous intact PTH is suppressed during Teriparatide (rhPTH 1-34) administration in postmenopausal women with established osteoporosis.

作者信息

Anastasilakis Athanasios D, Polyzos Stergios A, Goulis Dimitrios G, Slavakis Aristides, Efstathiadou Zoe, Kita Marina, Koukoulis George, Avramidis Avraam

机构信息

Department of Endocrinology, Hippocration General Hospital, Thessaloniki, Greece.

出版信息

Endocr J. 2008 Jul;55(3):613-6. doi: 10.1507/endocrj.k07e-123. Epub 2008 Jun 3.

Abstract

INTRODUCTION

Teriparatide (recombinant human PTH 1-34/TPTD) is an osteoanabolic agent available for osteoporosis treatment. The aim of this prospective trial was to evaluate the acute and chronic effects of TPTD in endogenous intact PTH (iPTH) levels in postmenopausal women with established osteoporosis.

MATERIALS AND METHODS

Thirty-six postmenopausal Caucasian women (age 66.6 1.4 years) with established osteoporosis received TPTD 20 mug once daily for eighteen months. Follow-up was continued for another six months after treatment discontinuation for a total of 24 months. Serum calcium, phosphate, total alkaline phosphatase (ALP) and iPTH were obtained from all women before and one hour, one day, as well as one, six, twelve, 18 and 24 months after treatment initiation. Lumbar spine bone mineral density was measured before, as well as twelve and eighteen months after treatment initiation.

RESULTS

iPTH levels decreased from the first hour of treatment, remained suppressed as long as TPTD was administered and increased after treatment discontinuation (p<0.001). Total ALP followed an opposite pattern. Serum calcium remained within normal range.

CONCLUSIONS

iPTH levels are suppressed rapidly and persistently during TPTD administration whereas they return to baseline after treatment discontinuation; therefore, they can serve as an index of patient's compliance to treatment.

摘要

引言

特立帕肽(重组人甲状旁腺激素1-34/TPTD)是一种可用于治疗骨质疏松症的骨合成代谢药物。这项前瞻性试验的目的是评估TPTD对已确诊骨质疏松症的绝经后女性内源性完整甲状旁腺激素(iPTH)水平的急性和慢性影响。

材料与方法

36名已确诊骨质疏松症的绝经后白人女性(年龄66.6±1.4岁)每天接受一次20微克的TPTD治疗,持续18个月。停药后继续随访6个月,共计24个月。在所有女性治疗开始前、治疗开始后1小时、1天、1个月、6个月、12个月、18个月和24个月时获取血清钙、磷、总碱性磷酸酶(ALP)和iPTH。在治疗开始前、治疗开始后12个月和18个月时测量腰椎骨密度。

结果

iPTH水平从治疗的第1小时开始下降,在持续给予TPTD期间一直受到抑制,停药后升高(p<0.001)。总ALP呈现相反的模式。血清钙保持在正常范围内。

结论

在给予TPTD期间,iPTH水平迅速且持续受到抑制,而停药后恢复到基线水平;因此,它们可作为患者治疗依从性的指标。

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