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特立帕肽与安慰剂对下肢应力性骨折女性患者骨生物标志物、骨结构及骨折愈合的短期影响:一项初步研究。

Short-term effects of teriparatide versus placebo on bone biomarkers, structure, and fracture healing in women with lower-extremity stress fractures: A pilot study.

作者信息

Almirol Ellen A, Chi Lisa Y, Khurana Bharti, Hurwitz Shelley, Bluman Eric M, Chiodo Christopher, Matzkin Elizabeth, Baima Jennifer, LeBoff Meryl S

机构信息

Department of Medicine, Brigham and Women's Hospital, USA.

Harvard Medical School, Boston, MA, USA.

出版信息

J Clin Transl Endocrinol. 2016 May 30;5:7-14. doi: 10.1016/j.jcte.2016.05.004. eCollection 2016 Sep.

Abstract

AIMS

In this pilot, placebo-controlled study, we evaluated whether brief administration of teriparatide (TPTD) in premenopausal women with lower-extremity stress fractures would increase markers of bone formation in advance of bone resorption, improve bone structure, and hasten fracture healing according to magnetic resonance imaging (MRI).

METHODS

Premenopausal women with acute lower-extremity stress fractures were randomized to injection of TPTD 20-µg subcutaneous (s.c.) (n = 6) or placebo s.c. (n = 7) for 8 weeks. Biomarkers for bone formation N-terminal propeptide of type I procollagen (P1NP) and osteocalcin (OC) and resorption collagen type-1 cross-linked C-telopeptide (CTX) and collagen type 1 cross-linked N-telopeptide (NTX) were measured at baseline, 4 and 8 weeks. The area between the percent change of P1NP and CTX over study duration is defined as the anabolic window. To assess structural changes, peripheral quantitative computed topography (pQCT) was measured at baseline, 8 and 12 weeks at the unaffected tibia and distal radius. The MRI of the affected bone assessed stress fracture healing at baseline and 8 weeks.

RESULTS

After 8 weeks of treatment, bone biomarkers P1NP and OC increased more in the TPTD- versus placebo-treated group (both p ≤ 0.01), resulting in a marked anabolic window (p ≤ 0.05). Results from pQCT demonstrated that TPTD-treated women showed a larger cortical area and thickness compared to placebo at the weight bearing tibial site, while placebo-treated women had a greater total tibia and cortical density. No changes at the radial sites were observed between groups. According to MRI, 83.3% of the TPTD- and 57.1% of the placebo-treated group had improved or healed stress fractures (p = 0.18).

CONCLUSIONS

In this randomized, pilot study, brief administration of TPTD showed anabolic effects that TPTD may help hasten fracture healing in premenopausal women with lower-extremity stress fractures. Larger prospective studies are warranted to determine the effects of TPTD treatment on stress fracture healing in premenopausal women.

摘要

目的

在这项先导性、安慰剂对照研究中,我们评估了对患有下肢应力性骨折的绝经前女性短期给予特立帕肽(TPTD)是否会在骨吸收之前增加骨形成标志物、改善骨结构,并根据磁共振成像(MRI)加速骨折愈合。

方法

患有急性下肢应力性骨折的绝经前女性被随机分为皮下注射20μg TPTD组(n = 6)或皮下注射安慰剂组(n = 7),为期8周。在基线、第4周和第8周测量骨形成生物标志物I型前胶原N端前肽(P1NP)和骨钙素(OC)以及骨吸收标志物I型胶原交联C末端肽(CTX)和I型胶原交联N末端肽(NTX)。在研究期间,P1NP和CTX百分比变化之间的面积定义为合成代谢窗口。为了评估结构变化,在基线、第8周和第12周对未受影响的胫骨和桡骨远端进行外周定量计算机断层扫描(pQCT)测量。在基线和第8周对受影响骨骼进行MRI评估应力性骨折愈合情况。

结果

治疗8周后,与安慰剂治疗组相比,TPTD治疗组的骨生物标志物P1NP和OC升高更为明显(均p≤0.01),从而形成了明显的合成代谢窗口(p≤0.05)。pQCT结果表明,与安慰剂相比,TPTD治疗的女性在负重胫骨部位的皮质面积和厚度更大,而安慰剂治疗的女性胫骨总体积和皮质密度更大。两组之间在桡骨部位未观察到变化。根据MRI,TPTD治疗组83.3%的女性和安慰剂治疗组57.1%的女性应力性骨折得到改善或愈合(p = 0.18)。

结论

在这项随机先导性研究中,短期给予TPTD显示出合成代谢作用,TPTD可能有助于加速患有下肢应力性骨折的绝经前女性的骨折愈合。需要开展更大规模的前瞻性研究来确定TPTD治疗对绝经前女性应力性骨折愈合的影响。

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