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绝经后骨质疏松症女性中特立帕肽和地舒单抗对激活素、卵泡抑素和抑制素的比较作用。

The comparative effect of teriparatide and denosumab on activins, follistatins, and inhibins in women with postmenopausal osteoporosis.

机构信息

Department of Endocrinology, 424 Military General Hospital, 56429, Thessaloniki, Greece.

First Laboratory of Pharmacology, Medical School, Aristotle University of Thessaloniki, 54124, Thessaloniki, Greece.

出版信息

J Bone Miner Res. 2024 Sep 2;39(9):1306-1314. doi: 10.1093/jbmr/zjae106.

Abstract

The activins-follistatins-inhibins (AFI) hormonal system affects bone metabolism. Treatments that alter bone metabolism may also alter the AFI molecules. In this non-randomized, open-label, head-to-head comparative study, circulating levels of the AFI system were evaluated in postmenopausal women with osteoporosis treated for 12 mo with either teriparatide (n = 23) or denosumab (n = 22). Τeriparatide treatment increased activin B (P=.01) and activin AB (P=.004) and the ratios activin A/follistatin (P=.006), activin B/follistatin (P=.007), activin AB/follistatin (P<.001), and activin AB/ follistatin-like 3 (FSTL3) (P=.034). The significant P for trend in group × time interactions of activins B and AB and of the ratio activin AB/FSTL3 remained robust after adjustment for BMI and LS BMD but it was lost for activin B after adjustment for previous antiresorptive treatment. The effect of teriparatide on BMD was attenuated when it was adjusted for baseline activins levels or their 12-mo changes. No changes were observed after denosumab treatment. In conclusion, activins B and AB, as well as the ratios of all activins to follistatin and of activin AB to FSTL3 increased with teriparatide treatment, possibly in a compensatory manner. Future studies are needed to study the potentially important role activins may play in bone biology and any associations with the effect of teriparatide on BMD. Clinical Trials identifier: NCT04206618. ClinicalTrials.gov  https://clinicaltrials.gov/search?term=NCT04206618.

摘要

激活素-卵泡抑素-抑制素(AFI)激素系统影响骨代谢。改变骨代谢的治疗方法也可能改变 AFI 分子。在这项非随机、开放标签、头对头的比较研究中,评估了接受骨质疏松症治疗的绝经后妇女的 AFI 系统的循环水平,这些患者接受了为期 12 个月的特立帕肽(n=23)或地舒单抗(n=22)治疗。特立帕肽治疗增加了激活素 B(P=.01)和激活素 AB(P=.004),以及激活素 A/卵泡抑素(P=.006)、激活素 B/卵泡抑素(P=.007)、激活素 AB/卵泡抑素(P<.001)和激活素 AB/卵泡抑素样 3(FSTL3)(P=.034)的比值。在调整 BMI 和 LS BMD 后,激活素 B 和 AB 以及激活素 AB/FSTL3 比值的组×时间交互作用的显著 P 值仍然稳健,但在调整先前的抗吸收治疗后,激活素 B 的 P 值则失去了稳健性。当特立帕肽对 BMD 的影响通过调整基线激活素水平或其 12 个月的变化来调整时,其效果减弱。地舒单抗治疗后没有观察到变化。总之,特立帕肽治疗后,激活素 B 和 AB 以及所有激活素与卵泡抑素的比值以及激活素 AB 与 FSTL3 的比值增加,可能以代偿方式增加。需要进一步的研究来研究激活素在骨生物学中的潜在重要作用及其与特立帕肽对 BMD 的影响的任何关联。临床试验标识符:NCT04206618。ClinicalTrials.gov 网站:https://clinicaltrials.gov/search?term=NCT04206618。

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