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甲状旁腺功能减退症患者口服人甲状旁腺激素(1-34)的安全性和疗效:一项开放标签研究。

Safety and Efficacy of Oral Human Parathyroid Hormone (1-34) in Hypoparathyroidism: An Open-Label Study.

机构信息

Endocrine Research Center, Lin Medical Center, Clalit Health Services, Haifa, Israel.

Hadassah Medical Center, Hebrew University Medical School, Jerusalem, Israel.

出版信息

J Bone Miner Res. 2021 Jun;36(6):1060-1068. doi: 10.1002/jbmr.4274. Epub 2021 Mar 5.

DOI:10.1002/jbmr.4274
PMID:33666947
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8252608/
Abstract

The standard treatment of primary hypoparathyroidism (hypoPT) with oral calcium supplementation and calcitriol (or an analog), intended to control hypocalcemia and hyperphosphatemia and avoid hypercalciuria, remains challenging for both patients and clinicians. In 2015, human parathyroid hormone (hPTH) (1-84) administered as a daily subcutaneous injection was approved as an adjunctive treatment in patients who cannot be well controlled on the standard treatments alone. This open-label study aimed to assess the safety and efficacy of an oral hPTH(1-34) formulation as an adjunct to standard treatment in adult subjects with hypoparathyroidism. Oral hPTH(1-34) tablets (0.75 mg human hPTH(1-34) acetate) were administered four times daily for 16 consecutive weeks, and changes in calcium supplementation and alfacalcidol use, albumin-adjusted serum calcium (ACa), serum phosphate, urinary calcium excretion, and quality of life throughout the study were monitored. Of the 19 enrolled subjects, 15 completed the trial per protocol. A median 42% reduction from baseline in exogenous calcium dose was recorded (p = .001), whereas median serum ACa levels remained above the lower target ACa levels for hypoPT patients (>7.5 mg/dL) throughout the study. Median serum phosphate levels rapidly decreased (23%, p = .0003) 2 hours after the first dose and were maintained within the normal range for the duration of the study. A notable, but not statistically significant, median decrease (21%, p = .07) in 24-hour urine calcium excretion was observed between the first and last treatment days. Only four possible drug-related, non-serious adverse events were reported over the 16-week study, all by the same patient. A small but statistically significant increase from baseline quality of life (5%, p = .03) was reported by the end of the treatment period. Oral hPTH(1-34) treatment was generally safe and well tolerated and allowed for a reduction in exogenous calcium supplementation, while maintaining normocalcemia in adult patients with hypoparathyroidism. © 2021 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).

摘要

原发性甲状旁腺功能减退症(简称 hypoPT)的标准治疗方法是口服钙剂和骨化三醇(或类似物),以控制低钙血症和高磷血症并避免高钙尿症,但对患者和临床医生来说仍然具有挑战性。2015 年,人甲状旁腺激素(hPTH)(1-84)作为每日皮下注射剂被批准作为不能单独通过标准治疗得到良好控制的患者的辅助治疗。这项开放标签研究旨在评估口服 hPTH(1-34)制剂作为辅助标准治疗在甲状旁腺功能减退症成年患者中的安全性和有效性。口服 hPTH(1-34)片剂(0.75mg 人 hPTH(1-34)醋酸盐)每天给药 4 次,连续 16 周,整个研究期间监测钙补充剂和骨化三醇使用、白蛋白校正血清钙(ACa)、血清磷酸盐、尿钙排泄和生活质量的变化。19 名入组受试者中,15 名按方案完成了试验。与基线相比,外源性钙剂量中位数降低了 42%(p=0.001),而整个研究过程中血清 ACa 水平中位数均保持在甲状旁腺功能减退症患者的较低目标 ACa 水平(>7.5mg/dL)以上。中位血清磷酸盐水平在首次给药后 2 小时迅速下降(23%,p=0.0003),并在整个研究期间维持在正常范围内。首次和最后一次治疗日之间观察到 24 小时尿钙排泄中位数显著但无统计学意义的下降(21%,p=0.07)。在 16 周的研究中,仅报告了 4 例可能与药物相关的非严重不良事件,均由同一名患者报告。治疗结束时,报告了生活质量略有但有统计学意义的改善(5%,p=0.03)。口服 hPTH(1-34)治疗总体安全且耐受良好,并允许减少外源性钙补充剂,同时维持甲状旁腺功能减退症成年患者的血钙正常。 © 2021 作者。骨矿研究杂志由 Wiley 期刊出版公司代表美国骨矿研究协会(ASBMR)出版。

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