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Repository corticotropin injection (H.P. Acthar gel) for the treatment of sarcoidosis-induced hypercalciuria and vitamin D dysregulation: a pilot open label study

机译:储存性促肾上腺皮质激素注射液(H.P. Acthar凝胶)用于治疗结节病引起的高钙尿症和维生素D失调:一项开放性试验性研究

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摘要

Vitamin D dysregulation may occur in sarcoidosis patients and result in hypercalciuria, hypercalcemia, nephrolithiasis, and renal impairment. We performed an open label pilot study of highly purified (H.P.) Acthar® Gel (repository corticotropin injection) (RCI) on patients with sarcoidosis-induced vitamin D dysregulation and hypercalciuria. Nine patients with sarcoidosis-induced vitamin D dysregulation and hypercalciuria on stable maintenance anti-sarcoidosis therapy received 80 units of RCI subcutaneously twice weekly for 12 weeks. 24-hour urinary calcium excretion was measured at baseline and at 12 weeks. Other parameters measured over 16 weeks (including 4 weeks post the last RCI dose) included the following serum values: calcium, 25-OH vitamin D, 1,25- diOH vitamin D and serum parathyroid hormone (PTH). In addition, the Sarcoidosis Health Questionnaire (SHQ) and Short Form-36 (SF-36) as well as a urinary symptom score were measured in all subjects. There was no significant change in the 24-hour urinary calcium excretion over 12 weeks of the study. However, there was evidence that RCI improved sarcoidosis-induced vitamin D dysregulation in that the serum 1,25- diOH vitamin D level significantly declined over 12 weeks. There was also improvement in most of the domains of the quality of life measures, although only a few of them reached statistical significance. There was also a trend toward improvement in urinary symptoms over the study period. The was evidence of the development corticosteroid side effects in the cohort, in that weight significantly increased over the study period. In this small pilot open label trial, 12 weeks of RCI did not significantly improve sarcoidosis-induced hypercalciuria. However, some statistically significant changes in serum vitamin D and PTH levels were demonstrated that were consistent with some amelioration of sarcoidosis-induced vitamin D dysregulation. Several corticosteroid-related side effects were demonstrated in this cohort.
机译:结节病患者可能发生维生素D失调,并导致高钙尿症,高血钙,肾结石和肾功能不全。我们对结节病诱发的维生素D失调和高钙尿症患者进行了高纯度(H.P.)Acthar®凝胶(贮库促肾上腺皮质激素注射)(RCI)的开放标签先导研究。 9名结节病诱发的维生素D失调和钙化过多的患者在稳定维持抗结节病治疗的情况下,每周两次皮下注射80单位RCI,共12周。在基线和第12周测量24小时尿钙排泄。在16周(包括最后一次RCI剂量后的4周)内测量的其他参数包括以下血清值:钙,25-OH维生素D,1,25-diOH维生素D和血清甲状旁腺激素(PTH)。此外,在所有受试者中均测量了结节病健康问卷(SHQ)和简短表格36(SF-36)以及尿液症状评分。在研究的12周内,24小时尿钙排泄没有明显变化。但是,有证据表明,RCI可改善结节病所致的维生素D失调,因为血清1,25-二羟基维生素D水平在12周内显着下降。生活质量衡量的大多数领域也有所改善,尽管只有少数达到统计学意义。在研究期间,还有尿毒症状改善的趋势。这是该人群中发展皮质类固醇副作用的证据,因为体重在研究期间显着增加。在这项小型的开放标签试验中,RCI的12周没有明显改善结节病引起的高钙尿症。然而,已证明血清维生素D和PTH水平在统计学上有显着变化,这与结节病引起的维生素D失调有所改善相一致。在该队列中证实了几种与皮质类固醇相关的副作用。

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