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地诺单抗治疗肥大细胞增多症相关骨质疏松症:病例系列

Denosumab for the Treatment of Mastocytosis-Related Osteoporosis: A Case Series.

作者信息

Orsolini Giovanni, Gavioli Irene, Tripi Gaia, Viapiana Ombretta, Gatti Davide, Idolazzi Luca, Zanotti Roberta, Rossini Maurizio

机构信息

Rheumatology Section, Department of Medicine, University of Verona, Piazzale L. Scuro 10, 37134, Verona, Italy.

Hematology Section, Department of Medicine, University of Verona, Verona, Italy.

出版信息

Calcif Tissue Int. 2017 Jun;100(6):595-598. doi: 10.1007/s00223-017-0241-z. Epub 2017 Feb 22.

Abstract

The purpose of this study was to investigate the therapeutic effect of denosumab, an anti-RANKL monoclonal antibody for the treatment of bone loss in indolent systemic mastocytosis (ISM) patients intolerant to bisphosphonates. Four patients underwent upon informed consent a treatment with denosumab 60 mg administered subcutaneously every 6 months with the same regimen used for postmenopausal osteoporosis. Bone mineral density (BMD) was measured at lumbar and femoral sites at baseline and after 1 year. C-terminal telopeptide of collagen type I (CTX), bone alkaline phosphatase (bALP) and tryptase serum level were determined at baseline and after 12 months with fasting blood samples withdrawals. BMD increased significantly at both sites during the 12 months; all the patients had an important decrease of serum CTX and of lesser extent of bALP serum levels. After denosumab treatment, a decrease in serum tryptase level was observed in all the patients. No adverse events or new fractures occurred. Denosumab seems to be a valid alternative for the treatment of bone loss in ISM. RANKL might be of key importance in the pathogenesis of ISM bone involvement.

摘要

本研究的目的是调查地诺单抗(一种抗RANKL单克隆抗体)对不耐受双膦酸盐的惰性系统性肥大细胞增多症(ISM)患者骨质流失的治疗效果。4例患者在获得知情同意后,接受了地诺单抗治疗,每6个月皮下注射60mg,采用与绝经后骨质疏松症相同的治疗方案。在基线和1年后测量腰椎和股骨部位的骨密度(BMD)。在基线和12个月后,通过采集空腹血样测定I型胶原C末端肽(CTX)、骨碱性磷酸酶(bALP)和类胰蛋白酶血清水平。在12个月期间,两个部位的骨密度均显著增加;所有患者的血清CTX均显著降低,bALP血清水平降低程度较小。地诺单抗治疗后,所有患者的血清类胰蛋白酶水平均降低。未发生不良事件或新的骨折。地诺单抗似乎是治疗ISM骨质流失的有效替代药物。RANKL可能在ISM骨受累的发病机制中起关键作用。

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