Reid Ian R, Sharma Sonakshi, Kalluru Ramanamma, Eagleton Carl
Department of Medicine, Faculty of Medical and Health Sciences, University of Auckland, Private Bag 92019, Auckland, New Zealand.
Department of Endocrinology, Auckland District Health Board, Auckland, New Zealand.
Calcif Tissue Int. 2016 Sep;99(3):322-5. doi: 10.1007/s00223-016-0150-6. Epub 2016 May 18.
Paget's disease is a condition involving focal overactivity of bone cells (osteoblasts and osteoclasts), which can result in significant skeletal morbidity. It is unclear in which bone cells the causative lesion resides. It is managed effectively with potent bisphosphonates, but treatment is difficult if these drugs are contraindicated. We describe a 75-year-old woman with Paget's disease involving the skull who was intolerant of bisphosphonates, so was treated with denosumab. This intervention normalized serum alkaline phosphatase for 4-8 months after each injection and led to some symptomatic improvement. Scintigraphic activity in the lesion was improved but not normalized. We conclude that reduction in RANKL activity by denosumab only partially corrects pagetic activity, indicating that the osteoclast overactivity of Paget's disease is not wholly mediated by RANKL. Denosumab has some clinical utility in Paget's disease and may become a second-line agent in those with contraindications to intravenous bisphosphonates.
佩吉特病是一种涉及骨细胞(成骨细胞和破骨细胞)局灶性过度活跃的病症,可导致严重的骨骼病变。致病病变存在于哪种骨细胞尚不清楚。强效双膦酸盐可有效治疗该病,但如果这些药物禁忌,则治疗困难。我们描述了一名75岁患有累及颅骨的佩吉特病的女性,她不耐受双膦酸盐,因此接受了地诺单抗治疗。每次注射后,这种干预使血清碱性磷酸酶在4 - 8个月内恢复正常,并带来了一些症状改善。病变部位的骨闪烁显像活性有所改善但未恢复正常。我们得出结论,地诺单抗降低RANKL活性仅部分纠正了佩吉特病的病变活性,这表明佩吉特病的破骨细胞过度活跃并非完全由RANKL介导。地诺单抗在佩吉特病中有一定临床应用价值,可能成为静脉注射双膦酸盐有禁忌者的二线药物。