Precision Medicine in the Medical, Surgical and Critical Care Areas, University of Palermo, 90100 Palermo, Italy.
Section of Pharmacology, Department of Biomedical and Biotechnological Sciences, University of Catania, 37100 Catania, Italy.
Medicina (Kaunas). 2024 Oct 24;60(11):1752. doi: 10.3390/medicina60111752.
: Mastocytosis (MS) is a rare disease that can involve various organs, including the bone. Given the incidence of the disease in the global population, MS poses a challenge for physicians, and early therapeutic intervention in the initial stages could significantly impact the quality of life of affected patients. : The aim of this scoping review was to provide an overview of secondary osteoporosis in systemic mastocytosis (SM), focusing on the heterogeneity of its manifestations, the benefits of early diagnosis, and appropriate pharmacological treatment. : A technical expert panel (TEP) consisting of 8 physicians with expertise in metabolic bone diseases conducted the review following the PRISMA-ScR model. A strength of this study is that it provides various therapeutic approaches for patients with bone involvement in SM, although the limited available literature on the topic constituted a limitation. The TEP sought evidence regarding the following diagnostic and therapeutic modalities in the management of SM: "bisphosphonate therapy", "zoledronic acid therapy", "denosumab therapy", "IFN-alpha therapy", and "IFN-alpha therapy in combination with pamidronate". : Clinical data showed a correlation between densitometric outcomes, serum tryptase levels, and mast cell infiltration in the bone marrow, between increased bone mineral density and the presence of osteosclerosis in cases of advanced SM, between the severity of osteoporosis and hypertryptasemia, and also provided results on the long-term effects of bisphosphonate therapy, the therapeutic efficacy of zoledronic acid administration, the positive effect of denosumab on the reduction of serum tryptase levels (even if is proved in a limited numbers of cases) and the prevention of new fractures, and the effect of IFN-alpha in more severe cases of SM, either alone or in combination with pamidronate. : Studies have demonstrated the effectiveness of various treatments depending on the form of mastocytosis, whether indolent systemic or advanced systemic, in the prognosis of the disease. However, this role should be further investigated in additional clinical studies, considering the limited data on the use of these interventions.
肥大细胞增多症(MS)是一种罕见的疾病,可累及包括骨骼在内的各种器官。鉴于该病在全球人群中的发病率,MS 对医生构成了挑战,在初始阶段进行早期治疗干预可能会显著影响受影响患者的生活质量。本综述的目的是概述系统性肥大细胞增多症(SM)中的继发性骨质疏松症,重点关注其表现的异质性、早期诊断的益处以及适当的药物治疗。一个由 8 名代谢性骨病专家组成的技术专家小组(TEP)按照 PRISMA-ScR 模型进行了审查。本研究的一个优势在于,它为骨骼受累的 SM 患者提供了各种治疗方法,尽管该主题的可用文献有限是一个限制。TEP 寻求有关以下诊断和治疗方法的证据,以管理 SM:“双膦酸盐治疗”、“唑来膦酸治疗”、“地舒单抗治疗”、“IFN-α 治疗”和“IFN-α 联合帕米膦酸治疗”。临床数据显示,骨密度计结果、血清胰蛋白酶水平和骨髓中肥大细胞浸润之间存在相关性,在晚期 SM 中,骨矿物质密度增加与骨硬化存在之间存在相关性,骨质疏松症的严重程度与高胰蛋白酶血症之间存在相关性,还提供了关于双膦酸盐治疗的长期效果、唑来膦酸给药的治疗效果、地舒单抗对降低血清胰蛋白酶水平的积极影响(即使在有限数量的病例中得到证实)和预防新骨折的效果,以及 IFN-α 在更严重的 SM 中的作用,无论是单独使用还是与帕米膦酸联合使用。研究表明,各种治疗方法取决于肥大细胞增多症的形式,无论是惰性系统性还是晚期系统性,对疾病的预后都有效。然而,考虑到这些干预措施使用的数据有限,应在更多的临床研究中进一步探讨这一作用。