Prevalence, pathogenesis, and treatment options for mastocytosis-related osteoporosis

被引:0
作者
M. Rossini
R. Zanotti
G. Orsolini
G. Tripi
O. Viapiana
L. Idolazzi
A. Zamò
P. Bonadonna
V. Kunnathully
S. Adami
D. Gatti
机构
[1] University of Verona,Rheumatology Unit, Department of Medicine
[2] University of Verona,Hematology Section, Department of Medicine
[3] University of Verona,Department of Pathology and Diagnostics
[4] Azienda Ospedaliera Universitaria Integrata of Verona,Allergy Unit
来源
Osteoporosis International | 2016年 / 27卷
关键词
Bisphosphonate; Bone mineral density; Bone turnover markers; Denosumab; Mastocytosis; Osteoporosis; Zoledronate;
D O I
暂无
中图分类号
学科分类号
摘要
Mastocytosis is a rare condition characterized by abnormal mast cell proliferation and a broad spectrum of manifestations, including various organs and tissues. Osteoporosis is one of the most frequent manifestations of systemic mastocytosis, particularly in adults. Osteoporosis secondary to systemic mastocytosis is a cause of unexplained low bone mineral density that should be investigated when accompanied by suspicious clinical elements. Bone involvement is often complicated by a high recurrence of fragility fractures, mainly vertebral, leading to severe disability. The mechanism of bone loss is the result of different pathways, not yet fully discovered. The main actor is the osteoclast with a relative or absolute predominance of bone resorption. Among the stimuli that drive osteoclast activity, the most important one seems to be the RANK-RANKL signaling, but also histamine and other cytokines play a significant role in the process. The central role of osteoclasts made bisphosphonates, as anti-resorptive drugs, the most rational treatment for bone involvement in systemic mastocytosis. There are a few small studies supporting this approach, with large heterogeneity of drug and administration scheme. Currently, zoledronate has the best evidence in terms of gain in bone mineral density and bone turnover suppression, two surrogate markers of anti-fracture efficacy.
引用
收藏
页码:2411 / 2421
页数:10
相关论文
共 425 条
  • [1] Krishnaswamy G(2006)The human mast cell: an overview Methods Mol Biol 315 13-34
  • [2] Ajitawi O(2010)Pathogenesis, classification and treatment of mastocytosis: state of the art in 2010 and future perspectives Expert Rev Hematol 3 497-516
  • [3] Chi DS(1994)The riddle of the mast cell: kit(CD117)-ligand as the missing link? Immunol Today 15 111-114
  • [4] Arock M(1999)Demonstration that human mast cells arise from a progenitor cell population that is CD34(+), c-kit(+), and expresses aminopeptidase N (CD13) Blood 94 2333-2342
  • [5] Valent P(2013)Primary mast cell disorders in children Curr Allergy Asthma Rep 13 693-701
  • [6] Valent P(2012)Diagnosis, progression patterns and prognostication in mastocytosis Expert Rev Hematol 5 261-274
  • [7] Kirshenbaum AS(2013)Mastocytosis: a paradigmatic example of a rare disease with complex biology and pathology Am J Cancer Res 3 159-172
  • [8] Goff JP(2008)Gastrointestinal manifestations of systemic mastocytosis World J Gastroenterol 14 7005-7008
  • [9] Semere T(2013)Systemic mastocytosis in adults: 2013 update on diagnosis, risk stratification, and management Am J Hematol 88 612-624
  • [10] Foster B(2012)Systemic mastocytosis with associated clonal hematologic nonmast cell lineage disease: a clinicopathologic review Arch Pathol Lab Med 136 832-838