Taxonomy of rare genetic metabolic bone disorders

被引:26
作者
Masi, L. [1 ]
Agnusdei, D. [2 ]
Bilezikian, J. [3 ]
Chappard, D. [4 ]
Chapurlat, R. [5 ]
Cianferotti, L. [1 ]
Devolgelaer, J. -P. [6 ]
El Maghraoui, A. [7 ]
Ferrari, S. [8 ]
Javaid, M. K. [9 ]
Kaufman, J. -M. [10 ]
Liberman, U. A. [11 ,12 ]
Lyritis, G. [13 ]
Miller, P. [14 ]
Napoli, N. [15 ]
Roldan, E. [16 ]
Papapoulos, S. [17 ]
Watts, N. B. [18 ]
Brandi, M. L. [1 ]
机构
[1] Univ Florence, Univ Hosp Florence, Dept Surg & Translat Med, Metab Bone Dis Unit, Florence, Italy
[2] Eli Lilly & Co, Florence, Italy
[3] Columbia Univ, Coll Phys & Surg, New York, NY USA
[4] LUNAM Univ, IRIS IBS, GEROM Grp Etud Remodelage Osseux & BioMat LHEA, Angers, France
[5] Univ Lyon, Hosp Civils Lyon, Dept Rheumatol, INSERM UMR 1033, Lyon, France
[6] Clin Univ UCL St Luc, Dept Med Interne, Brussels, Belgium
[7] Hop Militaire Mohammed V, Serv Rhumatol, Rabat, Morocco
[8] Univ Hosp Geneva, Fac Med, Div Bone Dis, Geneva, Switzerland
[9] Univ Oxford, Oxford NIHR Musculoskeletal Biomed Res Unit, Oxford, England
[10] Ghent Univ Hosp, Dept Endocrinol, Ghent, Belgium
[11] Tel Aviv Univ, Sackler Sch Med, Dept Physiol & Pharmacol, IL-69978 Tel Aviv, Israel
[12] Tel Aviv Univ, Sackler Sch Med, Felsenstein Med Res Ctr, IL-69978 Tel Aviv, Israel
[13] Univ Athens, Lab Res Musculoskeletal Syst, Athens, Greece
[14] Univ Colorado, Hlth Sci Ctr, Colorado Ctr Bone Res, Lakewood, CO USA
[15] Univ Campus Biomed Roma, Div Endocrinol & Diabet, Rome, Italy
[16] Gador SA, Dept Clin Pharmacol, Buenos Aires, DF, Argentina
[17] Leiden Univ, Med Ctr, Ctr Bone Qual, Leiden, Netherlands
[18] Mercy Hlth Osteoporosis & Bone Hlth Serv, Cincinnati, OH USA
关键词
Bone metabolism; Genetic bone diseases; Metabolic bone diseases; Rare bone diseases; Taxonomy; VACUOLAR PROTON PUMP; BIOCHEMICAL MARKERS; OSTEOPETROSIS; OSTEOCYTES; DISEASES; RESORPTION; OSTEOPOROSIS; MECHANISMS; OSTEOBLAST; MEMBRANE;
D O I
10.1007/s00198-015-3188-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The Summary This article reports a taxonomic classification of rare skeletal diseases based on metabolic phenotypes. It was prepared by The Skeletal Rare Diseases Working Group of the International Osteoporosis Foundation (IOF) and includes 116 OMIM phenotypes with 86 affected genes. Introduction Rare skeletal metabolic diseases comprise a group of diseases commonly associated with severe clinical consequences. In recent years, the description of the clinical phenotypes and radiographic features of several genetic bone disorders was paralleled by the discovery of key molecular pathways involved in the regulation of bone and mineral metabolism. Including this information in the description and classification of rare skeletal diseases may improve the recognition and management of affected patients. Methods IOF recognized this need and formed a Skeletal Rare Diseases Working Group (SRD-WG) of basic and clinical scientists who developed a taxonomy of rare skeletal diseases based on their metabolic pathogenesis. Results This taxonomy of rare genetic metabolic bone disorders (RGMBDs) comprises 116 OMIM phenotypes, with 86 affected genes related to bone and mineral homeostasis. The diseases were divided into four major groups, namely, disorders due to altered osteoclast, osteoblast, or osteocyte activity; disorders due to altered bone matrix proteins; disorders due to altered bone microenvironmental regulators; and disorders due to deranged calciotropic hormonal activity. Conclusions This article provides the first comprehensive taxonomy of rare metabolic skeletal diseases based on deranged metabolic activity. This classification will help in the development of common and shared diagnostic and therapeutic pathways for these patients and also in the creation of international registries of rare skeletal diseases, the first step for the development of genetic tests based on next generation sequencing and for performing large intervention trials to assess efficacy of orphan drugs.
引用
收藏
页码:2529 / 2558
页数:30
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