Literature DB >> 28627475

Joint-specific risk of impaired function in fibrodysplasia ossificans progressiva (FOP).

Robert J Pignolo1, Blythe P Durbin-Johnson2, David M Rocke3, Frederick S Kaplan4.   

Abstract

BACKGROUND: Fibrodysplasia ossificans progressiva (FOP) causes progressive disability due to heterotopic ossification from episodic flare-ups. Using data from 500 FOP patients (representing 63% of all known patients world-wide), age- and joint-specific risks of new joint involvement were estimated using parametric and nonparametric statistical methods.
RESULTS: Compared to data from a 1994 survey of 44 individuals with FOP, our current estimates of age- and joint-specific risks of new joint involvement are more accurate (narrower confidence limits), based on a wider range of ages, and have less bias due to its greater comprehensiveness (captures over three-fifths of the known FOP patients worldwide). For the neck, chest, abdomen, and upper back, the estimated hazard decreases over time. For the jaw, lower back, shoulder, elbow, wrist, fingers, hip, knee, ankle, and foot, the estimated hazard increases initially then either plateaus or decreases. At any given time and for any anatomic site, the data indicate which joints are at risk.
CONCLUSIONS: This study of approximately 63% of the world's known population of FOP patients provides a refined estimate of risk for new involvement at any joint at any age, as well as the proportion of patients with uninvolved joints at any age. Importantly, these joint-specific survival curves can be used to facilitate clinical trial design and to determine if potential treatments can modify the predicted trajectory of progressive joint dysfunction.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  ACVR1; Bone morphogenetic protein signaling; Fibrodysplasia ossificans progressiva; Heterotopic ossification; Joint survival; Risk

Mesh:

Substances:

Year:  2017        PMID: 28627475     DOI: 10.1016/j.bone.2017.06.009

Source DB:  PubMed          Journal:  Bone        ISSN: 1873-2763            Impact factor:   4.398


  6 in total

Review 1.  Fibrodysplasia ossificans progressiva (FOP): A disorder of osteochondrogenesis.

Authors:  Frederick S Kaplan; Mona Al Mukaddam; Alexandra Stanley; O Will Towler; Eileen M Shore
Journal:  Bone       Date:  2020-07-27       Impact factor: 4.398

2.  Compartment Syndrome of the Thigh in a Patient with Fibrodysplasia Ossificans Progressiva.

Authors:  Frederick S Kaplan; Mona Al Mukaddam; Robert J Pignolo
Journal:  J Orthop Case Rep       Date:  2020 May-Jun

Review 3.  Limitations of Jaw Movement in Fibrodysplasia Ossificans Progressiva: A Review.

Authors:  Ton Schoenmaker; Amine Dahou Bouchankouk; Semih Özkan; Marjolijn Gilijamse; Elinor Bouvy-Berends; Coen Netelenbos; Frank Lobbezoo; Elisabeth Marelise W Eekhoff; Teun J de Vries
Journal:  Front Med (Lausanne)       Date:  2022-03-22

4.  Fibrodysplasia ossificans progressiva: A rare disease with spinal deformity and severe hip dysfunction.

Authors:  Dong Sun; Peng Liu; Zhaolin Wang; Jianhu Mu; Jian Cao
Journal:  Front Pediatr       Date:  2022-09-15       Impact factor: 3.569

5.  Palovarotene reduces heterotopic ossification in juvenile FOP mice but exhibits pronounced skeletal toxicity.

Authors:  John B Lees-Shepard; Sarah-Anne E Nicholas; Sean J Stoessel; Parvathi M Devarakonda; Michael J Schneider; Masakazu Yamamoto; David J Goldhamer
Journal:  Elife       Date:  2018-09-18       Impact factor: 8.140

6.  Whole-body Computed Tomography Versus Dual Energy X‑ray Absorptiometry for Assessing Heterotopic Ossification in Fibrodysplasia Ossificans Progressiva.

Authors:  Sarah E Warner; Frederick S Kaplan; Robert J Pignolo; Stacy E Smith; Edward C Hsiao; Carmen De Cunto; Maja Di Rocco; Kathleen Harnett; Donna Grogan; Harry K Genant
Journal:  Calcif Tissue Int       Date:  2021-07-31       Impact factor: 4.333

  6 in total

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