Literature DB >> 28943457

Clinical staging of Fibrodysplasia Ossificans Progressiva (FOP).

Robert J Pignolo1, Frederick S Kaplan2.   

Abstract

Fibrodyplasia ossificans progressiva (FOP) is an ultra-rare genetic condition of heterotopic ossification (HO) that results in progressive loss of joint function, ultimately rendering movement impossible. Death is most commonly the result of thoracic insufficiency syndrome, or complications related to recurrent respiratory infections. There are no current treatments for FOP, but early and emerging clinical trials offer hope for this devastating disease. With the recent reporting of a comprehensive global natural history study, scales to assess joint dysfunction, and a more accurate prediction of joint survival, it is now possible to construct a conceptual framework for the clinical staging of FOP. Based on assessment of FOP features in seven areas, it is possible to assign five clinical stages. FOP features include flare-up activity, body regions affected, thoracic insufficiency, other complications, activities of daily living (ADLs), ambulatory status, and the cumulative joint involvement scale (CAJIS) score. Assessments of these features assign an individual with FOP to early/mild, moderate, severe, profound, or late-stage disease. These criteria seek to be flexible enough to be used by clinicians without reliance on advanced imaging or specialized testing, as well as by investigators involved in research or clinical trial studies who would have these tools available. These staging measures for FOP assess the influence of HO and accelerated joint dysfunction (due to congenital abnormalities) on the ability to perform common functional activities, and thus a delay or lack of progression from one stage to the next represents the ultimate test of efficacy for drug trials. This framework will serve both as a prediction tool for FOP progression as well as a critical opportunity to substantiate therapeutic interventions. The staging system proposed here will permit an accurate assessment of severity to appropriately develop or revise clinical plans of care, define operational research criteria, and identify the effectiveness of interventions. Ultimately, this clinical staging will aid the field in moving toward earlier intervention at a stage where disease-modifying therapies may be most efficacious.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Fibrodysplasia ossificans progressiva (FOP); Heterotopic ossification; Staging

Mesh:

Year:  2017        PMID: 28943457     DOI: 10.1016/j.bone.2017.09.014

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


  5 in total

1.  Clearance of Senescent Cells From Injured Muscle Abrogates Heterotopic Ossification in Mouse Models of Fibrodysplasia Ossificans Progressiva.

Authors:  Haitao Wang; Qiang Zhang; Frederick S Kaplan; Robert J Pignolo
Journal:  J Bone Miner Res       Date:  2021-10-25       Impact factor: 6.390

Review 2.  Do Interactions of Vitamin D3 and BMP Signaling Hold Implications in the Pathogenesis of Fibrodysplasia Ossificans Progressiva?

Authors:  Jessica L Pierce; Daniel S Perrien
Journal:  Curr Osteoporos Rep       Date:  2021-04-14       Impact factor: 5.163

3.  Atypical Presentation of Fibrodysplasia Ossificans Progressiva: A Case Report and Review of Literature.

Authors:  Vivek Tiwari; Prateek Behera; Radha Sarawagi; Babu Mohammed Rafi; Saurabh Sahu; Hemanth Raj; Manish Rajpoot
Journal:  Cureus       Date:  2018-07-10

4.  Cercosporamide inhibits bone morphogenetic protein receptor type I kinase activity in zebrafish.

Authors:  Jelmer Hoeksma; Gerard C M van der Zon; Peter Ten Dijke; Jeroen den Hertog
Journal:  Dis Model Mech       Date:  2020-09-24       Impact factor: 5.758

Review 5.  Current challenges and opportunities in the care of patients with fibrodysplasia ossificans progressiva (FOP): an international, multi-stakeholder perspective.

Authors:  Robert J Pignolo; Christopher Bedford-Gay; Amanda Cali; Michelle Davis; Patricia L R Delai; Kristi Gonzales; Candace Hixson; Alastair Kent; Hope Newport; Manuel Robert; Christiaan Scott; Frederick S Kaplan
Journal:  Orphanet J Rare Dis       Date:  2022-04-18       Impact factor: 4.303

  5 in total

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