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Natural history of fibrodysplasia ossificans progressiva: cross-sectional analysis of annotated baseline phenotypes

BACKGROUND: Fibrodysplasia Ossificans Progressiva (FOP; OMIM#135100) is an ultra-rare, severely disabling genetic disease characterized by congenital malformation of the great toes and progressive heterotopic ossification (HO) in muscles, tendons, ligaments, fascia, and aponeuroses often preceded by...

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Autores principales: Pignolo, Robert J., Baujat, Geneviève, Brown, Matthew A., De Cunto, Carmen, DiRocco, Maja, Hsiao, Edward C., Keen, Richard, Al Mukaddam, Mona, Sang, Kim-Hanh Le Quan, Wilson, Amy, White, Barbara, Grogan, Donna R., Kaplan, Frederick S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6499994/
https://www.ncbi.nlm.nih.gov/pubmed/31053156
http://dx.doi.org/10.1186/s13023-019-1068-7
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author Pignolo, Robert J.
Baujat, Geneviève
Brown, Matthew A.
De Cunto, Carmen
DiRocco, Maja
Hsiao, Edward C.
Keen, Richard
Al Mukaddam, Mona
Sang, Kim-Hanh Le Quan
Wilson, Amy
White, Barbara
Grogan, Donna R.
Kaplan, Frederick S.
author_facet Pignolo, Robert J.
Baujat, Geneviève
Brown, Matthew A.
De Cunto, Carmen
DiRocco, Maja
Hsiao, Edward C.
Keen, Richard
Al Mukaddam, Mona
Sang, Kim-Hanh Le Quan
Wilson, Amy
White, Barbara
Grogan, Donna R.
Kaplan, Frederick S.
author_sort Pignolo, Robert J.
collection PubMed
description BACKGROUND: Fibrodysplasia Ossificans Progressiva (FOP; OMIM#135100) is an ultra-rare, severely disabling genetic disease characterized by congenital malformation of the great toes and progressive heterotopic ossification (HO) in muscles, tendons, ligaments, fascia, and aponeuroses often preceded by painful, recurrent soft tissue swelling (flare-ups). The formation of HO leads to progressive disability, severe functional limitations in joint mobility, and to a shortened life-span. In this prospective natural history study, we describe the baseline, cross-sectional disease phenotype of 114 individuals with FOP. METHODS: All subjects underwent protocol-specified baseline assessments to determine their disease status. Cross-sectional analyses were performed using linear regression in which functional evaluations (Cumulative Analogue Joint Involvement Scale [CAJIS] and the FOP-Physical Function Questionnaire [FOP-PFQ]) and the burden of HO as measured by low-dose whole body CT (volume of HO and number of body regions with HO) were assessed. RESULTS: Findings from 114 subjects (age range 4 to 56 years) were evaluated. While subject age was significantly (p < 0.0001) correlated with increased CAJIS (r = 0.66) and FOP-PFQ scores (r = 0.41), the estimated mean increases per year (based on cross-sectional average changes over time) were small (0.47 units and 1.2%, respectively). There was also a significant (p < 0.0001) correlation between baseline age and HO volume (r = 0.56), with an estimated mean increase of 25,574 mm(3)/year. There were significant (p < 0.0001) correlations between the objective assessment of HO volume and clinical assessments of CAJIS (r = 0.57) and FOP-PFQ (r = 0.52). CONCLUSIONS: Based on the cross-sectional analysis of the baseline data, functional and physical disability as assessed by CAJIS and the FOP-PFQ increased over time. Although longitudinal data are not yet available, the cross-sectional analyses suggest that CAJIS and FOP-PFQ are not sensitive to detect substantial progression over a 1- to 2-year period. Future evaluation of longitudinal data will test this hypothesis. The statistically significant correlations between HO volume and the functional endpoints, and the estimated average annual increase in total HO volume, suggest that the formation of new HO will be measurable over the relative short-term course of a clinical trial, and represents an endpoint that is clinically meaningful to patients. TRIAL REGISTRATION: This study (NCT02322255) was first posted on 23 December, 2014. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13023-019-1068-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-64999942019-05-09 Natural history of fibrodysplasia ossificans progressiva: cross-sectional analysis of annotated baseline phenotypes Pignolo, Robert J. Baujat, Geneviève Brown, Matthew A. De Cunto, Carmen DiRocco, Maja Hsiao, Edward C. Keen, Richard Al Mukaddam, Mona Sang, Kim-Hanh Le Quan Wilson, Amy White, Barbara Grogan, Donna R. Kaplan, Frederick S. Orphanet J Rare Dis Research BACKGROUND: Fibrodysplasia Ossificans Progressiva (FOP; OMIM#135100) is an ultra-rare, severely disabling genetic disease characterized by congenital malformation of the great toes and progressive heterotopic ossification (HO) in muscles, tendons, ligaments, fascia, and aponeuroses often preceded by painful, recurrent soft tissue swelling (flare-ups). The formation of HO leads to progressive disability, severe functional limitations in joint mobility, and to a shortened life-span. In this prospective natural history study, we describe the baseline, cross-sectional disease phenotype of 114 individuals with FOP. METHODS: All subjects underwent protocol-specified baseline assessments to determine their disease status. Cross-sectional analyses were performed using linear regression in which functional evaluations (Cumulative Analogue Joint Involvement Scale [CAJIS] and the FOP-Physical Function Questionnaire [FOP-PFQ]) and the burden of HO as measured by low-dose whole body CT (volume of HO and number of body regions with HO) were assessed. RESULTS: Findings from 114 subjects (age range 4 to 56 years) were evaluated. While subject age was significantly (p < 0.0001) correlated with increased CAJIS (r = 0.66) and FOP-PFQ scores (r = 0.41), the estimated mean increases per year (based on cross-sectional average changes over time) were small (0.47 units and 1.2%, respectively). There was also a significant (p < 0.0001) correlation between baseline age and HO volume (r = 0.56), with an estimated mean increase of 25,574 mm(3)/year. There were significant (p < 0.0001) correlations between the objective assessment of HO volume and clinical assessments of CAJIS (r = 0.57) and FOP-PFQ (r = 0.52). CONCLUSIONS: Based on the cross-sectional analysis of the baseline data, functional and physical disability as assessed by CAJIS and the FOP-PFQ increased over time. Although longitudinal data are not yet available, the cross-sectional analyses suggest that CAJIS and FOP-PFQ are not sensitive to detect substantial progression over a 1- to 2-year period. Future evaluation of longitudinal data will test this hypothesis. The statistically significant correlations between HO volume and the functional endpoints, and the estimated average annual increase in total HO volume, suggest that the formation of new HO will be measurable over the relative short-term course of a clinical trial, and represents an endpoint that is clinically meaningful to patients. TRIAL REGISTRATION: This study (NCT02322255) was first posted on 23 December, 2014. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13023-019-1068-7) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-03 /pmc/articles/PMC6499994/ /pubmed/31053156 http://dx.doi.org/10.1186/s13023-019-1068-7 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Pignolo, Robert J.
Baujat, Geneviève
Brown, Matthew A.
De Cunto, Carmen
DiRocco, Maja
Hsiao, Edward C.
Keen, Richard
Al Mukaddam, Mona
Sang, Kim-Hanh Le Quan
Wilson, Amy
White, Barbara
Grogan, Donna R.
Kaplan, Frederick S.
Natural history of fibrodysplasia ossificans progressiva: cross-sectional analysis of annotated baseline phenotypes
title Natural history of fibrodysplasia ossificans progressiva: cross-sectional analysis of annotated baseline phenotypes
title_full Natural history of fibrodysplasia ossificans progressiva: cross-sectional analysis of annotated baseline phenotypes
title_fullStr Natural history of fibrodysplasia ossificans progressiva: cross-sectional analysis of annotated baseline phenotypes
title_full_unstemmed Natural history of fibrodysplasia ossificans progressiva: cross-sectional analysis of annotated baseline phenotypes
title_short Natural history of fibrodysplasia ossificans progressiva: cross-sectional analysis of annotated baseline phenotypes
title_sort natural history of fibrodysplasia ossificans progressiva: cross-sectional analysis of annotated baseline phenotypes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6499994/
https://www.ncbi.nlm.nih.gov/pubmed/31053156
http://dx.doi.org/10.1186/s13023-019-1068-7
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