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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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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. |
format | Online Article Text |
id | pubmed-6499994 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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