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Initial report of the osteogenesis imperfecta adult natural history initiative
BACKGROUND: A better understanding of the natural history of osteogenesis imperfecta (OI) in adulthood should improve health care for patients with this rare condition. METHODS: The Osteogenesis Imperfecta Foundation established the Adult Natural History Initiative (ANHI) in 2010 to give voice to th...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4650321/ https://www.ncbi.nlm.nih.gov/pubmed/26578084 http://dx.doi.org/10.1186/s13023-015-0362-2 |
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author | Tosi, Laura L. Oetgen, Matthew E. Floor, Marianne K. Huber, Mary Beth Kennelly, Ann M. McCarter, Robert J. Rak, Melanie F. Simmonds, Barbara J. Simpson, Melissa D. Tucker, Carole A. McKiernan, Fergus E. |
author_facet | Tosi, Laura L. Oetgen, Matthew E. Floor, Marianne K. Huber, Mary Beth Kennelly, Ann M. McCarter, Robert J. Rak, Melanie F. Simmonds, Barbara J. Simpson, Melissa D. Tucker, Carole A. McKiernan, Fergus E. |
author_sort | Tosi, Laura L. |
collection | PubMed |
description | BACKGROUND: A better understanding of the natural history of osteogenesis imperfecta (OI) in adulthood should improve health care for patients with this rare condition. METHODS: The Osteogenesis Imperfecta Foundation established the Adult Natural History Initiative (ANHI) in 2010 to give voice to the health concerns of the adult OI community and to begin to address existing knowledge gaps for this condition. Using a web-based platform, 959 adults with self-reported OI, representing a wide range of self-reported disease severity, reported symptoms and health conditions, estimated the impact of these concerns on present and future health-related quality of life (QoL) and completed a Patient-Reported Outcomes Measurement Information System (PROMIS®) survey of health issues. RESULTS: Adults with OI report lower general physical health status (p < .0001), exhibit a higher prevalence of auditory (58 % of sample versus 2–16 % of normalized population) and musculoskeletal (64 % of sample versus 1–3 % of normalized population) concerns than the general population, but report generally similar mental health status. Musculoskeletal, auditory, pulmonary, endocrine, and gastrointestinal issues are particular future health-related QoL concerns for these adults. Numerous other statistically significant differences exist among adults with OI as well as between adults with OI and the referent PROMIS® population, but the clinical significance of these differences is uncertain. CONCLUSIONS: Adults with OI report lower general health status but are otherwise more similar to the general population than might have been expected. While reassuring, further analysis of the extensive OI-ANHI databank should help identify areas of unique clinical concern and for future research. The OI-ANHI survey experience supports an internet-based strategy for successful patient-centered outcomes research in rare disease populations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13023-015-0362-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4650321 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46503212015-11-19 Initial report of the osteogenesis imperfecta adult natural history initiative Tosi, Laura L. Oetgen, Matthew E. Floor, Marianne K. Huber, Mary Beth Kennelly, Ann M. McCarter, Robert J. Rak, Melanie F. Simmonds, Barbara J. Simpson, Melissa D. Tucker, Carole A. McKiernan, Fergus E. Orphanet J Rare Dis Research BACKGROUND: A better understanding of the natural history of osteogenesis imperfecta (OI) in adulthood should improve health care for patients with this rare condition. METHODS: The Osteogenesis Imperfecta Foundation established the Adult Natural History Initiative (ANHI) in 2010 to give voice to the health concerns of the adult OI community and to begin to address existing knowledge gaps for this condition. Using a web-based platform, 959 adults with self-reported OI, representing a wide range of self-reported disease severity, reported symptoms and health conditions, estimated the impact of these concerns on present and future health-related quality of life (QoL) and completed a Patient-Reported Outcomes Measurement Information System (PROMIS®) survey of health issues. RESULTS: Adults with OI report lower general physical health status (p < .0001), exhibit a higher prevalence of auditory (58 % of sample versus 2–16 % of normalized population) and musculoskeletal (64 % of sample versus 1–3 % of normalized population) concerns than the general population, but report generally similar mental health status. Musculoskeletal, auditory, pulmonary, endocrine, and gastrointestinal issues are particular future health-related QoL concerns for these adults. Numerous other statistically significant differences exist among adults with OI as well as between adults with OI and the referent PROMIS® population, but the clinical significance of these differences is uncertain. CONCLUSIONS: Adults with OI report lower general health status but are otherwise more similar to the general population than might have been expected. While reassuring, further analysis of the extensive OI-ANHI databank should help identify areas of unique clinical concern and for future research. The OI-ANHI survey experience supports an internet-based strategy for successful patient-centered outcomes research in rare disease populations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13023-015-0362-2) contains supplementary material, which is available to authorized users. BioMed Central 2015-11-14 /pmc/articles/PMC4650321/ /pubmed/26578084 http://dx.doi.org/10.1186/s13023-015-0362-2 Text en © Tosi et al. 2015 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 Tosi, Laura L. Oetgen, Matthew E. Floor, Marianne K. Huber, Mary Beth Kennelly, Ann M. McCarter, Robert J. Rak, Melanie F. Simmonds, Barbara J. Simpson, Melissa D. Tucker, Carole A. McKiernan, Fergus E. Initial report of the osteogenesis imperfecta adult natural history initiative |
title | Initial report of the osteogenesis imperfecta adult natural history initiative |
title_full | Initial report of the osteogenesis imperfecta adult natural history initiative |
title_fullStr | Initial report of the osteogenesis imperfecta adult natural history initiative |
title_full_unstemmed | Initial report of the osteogenesis imperfecta adult natural history initiative |
title_short | Initial report of the osteogenesis imperfecta adult natural history initiative |
title_sort | initial report of the osteogenesis imperfecta adult natural history initiative |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4650321/ https://www.ncbi.nlm.nih.gov/pubmed/26578084 http://dx.doi.org/10.1186/s13023-015-0362-2 |
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