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Noncommunicable disease among adults with cerebral palsy: A matched cohort study
OBJECTIVE: To compare the incidence of noncommunicable diseases between adults with and without cerebral palsy (CP). METHODS: A cohort study was conducted using primary care data from the Clinical Practice Research Datalink. Cox models, stratified by matched set and adjusted for potential confounder...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6814410/ https://www.ncbi.nlm.nih.gov/pubmed/31462583 http://dx.doi.org/10.1212/WNL.0000000000008199 |
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author | Ryan, Jennifer M. Peterson, Mark D. Matthews, Anthony Ryan, Nicola Smith, Kimberley J. O'Connell, Neil E. Liverani, Silvia Anokye, Nana Victor, Christina Allen, Elizabeth |
author_facet | Ryan, Jennifer M. Peterson, Mark D. Matthews, Anthony Ryan, Nicola Smith, Kimberley J. O'Connell, Neil E. Liverani, Silvia Anokye, Nana Victor, Christina Allen, Elizabeth |
author_sort | Ryan, Jennifer M. |
collection | PubMed |
description | OBJECTIVE: To compare the incidence of noncommunicable diseases between adults with and without cerebral palsy (CP). METHODS: A cohort study was conducted using primary care data from the Clinical Practice Research Datalink. Cox models, stratified by matched set and adjusted for potential confounders, were fitted to compare the risk of any noncommunicable disease, cancer, cardiovascular disease, type 2 diabetes mellitus, and respiratory disease between adults with and without CP. RESULTS: The analysis included 1,705 adults with CP and 5,115 age-, sex-, and general practice–matched adults without CP. There was evidence from adjusted analyses that adults with CP had 75% increased risk of developing any noncommunicable disease compared to adults without CP (hazard ratio [HR] 1.75, 95% confidence interval [CI] 1.58–1.94). Specifically, they had increased risk of cardiovascular disease (HR 1.76, 95% CI 1.48–2.11) and respiratory disease (HR 2.61, 95% CI 2.14–3.19). There was no evidence of increased risk of cancer or type 2 diabetes mellitus. CONCLUSIONS: Adults with CP had increased risk of noncommunicable disease, specifically cardiovascular and respiratory disease. These findings highlight the need for clinical vigilance regarding identification of noncommunicable disease in people with CP and further research into the etiology and management of noncommunicable disease in this population. |
format | Online Article Text |
id | pubmed-6814410 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-68144102019-11-20 Noncommunicable disease among adults with cerebral palsy: A matched cohort study Ryan, Jennifer M. Peterson, Mark D. Matthews, Anthony Ryan, Nicola Smith, Kimberley J. O'Connell, Neil E. Liverani, Silvia Anokye, Nana Victor, Christina Allen, Elizabeth Neurology Article OBJECTIVE: To compare the incidence of noncommunicable diseases between adults with and without cerebral palsy (CP). METHODS: A cohort study was conducted using primary care data from the Clinical Practice Research Datalink. Cox models, stratified by matched set and adjusted for potential confounders, were fitted to compare the risk of any noncommunicable disease, cancer, cardiovascular disease, type 2 diabetes mellitus, and respiratory disease between adults with and without CP. RESULTS: The analysis included 1,705 adults with CP and 5,115 age-, sex-, and general practice–matched adults without CP. There was evidence from adjusted analyses that adults with CP had 75% increased risk of developing any noncommunicable disease compared to adults without CP (hazard ratio [HR] 1.75, 95% confidence interval [CI] 1.58–1.94). Specifically, they had increased risk of cardiovascular disease (HR 1.76, 95% CI 1.48–2.11) and respiratory disease (HR 2.61, 95% CI 2.14–3.19). There was no evidence of increased risk of cancer or type 2 diabetes mellitus. CONCLUSIONS: Adults with CP had increased risk of noncommunicable disease, specifically cardiovascular and respiratory disease. These findings highlight the need for clinical vigilance regarding identification of noncommunicable disease in people with CP and further research into the etiology and management of noncommunicable disease in this population. Lippincott Williams & Wilkins 2019-10-01 /pmc/articles/PMC6814410/ /pubmed/31462583 http://dx.doi.org/10.1212/WNL.0000000000008199 Text en Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Article Ryan, Jennifer M. Peterson, Mark D. Matthews, Anthony Ryan, Nicola Smith, Kimberley J. O'Connell, Neil E. Liverani, Silvia Anokye, Nana Victor, Christina Allen, Elizabeth Noncommunicable disease among adults with cerebral palsy: A matched cohort study |
title | Noncommunicable disease among adults with cerebral palsy: A matched cohort study |
title_full | Noncommunicable disease among adults with cerebral palsy: A matched cohort study |
title_fullStr | Noncommunicable disease among adults with cerebral palsy: A matched cohort study |
title_full_unstemmed | Noncommunicable disease among adults with cerebral palsy: A matched cohort study |
title_short | Noncommunicable disease among adults with cerebral palsy: A matched cohort study |
title_sort | noncommunicable disease among adults with cerebral palsy: a matched cohort study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6814410/ https://www.ncbi.nlm.nih.gov/pubmed/31462583 http://dx.doi.org/10.1212/WNL.0000000000008199 |
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