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Osteoarthritis and risk of mortality in the USA: a population-based cohort study
BACKGROUND: Osteoarthritis (OA) is the most common joint disease, but its association with mortality is unclear. METHODS: We analysed data on adult participants in the 1988–94 and 1999–2010 National Health and Nutrition Examination Surveys, followed for mortality through 2011. OA was defined by self...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7263761/ https://www.ncbi.nlm.nih.gov/pubmed/30169829 http://dx.doi.org/10.1093/ije/dyy187 |
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author | Mendy, Angelico Park, JuYoung Vieira, Edgar Ramos |
author_facet | Mendy, Angelico Park, JuYoung Vieira, Edgar Ramos |
author_sort | Mendy, Angelico |
collection | PubMed |
description | BACKGROUND: Osteoarthritis (OA) is the most common joint disease, but its association with mortality is unclear. METHODS: We analysed data on adult participants in the 1988–94 and 1999–2010 National Health and Nutrition Examination Surveys, followed for mortality through 2011. OA was defined by self-report, and in a subset of participants 60 years or older with knee X-rays, radiographic knee OA (RKOA) was defined as Kellgren–Lawrence score ≥2. Cox proportional hazards were used to determine the mortality hazard ratio (HR) associated with self-reported OA and RKOA, adjusting for covariates. RESULTS: The sample included 51 938 participants followed for a median 8.9 years; 2589 of them had knee X-rays and were followed for a median of 13.6 years. Self-reported OA and RKOA prevalences were 6.6% and 40.6%, respectively. Self-reported OA was not associated with mortality. RKOA was associated with an increased risk of mortality from cardiovascular diseases (CVD) {HR 1.43 [95% confidence interval (CI): 1.32, 1.64]}, diabetes [HR 2.04 (1.87, 2.23)] and renal diseases [HR 1.14 (1.04, 1.25)], but with a reduced risk of cancer mortality [HR 0.88 (0.80, 0.96)]. Participants with early RKOA onset (diagnosed before age 40) had a higher risk of mortality from all causes [HR 1.53 (1.43, 1.65)] and from diabetes [HR 7.18 (5.45, 9.45)]. Obese participants with RKOA were at increased risk of mortality from CVD [HR 1.89 (1.56, 2.29)] and from diabetes [HR: 3.42 (3.01, 3.88)]. CONCLUSIONS: Self-reported OA was not associated with mortality. RKOA was associated with higher CVD, diabetes and renal mortality, especially in people with early onset of the disease or with obesity. |
format | Online Article Text |
id | pubmed-7263761 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-72637612020-06-04 Osteoarthritis and risk of mortality in the USA: a population-based cohort study Mendy, Angelico Park, JuYoung Vieira, Edgar Ramos Int J Epidemiol Chronic Disease BACKGROUND: Osteoarthritis (OA) is the most common joint disease, but its association with mortality is unclear. METHODS: We analysed data on adult participants in the 1988–94 and 1999–2010 National Health and Nutrition Examination Surveys, followed for mortality through 2011. OA was defined by self-report, and in a subset of participants 60 years or older with knee X-rays, radiographic knee OA (RKOA) was defined as Kellgren–Lawrence score ≥2. Cox proportional hazards were used to determine the mortality hazard ratio (HR) associated with self-reported OA and RKOA, adjusting for covariates. RESULTS: The sample included 51 938 participants followed for a median 8.9 years; 2589 of them had knee X-rays and were followed for a median of 13.6 years. Self-reported OA and RKOA prevalences were 6.6% and 40.6%, respectively. Self-reported OA was not associated with mortality. RKOA was associated with an increased risk of mortality from cardiovascular diseases (CVD) {HR 1.43 [95% confidence interval (CI): 1.32, 1.64]}, diabetes [HR 2.04 (1.87, 2.23)] and renal diseases [HR 1.14 (1.04, 1.25)], but with a reduced risk of cancer mortality [HR 0.88 (0.80, 0.96)]. Participants with early RKOA onset (diagnosed before age 40) had a higher risk of mortality from all causes [HR 1.53 (1.43, 1.65)] and from diabetes [HR 7.18 (5.45, 9.45)]. Obese participants with RKOA were at increased risk of mortality from CVD [HR 1.89 (1.56, 2.29)] and from diabetes [HR: 3.42 (3.01, 3.88)]. CONCLUSIONS: Self-reported OA was not associated with mortality. RKOA was associated with higher CVD, diabetes and renal mortality, especially in people with early onset of the disease or with obesity. Oxford University Press 2018-12 2018-08-29 /pmc/articles/PMC7263761/ /pubmed/30169829 http://dx.doi.org/10.1093/ije/dyy187 Text en © The Author(s) 2018; all rights reserved. Published by Oxford University Press on behalf of the International Epidemiological Association http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Chronic Disease Mendy, Angelico Park, JuYoung Vieira, Edgar Ramos Osteoarthritis and risk of mortality in the USA: a population-based cohort study |
title | Osteoarthritis and risk of mortality in the USA: a population-based cohort study |
title_full | Osteoarthritis and risk of mortality in the USA: a population-based cohort study |
title_fullStr | Osteoarthritis and risk of mortality in the USA: a population-based cohort study |
title_full_unstemmed | Osteoarthritis and risk of mortality in the USA: a population-based cohort study |
title_short | Osteoarthritis and risk of mortality in the USA: a population-based cohort study |
title_sort | osteoarthritis and risk of mortality in the usa: a population-based cohort study |
topic | Chronic Disease |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7263761/ https://www.ncbi.nlm.nih.gov/pubmed/30169829 http://dx.doi.org/10.1093/ije/dyy187 |
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