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Inverse Association of Parkinson Disease With Systemic Lupus Erythematosus: A Nationwide Population-based Study
The effects of the inflammatory mediators involved in systemic lupus erythematous (SLE) on subsequent Parkinson disease have been reported, but no relevant studies have focused on the association between the 2 diseases. This nationwide population-based study evaluated the risk of Parkinson disease i...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4652833/ https://www.ncbi.nlm.nih.gov/pubmed/26579824 http://dx.doi.org/10.1097/MD.0000000000002097 |
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author | Liu, Feng-Cheng Huang, Wen-Yen Lin, Te-Yu Shen, Chih-Hao Chou, Yu-Ching Lin, Cheng-Li Lin, Kuen-Tze Kao, Chia-Hung |
author_facet | Liu, Feng-Cheng Huang, Wen-Yen Lin, Te-Yu Shen, Chih-Hao Chou, Yu-Ching Lin, Cheng-Li Lin, Kuen-Tze Kao, Chia-Hung |
author_sort | Liu, Feng-Cheng |
collection | PubMed |
description | The effects of the inflammatory mediators involved in systemic lupus erythematous (SLE) on subsequent Parkinson disease have been reported, but no relevant studies have focused on the association between the 2 diseases. This nationwide population-based study evaluated the risk of Parkinson disease in patients with SLE. We identified 12,817 patients in the Taiwan National Health Insurance database diagnosed with SLE between 2000 and 2010 and compared the incidence rate of Parkinson disease among these patients with that among 51,268 randomly selected age and sex-matched non-SLE patients. A Cox multivariable proportional-hazards model was used to evaluate the risk factors of Parkinson disease in the SLE cohort. We observed an inverse association between a diagnosis of SLE and the risk of subsequent Parkinson disease, with the crude hazard ratio (HR) being 0.60 (95% confidence interval 0.45–0.79) and adjusted HR being 0.68 (95% confidence interval 0.51–0.90). The cumulative incidence of Parkinson disease was 0.83% lower in the SLE cohort than in the non-SLE cohort. The adjusted HR of Parkinson disease decreased as the follow-up duration increased and was decreased among older lupus patients with comorbidity. We determined that patients with SLE had a decreased risk of subsequent Parkinson disease. Further research is required to elucidate the underlying mechanism. |
format | Online Article Text |
id | pubmed-4652833 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-46528332015-12-03 Inverse Association of Parkinson Disease With Systemic Lupus Erythematosus: A Nationwide Population-based Study Liu, Feng-Cheng Huang, Wen-Yen Lin, Te-Yu Shen, Chih-Hao Chou, Yu-Ching Lin, Cheng-Li Lin, Kuen-Tze Kao, Chia-Hung Medicine (Baltimore) Observational Study The effects of the inflammatory mediators involved in systemic lupus erythematous (SLE) on subsequent Parkinson disease have been reported, but no relevant studies have focused on the association between the 2 diseases. This nationwide population-based study evaluated the risk of Parkinson disease in patients with SLE. We identified 12,817 patients in the Taiwan National Health Insurance database diagnosed with SLE between 2000 and 2010 and compared the incidence rate of Parkinson disease among these patients with that among 51,268 randomly selected age and sex-matched non-SLE patients. A Cox multivariable proportional-hazards model was used to evaluate the risk factors of Parkinson disease in the SLE cohort. We observed an inverse association between a diagnosis of SLE and the risk of subsequent Parkinson disease, with the crude hazard ratio (HR) being 0.60 (95% confidence interval 0.45–0.79) and adjusted HR being 0.68 (95% confidence interval 0.51–0.90). The cumulative incidence of Parkinson disease was 0.83% lower in the SLE cohort than in the non-SLE cohort. The adjusted HR of Parkinson disease decreased as the follow-up duration increased and was decreased among older lupus patients with comorbidity. We determined that patients with SLE had a decreased risk of subsequent Parkinson disease. Further research is required to elucidate the underlying mechanism. Wolters Kluwer Health 2015-11-20 /pmc/articles/PMC4652833/ /pubmed/26579824 http://dx.doi.org/10.1097/MD.0000000000002097 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0, where it is permissible to download, share and reproduce the work in any medium, provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc-nd/4.0 |
spellingShingle | Observational Study Liu, Feng-Cheng Huang, Wen-Yen Lin, Te-Yu Shen, Chih-Hao Chou, Yu-Ching Lin, Cheng-Li Lin, Kuen-Tze Kao, Chia-Hung Inverse Association of Parkinson Disease With Systemic Lupus Erythematosus: A Nationwide Population-based Study |
title | Inverse Association of Parkinson Disease With Systemic Lupus Erythematosus: A Nationwide Population-based Study |
title_full | Inverse Association of Parkinson Disease With Systemic Lupus Erythematosus: A Nationwide Population-based Study |
title_fullStr | Inverse Association of Parkinson Disease With Systemic Lupus Erythematosus: A Nationwide Population-based Study |
title_full_unstemmed | Inverse Association of Parkinson Disease With Systemic Lupus Erythematosus: A Nationwide Population-based Study |
title_short | Inverse Association of Parkinson Disease With Systemic Lupus Erythematosus: A Nationwide Population-based Study |
title_sort | inverse association of parkinson disease with systemic lupus erythematosus: a nationwide population-based study |
topic | Observational Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4652833/ https://www.ncbi.nlm.nih.gov/pubmed/26579824 http://dx.doi.org/10.1097/MD.0000000000002097 |
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