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Association of visual impairment with risk for future Parkinson's disease
BACKGROUND: Although visual dysfunction is one of the most common non-motor symptoms among patients with Parkinson's disease (PD), it is not known whether visual impairment (VI) predates the onset of clinical PD. Therefore, we aim to examine the association of VI with the future development of...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8585627/ https://www.ncbi.nlm.nih.gov/pubmed/34805812 http://dx.doi.org/10.1016/j.eclinm.2021.101189 |
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author | Zhu, Zhuoting Hu, Wenyi Liao, Huan Tan, Zachary Chen, Yifan Shi, Danli Shang, Xianwen Zhang, Xueli Huang, Yu Yu, Honghua Wang, Wei He, Mingguang Yang, Xiaohong |
author_facet | Zhu, Zhuoting Hu, Wenyi Liao, Huan Tan, Zachary Chen, Yifan Shi, Danli Shang, Xianwen Zhang, Xueli Huang, Yu Yu, Honghua Wang, Wei He, Mingguang Yang, Xiaohong |
author_sort | Zhu, Zhuoting |
collection | PubMed |
description | BACKGROUND: Although visual dysfunction is one of the most common non-motor symptoms among patients with Parkinson's disease (PD), it is not known whether visual impairment (VI) predates the onset of clinical PD. Therefore, we aim to examine the association of VI with the future development of PD in the UK Biobank Study. METHODS: The UK Biobank Study is one of the largest cohort studies of health, enrolling over 500,000 participants aged 40–69 years between 2006 and 2010 across the UK. VI was defined as a habitual distance visual acuity (VA) worse than 0·3 logarithm of the minimum angle of resolution (LogMAR) in the better-seeing eye. Incident cases of PD were determined by self report data, hospital admission records or death records, whichever came first. Multivariable Cox proportional hazard regression models were used to investigate the association between VI and the risk of incident PD. FINDINGS: A total of 117,050 participants were free of PD at the baseline assessment. During the median observation period of 5·96 (IQR: 5·77–6·23) years, PD occurred in 222 (0·19%) participants. Visually impaired participants were at a higher risk of developing PD than non-VI participants (p < 0·001). Compared with the non-VI group, the adjusted hazard ratio was 2·28 (95% CI 1·29–4·05, p = 0·005) in the VI group. These results were consistent in the sensitivity analysis, where incident PD cases diagnosed within one year after the baseline assessment were excluded. INTERPRETATION: This cohort study found that VI was associated with an increased risk of incident PD, suggesting that VI may serve as a modifiable risk factor for prevention of future PD. |
format | Online Article Text |
id | pubmed-8585627 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-85856272021-11-18 Association of visual impairment with risk for future Parkinson's disease Zhu, Zhuoting Hu, Wenyi Liao, Huan Tan, Zachary Chen, Yifan Shi, Danli Shang, Xianwen Zhang, Xueli Huang, Yu Yu, Honghua Wang, Wei He, Mingguang Yang, Xiaohong EClinicalMedicine Research paper BACKGROUND: Although visual dysfunction is one of the most common non-motor symptoms among patients with Parkinson's disease (PD), it is not known whether visual impairment (VI) predates the onset of clinical PD. Therefore, we aim to examine the association of VI with the future development of PD in the UK Biobank Study. METHODS: The UK Biobank Study is one of the largest cohort studies of health, enrolling over 500,000 participants aged 40–69 years between 2006 and 2010 across the UK. VI was defined as a habitual distance visual acuity (VA) worse than 0·3 logarithm of the minimum angle of resolution (LogMAR) in the better-seeing eye. Incident cases of PD were determined by self report data, hospital admission records or death records, whichever came first. Multivariable Cox proportional hazard regression models were used to investigate the association between VI and the risk of incident PD. FINDINGS: A total of 117,050 participants were free of PD at the baseline assessment. During the median observation period of 5·96 (IQR: 5·77–6·23) years, PD occurred in 222 (0·19%) participants. Visually impaired participants were at a higher risk of developing PD than non-VI participants (p < 0·001). Compared with the non-VI group, the adjusted hazard ratio was 2·28 (95% CI 1·29–4·05, p = 0·005) in the VI group. These results were consistent in the sensitivity analysis, where incident PD cases diagnosed within one year after the baseline assessment were excluded. INTERPRETATION: This cohort study found that VI was associated with an increased risk of incident PD, suggesting that VI may serve as a modifiable risk factor for prevention of future PD. Elsevier 2021-11-06 /pmc/articles/PMC8585627/ /pubmed/34805812 http://dx.doi.org/10.1016/j.eclinm.2021.101189 Text en © 2021 Published by Elsevier Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research paper Zhu, Zhuoting Hu, Wenyi Liao, Huan Tan, Zachary Chen, Yifan Shi, Danli Shang, Xianwen Zhang, Xueli Huang, Yu Yu, Honghua Wang, Wei He, Mingguang Yang, Xiaohong Association of visual impairment with risk for future Parkinson's disease |
title | Association of visual impairment with risk for future Parkinson's disease |
title_full | Association of visual impairment with risk for future Parkinson's disease |
title_fullStr | Association of visual impairment with risk for future Parkinson's disease |
title_full_unstemmed | Association of visual impairment with risk for future Parkinson's disease |
title_short | Association of visual impairment with risk for future Parkinson's disease |
title_sort | association of visual impairment with risk for future parkinson's disease |
topic | Research paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8585627/ https://www.ncbi.nlm.nih.gov/pubmed/34805812 http://dx.doi.org/10.1016/j.eclinm.2021.101189 |
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