Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/114998
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dc.contributorSchool of Optometry-
dc.creatorDu, ZJ-
dc.creatorZhang, XY-
dc.creatorBulloch, G-
dc.creatorZhang, F-
dc.creatorHuang, Y-
dc.creatorWang, YX-
dc.creatorLiang, YY-
dc.creatorWu, GR-
dc.creatorZhu, ZT-
dc.creatorShang, XW-
dc.creatorHu, YJ-
dc.creatorYang, XH-
dc.creatorYu, HH-
dc.date.accessioned2025-09-02T00:32:01Z-
dc.date.available2025-09-02T00:32:01Z-
dc.identifier.issn2211-8160-
dc.identifier.urihttp://hdl.handle.net/10397/114998-
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.rights© 2025 The Author(s). This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (CC-BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. See http://creativecommons.org/licenses/by/4.0/.en_US
dc.rightsThe following publication Du, Z., Zhang, X., Bulloch, G., Zhang, F., Huang, Y., Wang, Y., Liang, Y., Wu, G., Zhu, Z., Shang, X., Hu, Y., Yang, X. and Yu, H. (2025) ‘Association Between Visual Acuity and Incident Atherosclerotic Cardiovascular Disease: A Longitudinal Test of Mediators’, Global Heart, 20(1), 19 is available at https://dx.doi.org/10.5334/gh.1406.en_US
dc.subjectVisual acuityen_US
dc.subjectAtherosclerotic cardiovascular diseaseen_US
dc.subjectMediatorsen_US
dc.subjectOlder adultsen_US
dc.subjectLongitudinalen_US
dc.titleAssociation between visual acuity and incident atherosclerotic cardiovascular disease: a longitudinal test of mediatorsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume20-
dc.identifier.issue1-
dc.identifier.doi10.5334/gh.1406-
dcterms.abstractBackground: Little is known about the prospective relationship between visual acuity (VA) and atherosclerotic cardiovascular disease (ASCVD) events and the extent to which this association is mediated via potential mediators. This study aims to investigate the relationship between VA and ASCVD events, including the mediation effects of potential factors.-
dcterms.abstractMethods: A prospective study was conducted using data from 110,522 participants in the UK Biobank, all of whom had baseline visual acuity (VA) measurements collected between 2006 and 2010. VA was assessed using the logarithm of the minimum angle of resolution (logMAR) chart, with the better-seeing eye selected for analysis. Incident ASCVD events were obtained from hospital admissions and death records up to April 2021. The longitudinalassociation between VA and ASCVD was examined using Cox proportional hazards models. A four-way decomposition mediation analysis was performed to quantify the indirect effects of hypertension, diabetes, depression, and socioeconomic status in mediating the relationship between VA and ASCVD.-
dcterms.abstractResults: Over an 11.13-year median follow-up, 5,496 ASCVD cases were recorded. A one-line worsening in VA (0.1 logMAR increase) was associated with an increased risk of ASCVD (HR = 1.63; 95%CI = 1.35-1.96, P < 0.001). Mediation analysis showed that hypertension, diabetes, depression, and Townsend deprivation index contributed 3.8%, 3.3%, 5.7%, and 5.9% to this association, respectively (all P < 0.05). Notably, depression was the strongest mediator, accounting for 10.0% of the association in women (P < 0.05).-
dcterms.abstractConclusions: Our study demonstrates that visual decline is associated with an increased risk of ASCVD. Early intervention through regular eye exams can help mitigate the risk of ASCVD in middle-aged and older adults. Additionally, mental health is a key mediator in the VA-ASCVD relationship, particularly among women.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationGlobal heart, 2025, v. 20, no. 1, 19-
dcterms.isPartOfGlobal heart-
dcterms.issued2025-
dc.identifier.isiWOS:001438191400001-
dc.identifier.artn19-
dc.description.validate202509 bcrc-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOSen_US
dc.description.fundingSourceSelf-fundeden_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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