Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0201000
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dc.titleAge-related macular degeneration and progression of coronary artery calcium: The multi-ethnic study of atherosclerosis
dc.contributor.authorFernandez A.B.
dc.contributor.authorBallard K.D.
dc.contributor.authorWong T.Y.
dc.contributor.authorGuo M.
dc.contributor.authorMcClelland R.L.
dc.contributor.authorBurke G.
dc.contributor.authorCotch M.F.
dc.contributor.authorKlein B.
dc.contributor.authorAllison M.
dc.contributor.authorKlein R.
dc.date.accessioned2019-11-01T08:14:03Z
dc.date.available2019-11-01T08:14:03Z
dc.date.issued2018
dc.identifier.citationFernandez A.B., Ballard K.D., Wong T.Y., Guo M., McClelland R.L., Burke G., Cotch M.F., Klein B., Allison M., Klein R. (2018). Age-related macular degeneration and progression of coronary artery calcium: The multi-ethnic study of atherosclerosis. PLoS ONE 13 (7) : e0201000. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0201000
dc.identifier.issn19326203
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/161222
dc.description.abstractBackground Age-related macular degeneration (AMD) shares many similarities with cardiovascular disease (CVD) pathophysiology. We sought to determine the relationship of AMD to the progression of coronary artery calcium (CAC) using data from the Multi-Ethnic Study of Atherosclerosis (MESA). Methods Our cohort consisted of 5803 adults aged 45 to 84 years free of known cardiovascular disease (CVD). Retinal photographs were taken during visit 2 (Aug 2002-Jan 2004). CAC was measured with computed tomography at visit 1 (July 2000-Aug 2002) and visit 5 (April 2010-Dec 2011) and changes between visits were determined. Results Participants were categorized as with (n = 244) and without AMD (n = 5559) at visit 2. At visit 5, 92 participants with and 2684 without AMD had CAC scores. Among those with detectable CAC at baseline (>0 at visit 1), CAC progression was greater in persons with compared to those without AMD after multivariable adjustment (530 ± 537 vs. 339 ± 426 Agatston units, P<0.01). Conclusions The presence of AMD in a diverse population without known clinical CVD independently predicted higher 10-year CAC progression in participants with baseline CAC >0. The retinal exam might be a useful tool for pre-clinical assessment and prevention of CVD events. © This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.
dc.rightsCC0 1.0 Universal
dc.rights.urihttp://creativecommons.org/publicdomain/zero/1.0/
dc.sourceUnpaywall 20191101
dc.subjectadult
dc.subjectage related macular degeneration
dc.subjectaged
dc.subjectArticle
dc.subjectcardiovascular disease
dc.subjectcardiovascular risk
dc.subjectclinical assessment
dc.subjectclinical research
dc.subjectcohort analysis
dc.subjectcomputer assisted tomography
dc.subjectcontrolled study
dc.subjectcoronary artery calcium score
dc.subjectdisease association
dc.subjectdisease classification
dc.subjectdisease course
dc.subjectdisease duration
dc.subjectethnic difference
dc.subjectfemale
dc.subjectfollow up
dc.subjecthuman
dc.subjectmajor clinical study
dc.subjectmale
dc.subjectpopulation distribution
dc.subjectretina image
dc.subjectatherosclerosis
dc.subjectcomplication
dc.subjectcoronary blood vessel
dc.subjectdisease exacerbation
dc.subjectethnology
dc.subjectmacular degeneration
dc.subjectmetabolism
dc.subjectmiddle aged
dc.subjectpathology
dc.subjectvery elderly
dc.subjectcalcium
dc.subjectAdult
dc.subjectAged
dc.subjectAged, 80 and over
dc.subjectAtherosclerosis
dc.subjectCalcium
dc.subjectCoronary Vessels
dc.subjectDisease Progression
dc.subjectFemale
dc.subjectHumans
dc.subjectMacular Degeneration
dc.subjectMale
dc.subjectMiddle Aged
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1371/journal.pone.0201000
dc.description.sourcetitlePLoS ONE
dc.description.volume13
dc.description.issue7
dc.description.pagee0201000
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