Please use this identifier to cite or link to this item: https://doi.org/10.1038/srep41492
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dc.titleRetinopathy Signs Improved Prediction and Reclassification of Cardiovascular Disease Risk in Diabetes: A prospective cohort study
dc.contributor.authorHo H.
dc.contributor.authorCheung C.Y.
dc.contributor.authorSabanayagam C.
dc.contributor.authorYip W.
dc.contributor.authorIkram M.K.
dc.contributor.authorOng P.G.
dc.contributor.authorMitchell P.
dc.contributor.authorChow K.Y.
dc.contributor.authorCheng C.Y.
dc.contributor.authorShyong Ta E.
dc.contributor.authorWong T.Y.
dc.date.accessioned2020-09-06T16:06:07Z
dc.date.available2020-09-06T16:06:07Z
dc.date.issued2017
dc.identifier.citationHo H., Cheung C.Y., Sabanayagam C., Yip W., Ikram M.K., Ong P.G., Mitchell P., Chow K.Y., Cheng C.Y., Shyong Ta E., Wong T.Y. (2017). Retinopathy Signs Improved Prediction and Reclassification of Cardiovascular Disease Risk in Diabetes: A prospective cohort study. Scientific Reports 7 : 41492. ScholarBank@NUS Repository. https://doi.org/10.1038/srep41492
dc.identifier.issn2045-2322
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/174496
dc.description.abstractCVD risk prediction in diabetics is imperfect, as risk models are derived mainly from the general population. We investigate whether the addition of retinopathy and retinal vascular caliber improve CVD prediction beyond established risk factors in persons with diabetes. We recruited participants from the Singapore Malay Eye Study (SiMES, 2004-2006) and Singapore Prospective Study Program (SP2, 2004-2007), diagnosed with diabetes but no known history of CVD at baseline. Retinopathy and retinal vascular (arteriolar and venular) caliber measurements were added to risk prediction models derived from Cox regression model that included established CVD risk factors and serum biomarkers in SiMES, and validated this internally and externally in SP2. We found that the addition of retinal parameters improved discrimination compared to the addition of biochemical markers of estimated glomerular filtration rate (EGFR) and high-sensitivity C-reactive protein (hsCRP). This was even better when the retinal parameters and biomarkers were used in combination (C statistic 0.721 to 0.774, p = 0.013), showing improved discrimination, and overall reclassification (NRI = 17.0%, p = 0.004). External validation was consistent (C-statistics from 0.763 to 0.813, p = 0.045; NRI = 19.11%, p = 0.036). Our findings show that in persons with diabetes, retinopathy and retinal microvascular parameters add significant incremental value in reclassifying CVD risk, beyond established risk factors. © 2017 The Author(s).
dc.publisherNature Publishing Group
dc.sourceUnpaywall 20200831
dc.subjectbiological marker
dc.subjectblood
dc.subjectcardiovascular disease
dc.subjectcomplication
dc.subjectdiabetic retinopathy
dc.subjectfemale
dc.subjecthuman
dc.subjectmale
dc.subjectmicrovasculature
dc.subjectmiddle aged
dc.subjectpathology
dc.subjectprospective study
dc.subjectreproducibility
dc.subjectretina blood vessel
dc.subjectrisk factor
dc.subjectBiomarkers
dc.subjectCardiovascular Diseases
dc.subjectDiabetic Retinopathy
dc.subjectFemale
dc.subjectHumans
dc.subjectMale
dc.subjectMicrovessels
dc.subjectMiddle Aged
dc.subjectProspective Studies
dc.subjectReproducibility of Results
dc.subjectRetinal Vessels
dc.subjectRisk Factors
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1038/srep41492
dc.description.sourcetitleScientific Reports
dc.description.volume7
dc.description.page41492
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