Please use this identifier to cite or link to this item: https://doi.org/10.1038/srep41492
Title: Retinopathy Signs Improved Prediction and Reclassification of Cardiovascular Disease Risk in Diabetes: A prospective cohort study
Authors: Ho 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. 
Keywords: biological marker
blood
cardiovascular disease
complication
diabetic retinopathy
female
human
male
microvasculature
middle aged
pathology
prospective study
reproducibility
retina blood vessel
risk factor
Biomarkers
Cardiovascular Diseases
Diabetic Retinopathy
Female
Humans
Male
Microvessels
Middle Aged
Prospective Studies
Reproducibility of Results
Retinal Vessels
Risk Factors
Issue Date: 2017
Publisher: Nature Publishing Group
Citation: Ho 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
Abstract: CVD 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).
Source Title: Scientific Reports
URI: https://scholarbank.nus.edu.sg/handle/10635/174496
ISSN: 2045-2322
DOI: 10.1038/srep41492
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