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A Diabetic Retinopathy Screening Tool for Low-Income Adults in Mexico

INTRODUCTION: A national diabetic retinopathy screening program does not exist in Mexico as of 2017. Our objective was to develop a screening tool based on a predictive model for early detection of diabetic retinopathy in a low-income population. METHODS: We analyzed biochemical, clinical, anthropom...

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Autores principales: Mendoza-Herrera, Kenny, Quezada, Amado D., Pedroza-Tobías, Andrea, Hernández-Alcaraz, Cesar, Fromow-Guerra, Jans, Barquera, Simón
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Centers for Disease Control and Prevention 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645201/
https://www.ncbi.nlm.nih.gov/pubmed/29023230
http://dx.doi.org/10.5888/pcd14.170157
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author Mendoza-Herrera, Kenny
Quezada, Amado D.
Pedroza-Tobías, Andrea
Hernández-Alcaraz, Cesar
Fromow-Guerra, Jans
Barquera, Simón
author_facet Mendoza-Herrera, Kenny
Quezada, Amado D.
Pedroza-Tobías, Andrea
Hernández-Alcaraz, Cesar
Fromow-Guerra, Jans
Barquera, Simón
author_sort Mendoza-Herrera, Kenny
collection PubMed
description INTRODUCTION: A national diabetic retinopathy screening program does not exist in Mexico as of 2017. Our objective was to develop a screening tool based on a predictive model for early detection of diabetic retinopathy in a low-income population. METHODS: We analyzed biochemical, clinical, anthropometric, and sociodemographic information from 1,000 adults with diabetes in low-income communities in Mexico (from 11,468 adults recruited in 2014–2016). A comprehensive ophthalmologic evaluation was performed. We developed the screening tool through the following stages: 1) development of a theoretical predictive model, 2) performance assessment and validation of the model using cross-validation and the area under the receiver operating characteristic curve (AUC ROC), and 3) optimization of cut points for the classification of diabetic retinopathy. We identified points along the AUC ROC that minimized the misclassification cost function and considered various scenarios of misclassification costs and diabetic retinopathy prevalence. RESULTS: Time since diabetes diagnosis, high blood glucose levels, systolic hypertension, and physical inactivity were considered risk factors in our screening tool. The mean AUC ROC of our model was 0.780 (validation data set). The optimized cut point that best represented our study population (z = −0.640) had a sensitivity of 82.9% and a specificity of 61.9%. CONCLUSION: We developed a low-cost and easy-to-apply screening tool to detect people at high risk of diabetic retinopathy in Mexico. Although classification performance of our tool was acceptable (AUC ROC > 0.75), error rates (precision) depend on false-negative and false-positive rates. Therefore, confirmatory assessment of all cases is mandatory.
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spelling pubmed-56452012017-10-31 A Diabetic Retinopathy Screening Tool for Low-Income Adults in Mexico Mendoza-Herrera, Kenny Quezada, Amado D. Pedroza-Tobías, Andrea Hernández-Alcaraz, Cesar Fromow-Guerra, Jans Barquera, Simón Prev Chronic Dis Original Research INTRODUCTION: A national diabetic retinopathy screening program does not exist in Mexico as of 2017. Our objective was to develop a screening tool based on a predictive model for early detection of diabetic retinopathy in a low-income population. METHODS: We analyzed biochemical, clinical, anthropometric, and sociodemographic information from 1,000 adults with diabetes in low-income communities in Mexico (from 11,468 adults recruited in 2014–2016). A comprehensive ophthalmologic evaluation was performed. We developed the screening tool through the following stages: 1) development of a theoretical predictive model, 2) performance assessment and validation of the model using cross-validation and the area under the receiver operating characteristic curve (AUC ROC), and 3) optimization of cut points for the classification of diabetic retinopathy. We identified points along the AUC ROC that minimized the misclassification cost function and considered various scenarios of misclassification costs and diabetic retinopathy prevalence. RESULTS: Time since diabetes diagnosis, high blood glucose levels, systolic hypertension, and physical inactivity were considered risk factors in our screening tool. The mean AUC ROC of our model was 0.780 (validation data set). The optimized cut point that best represented our study population (z = −0.640) had a sensitivity of 82.9% and a specificity of 61.9%. CONCLUSION: We developed a low-cost and easy-to-apply screening tool to detect people at high risk of diabetic retinopathy in Mexico. Although classification performance of our tool was acceptable (AUC ROC > 0.75), error rates (precision) depend on false-negative and false-positive rates. Therefore, confirmatory assessment of all cases is mandatory. Centers for Disease Control and Prevention 2017-10-12 /pmc/articles/PMC5645201/ /pubmed/29023230 http://dx.doi.org/10.5888/pcd14.170157 Text en https://creativecommons.org/licenses/by/4.0/This is a publication of the U.S. Government. This publication is in the public domain and is therefore without copyright. All text from this work may be reprinted freely. Use of these materials should be properly cited.
spellingShingle Original Research
Mendoza-Herrera, Kenny
Quezada, Amado D.
Pedroza-Tobías, Andrea
Hernández-Alcaraz, Cesar
Fromow-Guerra, Jans
Barquera, Simón
A Diabetic Retinopathy Screening Tool for Low-Income Adults in Mexico
title A Diabetic Retinopathy Screening Tool for Low-Income Adults in Mexico
title_full A Diabetic Retinopathy Screening Tool for Low-Income Adults in Mexico
title_fullStr A Diabetic Retinopathy Screening Tool for Low-Income Adults in Mexico
title_full_unstemmed A Diabetic Retinopathy Screening Tool for Low-Income Adults in Mexico
title_short A Diabetic Retinopathy Screening Tool for Low-Income Adults in Mexico
title_sort diabetic retinopathy screening tool for low-income adults in mexico
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645201/
https://www.ncbi.nlm.nih.gov/pubmed/29023230
http://dx.doi.org/10.5888/pcd14.170157
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