Type 2 diabetes and cardiac autonomic neuropathy screening using dynamic pupillometry

Aim To determine if changes in pupillary response are useful as a screening tool for diabetes and to assess whether pupillometry is associated with cardiac autonomic neuropathy. Methods We conducted a cross‐sectional study with participants drawn from two settings: a hospital and a community site. A...

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Published inDiabetic medicine Vol. 32; no. 11; pp. 1470 - 1478
Main Authors Lerner, A. G., Bernabé-Ortiz, A., Ticse, R., Hernandez, A., Huaylinos, Y., Pinto, M. E., Málaga, G., Checkley, W., Gilman, R. H., Miranda, J. J.
Format Journal Article
LanguageEnglish
Published England Blackwell Publishing Ltd 01.11.2015
Wiley Subscription Services, Inc
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Summary:Aim To determine if changes in pupillary response are useful as a screening tool for diabetes and to assess whether pupillometry is associated with cardiac autonomic neuropathy. Methods We conducted a cross‐sectional study with participants drawn from two settings: a hospital and a community site. At the community site, individuals with newly diagnosed diabetes as well as a random sample of control individuals without diabetes, confirmed by oral glucose tolerance test, were selected. Participants underwent an LED light stimulus test and eight pupillometry variables were measured. Outcomes were diabetes, defined by oral glucose tolerance test, and cardiac autonomic dysfunction, determined by a positive readout on two of four diagnostic tests: heart rate response to the Valsalva manoeuvre; orthostatic hypotension; 30:15 ratio; and expiration‐to‐inspiration ratio. The area under the curve, best threshold, sensitivity and specificity of each pupillometry variable was calculated. Results Data from 384 people, 213 with diabetes, were analysed. The mean (±sd) age of the people with diabetes was 58.6 (±8.2) years and in the control subjects it was 56.1 (±8.6) years. When comparing individuals with and without diabetes, the amplitude of the pupil reaction had the highest area under the curve [0.69 (sensitivity: 78%; specificity: 55%)]. Cardiac autonomic neuropathy was present in 51 of the 138 people evaluated (37.0%; 95% CI 28.8–45.1). To diagnose cardiac autonomic neuropathy, two pupillometry variables had the highest area under the curve: baseline pupil radius [area under the curve: 0.71 (sensitivity: 51%; specificity: 84%)], and amplitude of the pupil reaction [area under the curve: 0.70 (sensitivity: 82%; specificity: 55%)]. Conclusions Pupillometry is an inexpensive technique to screen for diabetes and cardiac autonomic neuropathy, but it does not have sufficient accuracy for clinical use as a screening tool. What's new? Rapid, easy‐to‐implement, point‐of‐care, bloodless and laboratory‐free screening tools would advance the field of diabetes. Pupillometry is such a tool and was performed following an automated technique and using a portable computer to minimize measurement error, including operator‐dependent bias. The usefulness of pupillometry as a screening tool for Type 2 diabetes in clinical and community settings has not been previously explored. The results from this study showed that pupillometry was not good enough to recommend its usage as a screening tool. Our results do not exclude the usefulness of pupillometry for neuropathy diagnosis or for monitoring and patient follow‐up at clinical encounters.
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Table S1. Comparison of pupillometry values according to sociodemographic variables.
National Institute of Dental and Craniofacial Research
National Institute of Mental Health
ArticleID:DME12752
National Institute On Drug Abuse
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CRONICAS Cohort Study Group
Cardiovascular Disease: Antonio Bernabé-Ortiz, Juan P. Casas, George Davey Smith, Shah Ebrahim, Héctor H. García, Robert H. Gilman, Luis Huicho, Germán Málaga, J. Jaime Miranda, Víctor M. Montori, Liam Smeeth; Chronic Obstructive Pulmonary Disease: William Checkley, Gregory B. Diette, Robert H. Gilman, Luis Huicho, Fabiola León-Velarde, María Rivera, Robert A. Wise; Training and Capacity Building: William Checkley, Héctor H. García, Robert H. Gilman, J. Jaime Miranda, Katherine Sacksteder.
These authors contributed equally to the work.
ISSN:0742-3071
1464-5491
DOI:10.1111/dme.12752