Title
Tear biomarkers and corneal sensitivity as an indicator of neuropathy in type 2 diabetes
Date Issued
01 May 2020
Access level
open access
Resource Type
journal article
Author(s)
Iyengar M.F.
Soto L.F.
Huaylinos Y.
Velasquez R.
Publisher(s)
Elsevier Ireland Ltd
Abstract
Aims: Explore potential of 31 tear biomarkers involved in screening for diabetic peripheral neuropathy (DPN). Assess the utility of aesthesiometry for measuring corneal damage in DPN and determine optimal cutoff point for detecting DPN. Methods: Screening test pilot study recruited 90 participants from a tertiary hospital in Lima, Peru. Participants were grouped by diabetes and neuropathy status. Tears collected on Schirmer strips, and proteins measured by both ELISA and multiplex-bead assay. Corneal sensitivity was measured by aesthesiometry, and DPN by vibration perception threshold testing. Results: There were 89 participants included in the analysis. The mean age was 55.7 ± 1.46, and 58.4% were female. MMP-9 and TGF-alpha concentrations were higher in participants with DPN versus diabetes alone, though not significant. Aesthesiometry was decreased in individuals with DPN when compared to participants with diabetes alone (p < 0.01) and normal controls (p < 0.01). Optimal cutoff point for aesthesiometry was found to be 5.8 cm, with 79% sensitivity and 75% specificity. Conclusions: Tears are an insufficient standalone tool for detecting DPN based on the biomarkers analyzed. Aesthesiometry is a simple, inexpensive, and accurate method to assess corneal damage associated with moderate-severe DPN, and its integration into screening practices has potential to improve detection of DPN in poor-resource settings.
Volume
163
Language
English
OCDE Knowledge area
Endocrinología, Metabolismo (incluyendo diabetes, hormonas)
Subjects
Scopus EID
2-s2.0-85083579012
PubMed ID
Source
Diabetes Research and Clinical Practice
ISSN of the container
01688227
Sponsor(s)
This work was supported by the NIH Fogarty International Center Grant # D43TW009340 . The funder had no role in the design or conduct of this research.
The authors acknowledge Dr. Miguel Pinto and Dr. Jorge Reyes Diaz for providing the space to conduct the study, and CRONICAS for providing clinical testing equipment. We acknowledge Dr. Manuela Verastegui Pimentel for providing laboratory space and equipment, and Edith Malaga, Jessy Condori A?azco, Sussana Oad, Grace Trompeter, and Hannah Steinburg for assisting with study procedures. MI, AORA, and RG conceived the study and did the overall directing and planning. MI, YH, and RV designed the computational framework and timeframe of study and recruited participants. MI, LFS, DR, and ABO analyzed the data. MI, LFS, DR, and RV wrote the manuscript with input from ABO and RG. This work was supported by the NIH Fogarty International Center Grant #D43TW009340. The funder had no role in the design or conduct of this research.
Sources of information:
Directorio de Producción Científica
Scopus