Evidence map›Paper›PMID 32283127›Full record

ArticleDiabetes research and clinical practice2020

Tear biomarkers and corneal sensitivity as an indicator of neuropathy in type 2 diabetes.

Meera F Iyengar, Luis F Soto, David Requena, Andrea O Ruiz-Alejos, Yvonne Huaylinos, Ricardo Velasquez, Antonio Bernabe-Ortiz, Robert H Gilman

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In one paragraph

Article in Diabetes research and clinical practice, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.0field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 18 citations in OpenAlex.

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  11. Diabetic Corneal Neuropathy.Journal of clinical medicine · 2020
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 2 countries.

Meera F IyengarCRONICAS Centre of Excellence in Chronic Diseases, Universidad Peruana Cayetano Heredia, Lima, Peru; University of Texas Southwestern Medical Center, Dallas, TX, USA. Electronic address: iyengar.m27@gmail.com.
Luis F SotoLaboratorio de Bioinformática y Biología Molecular, Facultad de Ciencias y Filosofía, Universidad Peruana Cayetano Heredia, Lima 15102, Peru.
David RequenaDepartment of International Health, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA; Laboratory of Cellular Biophysics, The Rockefeller University, New York, New York, USA.
Andrea O Ruiz-AlejosCRONICAS Centre of Excellence in Chronic Diseases, Universidad Peruana Cayetano Heredia, Lima, Peru; Vanderbilt University, Nashville, TN, USA.
Yvonne HuaylinosDivision of Endocrinology, Department of Medicine, Hospital Nacional Cayetano Heredia, Lima, Peru.
Ricardo VelasquezDivision of Ophthalmology, Department of Surgery, Hospital Nacional Cayetano Heredia, Lima, Peru.
Antonio Bernabe-OrtizCRONICAS Centre of Excellence in Chronic Diseases, Universidad Peruana Cayetano Heredia, Lima, Peru.
Robert H GilmanCRONICAS Centre of Excellence in Chronic Diseases, Universidad Peruana Cayetano Heredia, Lima, Peru; Department of International Health, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA; Área de Investigación y Desarrollo, A.B. PRISMA, Lima, Peru.
Universidad Peruana Cayetano Heredia · PEHospital Nacional Cayetano Heredia · PERockefeller University · USThe University of Texas Southwestern Medical Center · US

Funding

UJMT – ORWH – Gazzetta, Issa-BoubeD43TW009340 · FIC · UNIV OF NORTH CAROLINA CHAPEL HILL · PI William Checkley, Benjamin H. Chi · 2017 to 2026
$14.8M
FIC NIH HHS D43 TW009340
6 · The paper itself

Abstract

aimsExplore 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.

methodsScreening 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.

resultsThere 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.

conclusionsTears 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.

Indexed as

BiomarkersCorneaDiabetes Mellitus, Type 2Diabetic NeuropathiesFemaleHumansMaleMiddle AgedPilot ProjectsTearsBiomarkersAesthesiometryCorneal neuropathyDiabetesDiabetic neuropathyTear biomarkersType 2 diabetes

Identifiers

PMID32283127
PMCPMC8944933
OpenAlexW3015267098

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.