Evidence map›Paper›PMID 41538794›Full record

Observational studyJMIR research protocols2026

Central Nervous System Mechanisms and Treatment Response in Chronic Ocular Surface Pain: Protocol for a Cross-Sectional Observational Phenotyping Study.

Lindsey B De Lott, Steven E Harte, Chelsea Kaplan, David A Williams, Roni Shtein, Maria A Woodward, Alexander Tsodikov, Tatiana Deveney, Anat Galor, Anne Shea and 4 more

Abstract readObservational Study
In one paragraph

Observational study in JMIR research protocols, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Lindsey B De LottDepartment of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, MI, United States.ORCID 0000-0003-2403-0207
Steven E HarteChronic Pain and Fatigue Research Center, Department of Anesthesiology, University of Michigan, Ann Arbor, MI, United States.ORCID 0000-0002-2929-8694
Chelsea KaplanChronic Pain and Fatigue Research Center, Department of Anesthesiology, University of Michigan, Ann Arbor, MI, United States.ORCID 0000-0001-9324-655X
David A WilliamsChronic Pain and Fatigue Research Center, Department of Anesthesiology, University of Michigan, Ann Arbor, MI, United States.ORCID 0000-0002-5052-4895
Roni ShteinDepartment of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, MI, United States.ORCID 0000-0001-8202-3270
Maria A WoodwardDepartment of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, MI, United States.ORCID 0000-0001-7060-9004
Alexander TsodikovBiostatistics, School of Public Health, University of Michigan, Ann Arbor, MI, United States.ORCID 0000-0003-4507-2879
Tatiana DeveneyDepartment of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, MI, United States.ORCID 0009-0009-2958-8032
Anat GalorBascom Palmer Eye Institute, University of Miami, Miami, FL, United States.ORCID 0000-0002-3026-6155
Anne SheaDepartment of Neurology, University of Michigan, Ann Arbor, MI, United States.ORCID 0009-0008-8581-042X
Charles SchultzDepartment of Neurology, University of Michigan, Ann Arbor, MI, United States.ORCID 0009-0007-6697-9636
Clare McKolayDepartment of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, MI, United States.ORCID 0009-0003-0243-2392
Kathy A ScottChronic Pain and Fatigue Research Center, Department of Anesthesiology, University of Michigan, Ann Arbor, MI, United States.ORCID 0009-0002-9451-2770
Daniel J ClauwChronic Pain and Fatigue Research Center, Department of Anesthesiology, University of Michigan, Ann Arbor, MI, United States.ORCID 0000-0002-8114-7818

Funding

Tear protein biomarkers of refractive surgery painR33EY032468 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI AICHER, SUE A, GALOR, ANAT · 2023 to 2025
$2.9M
Central nervous system mechanisms and treatment response in chronic ocular surface painR01EY036357 · NEI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Lindsey Blake De Lott · 2024 to 2026
$1.6M
CSRD VA I01 CX002015NEI NIH HHS R01 EY036357NEI NIH HHS R33 EY032468
6 · The paper itself

Abstract

backgroundChronic ocular surface pain (COSP), occurring either in isolation or as part of numerous ocular conditions, such as dry eye syndrome, is a leading cause of eye care visits in the United States. Conventional treatments directed at the ocular surface-the perceived pain source-are often inadequate for pain relief. We hypothesize that some individuals with COSP are experiencing symptoms driven by central nervous system (CNS) dysfunction, similar to chronic overlapping pain conditions, rather than solely pathological problems in the eye. Some individuals with chronic overlapping pain conditions (eg, fibromyalgia) show evidence of nociplastic pain mechanisms, where the pain results from amplified or dysregulated CNS signaling and sensory processing. Although data exist suggesting the presence of nociplastic pain features in COSP, there is a need for comprehensive studies.

objectiveOur aim is to rigorously define the role of nociplastic pain in COSP with a large, representative cohort of 200 participants with COSP using established clinical, neurobiological, and treatment response features. We propose that as sign and symptom discordance increases, features indicative of nociplastic pain will also increase.

methodsIn aim 1, we will clinically phenotype participants with COSP, using validated patient-reported outcome measures and standard ocular exams. In aim 2, we will compare the neurobiological features of nociplastic pain across the discordance spectrum among a subset of aim 1 participants using multimodal evoked sensory testing (pressure, thermal, and visual testing) at sites both local to and remote from the eye. Participants will also complete structural and functional brain magnetic resonance imaging to assess regions important for pain perception and modulation. In aim 3, we will examine and validate predictors of COSP pain responses before and after application of a topical anesthetic to the ocular surface, which should block peripherally induced discomfort to allow for clarification of pain origination.

resultsWe received funding for this project in August 2024. Recruitment and enrollment began in January 2025 after protocol development and piloting were completed. This study is ongoing with 59 participants enrolled and 51 participants completing the study visits as of January 2026.

conclusionsFindings from the study have the potential to fundamentally change the way ocular pain syndromes are conceptualized, diagnosed, and treated. This work will not only help identify new CNS-directed pain treatments for a subset of patients with COSP but also help us better understand why many peripherally directed therapies are destined to be ineffective in a subset of individuals experiencing COSP. INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/84240.

Indexed as

Central Nervous SystemChronic PainDry Eye SyndromesEye PainCross-Sectional StudiesHumansNociplastic PainPain MeasurementPhenotypechronic paindry eyenociplasticobservational studyocular painprotocol

Identifiers

PMID41538794
PMCPMC12856401

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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.