Skip to content
EvidenceHelixEvidenceLib · Scientific Encyclopedia
⌘ K

Scientific library

EvidenceLib encyclopediaAll articles A–Z2,835Open textbooks209Open-access articles1,406Cancer study catalog458How it is made

My workspace this browser

Saved pages0Notes & annotations0

Recently viewed

Explore by field

Cancer and Oncology182Genetics and Genomics170Neuroscience185Cardiovascular Medicine180Immunology142Pharmacology173Molecular Biology161Infectious Diseases150Rare and Inherited Diseases181Clinical Research173Anatomy and Physiology613Drugs and Chemicals621Psychiatry and Psychology185Public Health and Nutrition178Diagnostics and Medical Technology125Respiratory Medicine113Digestive System and Liver91Metabolism and Endocrine Disease177Bones, Joints, Muscles and Skin213Kidney, Urology and Women's Health173Eye, Ear, Nose and Throat55
Plans & pricingCompare EvidenceHelix workspace plans
Library›EvidenceLib›Eye, Ear, Nose and Throat›Uveitis

Continue where you left off ()

Explore more with EvidenceHelix Workspace

Compare studies, analyze evidence and create research reports with premium tools.

Explore Researcher plans

Research reading room

Uveitis

Eye, Ear, Nose and Throat · NLM MeSH · updated 2026-11-04 · version 1

Citations verified against PubMedNot yet clinician-reviewed9 referencesApproximately 4 min read

Inflammation of part or all of the uvea, the middle (vascular) tunic of the eye, and commonly involving the other tunics (sclera and cornea, and the retina).

Table of Contents

1. Definition2. Research landscape3. Reading the evidence4. Open-access studies5. Key reviews6. References7. About this article

Definition and research guide

This page combines a MeSH definition, publication statistics and selected research abstracts. It is a starting point for reading the literature, not a medical textbook or a systematic evidence review.

Content available: 3 complete abstracts (660 words), 9 references. Full article text is not stored or reproduced here; follow the PMID, DOI or PMC links to read the original sources and their access terms.

Definition

Inflammation of part or all of the uvea, the middle (vascular) tunic of the eye, and commonly involving the other tunics (sclera and cornea, and the retina). (Dorland, 27th ed)

Definition: NLM Medical Subject Headings (MeSH) scope note (Public domain (U.S. National Library of Medicine); attribution requested). View the MeSH record.

Also known as: Uveitides.

Where it fits in the MeSH classification

Broader topics
Uveal Diseases
Narrower topics
Panuveitis; Uveitis, Intermediate; Uveitis, Suppurative; Uveomeningoencephalitic Syndrome

Research landscape

PubMed indexes 37,433 records tagged with the MeSH heading “Uveitis” (counts retrieved 2026-11-04). 6,610 of them (17.7%) were published from 2020 onward, and the busiest period so far is through 1999 with 15,046 records.

Reviews account for 4,367 records (11.7%) and meta-analyses for 203. Randomized controlled trials number 455 (1.2%) as a share of all records on the topic. Randomized trials make up only a small share of this literature, so much of what is known comes from laboratory, observational or descriptive work.

PubMed records by publication periodthrough 1999: 15,046 records; 2000-2009: 6,931 records; 2010-2019: 8,846 records; 2020 onward: 6,610 records15,046through 19996,9312000-20098,8462010-20196,6102020 onward
Records in PubMed indexed with this heading, by publication period. Real counts from NCBI E-utilities; the final period covers only part of the current year. Volume reflects how much has been published, not how strong the evidence is.
Show the data
PeriodRecords
through 199915,046
2000-20096,931
2010-20198,846
2020 onward6,610
Share of records by publication typeReviews: 11.7 percent; Meta-analyses: 0.5 percent; Randomized controlled trials: 1.2 percentReviews11.7% (4,367)Meta-analyses0.5% (203)Randomized controlled trials1.2% (455)
Share of all PubMed records on this heading that carry each publication type. Types overlap with other records, so the shares do not sum to 100%.
Publication-type chart data
Publication types among 37,433 PubMed records
TypeRecordsShare
Reviews4,36711.7%
Meta-analyses2030.5%
Randomized controlled trials4551.2%

Method: PubMed query "Uveitis"[MeSH Terms] with publication-type and date filters, retrieved 2026-11-04.

Reading the evidence in eye, ear, nose and throat

Eye, hearing, nose and throat studies rely on specialist tests (visual acuity, eye pressure, audiograms, scopes) and on patient-reported symptoms, which vary between people and with age. Some conditions improve without treatment, so comparison groups matter. Nothing on this page is advice about diagnosis or treatment; sudden loss of sight or hearing needs urgent care from a qualified clinician. Check how the outcome was tested, the age of the people studied and how long they were followed.

Evidence from open-access studies

These open-access studies come from PubMed’s best-match results for this heading (papers whose main topic it is), ranked here by citation count, with one recent addition. Each abstract is reproduced in full under its recorded open licence so that you can read the authors’ own words. They illustrate the literature; they are not a systematic summary of it. Citation counts measure attention, not reliability or clinical benefit.

Study comparison — selected abstracts, not a systematic review
Study / authorsYearSource label / designEurope PMC citationsLicence / source
Sestrin2 Exerts a Novel Protective Effect Against LPS-Induced Ferroptosis via the Nrf2-SLC7A11-GPX4 Signaling Axis
Zhang X, Yin J, Yang Y, Peng J, Xu Y, Zhang W, et al.
2025Research article
Design not recorded in structured metadata
5cc by
PMID 41294929 · DOI · PMC12651112
Effectiveness and Safety of Baricitinib for Juvenile Idiopathic Arthritis-Associated Uveitis or Chronic Anterior Antinuclear Antibody-Positive Uveitis
Ramanan AV, Guly CM, Simonini G, Keller SY, Sen P, Holzkaemper T, et al.
2026Randomized controlled trial
Design not recorded in structured metadata
5cc by
PMID 40947519 · DOI · PMC13034097
Long-term outcomes of JIA-associated uveitis: a systematic review and meta-analysis
Scagnellato L, Cozzi G, Lorenzin M, Poncina G, Rizzetto S, Ramonda R
2025Meta-analysis
Design not recorded in structured metadata
5cc by
PMID 41314670 · DOI · PMC12666193

Sestrin2 Exerts a Novel Protective Effect Against LPS-Induced Ferroptosis via the Nrf2-SLC7A11-GPX4 Signaling Axis [1]

Research article Zhang X, Yin J, Yang Y, Peng J, Xu Y, Zhang W, et al. · · 2025 · cited 5 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Uveitis is a leading cause of visual impairment linked to systemic inflammatory diseases.
Closing excerpt
SESN2 plays a crucial role in protecting against inflammation and ferroptosis via the Nrf2 pathway, presenting a promising therapeutic target for uveitis management.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (229 words)

Uveitis is a leading cause of visual impairment linked to systemic inflammatory diseases. Current corticosteroid treatments are limited by significant long-term side effects. Sestrin 2 (SESN2), a stress-responsive antioxidant protein, is implicated in the regulation of ferroptosis and inflammation. This study investigates SESN2's role in modulating inflammation and ferroptosis in endotoxin-induced uveitis (EIU) models, aiming to develop safer therapeutic alternatives for uveitis management. C57BL/6 mice were subjected to EIU via intravitreal injection of lipopolysaccharide (LPS) with or without SESN2-overexpressing adeno-associated virus (AAV). Clinical evaluations, cytokine profiling, and ferroptosis marker assessments were conducted. Additionally, BV2 microglial cells were genetically modified to overexpress or silence SESN2, followed by analyses of inflammatory cytokine production, oxidative stress, ferroptosis-related pathways, mitochondrial function, and involvement of the Nrf2 signaling pathway. SESN2 expression was significantly reduced in vivo and in vitro following LPS treatment. AAV-mediated SESN2 overexpression suppressed inflammatory responses. Mechanistically, SESN2 inhibited ferroptosis by upregulating ferroptosis-resistant proteins (SLC7A11, GPX4) and reducing lipid peroxidation markers (4-HNE). In vitro, SESN2 overexpression reduced oxidative stress and ferroptosis, while SESN2 knockdown exacerbated these effects. SESN2's protective role was mediated by Nrf2 activation, enhancing antioxidant defenses and ferroptosis inhibition. Inhibition of Nrf2 reversed SESN2's protective effects, underscoring the importance of the p62/Nrf2/GPX4 axis in SESN2-mediated ferroptosis protection. SESN2 plays a crucial role in protecting against inflammation and ferroptosis via the Nrf2 pathway, presenting a promising therapeutic target for uveitis management.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 41294929 · DOI · PMC12651112

Effectiveness and Safety of Baricitinib for Juvenile Idiopathic Arthritis-Associated Uveitis or Chronic Anterior Antinuclear Antibody-Positive Uveitis [2]

Randomized controlled trial Ramanan AV, Guly CM, Simonini G, Keller SY, Sen P, Holzkaemper T, et al. · · 2026 · cited 5 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
ObjectiveTo evaluate the efficacy and safety of baricitinib in pediatric patients with active juvenile idiopathic arthritis-associated uveitis (JIA-U) or chronic anterior antinuclear antibody-positive uveitis, who had an inadequate response to methotrexate (MTX) or biologic disease-modifying antirheumatic drugs (bDMARDs).
Closing excerpt
Baricitinib safety profile in this study was consistent with previous studies in children and adults with other diseases.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (260 words)

ObjectiveTo evaluate the efficacy and safety of baricitinib in pediatric patients with active juvenile idiopathic arthritis-associated uveitis (JIA-U) or chronic anterior antinuclear antibody-positive uveitis, who had an inadequate response to methotrexate (MTX) or biologic disease-modifying antirheumatic drugs (bDMARDs).MethodsJUVE-BRIGHT was an open-label, active-controlled phase-3 multicenter trial that used a novel design, including 1:1 randomization to an active reference arm. The primary efficacy endpoint was the proportion of responders at week 24 (W24), defined according to the Standardization of Uveitis Nomenclature (SUN) criteria as a two-step decrease in the level of inflammation (anterior chamber cells) or decrease to zero through W24 in the most severely affected eye at baseline. Study success was based on a prespecified Bayesian success rule: the study was deemed successful if there was >80% posterior probability that the baricitinib SUN criteria response rate at W24 was at least 57%.ResultsThis study enrolled 30 pediatric patients. The study primary endpoint was not met. In the baricitinib group, 36.8% of MTX-inadequate responder (MTX-IR) and bDMARD-IR patients and 20% of MTX-IR patients achieved a two-step decrease in SUN criteria at W24. Eight patients (33.3%) achieved a response at W24, resulting in 1.03% posterior probability of a response rate of >57%. Safety data were consistent with the established safety profile in other baricitinib indications in pediatric and adult patients.ConclusionAlthough the primary endpoint was not met, the data provide important information on baricitinib for the treatment of children with JIA-U refractory to both MTX and bDMARDs. Baricitinib safety profile in this study was consistent with previous studies in children and adults with other diseases.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 40947519 · DOI · PMC13034097

Long-term outcomes of JIA-associated uveitis: a systematic review and meta-analysis [3]

Meta-analysis Scagnellato L, Cozzi G, Lorenzin M, Poncina G, Rizzetto S, Ramonda R · · 2025 · cited 5 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Background and aimJuvenile idiopathic arthritis-associated uveitis (JIAU) is a potentially blinding condition beginning in childhood.
Closing excerpt
ConclusionLong-term prevalence and cumulative incidence of JIAU complications may persist in adulthood, with >10% developing severe visual impairment despite biologic therapy.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (171 words)

Background and aimJuvenile idiopathic arthritis-associated uveitis (JIAU) is a potentially blinding condition beginning in childhood. Flare-ups may occur throughout life, leading to cumulative ocular damage. This systematic review aimed to summarise the latest evidence on long-term ocular damage in adults with JIAU, focusing on studies published in the past 20 years.MethodsThe review protocol was registered in PROSPERO (ID 1033522). We included human studies on JIAU with at least 5 years of follow-up and/or young people ≥18 years old, published after 2000. Study quality was assessed using the Newcastle-Ottawa Scale. We extracted the cumulative incidence of complications and performed a meta-analysis to obtain pooled estimates (PE), assess heterogeneity, sensitivity, robustness and reporting bias using R packages.Results22 retrospective or cohort studies were eligible, encompassing 2208 long-term JIAU cases. Study quality was rated as good in 10, fair in 7 and poor in 5. Despite high heterogeneity (p50% biologic exposure, PE were numerically lower.ConclusionLong-term prevalence and cumulative incidence of JIAU complications may persist in adulthood, with >10% developing severe visual impairment despite biologic therapy.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 41314670 · DOI · PMC12666193

Key reviews and meta-analyses

The most cited review-type papers among PubMed’s best-match results for this heading, listed with bibliographic details only. Follow the links for the full text and access terms.

  • Research article HLA-B51/B5 and the risk of Behçet's disease: a systematic review and meta-analysis of case-control genetic association studies [4]
    de Menthon M, Lavalley MP, Maldini C, Guillevin L, Mahr A · Arthritis Rheum · 2009 · cited 323 times (Europe PMC)
  • Research article Prevalence of extra-articular manifestations in patients with ankylosing spondylitis: a systematic review and meta-analysis [5]
    Stolwijk C, van Tubergen A, Castillo-Ortiz JD, Boonen A · Ann Rheum Dis · 2015 · cited 305 times (Europe PMC)
  • Research article Outcomes of cataract surgery in patients with uveitis: a systematic review and meta-analysis [6]
    Mehta S, Linton MM, Kempen JH · Am J Ophthalmol · 2014 · cited 102 times (Europe PMC)
  • Research article Current evidence of methotrexate efficacy in childhood chronic uveitis: a systematic review and meta-analysis approach [7]
    Simonini G, Paudyal P, Jones GT, Cimaz R, Macfarlane GJ · Rheumatology (Oxford) · 2013 · cited 94 times (Europe PMC)
  • Research article Behçet's Syndrome [8]
    Saadoun D, Bodaghi B, Cacoub P · N Engl J Med · 2024 · cited 81 times (Europe PMC)
  • Research article Current evidence of anti-tumor necrosis factor α treatment efficacy in childhood chronic uveitis: a systematic review and meta-analysis approach of individual drugs [9]
    Simonini G, Druce K, Cimaz R, Macfarlane GJ, Jones GT · Arthritis Care Res (Hoboken) · 2014 · cited 78 times (Europe PMC)

References

  1. Zhang X, Yin J, Yang Y, Peng J, Xu Y, Zhang W, et al.. Sestrin2 Exerts a Novel Protective Effect Against LPS-Induced Ferroptosis via the Nrf2-SLC7A11-GPX4 Signaling Axis. . 2025. PMID 41294929 · DOI · PMC12651112
  2. Ramanan AV, Guly CM, Simonini G, Keller SY, Sen P, Holzkaemper T, et al.. Effectiveness and Safety of Baricitinib for Juvenile Idiopathic Arthritis-Associated Uveitis or Chronic Anterior Antinuclear Antibody-Positive Uveitis. . 2026. PMID 40947519 · DOI · PMC13034097
  3. Scagnellato L, Cozzi G, Lorenzin M, Poncina G, Rizzetto S, Ramonda R. Long-term outcomes of JIA-associated uveitis: a systematic review and meta-analysis. . 2025. PMID 41314670 · DOI · PMC12666193
  4. de Menthon M, Lavalley MP, Maldini C, Guillevin L, Mahr A. HLA-B51/B5 and the risk of Behçet's disease: a systematic review and meta-analysis of case-control genetic association studies. Arthritis Rheum. 2009. PMID 19790126 · DOI · PMC3867978
  5. Stolwijk C, van Tubergen A, Castillo-Ortiz JD, Boonen A. Prevalence of extra-articular manifestations in patients with ankylosing spondylitis: a systematic review and meta-analysis. Ann Rheum Dis. 2015. PMID 23999006 · DOI
  6. Mehta S, Linton MM, Kempen JH. Outcomes of cataract surgery in patients with uveitis: a systematic review and meta-analysis. Am J Ophthalmol. 2014. PMID 24983790 · DOI
  7. Simonini G, Paudyal P, Jones GT, Cimaz R, Macfarlane GJ. Current evidence of methotrexate efficacy in childhood chronic uveitis: a systematic review and meta-analysis approach. Rheumatology (Oxford). 2013. PMID 22879466 · DOI
  8. Saadoun D, Bodaghi B, Cacoub P. Behçet's Syndrome. N Engl J Med. 2024. PMID 38354143 · DOI
  9. Simonini G, Druce K, Cimaz R, Macfarlane GJ, Jones GT. Current evidence of anti-tumor necrosis factor α treatment efficacy in childhood chronic uveitis: a systematic review and meta-analysis approach of individual drugs. Arthritis Care Res (Hoboken). 2014. PMID 24740981 · DOI

About this article

Sources
NLM Medical Subject Headings (definition, synonyms); NCBI PubMed (counts, identifiers); Europe PMC (open-access abstracts and citation counts).
Verification
Every reference was resolved against PubMed on 2026-11-04; title, year and DOI matched.
Review state
automated source verified; no human expert review has been recorded yet.
Version
1, last updated 2026-11-04.

See how EvidenceLib is built. Spotted an error? Email support@evidencehelix.com.

Evidence strength

EvidenceHelix's computed view of the study designs behind this topic: how common meta-analyses, randomized trials and reviews are, how recent the literature is, and a plain-language reading. It describes the design mix of the literature. It is not a quality appraisal of any study, and it is not medical advice.

Included with the Researcher plan

Reading every article stays free. This computed view is part of the paid plans.

See plans Sign in

Your notes

Notes and highlights stay in this browser only; they are not sent to EvidenceHelix.

Related research topics

  • ChorioretinitisEye, Ear, Nose and Throat
  • IridocyclitisEye, Ear, Nose and Throat
  • IritisEye, Ear, Nose and Throat
  • PanuveitisEye, Ear, Nose and Throat
  • SacroiliitisBones, Joints, Muscles and Skin
  • AniseikoniaEye, Ear, Nose and Throat

All 51 articles in Eye, Ear, Nose and Throat →

At a glance

37,433
PubMed records on this heading
18%
published since 2020
4,367
review articles
455
randomized trials
9
verified references below

Counts come from PubMed on 2026-11-04; they show how much has been written, not how strong the evidence is.

Related topics See all →

  • ChorioretinitisEye, Ear, Nose and Throat
  • IridocyclitisEye, Ear, Nose and Throat
  • IritisEye, Ear, Nose and Throat
  • PanuveitisEye, Ear, Nose and Throat
  • SacroiliitisBones, Joints, Muscles and Skin

My notes & annotations (0)

Nothing yet. Select text and press Highlight, or write a note in the Notes tab. Stored in this browser only.

Sources

  • NLM MeSH record ↗
  • PubMed search used ↗

EvidenceLib is a research-education resource, not medical advice. It does not diagnose, prescribe or recommend starting, stopping or changing any treatment. Talk to a qualified clinician about your own situation. Methods, sources and licences · Rights and removal requests · Legal · Support