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Ocular Surface Changes and Meibomian Gland Dysfunction in Rheumatologic Patients

Ocular Surface Changes and Meibomian Gland Dysfunction in Rheumatologic Patients: A Cross-Sectional Analytical Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07810569
Enrollment
150
Registered
2026-09-09
Start date
2026-10-01
Completion date
2027-11-01
Last updated
2026-09-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ankylosing Spondylitis, Dry Eye Syndromes, Meibomian Gland Dysfunction, Psoriatic Arthritis, Rheumatoid Arthritis, Sjogren's Syndrome, Systemic Lupus Erythematosus

Keywords

Ocular Surface Disease, Meibography, Meiboscore, Non-Invasive Tear Break-Up Time, Tear Meniscus Height, Ocular Surface Disease Index, Autoimmune Rheumatic Diseases, Corneal Fluorescein Staining

Brief summary

This observational study aims to assess the frequency and severity of Meibomian Gland Dysfunction (MGD) and associated ocular surface changes in patients with systemic autoimmune rheumatic diseases compared with healthy volunteers. Meibomian glands are specialized glands in the eyelids that produce the lipid layer of tears, preventing tear evaporation. Systemic inflammation in rheumatologic conditions may affect these glands, leading to dry eye symptoms and ocular surface damage. A total of 150 participants (120 rheumatologic patients and 30 healthy controls) will be evaluated in a single cross-sectional examination. Rheumatologic diagnoses include Rheumatoid Arthritis, Systemic Lupus Erythematosus, Sjogren's Syndrome, Ankylosing Spondylitis, and Psoriatic Arthritis. Participants will undergo a standardized series of non-invasive and minimally invasive eye examinations, including: * An ocular symptom questionnaire (Ocular Surface Disease Index) * Non-contact infrared meibography to assess meibomian gland loss (Meiboscore) * Non-invasive tear break-up time (NIBUT) and tear meniscus height measurements * Slit-lamp biomicroscopy and corneal fluorescein staining The study also examines how meibomian gland alterations correlate with systemic disease activity scores and inflammatory blood markers.

Interventions

None listed

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Age 18 years or older * Ability to provide written informed consent * For rheumatologic patients: Confirmed clinical diagnosis of one of the following autoimmune diseases: * Rheumatoid Arthritis (2010 ACR/EULAR classification criteria) * Systemic Lupus Erythematosus (2019 EULAR/ACR classification criteria) * Sjogren's Syndrome (2016 ACR/EULAR classification criteria) * Ankylosing Spondylitis (modified New York criteria) * Psoriatic Arthritis (CASPAR criteria) * For healthy controls: Age- and sex-matched individuals with no systemic autoimmune disease and no current ocular surface complaints

Exclusion criteria

* Chronic use of topical antiglaucoma eye drops * Ocular surgery within the past 6 months * Active ocular infection or active uveitis * Contact lens wearers who have not discontinued wear for at least 2 weeks * History of ocular chemical burns * Pregnancy or lactation * Incomplete rheumatologic records or missing essential laboratory data

Design outcomes

Primary

MeasureTime frameDescription
Meibomian Gland Loss Assessed by MeiboscoreBaselineMeibomian gland drop-out is evaluated using non-contact infrared meibography and graded according to the Meiboscore scale for each eyelid (upper and lower): Grade 0 (no loss of meibomian glands), Grade 1 (gland loss involving less than one-third of the total area), Grade 2 (gland loss involving between one-third and two-thirds of the total area), and Grade 3 (gland loss involving more than two-thirds of the total area). Scores for the upper and lower eyelids are summed to yield a total Meiboscore per eye ranging from 0 to 6, where higher scores indicate greater meibomian gland loss and atrophy.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 10, 2026