Skip to content

Characteristics of Ankylosing Spondylitis Associated Uveitis

Characteristics of Ankylosing Spondylitis Associated Uveitis: A Retrospective Study in Egyptian Patients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07113834
Acronym
uveitis
Enrollment
22
Registered
2025-08-11
Start date
2023-09-01
Completion date
2024-08-01
Last updated
2025-08-11

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

Conditions

Uveitis

Keywords

Ankylosing Spondylitis, Uveitis

Brief summary

This study aims to understand the clinical characteristics associated with AAU in Egyptian AS patients, and the prognostic factors, in terms of the Corrected Distance Visual Acuity (CDVA).

Detailed description

This is a one-year retrospective cohort study conducted at the Spine and Ophthalmology Clinics of Benha University - Faculty of Medicine, Egypt, between September 2023 and August 2024. The study aims to characterize the clinical features and identify prognostic factors affecting visual outcomes in patients with Ankylosing Spondylitis-associated Anterior Uveitis (ASAAU). Patients included in this study were Egyptian nationals who initially presented to the Spine Clinic with systemic symptoms of ankylosing spondylitis (AS) and were subsequently referred to the Ophthalmology Clinic due to ophthalmic complaints. Only patients who were confirmed to have both AS (diagnosed according to the Modified New York criteria and radiographic imaging) and anterior uveitis (confirmed by slit-lamp examination and supported by Optical Coherence Tomography \[OCT\] and Fluorescein Angiography \[FA\]) were enrolled. The final sample included 26 eyes from 22 patients who fulfilled the inclusion criteria. Patients were excluded if they were non-Egyptian, had other systemic autoimmune or immunologic conditions, had uveitis due to secondary causes, had undergone ocular surgeries, did not receive uveitis treatment, were lost to follow-up, or had incomplete medical records.

Interventions

DRUGAdalimumab

A tumor necrosis factor-alpha (TNF-α) inhibitor used as a biologic agent for the treatment of ankylosing spondylitis. Administered subcutaneously as part of systemic immunomodulatory therapy.

Oral or intravenous corticosteroids (e.g., prednisolone) used to suppress systemic inflammation in cases of active AS or severe uveitis.

Sponsors

Benha University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Egyptian nationality. Age: ≥ 18 years. Confirmed diagnosis of Ankylosing Spondylitis (AS) according to the Modified New York Criteria, including: Clinical symptoms (e.g., chronic inflammatory back pain, reduced lumbar motion, reduced chest expansion) Radiographic evidence of sacroiliitis. Confirmed diagnosis of Acute Anterior Uveitis (AAU) based on: Ophthalmologic examination (e.g., slit-lamp biomicroscopy) Ancillary testing (e.g., Optical Coherence Tomography \[OCT\] and/or Fluorescein Angiography \[FA\]). Presentation to the Spine Clinic of Benha University - Faculty of Medicine between September 2023 and August 2024 with ophthalmic complaints, subsequently referred to the Ophthalmology Clinic. Complete medical and ophthalmologic records available. Received treatment for both AS and AAU. At least one follow-up visit after initiation of treatment.

Exclusion criteria

* Non-Egyptian patients. History of other systemic autoimmune or immunological diseases (e.g., sarcoidosis, Behçet's disease, systemic lupus erythematosus). Uveitis due to non-autoimmune secondary causes (e.g., infectious uveitis, trauma-related uveitis). History of ocular surgery prior to the episode of AAU

Design outcomes

Primary

MeasureTime frameDescription
Change in Corrected Distance Visual Acuity (CDVA)Baseline and 3-month follow-upCDVA was assessed at baseline (initial presentation) and after treatment (follow-up average of 3 months), using the Logarithm of the Minimum Angle of Resolution (logMAR) scale. Improvement or deterioration in CDVA was evaluated in relation to clinical characteristics, treatment modalities, and complication development.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026