Evidence map›Paper›PMID 40349258›Full record

ArticleRheumatology international2025

High prevalence of HLA-B51 and ocular involvement in Behçet's disease: a multicenter cross-sectional study.

Shamma Ahmad Al Nokhatha, Najla Aljaberi, Jawaher Al Zeyoudi, Ahlam Almarzooqi, Farah Soukieh, Mumtaz Khan

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Rheumatology international, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Genomic network analysis links uveitis with systemic inflammatory diseases.medRxiv : the preprint server for health sciences · 2026
    Article
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

6 authors.

Shamma Ahmad Al NokhathaRheumatology Division, Department of Rheumatology, Tawam Hospital, Al Ain, United Arab Emirates. shamma.alnokhatha@gmail.com.ORCID http://orcid.org/0000-0001-8720-867X
Najla AljaberiInternal Medicine Department, College of Medicine and Health Sciences, UAE University, Al Ain, United Arab Emirates.ORCID http://orcid.org/0000-0002-1390-7934
Jawaher Al ZeyoudiDivision of Rheumatology, Department of Rheumatology, Sheikh Shakhbout Medical City, Abu Dhabi, United Arab Emirates.ORCID http://orcid.org/0000-0001-9281-8341
Ahlam AlmarzooqiDepartment of Rheumatology, Al Qassimi Hospital, Emirates Health Services, Sharjah, United Arab Emirates.ORCID http://orcid.org/0000-0001-6169-7284
Farah SoukiehDepartment of Internal Medicine, Al Qassimi Hospital, Emirates Health Services, Sharjah, United Arab Emirates.ORCID http://orcid.org/0009-0000-6256-6489
Mumtaz KhanDivision of Rheumatology, Department of Rheumatology, Sheikh Shakhbout Medical City, Abu Dhabi, United Arab Emirates.ORCID http://orcid.org/0000-0002-3657-0449

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Behçet's disease (BD) is a rare multisystem vasculitis. Globally, BD exhibits a unique geographic distribution, with the highest prevalence along the historic Silk Road. To study the demographics, clinical characteristics, and outcomes of BD in the United Arab Emirates (UAE). A multicenter retrospective chart review study was conducted at hospitals in the UAE from 2008 to 2024. All adult and pediatric patients who were diagnosed with BD by a rheumatologist and treated within the timeframe were included in the study while those who received any alternative final diagnosis were excluded. The results were analyzed using descriptive and inferential statistics. One hundred and twenty-three patients were treated and monitored for BD. Most were female (n = 70, 57%). Their median age was 32 years (24-41), and approximately two-thirds were Emirati (n = 82, 67%). Twelve patients (10%) had a family history of BD, including 7 (6%) with first-degree BD. The time from the initial symptoms to diagnosis was 11.9 months (2.3-31.0). The most common clinical manifestations were oral ulcers (n = 99, 81%), arthralgia (n = 63, 51%), genital ulcers (n = 62, 50%), and ocular involvement (n = 37, 30%). Most of the patients were HLA-B51 positive (n = 92, 84%). At diagnosis, 36 (29%) met the ISG criteria, 73 (59%) met the ICBD criteria, and 50 (41%) met neither criteria. The male patients exhibited more major organ involvement (ocular, neurological, vascular, and cardiac), greater use of corticosteroids and anti-TNFa medications, and greater disease activity than the female patients. Among the patients with isolated ocular manifestations (n = 9) who met neither classification criteria, most were female (56%), with a median age of 37 years (26.5-3.5). None had a family history of autoimmune conditions, and all were HLA-B51 positive. Most of these patients (n = 8, 89%) received corticosteroids, 5 (56%) received azathioprine, and 2 (22%) received anti-TNFa therapies. These findings provide insights into the clinical profile of BD in the UAE. Notably, we found a high proportion of patients with positive HLA-B51 and ocular manifestation. Further research with larger sample sizes is needed to better understand these associations.

Indexed as

Behcet SyndromeHLA-B51 AntigenAdultCross-Sectional StudiesFemaleHumansMalePrevalenceRetrospective StudiesUnited Arab EmiratesYoung AdultHLA-B51 AntigenBehçet’sColchicineHLA-B51United Arab EmiratesUveitisVasculitis

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Registered trials

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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.