Serum circRNA-FUNDC1 and TNF-α were significantly upregulated in Behçet's disease patients compared to healthy controls, with both biomarkers tending to elevate with disease activity, suggesting potential roles as diagnostic biomarkers.
Key Findings
Results
CircRNA-FUNDC1 and TNF-α were significantly upregulated in Behçet's disease patients compared to healthy controls.
One hundred participants were enrolled: 50 BD patients and 50 healthy matched controls
Both circRNA-FUNDC1 and TNF-α showed upregulation with p < 0.0001 in the BD group versus controls
CircRNA-FUNDC1 was measured by quantitative real-time PCR and TNF-α by ELISA
A 5 mL blood sample was drawn from each subject for analysis
Results
Both circRNA-FUNDC1 and TNF-α levels were higher in active BD patients than in inactive BD patients.
Disease activity was assessed using the Behçet Disease Current-Activity Form score (BDCAF)
Both biomarkers tended to elevate with disease activity
Specific p-values for active versus inactive comparison were not separately reported in the abstract
The trend was consistent across both biomarkers
Results
CircRNA-FUNDC1 levels were significantly higher in BD patients without musculoskeletal and CNS manifestations compared to those with these manifestations.
CircRNA-FUNDC1 was higher in patients with negative musculoskeletal manifestations (p = 0.007)
CircRNA-FUNDC1 was higher in patients with negative CNS manifestations (p = 0.037)
This inverse relationship suggests differential expression patterns based on organ involvement
Results
TNF-α levels were significantly elevated in BD patients with oral ulcers and positive skin manifestations.
TNF-α was higher in patients with oral ulcers (p = 0.041)
TNF-α was higher in patients with positive skin manifestations compared to those without (p = 0.025)
These associations suggest TNF-α may be linked to specific mucocutaneous disease features in BD
Results
CircRNA-FUNDC1 levels varied significantly based on the type of medication patients were receiving.
CircRNA-FUNDC1 was higher in patients taking Azathioprine (p = 0.019)
CircRNA-FUNDC1 was higher in patients taking steroids (p = 0.035)
CircRNA-FUNDC1 was lower in patients taking cyclosporin (p = 0.049)
TNF-α tended to be elevated in patients taking Hydroxychloroquine compared to those who did not (p = 0.040)
Discussion
The authors propose that upregulated circRNA-FUNDC1 and TNF-α may improve understanding of the molecular mechanisms underlying Behçet's disease.
The study is among the first to evaluate serum circRNA-FUNDC1 specifically in BD patients
Both biomarkers were characterized as potential diagnostic biomarkers for BD
The authors suggest a potential role for these molecules in the inflammatory autoimmune processes characteristic of BD, which involves relapsing genital ulcers, ocular involvement, and intestinal disorders
What This Means
This research suggests that two biological molecules — a type of genetic material called circular RNA FUNDC1 (circRNA-FUNDC1) and a well-known inflammatory protein called TNF-α — are present at significantly higher levels in the blood of people with Behçet's disease (BD) compared to healthy individuals. BD is a rare inflammatory condition that causes recurring mouth sores, genital ulcers, eye inflammation, and other symptoms. The study measured these molecules in 50 BD patients and 50 healthy matched controls, finding that both were markedly elevated in BD patients and that their levels rose further when the disease was more active.
The study also found that these biomarkers behaved differently depending on which symptoms patients had. For example, TNF-α was higher in patients who had oral ulcers or skin problems, while circRNA-FUNDC1 was paradoxically higher in patients who did NOT have musculoskeletal or nervous system involvement. Additionally, the medications patients were taking appeared to influence biomarker levels — patients on cyclosporin had lower circRNA-FUNDC1, while those on azathioprine or steroids had higher levels.
This research suggests that measuring circRNA-FUNDC1 and TNF-α in blood samples could potentially help doctors diagnose Behçet's disease and track its activity over time. These findings also point toward possible molecular pathways involved in BD, which could eventually help in understanding why the disease behaves the way it does and potentially guide future treatment strategies. However, further larger studies would be needed to confirm these findings and establish clinical utility.
Marzouk R, Kamel M, Shaker O, Gameil M, Amrousy Y, El Kosaier M, et al.. (2026). Upregulation of serum circular RNA FUNDC1 and TNF-α in Behçet's disease: potential diagnostic biomarkers.. Scientific reports. https://doi.org/10.1038/s41598-026-66489-y