Purpose: To evaluate the efficacy of adalimumab (ADA) treatment in non-infectious uveitis and the effect of disease duration, age, and etiology on treatment outcome.

Methods: This retrospective study included patients with active non-infectious uveitis who were on ADA treatment with at least 3 months follow-up from a single tertiary care center. Uveitis type, any associated systemic disease, uveitis duration before ADA, duration of ADA treatment, best-corrected visual acuity (BCVA), anterior chamber cell (ACC) grade, vitritis grade, intraocular pressure (IOP) values, central macular thickness (CMT), fundus fluorescein angiography (FFA) score, complications and relapse rate were recorded.

Results: A total of 146 eyes of 77 patients (women=41, men=36) were included in the analysis. The mean age was 25.1±15.7 years. BCVA showed no significant improvement overall (+0.08, P=0.059) following ADA treatment. A weak negative correlation was found between the change in BCVA from baseline to final follow-up and disease duration before initiating ADA (r=-0.22, P=0.005). ACC and vitritis grade decreased significantly (-0.50, p<0.001; -0.51, P<0.001; respectively). The decrease in CMT was not significant (-18.6, P=0.390). Twenty patients (25.9%) experienced a relapse during treatment, and the mean relapse time was 24.9 months (95%CI: 21.0-28.9). Eleven (14.1%) of the patients required systemic corticosteroids as bridge therapy before ADA treatment and to suppress relapse while on ADA treatment. The mean dose of methylprednisolone decreased from 55.2±20.3mg to 12.3±18.0mg, and corticosteroids were discontinued in 7 of these patients.

Conclusion: ADA effectively controls intraocular inflammation and maintains visual stability in patients with non-infectious uveitis. Although BCVA did not show a statistically significant improvement overall, initiating ADA treatment early was correlated with better visual outcomes in some patients, particularly those who began treatment shortly after their disease onset. The corticosteroid burden was reduced.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jfo.2025.104457DOI Listing

Publication Analysis

Top Keywords

ada treatment
16
non-infectious uveitis
12
care center
8
disease duration
8
duration ada
8
vitritis grade
8
ada
6
uveitis
5
treatment
5
outcomes non-infectious
4

Similar Publications

Noninvasive ocular delivery of adalimumab-loaded nanostructured lipid carriers for targeted retinitis pigmentosa therapy.

Biomed Pharmacother

March 2025

Group of Pathophysiology and Therapies for Vision Disorders, Príncipe Felipe Research Center (CIPF), Eduardo Primo Yúfera 3, Valencia 46012, Spain; Joint Research Unit on Rare Diseases CIPF-Health Research Institute Hospital La Fe (IIS-La Fe), Valencia 46026, Spain; Biomedical Research Networking Center in Rare Diseases (CIBER-ER), Institute of Health Carlos III, Monforte de Lemos, 3-5. Pabellón 11, Madrid 28029, Spain; Catholic University of Valencia (UCV), Faculty of Health Sciences, Quevedo, 2, Valencia 46001, Spain. Electronic address:

Retinitis pigmentosa is a genetically heterogeneous retinal degeneration process. There is hardly any treatment available. It is associated with extensive chronic inflammation and the release of proinflammatory cytokines such as TNFα.

View Article and Find Full Text PDF

Familial chylomicronemia syndrome and treatments to target hepatic APOC3 mRNA.

Atherosclerosis

January 2025

Division of Endocrinology and Metabolism, Department of Medicine, M0682, University of California San Diego, 9500 Gilman Dr, La Jolla, CA, USA. Electronic address:

Familial chylomicronemia syndrome (FCS) is a rare, recessive monogenic disorder characterized by severely elevated plasma triglyceride (TG) levels due to absent or markedly impaired lipoprotein lipase activity, leading to a greatly increased risk of acute pancreatitis. Naturally occurring very low levels of apoC-III are associated with low TG levels; thus, apoC-III is a target for TG lowering, and therapies have been developed to reduce apoC-III. Strategies to inhibit hepatic apoC-III synthesis include antisense oligonucleotides (ASOs) and small interfering RNAs (siRNAs).

View Article and Find Full Text PDF

Background: There is low-certainty evidence on the impact of extended pharmacological prophylaxis on venous thromboembolism-associated morbidity and mortality. The aim of this study was to determine the efficacy and safety of extended prophylaxis after major abdominopelvic surgery for the prevention of clinically relevant venous thromboembolism after hospital discharge.

Methods: CArdiovaSCulAr outcomes after major abDominal surgEry (CASCADE) was a prospective, international, cohort study into which consecutive adult patients undergoing major abdominopelvic surgery were enrolled (January-May 2022).

View Article and Find Full Text PDF

Using Pharmacokinetic and Pharmacodynamic Analysis to Optimize the Dosing Regimens of Fanastomig (EMB-02) in Patients With Advanced Solid Tumors.

CPT Pharmacometrics Syst Pharmacol

March 2025

Hanghai EpimAb Biotherapeutics Co., Ltd, Shanghai EpimAb Biotherapeutics, Shanghai, China.

Fanastomig (also known as EMB-02) is a bispecific antibody targeting programmed cell death protein-1(PD-1) and lymphocyte activation gene-3 (LAG-3), developed for the treatment of advanced solid tumors. A first-in-human (FIH) Phase I study (NCT04618393) evaluated safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), immunogenicity, and clinical efficacy of Fanastomig in patients with advanced solid tumors. To determine the recommended Phase II dose (RP2D), population pharmacokinetics (PopPK), and exposure and response analysis (E-R) were conducted.

View Article and Find Full Text PDF

Impact of Big Data Analytics on Emergency Department Efficiency in Saudi Ministry of Health Hospitals: A Retrospective Data Analysis.

Risk Manag Healthc Policy

March 2025

Passionate Healthcare Strategist | Change Leader & Trusted Consultant | Driving Operational Excellence & Innovation in Healthcare and Beyond at Ascend Solutions, Western Region, Saudi Arabia.

Background: The integration of big data analytics in healthcare has become essential for enhancing operational performance, particularly within Emergency Departments (EDs), where efficiency improvements can significantly impact patient satisfaction and resource utilization.

Aim: This study examines the impact of big data analytics on ED performance metrics within Saudi Arabia's Ministry of Health (MOH) hospitals, with a focus on key performance indicators (KPIs) and the effectiveness of the Ada'a Health Program in optimizing ED operations.

Methods: A retrospective observational study was conducted across 10 hospitals in five regions of Saudi Arabia.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!