Purpose: This study was conducted to explore the association of autophagy-related genes (ATGs) single nucleotide polymorphisms (SNPs) with Behçet's disease (BD) and Vogt-Koyanagi-Harada (VKH) syndrome in a Chinese Han population.

Methods: A two-stage association study was carried out in 940 BD, 1061 VKH, and 2007 healthy controls. Genotyping for genetic variants of 10 autophagy family genes (ATG5, ATG7, ATG10, ATG16L1, IRGM, LKKR2, ATG2A, DAP, ULK1, and TSC1) was performed using PCR-restriction fragment length polymorphism (PCR-RFLP) or TaqMan SNP assays. Gene expression was quantified by real-time PCR.

Results: In the cohort of BD patients, we observed that the TT genotype of rs573775/ATG5 decreased susceptibility to BD (Pc = 8.35 × 10-6, OR = 0.490). In the case of VKH patients, the AC genotype of rs4703863/ATG10 increased susceptibility to VKH syndrome (Pc = 9.94 × 10-5, OR = 1.444), whereas the A allele and AA genotype of rs4703863 (Pc = 7.06 × 10-5, OR = 0.745; Pc = 6.34 × 10-6, OR = 0.669, respectively) acted as protective factors for VKH. Functional experiments showed an increased ATG5 expression by LPS stimulated PBMCs in TT cases of rs573775 compared with controls. The level of ATG5 mRNA in active BD patients not receiving immunosuppression was significantly higher than that in healthy controls.

Conclusions: This study demonstrated an association of ATG5 rs573775 with BD and ATG10 rs4703863 with VKH syndrome in a Chinese Han population. Furthermore, a variant of the ATG5 gene was shown to be correlated with ATG5 expression.

Download full-text PDF

Source
http://dx.doi.org/10.1167/iovs.15-18035DOI Listing

Publication Analysis

Top Keywords

vkh syndrome
16
syndrome chinese
12
chinese han
12
association atg5
8
atg5 gene
8
gene polymorphisms
8
behçet's disease
8
han population
8
atg5 expression
8
vkh
7

Similar Publications

Pattern of Uveitis in Northern Vietnam.

Ocul Immunol Inflamm

December 2024

Department of Ophthalmology, Hanoi Medical University, Hanoi, Vietnam.

Purpose: To characterize the spectrum of uveitis in patients visiting three tertiary hospitals in Hanoi, Vietnam.

Methods: This study collected prospective and multicenter data from patients diagnosed with uveitis at three tertiary hospitals in Hanoi City, Vietnam, between January 2022 and January 2024. Data on age, sex, clinical and laboratory findings, and etiology were collected.

View Article and Find Full Text PDF

To present a case of a young adult with bilateral chronic posterior uveitis resulting from Vogt-Koyanagi-Harada (VKH) disease treated with mycophenolate mofetil who subsequently developed vitreoretinal lymphoma in the right eye. A case and its findings were analyzed. A 34-year-old Hispanic woman presented with an 8-year history of chronic recurrent posterior uveitis in both eyes secondary to VKH disease.

View Article and Find Full Text PDF
Article Synopsis
  • The study assessed contrast sensitivity function (CSF) in patients recovering from Vogt-Koyanagi-Harada (VKH) disease, particularly focusing on those with and without sunset glow fundus (SGF).
  • Patients with SGF exhibited significantly impaired CSF compared to normal controls, especially at medium and high spatial frequencies, while no notable differences were found between the non-SGF group and controls.
  • The results indicate that despite good visual acuity recovery, both CSF and outer retinal thickness were reduced in VKH patients, suggesting that CSF is a valuable measure for evaluating functional vision in these cases.
View Article and Find Full Text PDF

Introduction: Vogt-Koyanagi-Harada (VKH) disease is a multisystem syndrome characterized by uveitis and exudative retinal detachments in the absence of ocular trauma or surgery. Neurological and cutaneous manifestations can also occur. Prior case reports have associated immune checkpoint inhibitors with a VKH-like disease.

View Article and Find Full Text PDF

Effects of pregnancy on the clinical course and treatment outcomes of Vogt-Koyanagi-Harada disease.

Indian J Ophthalmol

January 2025

Smt. Kannuri Santhamma Center for Vitreoretinal Diseases, Kallam Anji Reddy Campus Anant Bajaj Retina Institute, L V Prasad Eye Institute, Hyderabad, Telangana, India.

Purpose: To describe the clinical course and treatment outcomes of Vogt-Koyanagi-Harada (VKH) disease during pregnancy.

Methods: This retrospective study compares the clinical course and outcomes in pregnant and nonpregnant women with VKH. All VKH patients who were pregnant at presentation or on follow up and age-matched nonpregnant female controls during the study period (2013-2022) were included.

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!