CFH I62V as a Putative Genetic Marker for Posner-Schlossman Syndrome

Abstract

Objective: Posner-Schlossman syndrome (PSS), also known as glaucomatocyclitic crisis, is an ocular condition characterized by recurrent attacks of anterior uveitis and raised intraocular pressure. Previous studies by our team and others have identified the genetic association of complement pathway genes with uveitis and glaucoma. This study aimed to investigate the complement genes in PSS patients with the view of elucidating the genetic background of the disease.Methods: A total of 331 subjects (56 PSS patients and 275 controls) were recruited for this study. We selected 27 variants in six complement pathway genes (SERPING1, C2, CFB, CFH, C3, and C5) and detected them using TaqMan single nucleotide polymorphism (SNP) Genotyping Assays. Univariate SNP association analysis, haplotype-based association analysis, gene-gene interaction analysis among complement genes, and genotype-phenotype correlation analysis were performed.Results: Among the 27 variants of six complement pathway genes, the functional variant I62V (rs800292) at the CFH gene was found to be significantly associated with PSS; there was a significant increase in the frequency of A allele and AA homozygosity in PSS patients than in controls (P = 1.79 × 10−4; odds ratio (OR) 2.18, 95% CI: 1.44–3.29; P = 4.65 × 10−4; OR 3.66, 95% CI: 1.70–7.85, respectively). The additive effect of CFH-rs800292 and SERPING1-rs3824988 was identified with an OR of 12.50 (95% CI: 2.16–72.28). Genotype-phenotype analysis indicated that the rs800292 AA genotype was associated with a higher intraocular pressure and higher frequency of recurrence. Unlike a high proportion of human leukocyte antigen (HLA)-B27 positivity in anterior uveitis, only 3 in 56 (5.36%) PSS patients were HLA-B27 positive. In addition, one haplotype block (GC) in the SERPING1 gene showed a nominal association with PSS with an increased risk of 2.04 (P = 0.01; 95% CI: 1.18–3.53), but the P-value could not withstand the Bonferroni correction (Pcorr > 0.05).Conclusion: This study revealed a genetic association of a CFH variant with PSS as well as its clinical parameters, implying that the alternative complement pathway might play an important role in the pathogenesis of PSS. Further studies to enrich the understanding of the genetic background of PSS and the role of the complement system in ocular inflammation are warranted.

Clinical Characteristics of Posner‐Schlossman Syndrome Patients in China

“…Underlying mechanisms of the privilege distribution in male cases are still waiting to be elucidated. It was referred that the disease was related to the balancebreaking of the immune status [9,10], and the alternative complement pathway might play an important role in the pathogenesis of PSS [11]. Maintaining a properly functioning adaptive immune system required a proper balance between stimulatory and inhibitory signals [12,13].…”

Assessment of anxiety and depression in patients with Posner-Schlossman syndrome

“…Patients with PSS usually have characteristic clinical manifestations, recurrent acute anterior segment inflammation, markedly increased IOP, mild blur vision, with a vulnerable age of 20–50 years [ 20 , 21 ]. The pathophysiology of PSS is however not well understood; viral infection, genetic susceptibility, vascular endothelial dysfunction, and autoimmune diseases have been reported to be as risk factors that contribute to PSS onset and severity [ 21 ].…”

Long term outcome and prognostic indicators in Posner Schlossman syndrome

“…4 The aetiology of PSS is considered multifactorial. Vascular endothelial dysfunction 8 and genetic predisposition, [9][10][11] autoimmunity and allergy have been suggested as factors contributing towards PSS development. However, more recent literature suggests a causative association between PSS and herpes viridae, most predominantly human cytomegalovirus (CMV), 12 (Table 2).…”