Abstract

Purpose Increased evidence reveals that uric acid (UA) may have an important neuroprotective effect through its antioxidant properties. The aim of the present study was to investigate the relationship between pretreatment serum UA levels and the progression of newly diagnosed primary angle-closure glaucoma (PACG). Methods This prospective observational cohort study included 64 patients with newly diagnosed PACG who were followed up for a mean period of 12.77 months (range: 3–28 months). All subjects underwent a complete ophthalmological examination during the baseline and final follow-up visits, together with the acquisition of blood samples for UA measurements. During the follow-up period, the progression of PACG was defined as a clinical diagnosis of medically uncontrolled intraocular pressure and a loss of visual field with a mean deviation of >1 dB/year. Univariable and multivariable Cox regression models were used to investigate the association between baseline serum UA levels and the progression of PACG. The cumulative probability of progression of glaucoma was analyzed using the Kaplan-Meier method. Results During follow-up, 32 subjects were defined as progressive PACG, among whom baseline UA values were significantly higher in nonprogressing subjects than in progressing subjects (0.314 ± 0.069 mmol/l versus [vs.] 0.258 ± 0.069 mmol/l, respectively; P = 0.002). Similar results were also observed in male and female subgroups (P < 0.05). In a multivariable model, a decreased baseline serum UA level was associated with an increased risk for progressing PACG: both in male (hazard ratio [HR] 6.088 [95% confidence interval (CI) 1.163–31.8638]; P = 0.032) and female subjects (HR 3.565 [95% CI 1.131–11.236]; P = 0.030). Subjects with high UA levels demonstrated higher cumulative probabilities of nonprogressing PACG than those with low UA levels (male [16.67% vs. 80.00%; P = 0.0084] and female [29.41% vs. 68.00%; P = 0.0182]). Conclusion An association between high baseline serum UA levels and a decreased risk for progressing PACG was found. This primary finding suggests that high serum UA levels may have a protective role against PACG and could slow disease progression.

Highlights

  • Uric acid (UA), the naturally occurring end-product of purine metabolism in humans, is a powerful water-soluble radical scavenger [1]

  • This was determined using the following methods: a glaucoma hemifield test with outside normal limits that included a cluster of ≥3 nonedge contiguous points on the pattern deviation plot that crossed the horizontal meridian and had a probability of

  • After adjusting the multivariable model for age, hypertension, diabetes, intraocular pressure (IOP), vertical cup-disk ratio (VCDR), central corneal thickness (CCT), anterior chamber depth (ACD), axial length (AL), and mean deviation (MD), lower pretreatment levels of UA remained a risk factor that predicted the progression of primary angle-closure glaucoma (PACG) in both male (HR 6.088 [95% CI 1.163– 31.8638]; P = 0 032) and female (HR 3.565 [95% CI 1.131– 11.236]; P = 0 030) subjects

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Summary

Introduction

Uric acid (UA), the naturally occurring end-product of purine metabolism in humans, is a powerful water-soluble radical scavenger [1]. A previous study reported significantly lower serum UA levels in patients with PACG [25] and primary open-angle glaucoma [26]. These low levels were negatively associated with disease severity. Keller et al [29] reported that UA could protect hippocampal neurons against apoptosis by preventing mitochondrial superoxide accumulation and consequent peroxynitrite production and mitochondrial dysfunction Overall, these studies suggest that higher serum UA levels could have a similar protective role in PACG. To obtain a potentially simple, rapid, and reliable prognostic parameter, this study investigated potential associations between pretreatment serum UA levels and the progression of PACG

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