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Alterations in anterior chamber depth in primary open-angle glaucoma patients during latanoprost therapy. | LitMetric

AI Article Synopsis

  • The study aimed to assess how latanoprost therapy affects anterior chamber depth (ACD) in patients with primary open-angle glaucoma (POAG).
  • It involved 66 newly diagnosed POAG patients on latanoprost and a control group of 50 untreated ocular hypertensive patients, measuring ACD before and after treatment.
  • Results showed a significant reduction in ACD after 3 months of latanoprost treatment in the POAG group, but no impact on visual acuity or refractive status was observed, leaving the clinical significance of the ACD changes unclear.

Article Abstract

Purpose: The aim of this study was to evaluate changes in the anterior chamber depth (ACD) in primary open-angle glaucoma (POAG) patients during latanoprost therapy.

Methods: We carried out a prospective study in which we enrolled 66 newly diagnosed POAG patients treated with latanoprost 0.005% (group 1) and 50 ocular hypertensive and ⁄ or glaucoma suspect cases who were given no therapy (group 2 [control]). Measurements of the ACD were performed by A-scan ultrasonography before and after cycloplegia at baseline and at 3 months of latanoprost therapy. Differences in ACD and their correlations with the ocular hypotensive effect of the agent as well as the clinical significance of changes in ACD were analysed using Student’s t-test and Pearson’s correlation coefficient. Statistical significance was set at p < 0.05.

Results: Mean baseline ACD was 3.13 ± 0.35 mm (range 2.45–3.84 mm) in group 1 and 3.14 ± 0.36 mm (range 2.54–3.80 mm) in group 2 (p = 0.89). At 1 hour after instillation of cyclopentolate 1%, mean ACD in groups 1 and 2 was 3.18 ± 0.38 mm (range 2.45–3.92 mm) and 3.19 ± 0.37 mm (range 2.56–3.91 mm), respectively (p = 0.91). After 3 months of treatment, mean ACD in group 1 both without (3.05 ± 0.36 mm, range 2.14–3.76 mm) and with (3.09 ± 0.4 mm, range 2.20–3.96 mm) cycloplegia was significantly reduced compared with baseline values (p < 0.001 for both). However, there was no significant difference between mean ACD at baseline and that at month 3 in group 2. No correlation was demonstrated between the changes in ACD and the ocular hypotensive effect of latanoprost (p = 0.96, r = – 0.006). There were no changes in refractive status or visual acuity.

Conclusions: The overall results seem to suggest that latanoprost decreases mean ACD in patients with POAG. The clinical significance of this effect is uncertain.

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Source
http://dx.doi.org/10.1111/j.1755-3768.2009.01683.xDOI Listing

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