Risk factors for visual field progression in the low-pressure glaucoma treatment study

Am J Ophthalmol. 2012 Oct;154(4):702-11. doi: 10.1016/j.ajo.2012.04.015. Epub 2012 Jul 25.

Abstract

Purpose: To investigate risk factors associated with visual field progression in the Low-pressure Glaucoma Treatment Study, a prospective trial designed to compare the effects of the alpha2-adrenergic agonist brimonidine tartrate 0.2% to the beta-adrenergic antagonist timolol maleate 0.5% on visual function in low-pressure glaucoma.

Design: Prospective cohort study.

Methods: Low-pressure Glaucoma Treatment Study patients with ≥5 visual field tests during follow-up were included. Progression was determined using pointwise linear regression analysis, defined as the same 3 or more visual field locations with a slope more negative than -1.0 dB/year at P < 5%, on 3 consecutive tests. Ocular and systemic risk factors were analyzed using Cox proportional hazards model and further tested for independence in a multivariate model.

Results: A total of 253 eyes of 127 subjects (mean age, 64.7 ± 10.9 years; mean follow-up, 40.6 ± 12 months) were analyzed. Eyes randomized to timolol progressed faster than those randomized to brimonidine (mean rates of progression, -0.38 ± 0.9 vs 0.02 ± 0.7 dB/y, P < .01). In the final multivariate model adjusting for all tested covariates, older age (hazard ratio [HR] = 1.41/decade older, 95% confidence interval [CI] = 1.05 to 1.90, P = .022), use of systemic antihypertensives (HR = 2.53, 95% CI = 1.32 to 4.87, P = .005), and mean ocular perfusion pressure (HR = 1.21/mm Hg lower, 95% CI = 1.12 to 1.31, P < .001) were associated with progression whereas randomization to brimonidine revealed a protective effect (HR = 0.26, 95% CI = 0.12 to 0.55, P < .001).

Conclusions: While randomization to brimonidine 0.2% was protective compared to timolol 0.5%, lower mean ocular perfusion pressure increased the risk for reaching a progression outcome in the Low-pressure Glaucoma Treatment Study. This suggests that the beneficial effect of randomization to the brimonidine arm was independent of possible differences in ocular perfusion pressures between the 2 treatment arms. The current results and large number of drop-outs in the brimonidine 0.2% arm suggest that more research is necessary before altering clinical practice paradigms.

Trial registration: ClinicalTrials.gov NCT00317577.

Publication types

  • Comparative Study
  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Topical
  • Adrenergic alpha-2 Receptor Agonists / administration & dosage*
  • Adrenergic beta-Antagonists / administration & dosage*
  • Aged
  • Brimonidine Tartrate
  • Disease Progression
  • Double-Blind Method
  • Female
  • Follow-Up Studies
  • Gonioscopy
  • Humans
  • Intraocular Pressure / drug effects
  • Low Tension Glaucoma / drug therapy*
  • Low Tension Glaucoma / physiopathology
  • Male
  • Middle Aged
  • Ophthalmic Solutions
  • Prospective Studies
  • Quinoxalines / administration & dosage*
  • Risk Factors
  • Timolol / administration & dosage*
  • Vision Disorders / physiopathology*
  • Visual Acuity / physiology
  • Visual Field Tests
  • Visual Fields / physiology*

Substances

  • Adrenergic alpha-2 Receptor Agonists
  • Adrenergic beta-Antagonists
  • Ophthalmic Solutions
  • Quinoxalines
  • Brimonidine Tartrate
  • Timolol

Associated data

  • ClinicalTrials.gov/NCT00317577