Association of Long-Term Intraocular Pressure Variability and Rate of Ganglion Complex Thinning in Patients With Glaucoma.
Mahmoudinezhad Golnoush, Moghimi Sasan, Nishida Takashi, Walker Evan, Latif Kareem, Liebmann Jeffrey M, Fazio Massimo A, Girkin Christopher A, Zangwill Linda, Weinreb Robert N
AI Summary
This study found higher long-term IOP variability, not just mean IOP, independently linked to faster retinal ganglion cell thinning in glaucoma, suggesting it's a key therapeutic target.
Abstract
Purpose
To evaluate the association of mean intraocular pressure (IOP) and IOP variability (IOP fluctuation [SD of IOP] and the IOP range) with the rate of ganglion cell complex (GCC) layer thinning over time in patients with glaucoma.
Design
Prospective cohort study.
Methods
Participants with at least 4 visits and 2 years of follow-up of optical coherence tomography tests were included. A linear mixed-effect model was used to investigate the association of IOP parameters with the rates of GCC thinning. Subgroup analyses were conducted for eyes with early (MD ≥ -6 dB), and moderate to advanced stage (MD < -6 dB) at baseline.
Results
The cohort consisted of 369 eyes of 249 glaucoma patients (282 early glaucoma and 87 moderate to advanced glaucoma) with mean (standard deviation [SD]) age of 68.2 (10.7) years over 5.1 years of follow-up. The mean rate of GCC change was -0.59 (95% confidence interval [CI], -0.67 to -0.52) µm per year. In multivariable models, faster annual rate of GCC thinning was associated with a higher IOP fluctuation (-0.17 [95% CI, -0.23 to -0.11] µm per 1-mmHg higher, P < .001) or higher IOP range (-0.07 [95% CI, -0.09 to -0.05] µm per 1-mmHg higher, P < .001) after adjustment for mean IOP and other confounding factors. Similar results were found for early and moderate to advanced stages of glaucoma.
Conclusions
IOP variability showed an independent association with macular change in patients with glaucoma regardless of severity at baseline, even after adjustment for mean IOP, supporting its potential value as a therapeutic target for clinical decision-making.
MeSH Terms
Shields Classification
Key Concepts5
In patients with glaucoma, faster annual rate of ganglion cell complex (GCC) thinning was associated with a higher intraocular pressure (IOP) fluctuation (-0.17 [95% CI, -0.23 to -0.11] µm per 1-mmHg higher, P < .001) after adjustment for mean IOP and other confounding factors.
In patients with glaucoma, a higher intraocular pressure (IOP) range was associated with a faster annual rate of ganglion cell complex (GCC) thinning (-0.07 [95% CI, -0.09 to -0.05] µm per 1-mmHg higher, P < .001) after adjustment for mean IOP and other confounding factors.
The association between intraocular pressure (IOP) variability (IOP fluctuation and IOP range) and the rate of ganglion cell complex (GCC) thinning was similar for eyes with early glaucoma (MD ≥ -6 dB) and moderate to advanced stage glaucoma (MD < -6 dB) at baseline.
Intraocular pressure (IOP) variability showed an independent association with macular change (ganglion cell complex thinning) in patients with glaucoma regardless of severity at baseline, even after adjustment for mean IOP, supporting its potential value as a therapeutic target for clinical decision-making.
The mean rate of ganglion cell complex (GCC) change in a cohort of 369 eyes of 249 glaucoma patients was -0.59 (95% confidence interval [CI], -0.67 to -0.52) µm per year over 5.1 years of follow-up.
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