Visual acuity loss associated with excessive "dry macula" in exudative age-related macular degeneration
- PMID: 29503524
- PMCID: PMC5824750
- DOI: 10.2147/OPTH.S151999
Visual acuity loss associated with excessive "dry macula" in exudative age-related macular degeneration
Abstract
Purpose: To investigate the correlation between visual acuity and central macular thickness (CMT) and choroidal thickness (CCT) in patients with wet age-related macular degeneration (AMD).
Methods: In this retrospective analysis, 14 eyes that received >10 ranibizumab injections (based on pro re nata [PRN] regimen) and maintained initial visual acuity gain were analyzed. The following 5 parameters were measured at the foveal center: CMT (distance from the inner limiting membrane [ILM] to Bruch's membrane); central retinal thickness (CRT; distance from the ILM to the inner limit of the retinal pigment epithelium or subretinal fluid [SRF]); SRF thickness (SRFT); pigment epithelium detachment thickness (PEDT); and CCT. The correlation between the logarithm of the minimum angle of resolution (logMAR) best-corrected visual acuity (BCVA) and the 5 parameters was examined with generalized estimating equations.
Results: CMT, CRT, and CCT were negatively correlated with logMAR BCVA (P=0.031, 0.023, and 0.036, respectively) when only CMT values less than the thickness that maximized visual acuity for each eye were used for the analysis. Each 100-μm reduction in CMT, CRT, or CCT improved logMAR BCVA by -0.1, -0.08, or -0.07, respectively. SRFT and PEDT were not correlated with BCVA. The median CMT that maximized the visual acuity was 230 μm.
Conclusion: Dry macula with CMT <230 μm was associated with temporary decrease in visual acuity in AMD patients whose visual acuity was maintained with PRN regimen.
Keywords: age-related macular degeneration; dry macula; intravitreal injections; ranibizumab; visual acuity.
Conflict of interest statement
Disclosure HT reports grants and personal fees from Novartis Pharmaceuticals, personal fees from Bayer Yakuhin, personal fees from Santen Pharmaceutical, personal fees from Kowa Pharmaceutical, and personal fees from Tochigi Prefectural Ophthalmologists Association, outside the submitted work. YI reports personal fees from Novartis Pharmaceuticals, Mitsubishi-Tanabe Pharmaceutical, and Tochigi Prefectural Ophthalmologists Association, outside the submitted work. YY reports personal fees from Novartis Pharmaceuticals, Bayer Healthcare, and Santen Pharmaceutical, outside the submitted work. HK reports personal fees from Santen Pharmaceutical, Mitsubishi-Tanabe Pharmaceutical, and Senju Pharmaceutical, outside the submitted work. XT, SI, SS, YA, and YF report no conflicts of interest in this work.
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