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Proof of concept, randomized, placebo-controlled study of the effect of simvastatin on the course of age-related macular degeneration.

Authors :
Guymer RH
Baird PN
Varsamidis M
Busija L
Dimitrov PN
Aung KZ
Makeyeva GA
Richardson AJ
Lim L
Robman LD
Source :
PloS one [PLoS One] 2013 Dec 31; Vol. 8 (12), pp. e83759. Date of Electronic Publication: 2013 Dec 31 (Print Publication: 2013).
Publication Year :
2013

Abstract

Background: HMG Co-A reductase inhibitors are ubiquitous in our community yet their potential role in age-related macular degeneration (AMD) remains to be determined.<br />Objectives: To evaluate the effect of simvastatin on AMD progression and the effect modification by polymorphism in apolipoprotein E (ApoE) and complement factor H (CFH) genes.<br />Design: A proof of concept double-masked randomized controlled study.<br />Participants: 114 participants aged 53 to 91 years, with either bilateral intermediate AMD or unilateral non-advanced AMD (with advanced AMD in fellow eye), BCVA ≥ 20/60 in at least one eye, and a normal lipid profile.<br />Intervention: Simvastatin 40 mg/day or placebo, allocated 1:1.<br />Main Outcome Measures: Progression of AMD either to advanced AMD or in severity of non-advanced AMD. Results. The cumulative AMD progression rates were 70% in the placebo and 54% in the simvastatin group. Intent to treat multivariable logistic regression analysis, adjusted for age, sex, smoking and baseline AMD severity, showed a significant 2-fold decrease in the risk of progression in the simvastatin group: OR 0.43 (0.18-0.99), p = 0.047. Post-hoc analysis stratified by baseline AMD severity showed no benefit from treatment in those who had advanced AMD in the fellow eye before enrolment: OR 0.97 (0.27-3.52), p = 0.96, after adjusting for age, sex and smoking. However, there was a significant reduction in the risk of progression in the bilateral intermediate AMD group compared to placebo [adjusted OR 0.23 (0.07-0.75), p = 0.015]. The most prominent effect was observed amongst those who had the CC (Y402H) at risk genotype of the CFH gene [OR 0.08 (0.02-0.45), p = 0.004]. No evidence of harm from simvastatin intervention was detected.<br />Conclusion/significance: Simvastatin may slow progression of non-advanced AMD, especially for those with the at risk CFH genotype CC (Y402H). Further exploration of the potential use of statins for AMD, with emphasis on genetic subgroups, is warranted.<br />Trial Registration: Australian New Zealand Clinical Trial Registry (ANZCTR) ACTRN1260500032065.

Details

Language :
English
ISSN :
1932-6203
Volume :
8
Issue :
12
Database :
MEDLINE
Journal :
PloS one
Publication Type :
Academic Journal
Accession number :
24391822
Full Text :
https://doi.org/10.1371/journal.pone.0083759