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PLoS One. 2013 Dec 31;8(12):e83759. doi: 10.1371/journal.pone.0083759. eCollection 2013.

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

Author information

1
Centre for Eye Research Australia, University of Melbourne, Royal Victorian Eye and Ear Hospital, East Melbourne, Victoria, Australia.
2
Centre for Eye Research Australia, University of Melbourne, Royal Victorian Eye and Ear Hospital, East Melbourne, Victoria, Australia ; Biostatistics Unit, Faculty of Health, Deakin University, Burwood, Victoria, Australia.

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.

METHODOLOGY/PRINCIPAL FINDINGS:

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.

DESIGN:

A proof of concept double-masked randomized controlled study.

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.

INTERVENTION:

Simvastatin 40 mg/day or placebo, allocated 1:1.

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.

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.

TRIAL REGISTRATION:

Australian New Zealand Clinical Trial Registry (ANZCTR) ACTRN1260500032065.

PMID:
24391822
PMCID:
PMC3877099
DOI:
10.1371/journal.pone.0083759
[Indexed for MEDLINE]
Free PMC Article

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