Skip to main content
NCBI home page
Therapeutic Advances in Chronic Disease logoLink to Therapeutic Advances in Chronic Disease
. 2011 Sep;2(5):325–331. doi: 10.1177/2040622311415895

Age-Related Macular Degeneration: Current Treatment and Future Options

Tanya Moutray 2, Usha Chakravarthy 1
PMCID: PMC3513889  PMID: 23251758

Abstract

Age-related macular degeneration is the leading cause of visual impairment among older adults in the developed world. Epidemiological studies have revealed a number of genetic, ocular and environmental risk factors for this condition, which can be addressed by disease reduction strategies. We discuss the various treatment options for dry and exudative age-related macular degeneration available and explain how the recommended treatment depends on the exact type, location and extent of the degeneration. Currently, vascular endothelial growth factor (VEGF) inhibition therapy is the best available treatment for exudative age-related macular degeneration but is limited by the need for repeated intravitreal injections. The current treatment regime is being refined through research on optimal treatment frequency and duration and type of anti-VEGF drug. Different modes of drug delivery are being developed and in the future other methods of VEGF inhibition may be used.

Keywords: age-related macular degeneration, anti-VEGF, choroidal neovascularization

Introduction

Age-related macular degeneration (AMD) is the leading cause of visual impairment among older adults in the developed world [Klein et al. 1992]. Late clinical findings in AMD include geographical atrophy and neovascular AMD (nvAMD). It is estimated that a quarter of a million older adults in the UK are blind as a result of late AMD [Owen et al. 2003].

The pathophysiology of AMD includes diffuse thickening of the inner aspect of Bruch's membrane associated with soft drusen and may be accompanied by abnormalities of the retinal pigment epithelium (RPE) with focal hyperpigmentation. In patients with early AMD, visual function is good unless central geographical atrophy or nvAMD develops. Studies of the natural history show that severe visual loss, which is defined as a reduction of more than six lines of Snellen acuity, occurs in 21.3% of AMD patients at 6 months and 41.9% by 3 years [Wong et al. 2008]. The presence of large soft drusen and focal hyperpigmentation markedly increases the risk of developing late AMD [Cukras et al. 2010].

In exudative nvAMD, three patterns of choroidal neovascularization (CNV) have been defined: growth into the plane between the RPE and Bruch's membrane (type 1); growth between the retina and RPE (type 2); and retinal angiomatous proliferation within the retina (type 3). Blood and serum leak from these fenestrated vessels and cause separation of Bruch's membrane, the RPE and the retina from each other, leading to the accumulation of intraretinal fluid. This results in generalized thickening of the retina or the formation of cystic spaces, causing the photoreceptors to become misaligned, and eventually degenerative changes occur with cell loss and eventual fibrosis.

Current management strategies

An important aspect of AMD management is patient education, because early detection provides the greatest chance of successful treatment. Patients should be warned of the symptoms of incipient late nvAMD and of the increased risk of acquiring a similar nvAMD in the fellow eye if one eye has already been affected. They should also be informed that peripheral vision is almost always retained, even in advanced AMD. In advanced stages patients should also be referred for low vision aids and registration with blind services where appropriate.

Risk factor reduction

There are a number of risk factors associated with AMD progression, which may be addressed by disease reduction strategies. These risk factors include smoking, sunlight exposure and a low-antioxidant diet. Cigarette smoking is a well-established risk factor for the development of AMD [Thornton et al. 2005] and cessation is advised as there is a dose—response relationship with pack-years of smoking [Chakravarthy et al. 2007; Khan et al. 2006]. Wearing UV light protection is advisable from an early age to limit exposure of the macula to light of blue wavelengths [Ham et al. 1976]. The retina may be vulnerable to oxidative stress if the diet is low in antioxidants, as the ‘free radical’ theory of ageing proposes that oxygen radicals damage cells over time [Finkel and Holbrook, 2000]. Thus, eating a low-fat, balanced diet full of antioxidants, zinc and vitamin D is advised.

Late AMD

There are a number of treatment options for late AMD but the recommended treatment depends on the exact type, location and extent of AMD. In the 1980s and 1990s laser-based therapies were the mainstay of treatment. The Macular Photocoagulation Study Group (MPSG) used focal argon laser photocoagulation to destroy the neovascular complex with heavy confluent burns to try to prevent CNV enlargement or leakage, but recurrences were common [Macular Photocoagulation Study Group, 1991]. Photodynamic therapy (PDT) used with a photosensitive dye (verteporfin) to treat leaking vessels prevented moderate visual loss in predominantly classic lesions that involved the fovea [Bressler et al. 2002]. However, neither of these treatments were particularly successful in improving visual outcome.

Improved treatments have been developed using inhibitors against vascular endothelial growth factor (VEGF) as monotherapy or in combination with other treatments. VEGF increases vascular permeability and affects multiple components in angiogenesis that promote new vessel formation [Ferrara and Davis-Smyth, 1997]. VEGF also has important functions in vascular pathophysiology: in the process of ather-othrombosis it induces collateral circulation to protect against ischaemia in areas of vessel narrowing [Simons, 2005], and inside atherosclerotic plaques it promotes microvessel formation [Juan-Babot et al. 2003], which may disrupt vessels and cause intraplaque haemorrhage and disease progression.

Anti-VEGF monotherapies

Several inhibitors of VEGF have been investigated in the treatment of nvAMD and have been unequivocally shown to reduce exudative manifestations with significant beneficial effects on the maintenance of visual function [Rosenfeld et al. 2006; Gragoudas et al. 2004]. These drugs are injected into the vitreous cavity under local anaesthesia, where they reduce exudative manifestations in the macula. The following anti-angiogenic therapies are currently in use:

  • ranibizumab (Lucentis®, Genentech), a humanized Fab fragment of a monoclonal antibody that binds to and inhibits the action of all isoforms of VEGF-A;

  • bevacizumab (Avastin®, Roche), a humanized full-length antibody that is derived from the same monoclonal antibody as ranibizumab; there are no long-term results on the safety and effectiveness of intravitreal bevacizumab;

  • pegaptanib sodium (Macugen®, Eyetech/Pfizer), another therapy that blocks the activity of isoforms of VEGF-A but is rarely used in clinical practice as it is not as effective as ranibizumab or bevacizumab.

At present, the treatment of choice for any subfoveal CNV is ranibizumab 0.5 mg [Royal College of Ophthalmologists, 2009]. However, this treatment will only improve vision in a third of patients and some 10% will not respond to therapy. The criteria for continuation of treatment at 4-weekly intervals after the three initial loading doses of ranibizumab are:

  • persistent evidence of lesion activity;

  • the lesion continues to respond to repeated treatment;

  • absence of contraindications (see below) to continuing treatment.

However, despite being administered as an intraocular injection, these drugs may be detected in circulating blood [Gaudreault et al. 2005]. As VEGF has a role in thrombus formation and in the pathophysiology of atherosclerosis, the possibility of adverse cardiovascular effects similar to those reported for systemic anti-VEGF therapy in oncology, such as thrombosis, haemorrhage and hypertension, must be considered [Tunón et al. 2009]. The UK's Royal College of Ophthalmologists has recommended guidelines on temporarily discontinuing anti-VEGF treatment if a thromboembolic phenomenon, including myocardial infarction or cardiovascular accident, has occurred in the preceding 3 months, or if recurrent thromboembolic phenomena occur which are thought to be related to treatment with ranibizumab [Royal College of Ophthalmologists, 2009].

In the Minimally classic/occult trial of the Anti-VEGF antibody Ranibizumab in the treatment of Neovascular Age-related macular degeneration (MARINA) study, 716 patients with AMD received monthly intravitreal injections of 0.3 or 0.5 mg ranibizumab or a sham injection for 24 months [Rosenfeld et al. 2006]. In the ANti-VEGF antibody for the treatment of predominantly classic CHORoidal neovascularization in age-related macular degeneration (ANCHOR) study, 423 patients with AMD were randomized to receive monthly ranibizumab (0.3 or 0.5 mg) plus sham verteporfin therapy or sham injections plus active verteporfin therapy for 2 years [Brown et al. 2006]. Patients with previous cardiovascular disorders were not excluded from these trials, and no significant difference in the incidence of cardiovascular events was found. However, the sample sizes in these trials are insufficient to permit valid conclusions to be made about the presence or absence of such serious adverse events.

Comparison of anti-VEGF therapies, refinement of treatment strategies and combination therapies

Further refinement of the current treatment regime is needed through research on the optimal treatment frequency and duration and the type of anti-VEGF drug. Studies to compare ranibizumab and bevacizumab in the UK are the randomised controlled trial of alternative treatments to Inhibit VEGF in Age-related choroidal Neovascularisation (IVAN) study and the in USA the Comparison of Age-related Macular Degeneration Treatments Trials: Lucentis-Avastin Trial (CATT) study are ongoing.

There are a number of other agents previously studied, including PDT and steroids, that may be used in combination with any of the above treatments.

Combination therapies

Anti-VEGF monotherapy regimes merely reduce the exudative manifestations and do not cause permanent regression of new vessels in patients who are commenced on these treatments. They require monthly monitoring and treatment for many years. Thus, the burden on scant and stretched clinical resources grows inexorably. With this in mind, combination approaches are being considered using therapies that cause new vessel regression, such as photodynamic therapy and ionizing radiation.

Photodynamic therapy.

Combination treatments using ranibizumab or bevacizumab and PDT have yielded visual outcomes that are comparable to those given by ranibizumab alone, while the number of treatments required to maintain a dry macula is reduced slightly (CAVE and MONTBLANC trials) [Heier et al. 2006].

The PROTECT non-randomized trial found that same-day application of PDT and intravitreal ranibizumab followed by three monthly injections improved visual acuity by a mean of seven letters and retreatments were rarely required during the 9-month follow up [Schmidt-Erfurth et al. 2006]. The larger phase III SUMMIT trials (MONT BLANC, DENALI, EVEREST) will provide more robust information on the safety and efficacy of PDT combined with ranibizumab compared with ranibizumab monotherapy. Preliminary results of combination therapy for nvAMD have not lived up to the promise of significantly reducing the injection frequency and improving vision, except for the EVEREST study of idiopathic polypoidal choroidal vasculopathy (IPCV). This suggests that combination therapy with PDT and ranibizumab is more effective than monotherapy in the treatment of IPCV, where there is are significant differences in treatment frequency and outcome with combination therapy compared with mono-therapy with either ranibizumab or PDT alone [Lai, 2010].

In the CNV Secondary to AMD Treated with BEta RadiatioN Epiretinal Therapy (CABERNET) trial, we await the final results which are as yet unpublished. This study compares ranibizumab monotherapy with a single dose of epimacular brachytherapy of 16 Gy using strontium 90 beta radiation combined with ranibizumab. In this 2-year trial the need for retreatment is the primary outcome parameter. The I-Ray plus aNti-VEGF TREatment for Patients wIth Wet AMD (INTREPID) study is testing a single dose of 16 or 24 Gy of highly collimated photons delivered through the iRAY device combined with ranibizumab versus ranibizumab monotherapy. The primary outcome is again the number of retreatments needed.

Photodynamic therapy + anti-VEGF + dexamethasone.

Trials of triple therapy are under way to investigate the treatment of exudative AMD using PDT to eradicate the existing CNV, steroid to limit the inflammatory response and reduce further upregulation of VEGF, and anti-VEGF to prevent any further angiogenesis. The RADICAL (Reduced Fluence Visudyne Anti-VEGF-Dexamethasone In Combination for AMD Lesions) phase II multicentre study aims to determine whether proprietary verteporfin (Visudyne®, Novartis) combined with ranibizumab (Lucentis®, Genentech) (with or without dexamethasone) reduces retreatment rates compared with ranibizumab monotherapy. The overall results suggest that fewer retreatment visits were required with the combination therapies than with monotherapy, so that verteporfin combination therapy may be a potential cost-effective way to treat patients with nvAMD [Augustin et al. 2007].

Emerging therapies

Non-nvAMD

Preventative strategies for non-nvAMD are under investigation that target complement regulation as this is disrupted in AMD. Copaxone® (glatiramer acetate) is an anti-inflammatory agent given by subcutaneous injection that alters immunomodulatory gene expression and is being used in early AMD to reduce the size and extent of drusen [Arnon and Aharoni, 2009]. POT-4 is a derivative of the cyclic peptide Compstatin undergoing phase I testing and is directed against C3, which is a central component of all major complement activation pathways [Rakic, 2003]. ARC1905 is also undergoing study and is an aptamer that inhibits the pro-inflammatory C5 [Usui et al. 2004].

The use of topically administered AL-8309B (Alcon Laboratories) for the treatment of AMD-related geographical atrophy is currently under investigation in the double-masked, randomized phase III GATE trial [Singerman, 2009].

nvAMD

At present, anti-VEGF therapy is the best available treatment for nvAMD but is limited by the need for repeated intravitreal injections and its associated risks and burden on workload. Different methods of VEGF inhibition are being developed that target various stages in the signalling cascade that regulates VEGF production.

Upstream inhibitors

Inhibition of upstream factors in the signalling cascade that leads to angiogenesis includes a protein kinase called mTOR that regulates cell growth and proliferation. The mammalian target of rapamycin (mTOR) activates hypoxia-inducible factor 1 a (HIF-1 a), which causes transcription of multiple genes, including those that produce VEGF [Ma and Blenis, 2009]. Sirolimus (Rapamycin®, Macusight and Santen) is a broad-acting mTOR inhibitor given by the subconjunctival or intravitreal route under investigation in the EMERALD (Phase II Study of an Ocular Sirolimus (Rapamycin) Formulation in Combination With Lucentis® in Patients With Age-Related Macular Degeneration) trial [ClinicalTrials.gov identifier: NCT00766337].

Downstream inhibitors

Targets in the angiogenesis cycle include tyro-sine kinase receptors that are expressed in CNVs, such as topical TG100801 (Targegen) [ClinicalTrials.gov identifier: NCT00414999], AL39324 (Alcon) (in phase II testing, WALTZ trial) [ClinicalTrials.gov identifier: NCT00992563], oral vatalanib [ClinicalTrials.gov identifier: NCT00138632] and topical ATG-3 (Athenagen), which is a 7-nicotinic acetylcholine receptor antagonist.

Transmembrane proteins called integrins are essential in angiogenesis during endothelial cell migration and macrophage recruitment [Avraamides et al. 2008]. Phase I trials have been conducted with JM6427, which is a specific integrin antagonist [ClinicalTrials.gov identifier: NCT00536016], and volociximab, which is a monoclonal antibody that block binds integrin [ClinicalTrials.gov identifier: NCT00782093].

Platelet-derived growth factor (PDGF) acts as a mitogen for pericytes and is critical for blood vessel maintenance. E10030 (Ophthotech) is an anti-PDGF agent that, when combined with anti-VEGF, causes neovascular regression [ClinicalTrials.gov identifier: NCT01089517].

VEGF Trap

VEGF Trap is a VEGF—receptor fusion protein that binds all forms of VEGF-A. The Clinical Evaluation of Anti-Angiogenesis in the Retina Intravitreal Trial (CLEAR-IT) of VEGF Trap-Eye in patients with nvAMD found a mean gain in best corrected visual acuity (BCVA) from baseline of 7.3 letters at 3 months, 8.4 letters at 1 year and 7.1 letters at month 6 of the extension study (n = 117). Over the 15-month course of the “as required” Pro re nata (PRN) dosing phase, from month 3 of the original study to month 6 of the extension phase, patients received a mean of 3.5 injections of VEGF Trap-Eye. The visual outcome was similar to that with ranibizumab but with significantly reduced frequency of intravitreal injection [Nguyen et al. 2009].

The VEGF Trap-Eye: Investigation of Efficacy and Safety in Wet AMD (VIEW) study evaluated three dose levels of VEGF Trap-Eye in the treatment of nvAMD in the United States (VIEW 1) and globally (VIEW 2). A statistically significant mean improvement in vision of 10.9 letters was found at 52 weeks in the group injected monthly with VEGF Trap-Eye (2 mg) compared with eight letters in the ranibizumab (0.5 mg) group injected monthly. VEGF Trap-Eye (2 mg) injected every 2 months maintained vision at week 52, and was similar in efficacy and safety to ranibizumab dosed monthly. PRN dosing at least every 3 months (but not more often than monthly) is currently being evaluated.

Gene therapy

In AMD, a relatively small number of genes with large effect have been identified, several of which alter the alternative complement pathway. Drugs that inhibit complement activation represent a novel method of treatment in the future and major genetic factors are discussed below.

Genes associated with the complement cascade

Several genes that code for proteins involved in the complement cascade significantly increase the risk of AMD (such as variation in complement factor (CFH) and complement component 3) or decrease the risk of AMD (variation in complement component 2 and factor B and deletion of CFH-related genes CFHR1 and CFHR3). A mutation in complement factor H, a key regulator of the complement pathway, is strongly associated with increased risk of AMD as carriage of the Y402H polymorphism increases between 2- and 7-fold the risk of developing AMD. This gene polymorphism accounts for up to 50% of the population-attributable risk of AMD [Edwards et al. 2005; Haines et al. 2005].

Variation in C3 has been shown to increase the risk of developing AMD up to 2.6-fold [Yates et al. 2007]. A protective deletion of CFHR1 and 24CFHR3 occurs close to the CFH locus in 8% of AMD patients [Hughes et al. 2006] and a protective haplotype, reducing the risk of AMD, is associated with variation in complement factors C2 and factor B [Gold et al. 2006].

Chromosome 10q locus

Single-nucleotide polymorphisms (SNPs) in chromosome 10q26 are associated with an increased risk of AMD. Further functional studies are needed to confirm whether SNPs identified in the coding region of the LOC387715/ARMS2 (age-related maculopathy susceptibility 2) gene [Rivera et al. 2005] or located in the promoter region of HTRA1 (high temperature requirement factor A1) [Edwards et al. 2005; Haines et al. 2005] represent the true genetic risk variant at this locus. A major genetic risk factor for AMD occurs at this 10q26 locus, with an up to 10-fold increased risk of developing AMD [DeWan et al. 2006].

Other major genetic loci

Meta-analysis of whole genome linkage studies identified several significant genetic loci for AMD [Fisher et al. 2005] on chromosomes 1 (CFH locus), 10q, and 1q, 2 p, 3 p and 16, where undiscovered genetic variants are yet to be revealed.

Pharmacogenetic relationships

Some preliminary pharmacogenetic relationships have been reported to exist between genetic risk factors associated with AMD and the response to treatment. These pharmacogenetic associations could be used in the future to create a personalized therapeutic plan whereby patients with different genotypes are offered different treatments. For example, patients with the CFHY402H CC genotype had a significantly worse prognosis with intravitreal bevacizumab injections compared with those with the CFH TC or TT genotypes [Brantley et al. 2007]. There is also evidence that carriage of CFH or HTRA1 genetic variants can increase the risk of developing CNV or alter the phenotype of CNV [Leveziel et al. 2008; Weger et al. 2007].

Conclusion

Anti-VEGF therapy is the best available treatment for nvAMD. However, the current regime is being refined through research on optimal monotherapy and combination strategies. There is ongoing, exciting research looking at immunomodulation and targeting various inhibition sites in the angiogenesis pathway, which may be the future of AMD treatment.

Footnotes

This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors.

The authors declare no conflicts of interest in preparing this article.

References

  1. Arnon R., Aharoni R. (2009) Neuroprotection and neurogeneration in MS and its animal model EAE effected by glatiramer acetate. J Neural Transm 116: 1443–1449 [DOI] [PubMed] [Google Scholar]
  2. Augustin A.J., Puls S., Offermann I. (2007) Triple therapy for choroidal neovascularization due to age-related macular degeneration: Verteporfin PDT, bevacizumab, and dexamethasone. Retina 27: 133–140 [DOI] [PubMed] [Google Scholar]
  3. Avraamides C.J., Garmy-Sisini B., Varner J.A. (2008) Integrins in angiogenesis and lymphangiogenesis. Nat Rev Cancer 8: 604–617 [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Brantley M.A., Fang A.M., King J.M., Tewari A., Kymes S.M., Shiels A. (2007) Association of complement factor H and LOC387715 genotypes with response of exudative age-related macular degeneration to intravitreal bevacizumab. Ophthalmology 114: 2168–2173 [DOI] [PubMed] [Google Scholar]
  5. Bressler N.M., Arnold J., Benchaboune M., Blumenkranz M.S., Fish G.E., Gragoudas E.S., et al. (2002) Treatment of Age-Related Macular Degeneration with Photodynamic Therapy (TAP) Study Group. Verteporfin therapy of subfoveal choroidal neovascularization in patients with age-related macular degeneration: Additional information regarding baseline lesion composition's impact on vision outcomes. TAP Report No. 3. Arch Ophthalmol 120: 1443–1454 [DOI] [PubMed] [Google Scholar]
  6. Brown D.M., Kaiser P.K., Michels M., Soubrane G., Heier J.S., Kim R.Y., et al. for the ANCHOR Study Group. (2006) Ranibizumab versus verteporfin for neovascular age-related macular degeneration. N Engl J Med 355: 1432–1444 [DOI] [PubMed] [Google Scholar]
  7. Chakravarthy U., Augood C., Bentham G.C., de Jong P.T., Rahu M., Seland J., et al. (2007) Cigarette smoking and age-related macular degeneration in the EUREYE Study. Ophthalmology 114: 1157–1163 [DOI] [PubMed] [Google Scholar]
  8. Cukras C., Agron E., Klein M.L., Ferris F.L., III, Chew E.Y., Gensler G., et al. for the Age-Related Eye Disease Study Research Group. (2010) Natural history of drusenoid pigment epithelial detachment in age-related macular degeneration: Age-Related Eye Disease Study Report No. 28. Ophthalmology 117: 489–499 [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. DeWan A., Lui M., Hartman S., Zhang S.S., Liu D.T., Zhao C., et al. (2006) HTRA1 promoter polymorphism in wet age-related macular degeneration. Science 314: 989–992 [DOI] [PubMed] [Google Scholar]
  10. Edwards A.O., Ritter R., Abel K.J., Manning A., Panhuysen C., Farrer L.A. (2005) Complement factor H polymorphism and age-related macular degeneration. Science 308: 421–424 [DOI] [PubMed] [Google Scholar]
  11. Ferrara N., Davis-Smyth T. (1997) The biology of vascular endothelial growth factor. Endocr Rev 18: 4–25 [DOI] [PubMed] [Google Scholar]
  12. Finkel T., Holbrook N.J. (2000) Oxidants, oxidative stress and the biology of ageing. Nature 408: 239–247 [DOI] [PubMed] [Google Scholar]
  13. Fisher S.A., Abecasis G.R., Yashar B.M., Zareparsi S., Swaroop A., Iyengar S.K., et al. (2005) Meta-analysis of genome scans of age-related macular degeneration. Hum Mol Genet 14: 2257–2264 [DOI] [PubMed] [Google Scholar]
  14. Gaudreault J., Fei D., Rusit J., Suboc P., Shiu V. (2005) Preclinical pharmacokinetics of ranibizumab (rhuFabV2) after a single intravitreal administration. Invest Ophthalmol Vis Sci 46: 726–733 [DOI] [PubMed] [Google Scholar]
  15. Gold B., Merriam J.E., Zernant J., Hancox L.S., Taiber A.J., Gehrs K., et al. (2006) Variation in factor B (BF) and complement component 2 (C2) genes is associated with age-related macular degeneration. Nat Genet 38: 458–462 [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Gragoudas E.S., Adamis A., Cunningham E.T., Feinsod M., Guyer D.R. and for the VEGF Inhibition Study in Ocular Neovascularization Clinical Trial Group (2004) Pegaptanib for neovascular age-related macular degeneration. N Engl J Med 351: 2805–2816 [DOI] [PubMed] [Google Scholar]
  17. Haines J.L., Hauser M.A., Schmidt S., Scott W.K., Olson L.M., Gallins P., et al. (2005) Complement factor H variant increases the risk of age-related macular degeneration. Science 308: 419–421 [DOI] [PubMed] [Google Scholar]
  18. Haines J.L., Hauser M.A., Schmidt S., Scott W.K., Olson L.M., Gallins P., et al. (2005) Complement factor H variant increases the risk of age-related macular degeneration. Science 308: 419–421 [DOI] [PubMed] [Google Scholar]
  19. Ham W.T., Jr, Mueller H.A., Sliney D.H. (1976) Retinal sensitivity to damage from short wavelength light. Nature 260: 153–155 [DOI] [PubMed] [Google Scholar]
  20. Heier J.S., Boyer D.S., Ciulla T.A., Ferrone P.J., Jumper J.M., Gentile R.C., et al. for the FOCUS Study Group (2006) Ranibizumab combined with verteporfin photodynamic therapy in neovascular age-related macular degeneration: Year 1 results of the FOCUS Study. Arch Ophthalmol 124: 1532–1542, Erratum in: Arch Ophthalmol 2006; 125: 138. [DOI] [PubMed] [Google Scholar]
  21. Hughes A.E., Orr N., Esfandiary H., Diaz-Torres M., Goodship T., Chakravarthy U. (2006) A common CFH haplotype, with deletion of CFHR1 and CFHR3, is associated with lower risk of age-related macular degeneration. Nat Genet 38: 1173–1177 [DOI] [PubMed] [Google Scholar]
  22. Juan-Babot J.O., Martinez-Gonzalez J., Berrozpe M., Badimon L. (2003) Neovascularization in human coronary arteries with lesions of different severity. Rev Esp Cardiol 56: 978–986 [DOI] [PubMed] [Google Scholar]
  23. Khan J.C., Thurlby D.A., Shahid H., Clayton D.G., Yates J.R., Bradley M., et al. (2006) Genetic Factors in AMD Study. Smoking and age related macular degeneration: The number of pack years of cigarette smoking is a major determinant of risk for both geographic atrophy and choroidal neovascularisation. Br J Ophthalmol 90: 75–80 [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Klein R., Klein B.E., Linton K.L. (1992) Prevalence of age-related maculopathy. The Beaver Dam Eye Study. Ophthalmology 99: 933–943 [DOI] [PubMed] [Google Scholar]
  25. Lai T.Y. for the EVEREST Study Group (2010) Verteporfin PDT and ranibizumab combination therapy for symptomatic macular polypoidal choroidal vasculopathy (PCV): EVEREST results. Invest Ophthalmol Vis Sci 51: ARVO E—abstract 2228. [Google Scholar]
  26. Leveziel N., Zerbib J., Richard F., Querques G., Morineau G., Fremeaux-Bacchi V., et al. (2008) Genotype-phenotype correlations for exudative age-related macular degeneration associated with homo-zygous HTRA1 and CFH genotypes. Invest Ophthalmol Vis Sci 49: 3090–3094 [DOI] [PubMed] [Google Scholar]
  27. Ma X.M., Blenis J. (2009) Molecular mechanisms of mTOR-mediated translational control. Nat Rev Mol Cell Biol 10: 307–318 [DOI] [PubMed] [Google Scholar]
  28. Macular Photocoagulation Study Group. (1991) Argon laser photocoagulation for neovascular macu-lopathy. Five-year results from randomized clinical trials. Arch Ophthalmol 109: 1109–1114 [PubMed] [Google Scholar]
  29. Nguyen Q.D., Shah S.M., Browning D.J., Hudson H., Sonkin P., Hariprasad S.M., et al. (2009) A phase I study of intravitreal vascular endothelial growth factor trap-eye in patients with neovascular age-related macular degeneration. Ophthalmology 116: 2141–2148 [DOI] [PubMed] [Google Scholar]
  30. Owen C.G., Fletcher A.E., Donoghue M., Rudnicka A.R. (2003) How big is the burden of visual loss caused by age related macular degeneration in the United Kingdom?. Br J Ophthalmol 87: 312–317 [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Rakic J.M., Lambert V., Devy L., Lutton A., Carmeliet P., Claes C., et al. (2003) Placental growth factor, a member of the VEGF family, contributes to the development of choroidal neovascularization. Invest Ophthalmol Vis Sci 44: 3186–3193 [DOI] [PubMed] [Google Scholar]
  32. Rivera A., Fisher S.A., Fritsche L.G., Keilhauer C.N., Lichtner P., Meitinger T., et al. (2005) Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk. Hum Mol Genet 14: 3227–3236 [DOI] [PubMed] [Google Scholar]
  33. Rosenfeld P.J., Brown D.M., Heier J.S., Boyer D.S., Kaiser P.K., Chung C.Y., et al. (2006) Ranibizumab for neovascular age-related macular degeneration. N Engl J Med 355: 1419–1431 [DOI] [PubMed] [Google Scholar]
  34. Royal College of Ophthalmologists. (2009) Age-Related Macular Degeneration. Guidelines for Management, Royal College of Ophthalmologists: London [Google Scholar]
  35. Schmidt-Erfurth U.M., Gabel P., Hohman, T. for the PROTECT Study Group (2006) Preliminary results from an open-label, multicenter, phase II study assessing the effects of same-day administration of ranibizumab (Lucentis(TM)) and verteporfin PDT (PROTECT Study). In Program and Abstracts of the Association for Research in Vision and Ophthalmology, Fort Lauderdale, FL, 30 April-4 May, abstract 2960.
  36. Simons M. (2005) Angiogenesis: Where do we stand now?. Circulation 111: 1556–1566 [DOI] [PubMed] [Google Scholar]
  37. Singerman L.J. (2009) Advances in the management of dry age-related macular degeneration (AMD). Paper presented at the American Academy of Ophthalmology Annual Meeting, 24-27 October.
  38. Thornton J., Edwards R., Mitchell P., Harrison R.A., Buchan I., Kelly S.P., et al. (2005) Smoking and age-related macular degeneration: A review of associations. Eye 19: 935–944 [DOI] [PubMed] [Google Scholar]
  39. Tunón J., Ruiz-Moreno J.M., Martın-Ventura J.L., Blanco-Colio L.M., Lorenzo O., Egido J. (2009) Cardiovascular risk and antiangiogenic therapy for age-related macular degeneration. Surv Ophthalmol 54: 339–348 [DOI] [PubMed] [Google Scholar]
  40. Usui T., Ishida S., Yamashiro K., Kaji Y., Poulaki V., Moore J., et al. (2004) VEGF164(165) as the pathological isoform: Differential leukocyte and endothelial responses through VEGFR1 and VEGFR2. Invest Ophthalmol Vis Sci 45: 368–374 [DOI] [PubMed] [Google Scholar]
  41. Weger M., Renner W., Steinbrugger I., Köfer K., Wedrich A., Groselj-Strele A., et al. (2007) Association of the HTRA1-625 G>A promoter gene polymorphism with exudative age-related macular degeneration in a Central European population. Mol Vis 13: 1274–1279 [PubMed] [Google Scholar]
  42. Wong T., Chakravarthy U., Klein R., Mitchell P., Zlateva G., Buggage R., et al. (2008) The natural history and prognosis of neovascular age-related macular degeneration. A systematic review of the literature and meta-analysis. Ophthalmology 115: 116–126 [DOI] [PubMed] [Google Scholar]
  43. Yates J.R., Sepp T., Matharu B.K., Khan J.C., Thurlby D.A., Shahid H., et al. (2007) Complement C3 variant and the risk of age-related macular degeneration. N Engl J Med 357: 553–561 [DOI] [PubMed] [Google Scholar]

Articles from Therapeutic Advances in Chronic Disease are provided here courtesy of SAGE Publications

RESOURCES