Next Article in Journal
The Serum Profile of Transferrin Isoforms in Pancreatitis
Next Article in Special Issue
Subthreshold Exudative Choroidal Neovascularization (CNV): Presentation of This Uncommon Subtype and Other CNVs in Age-Related Macular Degeneration (AMD)
Previous Article in Journal
Chest X-ray Does Not Predict the Risk of Endotracheal Intubation and Escalation of Treatment in COVID-19 Patients Requiring Noninvasive Respiratory Support
Previous Article in Special Issue
Monthly Alternating Injections of Aflibercept and Bevacizumab for Neovascular Age-Related Macular Degeneration
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Case Report

Complete Resolution of Central Soft Drusen without Geographic Atrophy or Choroidal Neovascularization

1
Harvard Retinal Imaging Lab, Boston, MA 02114, USA
2
Retina Service, Massachusetts Eye and Ear, Department of Ophthalmology, Harvard Medical School, Boston, MA 02114, USA
*
Author to whom correspondence should be addressed.
J. Clin. Med. 2022, 11(6), 1637; https://doi.org/10.3390/jcm11061637
Submission received: 31 December 2021 / Revised: 3 March 2022 / Accepted: 14 March 2022 / Published: 16 March 2022

Abstract

:
The treatment and prevention of dry age-related macular degeneration (AMD) traditionally involve lifestyle modifications and antioxidant supplementation, including the AREDS2 formula. We present a case of a woman with dry AMD in her right eye with several large, confluent central drusen on her exam and optical coherence tomography B-scan. Over the course of a year, the drusen almost completely disappeared, but the retinal layers were preserved without the development of geographic atrophy or choroidal neovascularization. While the exact cause of this phenomenon is unclear, it was thought to be associated with this patient’s strict daily use of numerous dietary supplements. This case highlights the potential in exploring alternative medicine supplements in the treatment of AMD.

1. Introduction

Age-related macular degeneration (AMD) is the leading cause of irreversible vision loss in individuals 50 years of age or older in the developed world. Drusen are a clinical hallmark of AMD, as excess drusen lead to inflammation and damage of the retinal pigmentary epithelium (RPE) [1]. The advancement of AMD is marked by the development of geographic atrophy (GA) and/or choroidal neovascularization (CNV) due to the expression of angiogenic cytokines such as vascular endothelial growth factor (VEGF) [2]. Dry AMD is characterized by the presence of drusen, with the development of RPE changes and GA in more advanced stages, while wet AMD is defined by the presence of choroidal neovascularization and subretinal fluid or hemorrhage. Whereas wet AMD is commonly treated with anti-VEGF injections, current management of dry AMD is more conservative, including lifestyle modifications and antioxidant supplementation [1]. Herein, we report a unique case of a woman with dry AMD, who used an extensive list of daily dietary supplements and experienced the dramatic resolution of several large, central soft drusen over the course of a year without the development of GA or CNV.

2. Case Presentation

A 64 -year-old Caucasian woman presented for an annual follow-up of dry AMD in her right eye and wet AMD in her left eye. At her last appointment, both eyes were noted to have remained in stable condition since the last Avastin injection of her left eye three years before. At this current appointment, Snellen’s visual acuity (VA) of her right eye improved from 20/50+1 to 20/20−2, while VA in her left eye improved from 20/40+2 to 20/25+1. Of note, she had just undergone a cataract extraction in her right eye three weeks ago. Fundus exam was significant for a dramatic improvement in several large central, soft drusen in the right eye without evidence of subretinal fluid or hemorrhage. Baseline spectral-domain OCT (SD-OCT, SPECTRALIS® Heidelberg), taken a year prior, had shown the presence of large, central drusen with disruption of the outer nuclear layer (ONL) and external limiting membrane (ELM). (Figure 1a). These findings were confirmed on fundus autofluorescence (FAF), which showed a focal area of hyperfluorescence, corresponding to diffuse drusen. (Figure 2) At the current visit, SD-OCT confirmed dramatic regression of the drusen with preservation of the retinal layers, including the ONL. Some hyperreflective material at the level of the ONL can be seen and may represent the retention of material deposits. (Figure 1c) FAF images were not available for this current visit.
Fundus exam of the left eye was stable from the previous visit and showed large and intermediate drusen in a nummular pattern, with collapsed PED and focal atrophy. SD-OCT and FAF confirmed these findings. (Figure 1b,d and Figure 2 e–h)
Upon further questioning, the patient denied leading a particularly healthy lifestyle between her two visits. She revealed that she was a devout Christian and prayed regularly. Lastly, the patient divulged her extensive list of daily dietary supplements (Table 1), prescribed by her long-time orthomolecular specialist.

3. Discussion

This is a single case of a patient with near-complete resolution of central large, soft, confluent drusen with preservation of the retinal layers. While drusen resolution is generally regarded as beneficial for the AMD patient, its utility as a clinical trial endpoint is controversial, as not all cases of drusen regression are associated with VA improvement [2]. Drusen regression may occur spontaneously but most often precedes the appearance of new deposits or accompanies progression to late-stage AMD [2]. Progression to GA is more common than progression to choroidal neovascularization [2]. Only ~7% of drusen-only eyes demonstrate significant spontaneous regression without GA or CNV within 24 months [2].
Drusen regression without GA or CNV development has been noted after coincidental rhegmatogenous retinal detachment after vitrectomy with inner limiting membrane peel [3]. This phenomenon was attributed to the elimination of lipophilic material by a large volume of sub-retinal fluid, and stimulation of phagocytosis by surgery, respectively. Treatment with high-dose statins, as well as treatment with low energy photocoagulation and anti-VEGF, has been shown to induce drusen regression without the development of GA and with VA improvement [4,5]. Lastly, subthreshold nanosecond laser was also shown in a pilot study to provoke significant drusen reduction with improved visual function [6]. Although this patient’s VA improvement is confounded by her recent cataract surgery, the resolution of her central confluent drusen on clinical exam and imaging is striking. We were not able to obtain further follow-up from the patient, which may have been useful to confirm the lack of GA and CNV development in a longer time interval.
The exact reason for this patient’s drusen resolution is not completely understood. Aside from recent cataract surgery, the patient had not undergone any other intraocular surgeries, injections, or procedures. She did not take any statins. The dramatic regression of her drusen is especially interesting in the context of her cataract surgery, given that there is some thought that cataract surgery may exacerbate the progression to exudative AMD given its inflammatory effects. This effect is not confirmed, however, as recent reviews have been either inconclusive [7] or unable to find an association between the two [8].
Another possible reason for this phenomenon could be attributed to the patient’s diligent and extensive use of daily dietary supplements. Several of the patient’s supplements, such as lutein, zeaxanthin, Vitamin C and zinc, overlap with the AREDS2 formula, which has been shown to reduce progression to late AMD [9]. Notably, the patient does not take Vitamin E or copper, which are included in the AREDS2 formula [10]. Thus, it is important to consider the role of dietary supplements in the treatment of AMD, given the growing research interest in the role of microbiome and metabolome in this condition [11,12].
Carotenoids, such as lutein, zeaxanthin, and astaxanthin, exert antioxidant, anti-inflammatory and antiapoptotic activities. Thus, supplementation with carotenoids has been shown to reduce CNV risk and improve visual function, including visual acuity, contrast sensitivity and glare disability [13]. Meanwhile, there is evidence that antioxidants, vitamin C, magnesium, and zinc, can slow the progression of AMD [11], but literature regarding their efficacy is mixed [9,14]. Similarly, Vitamin A and D3, also on this patient’s list, have yielded positive but inconsistent studies regarding their efficacy in AMD prevention and treatment [9].
Other supplements on the patient’s list are promising for potential AMD treatments but still need further investigation. Vitamin K2 is implicated in age-related diseases [15]; however, to date, there is no published literature demonstrating its role in AMD treatment. Additionally, alpha-lipoic acid has also been studied in AMD treatment, showing some potential with evidence of antioxidant activity and possible improvement in visual function and quality of life [16,17]. However, its use is limited by gastrointestinal upset issues and failed to show improvement in visual acuity or GA in a recent clinical trial [18]. The last two supplements on the patient’s list—taurine and N-acetylcysteine—have both been shown to have a potential therapeutic effect on human donor RPE cells [19,20]. However, further investigation is needed to ascertain the clinical efficacy of these supplements on AMD treatment.
Beyond this patient’s list, other natural medicine supplements also demonstrate promise. Curcumin has been shown to be neuroprotective [21], with curcumin-based nutritional supplements showing potential to reduce injection burden in patients with wet AMD [22]. Moreover, given increasing evidence of the association between the intestinal microbiota and AMD, further exploration of probiotic treatment in this condition may also be fruitful.
If dietary supplements did contribute significantly to this phenomenon, the unilateral nature of this patient’s improvement should be discussed. Given that AMD is a heterogeneous disease with a variety of phenotypes, with varying sizes and types of drusen [23], it is important to note that the patient’s improvement in the right eye was limited to the central soft, and confluent drusen while some smaller, non-foveal drusen remained. In contrast, the same large and confluent drusen were not apparent in the left eye. In a pilot study of high-dose statins in AMD treatment, Vavvas et al. concluded the medication might have a particular role in a certain subset of AMD patients—namely, those with intermediate-high risk, large drusenoid deposits [5]. Likewise, dietary supplements may play a similar role in benefitting this specific subtype of AMD.

4. Conclusions

We describe a rare case of complete resolution of drusen in a patient with dry AMD. The exact treatment modality leading to this extent of dramatic improvement is mysterious and has not been reported before. Considering the morbidity related to the blindness associated with dry AMD, the authors believe this case can be an important step in exploring the efficacy of alternative modalities of treatment as a part of a multi-disciplinary approach via larger sample-sized controlled clinical trials.

Author Contributions

R.Z. described the case, collected the clinical data, and drafted the manuscript. I.G. helped draft and format the manuscript. J.B.M. performed overall supervision. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Written informed consent has been obtained from the patient to publish this paper.

Conflicts of Interest

J.B.M. is a consultant for Alcon, Allergan, Carl Zeiss, Sunovion and Genentech.

References

  1. Jager, R.D.; Mieler, W.F.; Miller, J. Age-Related macular degeneration. N. Engl. J. Med. 2008, 358, 2606–2617. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  2. Yehoshua, Z.; Wang, F.; Rosenfeld, P.J.; Penha, F.; Feuer, W.J.; Gregori, G. Natural history of drusen morphology in age-related macular degeneration using spectral domain optical coherence tomography. Ophthalmology 2011, 118, 2434–2441. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Dithmar, S.; Pollithy, S.; Ach, T. Disappearance of central confluent soft drusen following vitrectomy and ILM peeling. Eye 2013, 27, 779–781. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Kim, M.S.; Ryoo, N.-K.; Park, K.H. Laser and anti-vascular endothelial growth factor treatment for drusenoid pigment epithelial detachment in age-related macular degeneration. Sci. Rep. 2020, 10, 14370. [Google Scholar] [CrossRef] [PubMed]
  5. Vavvas, D.G.; Daniels, A.B.; Kapsala, Z.G.; Goldfarb, J.W.; Ganotakis, E.; Loewenstein, J.I.; Young, L.; Gragoudas, E.S.; Eliott, D.; Kim, I.; et al. Regression of some high-risk features of age-related macular degeneration (AMD) in patients receiving intensive statin treatment. EBioMedicine 2016, 5, 198–203. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Querques, G.; Sacconi, R.; Gelormini, F.; Borrelli, E.; Prascina, F.; Zucchiatti, I.; Querques, L.; Bandello, F. Subthreshold laser treatment for reticular pseudodrusen secondary to age-related macular degeneration. Sci. Rep. 2021, 11, 2193. [Google Scholar] [CrossRef] [PubMed]
  7. Casparis, H.; Lindsley, K.; Kuo, I.C.; Sikder, S.; Bressler, N.M. Surgery for cataracts in people with age-related macular degeneration. Cochrane Database Syst. Rev. 2012, 6, CD006757. [Google Scholar] [CrossRef] [Green Version]
  8. Kessel, L.; Erngaard, D.; Flesner, P.; Andresen, J.; Tendal, B.; Hjortdal, J. Cataract surgery and age-related macular degeneration. An evidence-based update. Acta Ophthalmol. 2015, 93, 593–600. [Google Scholar] [CrossRef] [PubMed]
  9. Agrón, E.; Mares, J.; Clemons, T.E.; Swaroop, A.; Chew, E.Y.; Keenan, T.D. Dietary nutrient intake and progression to late age-related macular degeneration in the age-related eye disease studies 1 and 2. Ophthalmology 2021, 128, 425–442. [Google Scholar] [CrossRef] [PubMed]
  10. Chew, E.Y.; Clemons, T.; SanGiovanni, J.P.; Danis, R.; Domalpally, A.; McBee, W.; Sperduto, R.; Ferris, F. The age-related eye disease study 2 (AREDS2). Ophthalmology 2012, 119, 2282–2289. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  11. Rinninella, E.; Mele, M.C.; Merendino, N.; Cintoni, M.; Anselmi, G.; Caporossi, A.; Gasbarrini, A.; Minnella, A.M. The role of diet, micronutrients and the gut microbiota in age-related macular degeneration: New Perspectives from the gut—Retina axis. Nutrients 2018, 10, 1677. [Google Scholar] [CrossRef] [Green Version]
  12. Brown, C.N.; Green, B.D.; Thompson, R.B.; Hollander, A.I.D.; Lengyel, I.; on behalf of the EYE-RISK consortium. Metabolomics and Age-Related Macular Degeneration. Metabolites 2018, 9, 4. [Google Scholar] [CrossRef] [Green Version]
  13. Giannaccare, G.; Pellegrini, M.; Senni, C.; Bernabei, F.; Scorcia, V.; Cicero, A.F.G. Clinical applications of astaxanthin in the treatment of ocular diseases: Emerging insights. Mar. Drugs 2020, 18, 239. [Google Scholar] [CrossRef] [PubMed]
  14. Khoo, H.E.; Ng, H.S.; Yap, W.-S.; Goh, H.J.H.; Yim, H.S. Nutrients for prevention of macular degeneration and eye-related diseases. Antioxidants 2019, 8, 85. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  15. Simes, D.C.; Viegas, C.S.B.; Araújo, N.; Marreiros, C. Vitamin K as a diet supplement with impact in human health: Current evidence in age-related diseases. Nutrients 2020, 12, 138. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  16. Tao, Y.; Jiang, P.; Wei, Y.; Wang, P.; Sun, X.; Wang, H. α-Lipoic acid treatment improves vision-related quality of life in patients with dry age-related macular degeneration. Tohoku J. Exp. Med. 2016, 240, 209–214. [Google Scholar] [CrossRef] [Green Version]
  17. Sun, Y.-D.; Dong, Y.-D.; Zhai, L.-L.; Fan, R.; Bai, Y.-L.; Jia, L.-H. Effect of (R)-α-Lipoic acid supplementation on serum lipids and antioxidative ability in patients with age-related macular degeneration. Ann. Nutr. Metab. 2012, 60, 293–297. [Google Scholar] [CrossRef]
  18. Kim, B.J.; Hunter, A.; Brucker, A.J.; Hahn, P.; Gehrs, K.; Patel, A.; Edwards, A.O.; Li, Y.; Khurana, R.N.; Nissim, I.; et al. Orally administered alpha lipoic acid as a treatment for geographic atrophy. Ophthalmol. Retin. 2020, 4, 889–898. [Google Scholar] [CrossRef]
  19. Shin, E.Y.; Park, J.H.; Shin, M.E.; Song, J.E.; Thangavelu, M.; Carlomagno, C.; Motta, A.; Migliaresi, C.; Khang, G. Injectable taurine-loaded alginate hydrogels for retinal pigment epithelium (RPE) regeneration. Mater. Sci. Eng. C 2019, 103, 109787. [Google Scholar] [CrossRef]
  20. Terluk, M.R.; Ebeling, M.C.; Fisher, C.R.; Kapphahn, R.J.; Yuan, C.; Kartha, R.V.; Montezuma, S.R.; Ferrington, D.A. N-Acetyl-L-cysteine protects human retinal pigment epithelial cells from oxidative damage: Implications for age-related macular degeneration. Oxidative Med. Cell. Longev. 2019, 2019, 5174957. [Google Scholar] [CrossRef] [Green Version]
  21. Baum, L.; Lam, C.W.K.; Cheung, S.K.-K.; Kwok, T.; Lui, V.; Tsoh, J.; Lam, L.; Leung, V.; Hui, E.; Ng, C.; et al. Six-Month randomized, placebo-controlled, double-blind, pilot clinical trial of curcumin in patients with alzheimer disease. J. Clin. Psychopharmacol. 2008, 28, 110–113. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. Allegrini, D.; Raimondi, R.; Angi, M.; Ricciardelli, G.; Montericcio, A.; Borgia, A.; Romano, M.R. Curcuma-Based nutritional supplement in patients with neovascular age-related macular degeneration. J. Med. Food 2021, 24, 1191–1196. [Google Scholar] [CrossRef] [PubMed]
  23. Miller, J.W. Age-Related Macular Degeneration Revisited—Piecing the puzzle: The LXIX Edward Jackson Memorial Lecture. Am. J. Ophthalmol. 2013, 155, 1–35.e13. [Google Scholar] [CrossRef] [PubMed]
Figure 1. SPECTRALIS® Heidelberg OCT B-scans showed (a) presence of several large central, soft, confluent drusen in the right eye and (b) collapsed PED and subretinal material without fluid in the left eye. One year later, follow-up B-scan of the (c) right eye showed dramatic, complete drusen regression centrally, without geographic atrophy or choroidal neovascularization. (d) Corresponding follow-up B-scan of the left eye showed no changes.
Figure 1. SPECTRALIS® Heidelberg OCT B-scans showed (a) presence of several large central, soft, confluent drusen in the right eye and (b) collapsed PED and subretinal material without fluid in the left eye. One year later, follow-up B-scan of the (c) right eye showed dramatic, complete drusen regression centrally, without geographic atrophy or choroidal neovascularization. (d) Corresponding follow-up B-scan of the left eye showed no changes.
Jcm 11 01637 g001
Figure 2. SPECTRALIS® Heidelberg multicolor (a,e) and fundus autofluorescence with near-infrared (b,f), blue (c,g), and green (d,h) reflectance taken one year prior showed focal areas of hyperfluorescence corresponding to diffuse drusen in both eyes. Multicolor and autofluorescence images were not available for the current visit.
Figure 2. SPECTRALIS® Heidelberg multicolor (a,e) and fundus autofluorescence with near-infrared (b,f), blue (c,g), and green (d,h) reflectance taken one year prior showed focal areas of hyperfluorescence corresponding to diffuse drusen in both eyes. Multicolor and autofluorescence images were not available for the current visit.
Jcm 11 01637 g002
Table 1. Daily dietary supplements prescribed to patient by orthomolecular medicine specialist.
Table 1. Daily dietary supplements prescribed to patient by orthomolecular medicine specialist.
Supplements Prescribed for AMDOther Supplements
SupplementDosageFrequencySupplementDosageFrequency
Vitamin D35000 IU4/dayNutrient 950 (no copper, no iron)1 cap2/day
Vitamin A10,000 IU1/dayMagtein667 mg7/day
Vitamin K2100 mcg6/dayCoenzyme Q10200 mg3/day
Ascorbyl Palmitate450 mg4/daySynthroid50 mcg2/day
(Vitamin C)Sodium ascorbateteaspoon3/4 for bfast, 1/2 for dinner
Astaxanthin4 mg2/dayAlpha Lipoic Acid600 mg1/day
Lutein20 mg4/dayEnteric coated aspirin81 mg1/day
Taurine500 mg4/dayMSM1000 mg4/day
Zeaxanthin4mg4/dayGlucosamine sulfate750 mg3/day
Magnesium Lethreonate667 mg8/dayQuercetinunknown
Zinc30 mg2/dayIodoral (Optomax)12.5 mg2/day
NAC (Swanson)600 mg2/dayPotassium citrate99 mg5/day
Sea salt 1/2 teaspoon per day on food
Melatonin10 mg
Turmeric 2/day
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Zeng, R.; Garg, I.; Miller, J.B. Complete Resolution of Central Soft Drusen without Geographic Atrophy or Choroidal Neovascularization. J. Clin. Med. 2022, 11, 1637. https://doi.org/10.3390/jcm11061637

AMA Style

Zeng R, Garg I, Miller JB. Complete Resolution of Central Soft Drusen without Geographic Atrophy or Choroidal Neovascularization. Journal of Clinical Medicine. 2022; 11(6):1637. https://doi.org/10.3390/jcm11061637

Chicago/Turabian Style

Zeng, Rebecca, Itika Garg, and John B. Miller. 2022. "Complete Resolution of Central Soft Drusen without Geographic Atrophy or Choroidal Neovascularization" Journal of Clinical Medicine 11, no. 6: 1637. https://doi.org/10.3390/jcm11061637

APA Style

Zeng, R., Garg, I., & Miller, J. B. (2022). Complete Resolution of Central Soft Drusen without Geographic Atrophy or Choroidal Neovascularization. Journal of Clinical Medicine, 11(6), 1637. https://doi.org/10.3390/jcm11061637

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop