Drusen

File:Macular Soft Drusen.jpg
Macular soft drusen in the right eye of a 70-year-old male.
Macular hard drusen in the right eye. 65-year-old diabetic woman.

Drusen, from the German word for node or geode (singular, "Druse"), are tiny yellow or white accumulations of extracellular material that build up between Bruch's membrane and the retinal pigment epithelium of the eye. The presence of a few small ("hard") drusen is normal with advancing age, and most people over 40 have some hard drusen.[1] However, the presence of larger and more numerous drusen in the macula is a common early sign of age-related macular degeneration (AMD).

## Contents

* 1 Classification
* 2 Pathophysiology
* 3 Diagnosis
* 4 Treatment
* 5 See also
* 6 Notes

## Classification

Drusen associated with aging and macular degeneration are distinct from another clinical entity, optic disc drusen, which is present on the optic nerve head.[2] Both age-related drusen and optic disc drusen can be observed by ophthalmoscopy. Optical coherence tomography scans of the orbits or head, calcification at the head of the optic nerve without change in size of globe strongly suggests drusen in a middle-age or elderly patient.

Whether drusen promote AMD or are symptomatic of an underlying process that causes both drusen and AMD is not known, but they are indicators of increased risk of the complications of AMD.[3]

'Hard drusen' may coalesce into 'soft drusen' which is a manifestation of macular degeneration.[4]

## Pathophysiology

Around 1850, three authors, Carl Wedl, Franciscus Donders, and Heinrich Müller, gave drusen different labels. Drusen, the hallmark of AMD, were first described in 1854 by Wedl.[5] Wedl named them colloid bodies of the choroid and thought that they were incompletely developed cells. Franciscus Donders[6] called them "Colloidkugeln" (colloid spheres). Later, Heinrich Müller named them by the German word for geode, based on their glittering appearance.[7] He was convinced that drusen originated from the nuclei of the pigment cells, which he believed to belong to the choroid.[8] In view of their location between the retinal pigment epithelium (RPE) and its vascular supply, the choriocapillaris, it is possible that drusen deprive the RPE and photoreceptor cells of oxygen and nutrients. In some cases, drusen develop above the so-called pillars of the choriocapillaris that is the area between two micro vessels;[9] although important variations are observed between different subtypes of AMD.

File:Drusen in OCT.pngDrusen in optical coherence tomography.

The source of the proteins and lipids in drusen is also not clear, with potential contributions by both the RPE and the choroid. Several trace elements are present in drusen,[10] probably the most concentrated being zinc.[11] The protein composition of drusen includes apolipoproteins and oxidized proteins, likely originating from blood, RPE, and photoreceptors.[12] Drusen composition also includes members of the complement system. Zinc in drusen has been suggested to play a role in drusen formation by precipitating and inhibiting the elements of the complement cascade, especially complement factor H.[11]

The presence of molecules that regulate inflammation in drusen has led some investigators to conclude that these deposits are product of the immune system.[13]

## Diagnosis

Usually being asymptomatic, drusen are typically found during routine eye exams where the pupils have been dilated.[14]

## Treatment

Laser treatment of drusen has been studied. While it is possible to eliminate drusen with this treatment strategy, it has been shown that this fails to reduce the risk of developing the choroidal neovascularisation which causes the blindness associated with age-related macular degeneration.[15]

## See also

* Optic disc drusen

## Notes

1. ↑ "Drusen prevalence and pigmentary changes in Caucasians aged 18-54 years". Eye (Lond) 26 (10): 1357–62. 2012. doi:10.1038/eye.2012.165. PMID 22899005.
2. ↑ "Optic nerve head drusen". Semin Ophthalmol 18 (4): 222–42. December 2003. doi:10.1080/08820530390895244. PMID 15513010.
3. ↑ "Age-Related Macular Degeneration". National Eye Institute. March 2008. http://www.nei.nih.gov/health/maculardegen/armd_facts.asp.
4. ↑ "Macular Degeneration types and risk factors". http://www.agingeye.net/maculardegen/maculardegeninformation.php.
5. ↑ Wedl C. Grundzüge der pathologischen Histologie Wien: Gerold, C; 1854
6. ↑ Donders FC (March 1855). "Beitrage zur pathologischen Anatomie des Auges". Graefes Arch Clin Exp Ophthalmol 1 (2): 106–18. doi:10.1007/BF02720791.
7. ↑ Müller H (January 1856). "Anatomische Beiträge zur Ophthalmologie – Untersuchungen über die Glashäute des Auges, insbesondere die Glaslamelle der Chorioidea und ihre senilen Veränderungen". Graefes Arch Clin Exp Ophthalmol 2 (2): 1–69. doi:10.1007/BF02720657.
8. ↑ de Jong PT. A Historical Analysis of the Quest for the Origins of Aging Macula Disorder, the Tissues Involved, and Its Terminology. Ophthalmol Eye Dis. 2016;8(Suppl 1):5-14. Published 2016 Nov 1. doi:10.4137/OED.S40523
9. ↑ "Association of drusen deposition with choroidal intercapillary pillars in the aging human eye". Invest. Ophthalmol. Vis. Sci. 45 (9): 2886–92. September 2004. doi:10.1167/iovs.03-1083. PMID 15326099. https://discovery.ucl.ac.uk/8034/1/8034.pdf.
10. ↑ "Element analysis of the early stages of age-related macular degeneration". Arch. Ophthalmol. 110 (3): 389–94. March 1992. doi:10.1001/archopht.1992.01080150087034. PMID 1543459.
11. ↑ 11.0 11.1 "High concentration of zinc in sub-retinal pigment epithelial deposits". Exp. Eye Res. 84 (4): 772–80. April 2007. doi:10.1016/j.exer.2006.12.015. PMID 17313944.
12. ↑ "Drusen proteome analysis: An approach to the etiology of age-related macular degeneration". Proc Natl Acad Sci USA 99 (23): 14682–87. November 12, 2002. doi:10.1073/pnas.222551899. PMID 12391305.
13. ↑ "An integrated hypothesis that considers drusen as biomarkers of immune-mediated processes at the RPE-Bruch's membrane interface in aging and age-related macular degeneration". Prog Retin Eye Res 20 (6): 705–32. November 2001. doi:10.1016/S1350-9462(01)00010-6. PMID 11587915.
14. ↑ "Drusen Diagnosis and Treatment". 4 March 2021. https://www.aao.org/eye-health/diseases/drusen-diagnosis.
15. ↑ "Laser treatment of drusen to prevent progression to advanced age-related macular degeneration". Cochrane Database Syst Rev 2015 (10): CD006537. 2015. doi:10.1002/14651858.CD006537.pub3. PMID 26493180.

Mishra S, Goel S, Roy SS, Garg B, Parvin M, Saurabh K, Roy R. Multimodal imaging characteristics of refractile drusen. Indian journal of ophthalmology. 2019 Jan;67(1):128.

Classification|

* ICD-10: H35.3, H47.3
* OMIM: 126700 Online Mendelian Inheritance in Man (OMIM) 126600 Online Mendelian Inheritance in Man (OMIM) 611040 Online Mendelian Inheritance in Man (OMIM) 603075 Online Mendelian Inheritance in Man (OMIM) 134370
* DiseasesDB: 29371

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External resources|

* eMedicine: search/Drusen

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