Drusen

Drusen
Macular soft drusen in the right eye of a 70-year-old male.
Classification and external resources
Specialty ophthalmology
ICD-10 H35.3, H47.3
OMIM 126700 126600 611040 603075 134370
DiseasesDB 29371
eMedicine topic list

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. However, the presence of larger and more numerous drusen in the macula is a common early sign of age-related macular degeneration (AMD).

Classification

Drusen are associated with aging and macular degeneration are distinct from another clinical entity, optic disc drusen, which is present on the optic nerve head.[1] 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.[2]

'Hard drusen' may coalesce into 'soft drusen' which is a manifestation of macular degeneration.[3]

Pathophysiology

Drusen were initially described by Franciscus Donders[4] who called them "Colloidkugeln" (colloid spheres). Later, Heinrich Müller named them for the German word for geode, based on their glittering appearance.[5] 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;[6] although important variations are observed between different subtypes of AMD.

Drusen 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,[7] probably the most concentrated being zinc.[8] The protein composition of drusen includes apolipoproteins and oxidized proteins, likely originating from blood, RPE, and photoreceptors.[9] Drusen composition also includes members of the complement system. Zinc in drusen have been suggested to play a role in drusen formation by precipitating and inhibiting the elements of the complement cascade, especially complement factor H.[8]

The presence of molecules that regulate inflammation in drusen has led some investigators to conclude that these deposits are product of the immune system.[10]

See also

Notes

  1. ↑ Davis PL, Jay WM (December 2003). "Optic nerve head drusen". Semin Ophthalmol. 18 (4): 222–42. PMID 15513010. doi:10.1080/08820530390895244.
  2. ↑ "Age-Related Macular Degeneration". National Eye Institute. March 2008. Retrieved 2008-05-21.
  3. ↑ http://www.agingeye.net/maculardegen/maculardegeninformation.php
  4. ↑ Donders FC (March 1855). "Beitrage zur pathologischen Anatomie des Auges". Graefes Arch Clin Exp Ophthalmol. 1 (2): 106–18. doi:10.1007/BF02720791.
  5. ↑ Müller H (January 1856). "Anatomische Beiträge zur Ophthalmologie - 1) 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.
  6. ↑ Lengyel I, Tufail A, Hosaini HA, Luthert P, Bird AC, Jeffery G (September 2004). "Association of drusen deposition with choroidal intercapillary pillars in the aging human eye". Invest. Ophthalmol. Vis. Sci. 45 (9): 2886–92. PMID 15326099. doi:10.1167/iovs.03-1083.
  7. ↑ van der Schaft TL, de Bruijn WC, Mooy CM, Ketelaars DA, de Jong PT (March 1992). "Element analysis of the early stages of age-related macular degeneration". Arch. Ophthalmol. 110 (3): 389–94. PMID 1543459. doi:10.1001/archopht.1992.01080150087034.
  8. 1 2 Lengyel I, Flinn JM, Peto T, et al. (April 2007). "High concentration of zinc in sub-retinal pigment epithelial deposits". Exp. Eye Res. 84 (4): 772–80. PMID 17313944. doi:10.1016/j.exer.2006.12.015.
  9. ↑ Crabb JW, Miyag M, Gu X, Shadrach K, West KA, Sakaguchi H, Kamei M, Hasan A, Yan L, Rayborn ME, Salomon RG, Hollyfield JG (November 12, 2002). "Drusen proteome analysis: An approach to the etiology of age-related macular degeneration". Proc Natl Acad Sci U S A. 99 (23): 14682–7. PMID 12391305. doi:10.1073/pnas.222551899.
  10. ↑ Hageman GS, Luthert PJ, Victor Chong NH, Johnson LV, Anderson DH, Mullins RF (November 2001). "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. PMID 11587915. doi:10.1016/S1350-9462(01)00010-6.
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