Choroid: Difference between revisions

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== Blood supply ==
== Blood supply ==
There are two circulations of the eye: the retinal (in the retina) and [[uvea]]l, supplied in humans by [[Ciliary arteries|posterior ciliary arteries]], originating from the [[ophthalmic artery]] (a branch of the [[internal carotid artery]]).<ref>[https://www.ncbi.nlm.nih.gov/books/NBK53329/ The Ocular Circulation]</ref> The arteries of the [[uvea]]l circulation, supplying the [[uvea]] and outer and middle layers of the retina, are branches of the ophthalmic artery and enter the eyeball without passing with the optic nerve. The retinal circulation, on the other hand, derives its circulation from the central retinal artery, also a branch of the ophthalmic artery, but passing in conjunction with the optic nerve.<ref name="eb">"Sensory Reception:  Human Vision: Structure and function of the Human Eye" vol. 27, p. 174  Encyclopædia Britannica,  1987</ref>  They branch in a segmental distribution to end arterioles and not [[anastomoses]]. This is clinically significant for diseases affecting  choroidal blood supply. The [[macula]] responsible for central vision and  the anterior part of the [[optic nerve]] are dependent on choroidal blood supply.<ref>{{cite journal | doi = 10.1136/bjo.59.11.631 | last1 = Hayreh | first1 = SS. |name-list-style=vanc |date=November 1975 | title = Segmental nature of the choroidal vasculature | journal = Br J Ophthalmol | volume = 59 | issue = 11| pages = 631–648 | pmid = 812547 | pmc = 1017426 }}</ref> The structure of choroidal vessels can be revealed by [[optical coherence tomography]], and blood flow can be revealed by [[Indocyanine green angiography]], and [[laser Doppler imaging]].<ref>Puyo, Léo, Michel Paques, Mathias Fink, José-Alain Sahel, and Michael Atlan. "Choroidal vasculature imaging with laser Doppler holography." Biomedical optics express 10, no. 2 (2019): 995–1012.</ref>
The human eye is supplied by two largely distinct vascular systems: the '''retinal circulation''', which nourishes the inner retina, and the '''uveal circulation''' (choroidal, ciliary body and iris), which nourishes the [[uvea]] and the outer retina (via the [[choroid]]). Both systems arise primarily from the [[ophthalmic artery]], a branch of the [[internal carotid artery]].<ref name="KielOcularCirc">{{Cite book|title=The Ocular Circulation|author=Kiel JW|publisher=NCBI Bookshelf|url=https://www.ncbi.nlm.nih.gov/books/NBK53329/|access-date=2025-12-24}}</ref>
 
The uveal circulation is supplied mainly by the [[Ciliary arteries|posterior ciliary arteries]] (short and long), which enter the globe independently of the [[optic nerve]]. These arteries provide the dominant blood supply to the choroid and contribute importantly to perfusion of the [[optic nerve head]] (including the anterior portion of the optic nerve).<ref name="Hayreh1975">{{cite journal |doi=10.1136/bjo.59.11.631 |last1=Hayreh |first1=S. S. |date=November 1975 |title=Segmental nature of the choroidal vasculature |journal=British Journal of Ophthalmology |volume=59 |issue=11 |pages=631–648 |pmid=812547 |pmc=1017426}}</ref>
The retinal circulation derives primarily from the [[central retinal artery]], which travels within the optic nerve and enters the eye at the [[optic disc]]. It then branches over the inner retinal surface into arterioles and capillaries supplying the nerve fiber and inner retinal layers.<ref name="KielOcularCirc" />
 
Retinal arteries behave as functional '''end-arteries''' with limited collateralization; consequently, focal obstruction can produce sectoral retinal ischemia. By contrast, the choroid exhibits a '''segmental''' vascular organization, and regional perfusion territories supplied by posterior ciliary arteries are clinically relevant because the [[macula]] and the anterior optic nerve (structures critical for central vision) depend strongly on choroidal perfusion.<ref name="Hayreh1975" />
 
=== Imaging the choroid and its blood flow ===
 
[[File:LDHvsICG.jpg|thumb|left|400px|Choroidal blood-flow contrast revealed with [[indocyanine green angiography]] (Spectralis, Heidelberg) and [[Laser Doppler holography]] (LDH).<ref name="Puyo2020STF" />]]
 
Structural features of the choroid can be assessed with [[optical coherence tomography]] (OCT), while choroidal vascular contrast is classically obtained with [[indocyanine green angiography]] (ICGA), an invasive dye-based method that is relatively robust for deeper choroidal vessels. [[Optical coherence tomography angiography]] (OCTA) provides non-invasive motion-contrast maps but can be limited by depth-dependent sensitivity, segmentation/projection artifacts, and reduced sensitivity for very slow flow or deeper large vessels.
 
[[File:Real-time fisheye Doppler holography of choroidal blood-flow.gif|thumb|right|Choroidal and retinal blood-flow imaging by real-time fisheye [[Laser Doppler holography]] (LDH).]]
 
Laser-Doppler–based approaches provide an additional, non-invasive route to choroidal flow contrast. In ophthalmology, [[Laser Doppler holography]] (LDH) is a full-field, camera-based implementation that uses [[digital holography]] and temporal demodulation of reconstructed optical fluctuations to generate Doppler power maps that highlight blood-flow–related signals in retinal and choroidal vessels.<ref name="Puyo2019Choroid">{{Cite journal|doi=10.1364/BOE.10.000995|doi-access=free|title=Choroidal vasculature imaging with laser Doppler holography|year=2019|last1=Puyo|first1=Léo|last2=Paques|first2=Michel|last3=Fink|first3=Mathias|last4=Sahel|first4=José-Alain|last5=Atlan|first5=Michael|journal=Biomedical Optics Express|volume=10|issue=2|pages=995–1012|pmid=30800528|pmc=6377881|arxiv=2106.00608}}</ref>
 
Signal-processing refinements (e.g., spatio-temporal filtering and decomposition methods) have been reported to improve visualization of slower flow components and enhance choroidal vessel contrast in LDH datasets.<ref name="Puyo2020STF">{{Cite journal|doi=10.1364/BOE.392699|doi-access=free|title=Spatio-temporal filtering in laser Doppler holography for retinal blood flow imaging|year=2020|last1=Puyo|first1=Léo|last2=Paques|first2=Michel|last3=Atlan|first3=Michael|journal=Biomedical Optics Express|volume=11|issue=6|pages=3274–3287|pmid=32637254|pmc=7316027}}</ref>
 
Wide-field extensions of Doppler holography have also been described in conference literature for imaging choroidal blood flow over larger posterior-pole regions, with the aim of visualizing major choroidal arteries/veins and outflow patterns (including drainage toward [[vortex vein]]s) that may be relevant in conditions such as the [[pachychoroid]] disease spectrum.<ref name="Atlan2025Widefield">{{Cite journal|last1=Atlan|first1=M.|year=2025|title=Wide-field Doppler Holography of Choroidal Blood Flow|journal=Investigative Ophthalmology & Visual Science|url=https://iovs.arvojournals.org/article.aspx?articleid=2810463|access-date=2025-12-24}}</ref>


[[File:LDHvsICG.jpg|thumb| left|400px|Choroidal blood flow revealed with ICG-angiography (Spectralis, Heidelberg) and [[laser Doppler imaging]]<ref>Léo Puyo, Michel Paques, and Michael Atlan, "Spatio-temporal filtering in laser Doppler holography for retinal blood flow imaging," Biomed. Opt. Express 11, 3274–3287 (2020)</ref>]]


===In bony fish===
===In bony fish===

Latest revision as of 23:29, 24 December 2025

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The choroid, also known as the choroidea or choroid coat, is a part of the uvea, the vascular layer of the eye. It contains connective tissues, and lies between the retina and the sclera. The human choroid is thickest at the far extreme rear of the eye (at 0.2 mm), while in the outlying areas it narrows to 0.1 mm.[1] The choroid provides oxygen and nourishment to the outer layers of the retina. Along with the ciliary body and iris, the choroid forms the uveal tract.

The structure of the choroid is generally divided into four layers (classified in order of furthest away from the retina to closest):

  • Haller's layer – outermost layer of the choroid consisting of larger diameter blood vessels;[1]
  • Sattler's layer – layer of medium diameter blood vessels;[1]
  • Choriocapillaris – layer of capillaries;[1] and
  • Bruch's membrane (synonyms: Lamina basalis, Complexus basalis, Lamina vitra) – innermost layer of the choroid.[1]

Blood supply

The human eye is supplied by two largely distinct vascular systems: the retinal circulation, which nourishes the inner retina, and the uveal circulation (choroidal, ciliary body and iris), which nourishes the uvea and the outer retina (via the choroid). Both systems arise primarily from the ophthalmic artery, a branch of the internal carotid artery.[2]

The uveal circulation is supplied mainly by the posterior ciliary arteries (short and long), which enter the globe independently of the optic nerve. These arteries provide the dominant blood supply to the choroid and contribute importantly to perfusion of the optic nerve head (including the anterior portion of the optic nerve).[3] The retinal circulation derives primarily from the central retinal artery, which travels within the optic nerve and enters the eye at the optic disc. It then branches over the inner retinal surface into arterioles and capillaries supplying the nerve fiber and inner retinal layers.[2]

Retinal arteries behave as functional end-arteries with limited collateralization; consequently, focal obstruction can produce sectoral retinal ischemia. By contrast, the choroid exhibits a segmental vascular organization, and regional perfusion territories supplied by posterior ciliary arteries are clinically relevant because the macula and the anterior optic nerve (structures critical for central vision) depend strongly on choroidal perfusion.[3]

Imaging the choroid and its blood flow

File:LDHvsICG.jpg
Choroidal blood-flow contrast revealed with indocyanine green angiography (Spectralis, Heidelberg) and Laser Doppler holography (LDH).[4]

Structural features of the choroid can be assessed with optical coherence tomography (OCT), while choroidal vascular contrast is classically obtained with indocyanine green angiography (ICGA), an invasive dye-based method that is relatively robust for deeper choroidal vessels. Optical coherence tomography angiography (OCTA) provides non-invasive motion-contrast maps but can be limited by depth-dependent sensitivity, segmentation/projection artifacts, and reduced sensitivity for very slow flow or deeper large vessels.

File:Real-time fisheye Doppler holography of choroidal blood-flow.gif
Choroidal and retinal blood-flow imaging by real-time fisheye Laser Doppler holography (LDH).

Laser-Doppler–based approaches provide an additional, non-invasive route to choroidal flow contrast. In ophthalmology, Laser Doppler holography (LDH) is a full-field, camera-based implementation that uses digital holography and temporal demodulation of reconstructed optical fluctuations to generate Doppler power maps that highlight blood-flow–related signals in retinal and choroidal vessels.[5]

Signal-processing refinements (e.g., spatio-temporal filtering and decomposition methods) have been reported to improve visualization of slower flow components and enhance choroidal vessel contrast in LDH datasets.[4]

Wide-field extensions of Doppler holography have also been described in conference literature for imaging choroidal blood flow over larger posterior-pole regions, with the aim of visualizing major choroidal arteries/veins and outflow patterns (including drainage toward vortex veins) that may be relevant in conditions such as the pachychoroid disease spectrum.[6]


In bony fish

Teleosts bear a body of capillaries adjacent to the optic nerve called the choroidal gland. Though its function is not known, it is believed to be a supplemental oxygen carrier.[7]

Mechanism

Melanin, a dark colored pigment, helps the choroid limit uncontrolled reflection within the eye that would potentially result in the perception of confusing images.

In humans and most other primates, melanin occurs throughout the choroid. In albino humans, frequently melanin is absent and vision is low. In many animals, however, the partial absence of melanin contributes to superior night vision. In these animals, melanin is absent from a section of the choroid and within that section a layer of highly reflective tissue, the tapetum lucidum, helps to collect light by reflecting it in a controlled manner. The uncontrolled reflection of light from dark choroid produces the photographic red-eye effect on photos, whereas the controlled reflection of light from the tapetum lucidum produces eyeshine (see Tapetum lucidum).

History

The choroid was first described by Democritus (c. 460 – c. 370 BCE) around 400 BCE, calling it the "chitoon malista somphos" (more spongy tunic [than the sclera]).[8] Democritus likely saw the choroid from dissections of animal eyes.[9]

About 100 years later, Herophilos (c. 335 – 280 BCE) also described the choroid from his dissections on eyes of cadavers.[10][11]

Clinical significance

Choroid is the most common site for metastasis in the eye due to its extensive vascular supply. The origin of the metastases are usually from breast cancer, lung cancer, gastrointestinal cancer, and kidney cancer. Bilateral choroidal metastases are usually due to breast cancer, while unilateral metastasis is due to lung cancer. Choroidal metastases should be differentiated from uveal melanoma, where the latter is a primary tumour arising from the choroid itself.[12]

See also

Additional images

References

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  1. a b c d e MRCOphth Sacs questions
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  7. "Eye (Vertebrate)" McGraw-Hill Encyclopedia of Science and Technology, vol. 6, 2007.
  8. Dolz-Marco, R., Gallego-Pinazo, R., Dansingani, K. K., & Yannuzzi, L. A. (2017). The history of the choroid. In J. Chhablani & J. Ruiz-Medrano (Eds.), Choroidal Disorders (Vol. 1–5, pp. 1–5). Academic Press. Script error: No such module "CS1 identifiers".
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  11. Reverón, R. (2015). Herophilos, the great anatomist of antiquity. Anatomy, 9(2), 108–111. Script error: No such module "CS1 identifiers". https://dergipark.org.tr/en/download/article-file/371071
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External links

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