The choroid is a thin, vascularized layer of tissue forming part of the uvea, the middle tunic of the eye, situated between the sclera (the white outer layer) and the retina at the back of the eyeball.[1] It spans the posterior two-thirds of the eye, extending from the optic nerve to the ora serrata, and is characterized by its dense network of blood vessels embedded in connective tissue rich in melanocytes.[2] With a thickness varying from approximately 100 to 370 micrometers depending on age, location, and measurement method (thickest subfoveally), the choroid plays a critical role in ocular physiology.[3][4][5]Structurally, the choroid consists of several distinct layers: the outermost suprachoroid, containing loose connective tissue and melanocytes; Haller's layer with large vessels; Sattler's layer with medium-sized vessels; and the innermost choriocapillaris, a capillary bed adjacent to Bruch's membrane, which separates it from the retinal pigment epithelium.[3] This multilayered organization supports its high blood flow—estimated at rates up to ten times that of the brain per unit weight—facilitating nutrient and oxygen delivery to the avascular outer retina and optic nerve head.[3] The melanin's abundance in the choroid absorbs stray light, preventing internal reflections that could degrade visual acuity and protecting photoreceptors from phototoxicity.[3]Beyond its vascular and optical functions, the choroid contributes to ocular homeostasis through barrier properties, thermoregulation, and modulation of eye growth. The choriocapillaris acts as a selective barrier, regulating fluid and protein exchange between the bloodstream and retinal interstitium via fenestrated endothelium.[3] It also secretes growth factors such as transforming growth factor-beta (TGF-β) and retinoic acid, influencing scleral remodeling and emmetropization—the process aligning refractive development with visual demands—and diurnal variations in choroidal thickness (approximately 20-35 micrometers) help maintain retinal apposition.[3][6] Clinically, choroidal dysfunction underlies conditions like choroiditis (inflammation), age-related macular degeneration (via impaired Bruch's membrane permeability), and myopia progression, often diagnosed through imaging modalities such as optical coherence tomography.[1][3]
Anatomy
Macroscopic structure
The choroid constitutes the middle vascular layer of the uvea, positioned between the sclera externally and the retina internally within the posterior segment of the eye.[7] It forms a thin, dark brown membrane due to its high melanin content, which aids in light absorption.[8] This layer covers the posterior two-thirds of the eyeball, extending from the optic disc posteriorly to the ora serrata anteriorly.[8]The choroid exhibits a roughly cup-shaped configuration that conforms to the spherical curvature of the eyeball.[2] Its thickness varies regionally, ranging from approximately 50 to 350 μm in adults, thickest in the subfoveal region, with greater dimensions observed temporally and in posterior areas compared to nasal and anterior regions.[7][9] At birth, the average thickness measures approximately 0.2 mm, progressively thinning to about 0.08 mm by age 90.The choroid adheres externally to the sclera via loose connective tissue forming the suprachoroidal space, a potential cavity that allows limited mobility between layers.[8] Internally, it connects to the retina through Bruch's membrane, a thin basal lamina.[8] This structure is perforated by the optic nerve at its posterior termination and by ciliary vessels, facilitating passage to adjacent ocular components.[7]Notable macroscopic features include the inner adjacency of the choriocapillaris, a capillaryplexus directly apposed to Bruch's membrane, and the presence of perivascular spaces surrounding larger vessels, which exhibit regional variations in density.[7]
Microscopic structure
The choroid exhibits a distinct layered organization at the microscopic level, typically divided into four principal layers from outer to inner: the suprachoroid, the vascular layer, the choriocapillaris, and the interface with Bruch's membrane.[3] The outermost suprachoroid, also known as the lamina fusca, consists of a thin layer of loose connective tissue rich in melanocytes and collagen fibers, which anchors the choroid to the sclera and contributes to its pigmentation.[10] Beneath this lies the vascular layer, subdivided into medium-sized vessels (Sattler's layer) and larger vessels (Haller's layer), forming a network that supports the choroid's high vascular density.[3] The innermost choriocapillaris is a lobular capillaryplexus directly adjacent to Bruch's membrane, facilitating nutrient exchange with the retina, while Bruch's membrane itself serves as a thin, pentalaminar extracellular barrier at the choroid-retinal pigment epithelium interface.[3]At the cellular level, the choroid is composed primarily of melanocytes, which provide dense pigmentation to absorb stray light and prevent internal reflections, particularly prominent in humans.[11] Endothelial cells line the extensive vascular network, with fibroblasts producing the supportive stroma and immune cells such as macrophages and dendritic cells residing within the tissue for local immune surveillance.[3]Pericytes and smooth muscle cells also contribute to vascular stability in the medium and large vessel layers.[12]The extracellular matrix of the choroid is characterized by loose connective tissue that accommodates its vascular elements, containing primarily collagen types I and III in the stroma, type IV in basement membranes, and elastin fibers that impart elasticity to the vessel walls.[13] This matrix supports the choroid's flexibility and permeability while maintaining structural integrity.[14]Notable microscopic features include the fenestrated endothelium of the choriocapillaris, which features numerous pores allowing high permeability for plasma components to reach the outer retina.[15] Additionally, the choroid lacks conventional lymphatic vessels, relying instead on venous drainage for fluid clearance.[16]
Vascular supply
The choroid receives its arterial supply primarily from the short posterior ciliary arteries, which arise as branches of the ophthalmic artery and typically number between 10 and 20 per eye. These arteries penetrate the sclera in a radial pattern surrounding the optic nerve head, branching into larger-caliber vessels that form the outer and middle vascular layers of the choroid, supplying the majority of its posterior and central extent.[17][18][19]Two long posterior ciliary arteries, also branching from the ophthalmic artery, provide supply to the anterior periphery of the choroid, extending forward to form an anastomotic ring near the ora serrata and contributing to the vascular network in this region.[20][18]Venous drainage from the choroid occurs through four to five vortex veins, which collect blood from postcapillary venules and pierce the sclera at sites posterior to the equator before emptying into the superior and inferior ophthalmic veins.[17][18][19]The choroid contains no true lymphatic vessels, though perivascular spaces surrounding the choroidal vasculature facilitate interstitialfluid movement and exchange.[21][22]The short posterior ciliary arteries account for the bulk of choroidal perfusion, penetrating the sclera at multiple discrete sites to distribute blood across the tissue; within the inner choriocapillaris layer, this results in a high vascular density organized into numerous lobules.[17][19][20]Choroidal blood flow is autoregulated mainly via a myogenic response in the smooth muscle cells of the medium and large vessels, helping maintain stable perfusion despite fluctuations in perfusion pressure.[23][24]The choroidal circulation features high blood flow rates with low oxygen extraction, typically around 3-5% from the blood passing through the tissue.[25][26]
Function
Nutritional support
The choroid plays a crucial role in oxygen delivery to the outer retina and retinal pigment epithelium (RPE) primarily through diffusion from the choriocapillaris, a fenestrated capillary layer adjacent to Bruch's membrane. This vascular network supplies the majority of oxygen required by the photoreceptors and outer retinal layers, where metabolic demand is high due to phototransduction processes. Studies indicate that under normal conditions, the choroid accounts for approximately 50-60% of total retinal oxygen consumption, with the potential to supply up to 97% of the oxygen needs between the choriocapillaris and deep retinal capillaries during hyperoxic states.[27][28] The exceptionally high blood flow rate in the choroid, estimated at around 800 ml per 100 g of tissue per minute—one of the highest in the body—facilitates this efficient oxygen transfer by maintaining a steep partial pressure gradient across the RPE.[3]Nutrient transport from the choroid to the outer retina occurs via passive diffusion and active mechanisms across Bruch's membrane, enabling the delivery of essential metabolites such as glucose, amino acids, and fatty acids. The fenestrated endothelium of the choriocapillaris allows high permeability to small molecules like glucose and amino acids for subsequent uptake by the RPE and photoreceptors. Glucose, the primary energy substrate for the retina, is shuttled through RPE transporters (e.g., GLUT1) from choroidal blood to support retinal glycolysis, while fatty acids contribute to photoreceptor membrane renewal. Additionally, the choroid facilitates vitamin A (retinol) transport to the RPE via the receptor STRA6, where it is converted to 11-cis-retinal for photoreceptor function in the visual cycle.[3][29][30]Waste removal from the outer retina is mediated by the choroid through the clearance of metabolic byproducts such as carbon dioxide (CO2) and lactate, which diffuse back across Bruch's membrane into the choriocapillaris for systemic elimination. Photoreceptors produce lactate via aerobic glycolysis (Warburg effect), which the RPE absorbs and exports to the choroid, preventing accumulation in the subretinal space. The choroid also supports RPE phagocytosis of shed photoreceptor outer segments by providing nutrients that sustain this energy-intensive process, indirectly aiding debris clearance. This bidirectional exchange is enhanced by the choriocapillaris's fenestrations, which permit rapid diffusion of waste products.[31][32]Specific mechanisms underlying these functions include the high permeability of the choriocapillaris's fenestrated capillaries, which lack a continuous basement membrane and allow selective passage of plasma components up to the size of small proteins while restricting larger molecules. This structure optimizes nutrient influx and waste efflux. Furthermore, the choroid contributes to pH and ion balance in the outer retina by supporting RPE-mediated bicarbonate (HCO3-) transport; the RPE uses Na+/HCO3- cotransporters to move bicarbonate from the subretinal space to choroidal blood, buffering CO2-induced acidosis and maintaining stable extracellular pH for retinalhomeostasis. Diurnal fluctuations in choroidal blood flow and thickness further aid in maintaining retinalapposition and temperature stability.[33][34][3]
Thermoregulation and barrier functions
The choroid plays a crucial role in thermoregulation of the retina through its extensive vascular network, which facilitates heat dissipation from retinal metabolic activity and lightabsorption. The high bloodflow in the choroid, accounting for approximately 85% of the ocular blood supply, acts as a heat sink to stabilize retinal temperature, preventing overheating during exposure to intense light or increased metabolic demands.[3] This modulation occurs via both passive mechanisms, such as convective heat transfer through the choriocapillaris, and active neural regulation, where sympathetic innervation adjusts choroidal bloodflow in response to thermal loads, ensuring the retina maintains a temperature gradient conducive to optimal photoreceptor function.[35][36]In addition to thermoregulation, the choroid contributes to barrier functions as part of the outer blood-retinal barrier (oBRB), where the fenestrated endothelium of the choriocapillaris interacts with Bruch's membrane and the retinal pigment epithelium (RPE) to regulate the passage of molecules and fluids. Although the choriocapillaris features fenestrations that allow permeability, the overall oBRB integrity relies on tight junctions primarily in the RPE, which prevent unregulated leakage from the choroidal vasculature into the subretinal space.[37] This structure enables the choroid to maintain ion and fluid balance in the retina, actively pumping ions and water to counteract osmotic pressures and inhibit retinal edema under normal conditions.[38] The choroidal blood flow dynamics further support this by facilitating rapid clearance of excess interstitial fluid, ensuring the virtual subretinal space remains free of accumulation.[22]The choroid also supports immune modulation by housing resident immune cells, including macrophages, dendritic cells, and mast cells, which conduct surveillance for pathogens entering via the vascular supply outside the blood-retinal barrier. These cells detect microbial threats and initiate localized inflammatory responses without compromising retinal integrity, serving as a frontline defense in the uvea.[39] Complementing this, choroidal melanocytes produce melanin, whose content varies with individual pigmentation levels and enhances UV protection by absorbing ultraviolet radiation and stray light to minimize phototoxicity.[40] This melanin scavenging of reactive oxygen species further reduces oxidative damage to adjacent retinal tissues, linking pigmentation density directly to ocular resilience against environmental stressors.[40]
Development and comparative aspects
Embryonic development
The choroid originates from mesenchyme derived from the mesoderm, which condenses into layers proximal to the optic cup during early eye development.[41] Melanocytes within the choroid arise from neural crest cells, which migrate and differentiate into pigmented cells that contribute to the choroid's pigmentation.[42] This process begins around the fourth week of gestation, when a primitive vascular plexus forms from mesenchymal cells surrounding the optic cup, marking the initial establishment of the choroidal vasculature.[41][43]By the sixth week of gestation, mesenchymal tissue invades the space between the optic cup and sclera, initiating vascular invasion and the formation of the choriocapillaris layer through angiogenesis.[41] This angiogenesis is primarily driven by vascular endothelial growth factor (VEGF) secreted by the retinal pigment epithelium (RPE), which induces endothelial cell proliferation and capillary formation adjacent to the RPE.[44] Simultaneously, melanoblasts migrate from the neural crest into the developing choroid, integrating with the vascular elements to provide pigmentation.[42] The choroidal fissure, an embryonic indentation in the optic cup, closes by the seventh week, a critical event that ensures proper formation of the choroid and prevents coloboma, a congenital defect resulting from incomplete closure.[45]The choriocapillaris fully differentiates by the eighth week, supporting the inner choroidal layers, while the complete layering of the choroid— including the Haller's large vessels, Sattler's medium vessels, and choriocapillaris—is achieved by the third month of gestation.[41] During this early phase, the retina remains avascular overall, with its outer layers receiving nutrition from the maturing choroidal vasculature and its inner layers and the lens supplied by the transient hyaloid artery, which regresses as the inner retinal vessels develop in the later stages of gestation and postnatally.[20][46] Maturation of the choroid continues postnatally, with refinements in vascular density and pigmentation occurring after birth.[41]
Variations across vertebrates
The choroid exhibits significant structural variations across vertebrate classes, reflecting evolutionary adaptations to diverse visual demands and environmental transitions from aquatic to terrestrial habitats. Over approximately 540 million years, the choroid has evolved to support increasing retinal metabolic needs, transitioning from simple diffusive supply in early aquatic forms to more complex vascular and supplemental structures in terrestrial lineages.[47] In cartilaginous fish such as sharks, the choroid features prominent iridescent layers formed by guanine crystals in the choroidal tapetum lucidum, which enhance low-light vision and contribute to camouflage by reflecting ambient light to disrupt silhouettes in marine environments.[48] Bony fish (teleosts) show a less developed choriocapillaris compared to terrestrial vertebrates, relying instead on rectangular choroidal glands—vascular networks akin to pseudobranch functions—that concentrate oxygen for retinal nutrition, particularly in species with thick retinas.[49] These glands, often forming a rete mirabile, underscore the choroid's role in gas exchange adaptations during early vertebrateevolution in aquatic settings.[47]In amphibians, the choroid maintains a primarily diffusive vascular supply to support thin retinas, evolving as a bridge in the aquatic-to-terrestrial transition where ocular demands shifted with emerging aerial vision.[47] Reptiles exhibit a thicker choroid with the conus papillaris, a vascular projection analogous to the avian pecten, which supplements choroidal circulation to nourish avascular regions of the retina and reduce dependence on diffusion alone.[47] Birds possess an even more specialized choroid, featuring the pecten oculi—a pigmented, comb-like vascular structure extending into the vitreous humor—that provides direct nutritional support to the metabolically active, avascular retina, enhancing efficiency in high-acuity vision for flight and predation.[50] This adaptation likely co-evolved with uric acidmetabolism in sauropsids, distinguishing reptilian and avian choroids from those in earlier lineages.[51]Among mammals, the choroid generally mirrors the human configuration with high vascular density in the choriocapillaris to sustain outer retinal layers, though pigmentation varies notably; in albinos, reduced melanin in choroidal melanocytes leads to hypopigmentation, altering light scattering and contributing to visual pathway anomalies.[52] These interclass differences highlight the choroid's evolutionary plasticity, from guanine-based reflectors in aquatic forms for enhanced sensitivity to specialized projections in sauropsids for optimized terrestrial nutrition.[47] In bony fish, melanocytes additionally incorporate guanine crystals forming a tapetal layer within the choroid, which reflects light back through the retina to improve vision in dim conditions.[53]
Clinical significance
Associated disorders
The choroid is susceptible to various inflammatory disorders, collectively termed choroiditis, which involve inflammation of the choroidal tissue often extending to the retina as chorioretinitis. These conditions can arise from infectious agents, such as Toxoplasma gondii, the most common cause of infectious chorioretinitis, leading to focal necrotizing lesions in the choroid and retina. Autoimmune-mediated forms, including serpiginous choroiditis, present as recurrent, asymmetrically bilateral inflammation characterized by grayish-white lesions at the optic disc margin that progress in a serpentine pattern, resulting from immune-mediated non-perfusion of the choriocapillaris and subsequent atrophy of the retinal pigment epithelium (RPE) and choroid. Pathophysiologically, these processes cause scarring, photoreceptor damage, and progressive vision loss due to disruption of the choriocapillaris and overlying retinal layers.Vascular disorders of the choroid include central serous chorioretinopathy (CSCR), a condition involving multifactorial choroidal circulatory disturbances that lead to hyperpermeability and fluid leakage from the choroid into the subretinal space, causing serous retinal detachment typically in the macula. In age-related macular degeneration (AMD), particularly the neovascular or wet form, choroidal neovascularization (CNV) develops as abnormal, fragile vessels proliferate from the choroid through Bruch's membrane into the sub-RPE space, driven by overexpression of vascular endothelial growth factor (VEGF) from dysfunctional RPE cells; this affects the choroid in nearly all wet AMD cases, which comprise about 10-15% of total AMD. These vascular changes compromise the blood-retinal barrier and contribute to macular edema, hemorrhage, and central vision impairment.Neoplastic conditions primarily affecting the choroid encompass choroidal melanoma, the most common primary intraocular malignancy, originating from uveal melanocytes in approximately 85-90% of uveal melanoma cases. This tumor arises sporadically in the choroid, with an annual incidence of 5-7.5 cases per million individuals, predominantly in those of European descent, and can lead to retinal detachment, vitreous hemorrhage, or metastasis to the liver in up to 50% of cases over time. Metastatic tumors to the choroid, often from breast or lung primaries, represent another neoplastic category, where tumor emboli lodge in the choroidal vasculature, causing multifocal yellow-white lesions and secondary retinal changes.Congenital anomalies include choroidal coloboma, a developmental defect resulting from incomplete closure of the embryonic optic fissure, leading to a gap-like absence of choroidal tissue, often accompanied by defects in the RPE and sclera, which increases the risk of retinal detachment or visual field defects. In albinism, particularly oculocutaneous forms, hypopigmentation of the choroid due to reduced melanin in the RPE and iris exposes underlying structures to excessive light, heightening phototoxicity and oxidative damage to the choroid and retina, thereby exacerbating risks of macular hypoplasia and nystagmus.
Diagnostic and therapeutic approaches
Optical coherence tomography (OCT) is a primary non-invasive imaging modality for evaluating choroidal structure, offering axial resolution of approximately 5-10 μm to assess thickness, subretinal fluid, and choroidal lesions.[54] Enhanced depth imaging OCT (EDI-OCT) and swept-source OCT (SS-OCT) enhance visualization of the choroid by improving penetration depth up to 2-3 mm, enabling precise measurement of choroidal thickness in conditions like age-related macular degeneration (AMD) and central serous chorioretinopathy.[55]Indocyanine green angiography (ICGA) provides detailed assessment of choroidal vascular flow and perfusion, particularly useful for detecting hypofluorescent lesions and neovascularization, and is preferred over fluorescein angiography (FA) due to its strong protein binding, which allows deeper penetration into choroidal tissues without significant leakage from retinal vessels.[55] Fundus autofluorescence (FAF) imaging aids in evaluating melanin distribution and lipofuscin accumulation in the choroid and retinal pigment epithelium, helping to identify patterns in inflammatory or degenerative disorders.[55]Ultrasound, including A-scan and B-scan modes, is employed for measuring tumor dimensions and acoustic properties in choroidal masses like melanomas, with resolutions sufficient for detecting extrascleral extension.[56]Fluorescein angiography assists in differentiating choroidal from retinal vascular abnormalities by highlighting leakage patterns, though it is less effective for deep choroidal structures compared to ICGA.[55]Therapeutic approaches for choroidal conditions target underlying vascular, inflammatory, or neoplastic processes. Intravitreal anti-vascular endothelial growth factor (anti-VEGF) injections, such as ranibizumab, are standard for choroidal neovascularization in AMD and pathologic myopia, inhibiting angiogenesis and reducing leakage with repeated dosing every 4-8 weeks initially.[57] Photodynamic therapy (PDT) using verteporfin, administered intravenously followed by laser activation, selectively occludes abnormal choroidal vessels in wet AMD and polypoidal choroidal vasculopathy, often combined with anti-VEGF for improved outcomes.[58] For inflammatory choroidopathies like Vogt-Koyanagi-Harada disease, systemic corticosteroids serve as first-line therapy to suppress acute inflammation, with transition to immunosuppressants such as cyclosporine or mycophenolate mofetil for steroid-sparing control in chronic cases.[59] Surgical interventions include pars plana vitrectomy to address vitreoretinal complications from choroidal tumors or detachments, often combined with endoresection to remove intraocular masses while preserving the globe.[60] In advanced choroidal melanoma with poor visual prognosis or complications, enucleation remains the definitive treatment to prevent metastasis.[60] Emerging therapies for choroidal melanoma include belzupacap sarotalocan (AU-011), a virus-like drug conjugate in phase 3 clinical trials as of 2025, showing promise for early-stage tumors with vision preservation, and proton beam therapy, which a 2025 meta-analysis confirmed achieves high local control rates (up to 95%) and overall survival benefits.[61][62]
Historical context
Early descriptions
The choroid, a vascular and pigmented layer of the eye, was first alluded to in ancient Greek texts as a spongy inner tunic distinct from the denser sclera. Around 400 BCE, Democritus of Abdera provided the earliest known description and illustration, referring to it as the "chitoon malista somphos" (more spongy tunic), emphasizing its porous, vascular nature compared to the outer coats. This observation laid the groundwork for later understandings of its membrane-like quality.[63]In the 2nd century AD, Galen of Pergamon advanced these ideas by systematically delineating the eye's layered structure in his anatomical treatises, identifying the choroid as one of the principal membranes alongside the cornea, sclera, lens capsule, and retina. He described it as the vascular tunic, highlighting its role in enclosing the eye's internal fluids and its resemblance to a skin-like sheath due to its thin, enveloping form—termed "choroeides" in Greek, evoking a membrane akin to the chorion (the fetal afterbirth sac). This nomenclature, rooted in Greek "chorioeidēs" (resembling the chorion), reflected its folded, vascular appearance in dissections, though early anatomists often confused it with adjacent structures like the retina, mistaking its pigmentation for part of the sensory layer.[64][65][66]Arabic scholars in the medieval period built upon Galenic foundations, incorporating empirical observations into comprehensive medical encyclopedias. Avicenna (Ibn Sina, 980–1037 AD) in his Canon of Medicine detailed the eye's tunics as part of the uvea, viewed as protective and nutritive.[67][68]During the Renaissance, anatomical precision improved through dissection and illustration. Andreas Vesalius, in his seminal 1543 work De Humani Corporis Fabrica, depicted the choroid as an integral component of the uvea, illustrating its continuity with the iris and ciliary body in cross-sectional views of the eye, thereby correcting some Galenic inaccuracies about layer separations. Gabriele Falloppio, in his 1561 Observationes Anatomicae, expanded on Vesalius's work in ocular anatomy.[66][69]In the 17th and 18th centuries, techniques like vascular injection revealed the choroid's intricate blood supply. Frederik Ruysch, in the 1690s and early 1700s, pioneered wax injections into ocular vessels, vividly demonstrating the choroid's dense capillary network and its role in circulation, which his son later termed the "tunica Ruyschiana" for the complex including the retinal pigment epithelium and choriocapillaris. These efforts solidified the choroid's identity as a distinct, highly vascular entity before microscopic advancements.[63][70]
Modern advancements
In the 19th century, significant progress in choroidal anatomy was made through histological studies, with Karl Bruch identifying and describing Bruch's membrane in 1844 as a distinct layer separating the choroid from the retina.[71] This discovery, detailed in Bruch's doctoral thesis, highlighted the membrane's role as a thin, acellular structure essential for choroidal-retinal interactions.[72] Concurrently, histologists such as Albert von Kölliker advanced the understanding of choroidal layering using improved microscopy techniques, delineating the vascular and stromal components in the mid-1800s and establishing the foundational multilayered organization observed in modern histology.[73]The 20th century brought technological innovations that revealed choroidal function and microstructure. In the 1950s, Harold R. Novotny and David L. Alvis pioneered fluorescein angiography, first demonstrated in 1959, which allowed noninvasive visualization of choroidal blood flow by injecting sodium fluorescein and capturing serial fundus images.[74] This technique revolutionized the assessment of choroidal circulation, enabling the detection of vascular leaks and perfusion abnormalities.[75] By the 1960s, electron microscopy provided ultrastructural insights, with studies revealing the fenestrated endothelium of the choriocapillaris, a key feature facilitating nutrient exchange with the retina, as documented in early examinations of human choroidal tissue.[76] In the 1970s, Anders Bill's quantitative studies in animal models, such as cats, measured choroidal blood flow rates and oxygen extraction, demonstrating high flow volumes—up to 50 times that of the retina—and its sensitivity to intraocular pressure changes.[77]Sohan Hayreh's research during this period further elucidated choroidal hemodynamics, showing limited autoregulation in the choroidal vasculature compared to the retina, with blood flow responding passively to systemic pressure variations in primate and human studies from the 1960s to 1990s.[78] Entering the 21st century, optical coherence tomography (OCT), developed in the early 1990s, evolved to enable in vivo choroidal imaging; enhanced-depth imaging OCT in the 2000s allowed precise thickness mapping, revealing subfoveal choroidal thicknesses averaging 272–354 μm in healthy adults.[79] Genetic research linked choroidal alterations to age-related macular degeneration (AMD), with variants in the complement factor H (CFH) gene, such as Y402H identified in 2005, increasing AMD risk by impairing choroidal neovascularization regulation.[80]Post-2000 advancements in swept-source OCT have quantified dynamic choroidal changes, showing age-related thinning—at a rate of approximately 3 μm per year—and thinning during accommodation, up to 10-20 μm in young subjects, aiding in understanding adaptive vascular responses.[81][82] In the 2020s, integration of choroidal imaging with retinal studies via multimodal OCT and artificial intelligence has advanced personalized medicine, enabling risk stratification for AMD through combined genetic and vascular biomarkers to tailor therapies like anti-VEGF injections; as of 2025, AI models improve detection of choroidal neovascularization with over 90% accuracy in multimodal datasets.[83][84]