Molecular Classification
Other (Extracellular matrix structure), Basement membrane (specialized type)
Other Names
Lamina vitrea, Vitreous lamina, Membrane vitriae, Lamina basalis choroideae (Latin)
Disease Roles
Age-related macular degeneration (AMD)[1][3][5]Retinitis pigmentosa[3]Pseudoxanthoma elasticum[1][3]

Bruch's membrane Overview

Bruch's membrane is a thin (2–4 μm), acellular, five-layered extracellular matrix located between the retinal pigment epithelium (RPE) and the choriocapillaris within the eye. It serves as a semi-permeable barrier that regulates the exchange of nutrients, oxygen, metabolic waste products, lipids, vitamins, signaling molecules, and other factors essential for photoreceptor function between the retina/RPE complex and general circulation. The structure consists of five layers—two basement membranes on either side sandwiching collagenous zones with a central elastic fiber band. With age or disease states such as age-related macular degeneration or inherited disorders like pseudoxanthoma elasticum or Alport syndrome, Bruch’s membrane can thicken or accumulate lipid-rich deposits ("drusen"), impairing its transport functions. This dysfunction contributes to vision loss through mechanisms such as neovascularization or detachment of retinal layers. While crucial in ocular physiology and pathology—especially in diseases like AMD—Bruch’s membrane itself is not considered a direct therapeutic target like receptors or enzymes but rather an anatomical substrate involved in disease processes.[1][3][5]

Mechanism of Action

Biological Functions

Regulation of fluid and solute passage between the choroid and retina[1][3][5]
Physical support for retinal pigment epithelium (RPE) cells[6]
Acts as a molecular sieve for biomolecules, nutrients, oxygen, fluids, and metabolic waste products[3][5]
Involved in cell–cell communication and tissue remodeling in the eye[6]

Disease Associations

Age-related macular degeneration (AMD)[1][3][5]
Retinitis pigmentosa[3]
Pseudoxanthoma elasticum[1][3]
Sorsby's fundus dystrophy[3]
Malattia Leventinese[3]
Myopia-related pathology and trauma-induced defects leading to choroidal neovascularization[1]

Safety Considerations

No safety concerns listed

Associated Biomarkers

Biomarker
Drusen formation as an indicator of AMD progression related to Bruch's membrane changes[1][3]