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Optic Atrophy

Abstract
Optic atrophy is a pathological term referring to optic nerve shrinkage caused by the degeneration of retinal ganglion cell (RGC) axons. The term “optic atrophy” is regarded as a misnomer since atrophy implies disuse. Therefore, a better term for optic atrophy would be “optic neuropathy.” However, that term is also controversial since, in certain situations, such as primary optic atrophy or traumatic brain injury, optic neuropathy may not occur.[1] Optic atrophy is the end stage of a disease process affecting the retinogeniculate portion of the visual pathway, characterized by a non-specific sign of optic disc pallor. While the peripheral nervous system has an intrinsic ability for repair and regeneration, the central nervous system, for the most part, is incapable of such processes. The axons of the optic nerve are heavily myelinated by oligodendrocytes and reactive astrocytes, which express many inhibitory factors for axonal regeneration.[2] Thus, the optic nerve, with its 1.2 million fibers, behaves more like a white matter tract rather than a true peripheral nerve. The optic nerve head is supplied by pial capillaries that undergo degeneration contributing to the pallor of the optic disc seen in optic atrophy. It is this neuro-vascular degeneration which forms the foundation for the development of optic atrophy. When light is thrown on the fundus from a light source, it undergoes total internal reflection through the axonal fibers. Subsequently, reflection from the capillaries on the disc surface gives rise to the characteristic yellow-pink color of a healthy optic disc. In eyes with cataract, red color is exaggerated, giving rise to a hyperemic appearance of the disc. Conversely, in pseudophakic individuals, the disc may appear to have some degree of pallor. Usually, 4-6 weeks are required following axonal damage for the optic disc pallor to start developing. In severe cases, the disc ultimately becomes chalky white. The overlying axons and capillaries degenerate so that the white lamina cribrosa becomes visible. This contrasts sharply with the surrounding red-colored retina. The exact mechanisms responsible for the optic disc pallor seen in optic atrophy are not clearly elucidated. It is assumed that the loss of axonal fibers along with the rearrangement of astrocytes contributes to the disc pallor. Cogan and Walsh, as well as Hoyt, have mentioned optic disc pallor as a consequence of loss of smaller blood vessels and the variable amount of reactive gliosis and fibrosis, as the optic nerve shrinks due to various factors. The degenerated axons also lose the optical property of total internal reflection, leading to the pale optic disc seen in this condition.[3] Recognition of optic atrophy might prove to be life-saving for the patient. Therefore, it is imperative to have adequate knowledge regarding this fairly common condition. This review presents the basic concepts of optic atrophy.

Publisher

StatPearls Publishing
Treasure Island (FL)

Language

eng

PubMed ID

32644556

Citation

Ahmad SS, Kanukollu VM: Optic Atrophy. StatPearls. StatPearls Publishing, 2020, Treasure Island (FL).
Ahmad SS, Kanukollu VM. Optic Atrophy. StatPearls. StatPearls Publishing; 2020.
Ahmad SS & Kanukollu VM. (2020). Optic Atrophy. In StatPearls. Treasure Island (FL): StatPearls Publishing
Ahmad SS, Kanukollu VM. Optic Atrophy. StatPearls. Treasure Island (FL): StatPearls Publishing; 2020.
* Article titles in AMA citation format should be in sentence-case
TY - CHAP T1 - Optic Atrophy BT - StatPearls A1 - Ahmad,Syed Shoeb, AU - Kanukollu,Venkata M., Y1 - 2020/01// PY - 2020/7/10/pubmed PY - 2020/7/10/medline PY - 2020/7/10/entrez N2 - Optic atrophy is a pathological term referring to optic nerve shrinkage caused by the degeneration of retinal ganglion cell (RGC) axons. The term “optic atrophy” is regarded as a misnomer since atrophy implies disuse. Therefore, a better term for optic atrophy would be “optic neuropathy.” However, that term is also controversial since, in certain situations, such as primary optic atrophy or traumatic brain injury, optic neuropathy may not occur.[1] Optic atrophy is the end stage of a disease process affecting the retinogeniculate portion of the visual pathway, characterized by a non-specific sign of optic disc pallor. While the peripheral nervous system has an intrinsic ability for repair and regeneration, the central nervous system, for the most part, is incapable of such processes. The axons of the optic nerve are heavily myelinated by oligodendrocytes and reactive astrocytes, which express many inhibitory factors for axonal regeneration.[2] Thus, the optic nerve, with its 1.2 million fibers, behaves more like a white matter tract rather than a true peripheral nerve. The optic nerve head is supplied by pial capillaries that undergo degeneration contributing to the pallor of the optic disc seen in optic atrophy. It is this neuro-vascular degeneration which forms the foundation for the development of optic atrophy. When light is thrown on the fundus from a light source, it undergoes total internal reflection through the axonal fibers. Subsequently, reflection from the capillaries on the disc surface gives rise to the characteristic yellow-pink color of a healthy optic disc. In eyes with cataract, red color is exaggerated, giving rise to a hyperemic appearance of the disc. Conversely, in pseudophakic individuals, the disc may appear to have some degree of pallor. Usually, 4-6 weeks are required following axonal damage for the optic disc pallor to start developing. In severe cases, the disc ultimately becomes chalky white. The overlying axons and capillaries degenerate so that the white lamina cribrosa becomes visible. This contrasts sharply with the surrounding red-colored retina. The exact mechanisms responsible for the optic disc pallor seen in optic atrophy are not clearly elucidated. It is assumed that the loss of axonal fibers along with the rearrangement of astrocytes contributes to the disc pallor. Cogan and Walsh, as well as Hoyt, have mentioned optic disc pallor as a consequence of loss of smaller blood vessels and the variable amount of reactive gliosis and fibrosis, as the optic nerve shrinks due to various factors. The degenerated axons also lose the optical property of total internal reflection, leading to the pale optic disc seen in this condition.[3] Recognition of optic atrophy might prove to be life-saving for the patient. Therefore, it is imperative to have adequate knowledge regarding this fairly common condition. This review presents the basic concepts of optic atrophy. PB - StatPearls Publishing CY - Treasure Island (FL) UR - https://www.unboundmedicine.com/medline/citation/32644556/StatPearls:_Optic_Atrophy L2 - https://www.ncbi.nlm.nih.gov/books/NBK559130 DB - PRIME DP - Unbound Medicine ER -
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