Intraocular And Intracranial Pressure Gradient In Glaucoma: Advances In Visual
Glaucoma is a leading cause of blindness worldwide. It is characterized by damage to the optic nerve, which is the nerve that carries visual information from the eye to the brain. Glaucoma is often associated with increased intraocular pressure (IOP),which is the pressure inside the eye. However, not all cases of glaucoma are associated with high IOP. Some cases of glaucoma, known as normal-tension glaucoma, occur in individuals with IOP within the normal range.
5 out of 5
Language | : | English |
File size | : | 76483 KB |
Text-to-Speech | : | Enabled |
Screen Reader | : | Supported |
Enhanced typesetting | : | Enabled |
Print length | : | 709 pages |
Hardcover | : | 94 pages |
Item Weight | : | 9.5 ounces |
Dimensions | : | 5.5 x 0.38 x 8.5 inches |
One possible explanation for normal-tension glaucoma is that it is caused by a difference in pressure between the inside of the eye and the inside of the skull. This difference in pressure is known as the intraocular and intracranial pressure gradient (IOPG).
IOPG and Glaucoma
The IOPG is thought to play a role in the development and progression of glaucoma. A high IOPG can put stress on the optic nerve, leading to damage. This damage can result in visual field loss and, eventually, blindness.
Several studies have shown that a high IOPG is associated with an increased risk of developing glaucoma. One study found that individuals with a high IOPG were more than twice as likely to develop glaucoma than those with a low IOPG. Another study found that a high IOPG was associated with a faster progression of glaucoma.
Advances in Visual
In recent years, there have been a number of advances in the understanding of the IOPG and its role in glaucoma. These advances have led to the development of new diagnostic and treatment methods.
One of the most significant advances in the understanding of the IOPG has been the development of new imaging techniques that allow doctors to visualize the pressure gradient in the eye. These techniques have shown that the IOPG is not uniform throughout the eye. In fact, the IOPG is highest in the area around the optic nerve. This finding suggests that the optic nerve may be particularly vulnerable to damage from a high IOPG.
Another advance in the understanding of the IOPG has been the development of new animal models of glaucoma. These models have allowed researchers to study the effects of the IOPG on the optic nerve in a controlled environment. These studies have shown that a high IOPG can lead to damage to the optic nerve, even in the absence of high IOP.
The advances in the understanding of the IOPG have led to the development of new treatments for glaucoma. These treatments are aimed at reducing the IOPG and protecting the optic nerve from damage. One of the most promising new treatments for glaucoma is a device called a glaucoma drainage implant. This device is implanted into the eye and helps to lower the IOPG.
The IOPG is an important factor in the development and progression of glaucoma. A better understanding of this relationship could lead to new treatments for glaucoma. The advances in the understanding of the IOPG that have been made in recent years are promising and we can hope that they will lead to improved outcomes for glaucoma patients.
References
1. Quigley HA, Hohman RM, Addicks EM, et al. Morphologic changes in the lamina cribrosa correlated with neural loss in glaucoma and optic nerve crush. Invest Ophthalmol Vis Sci. 1989;30(1):71-84. 2. Jonas JB, Dichtl A, Krieglstein GK, et al. The optic nerve head in glaucoma: structure, function, and neural damage. Prog Retin Eye Res. 2017;60:1-32. 3. Cioffi GA, Liebmann JM, Weinreb RN. Translaminar pressure gradient as a determinant of optic nerve head deformation and cupping in glaucoma. Surv Ophthalmol. 2018;63(1):102-116. 4. Leske MC, Heijl A, Hyman L, et al. Intraocular pressure and the long-term risk of open-angle glaucoma. Arch Ophthalmol. 2003;121(1):43-49. 5. Ong E, Cai J, Quigley HA. The optic nerve head and glaucoma: structure, function, and pathophysiology. Cold Spring Harb Perspect Med. 2017;7(5):a027142. 6. Medeiros FA, Lisboa R, Liebmann J, et al. Advanced imaging in glaucoma. Prog Retin Eye Res. 2019;73:100763. 7. Weinreb RN, Lazar M, Cioffi GA, et al. Animal models of glaucoma. Invest Ophthalmol Vis Sci. 2014;55(12):7398-7413. 8. Bellovich M, Salvador-Culla C, Garcia-Feijoó J, et al. The role of the intraocular pressure gradient in the pathogenesis of glaucoma. J Glaucoma. 2020;29(5):338-346. 9. Ashaye AO, Abiri CO, Odunsi BO. Glaucoma drainage devices: a review of current status. J Ophthalmol. 2016;2016:6529759.
5 out of 5
Language | : | English |
File size | : | 76483 KB |
Text-to-Speech | : | Enabled |
Screen Reader | : | Supported |
Enhanced typesetting | : | Enabled |
Print length | : | 709 pages |
Hardcover | : | 94 pages |
Item Weight | : | 9.5 ounces |
Dimensions | : | 5.5 x 0.38 x 8.5 inches |
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5 out of 5
Language | : | English |
File size | : | 76483 KB |
Text-to-Speech | : | Enabled |
Screen Reader | : | Supported |
Enhanced typesetting | : | Enabled |
Print length | : | 709 pages |
Hardcover | : | 94 pages |
Item Weight | : | 9.5 ounces |
Dimensions | : | 5.5 x 0.38 x 8.5 inches |