glaucoma - escrs.org fileglaucoma is a neurodegenerative disease that affects the central visual...

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24 EUROTIMES | Volume 17 | Issue 7/8 T he study of brain changes in glaucoma may provide new insights into the pathobiology of glaucomatous damage and disease progression and stimulate new detection and therapeutic strategies to prevent blindness, according to Neeru Gupta MD, PhD. “There is now abundant evidence that glaucoma is a neurodegenerative disease that affects the central visual system. This is borne out by our own research over the last decade as well as work from other laboratories around the world. It is clear that if we want to do something about glaucoma we should be tackling the eye but also remembering that we need to follow up with the connections to the brain, focusing on structures such as the retinal ganglion cell and lateral geniculate nucleus,” Dr Gupta told delegates attending the World Glaucoma Congress. Dr Gupta, professor and Dorothy Pitts chair of ophthalmology and vision sciences, and laboratory medicine and pathobiology at St Michael’s Hospital, University of Toronto, said that it was important to consider other factors beyond optic disc changes in recognising and treating glaucoma. “If we want to move forward, it may be worthwhile to explore some of the processes that go into the visual aspects that take place in the brain,” she said. While a lot of work in glaucoma research and treatment has focused on measures to lower intraocular pressure, Dr Gupta said that the elephant in the room is the fact that many patients will continue to lose sight despite treatment. One promising avenue of research has been to focus on the target of retinal ganglion cells, the lateral geniculate nucleus (LGN), a structure located in the thalamus of the brain which serves as the primary relay centre for visual information received from the retina. Dr Gupta described the LGN as a very special structure exquisitely organised into six distinctive layers: the ventral two magnocellular layers and the dorsal four parvocellular layers. An additional set of neurons, known as the koniocellular sublayers, are found ventral to each of the magnocellular and parvocellular layers. In studies of experimental monkey glaucoma with optic nerve fibre loss, the LGN was shown to undergo significant degenerative changes, including overall LGN shrinkage and reduced neuron size and number, said Dr Gupta. There is also evidence that the same process holds true for humans. In 2006, Dr Gupta’s group published the results of a post-mortem human glaucoma case with bilateral visual-field loss in which reduced LGN and neuron size were observed by histomorphometry and ex vivo MRI scans compared with age-matched controls. In the same study, pre-chiasmal optic nerve and visual cortex changes were also seen. In 2009, Dr Gupta and colleagues looked at patients with glaucoma, and evaluated the structure of the LGN by MRI. This work provides evidence of significant LGN atrophy in human disease. New techniques The use of latest- generation imaging technologies, in particular MRI scanning techniques, is helping to transform understanding of the role of the brain in glaucoma, said Dr Gupta. Functional magnetic resonance imaging (fMRI), a non-invasive means of inferring function-specific neuronal activity, enables researchers to evaluate glaucomatous changes in neuronal activity throughout the visual pathway in vivo. Recent glaucoma research has focused on the potentially protective effects of memantine, a neuroprotective agent used in neurodegenerative diseases such as Parkinson’s disease and Alzheimer’s disease. In a 2006 study of memantine in monkey glaucoma, Yucel et al showed that memantine attenuates LGN neuron shrinkage. Following up this work, more recently, Dr Gupta’s group used Sholl analysis to demonstrate that dendrites in monkey LGN have reduced complexity. “We specifically evaluated dendrite complexity under the microscope and saw a significant increase in dendrite complexity in glaucoma subjects treated with oral memantine compared to those with glaucoma that received only vehicle. This tells us that there is an opportunity to change the wiring in the brain with new treatments as we learn more about visual system degeneration in glaucoma,” she said. contact Neeru Gupta [email protected] NEW STRATEGIES Other factors beyond optic disk changes should be considered when treating glaucoma By Dermot McGrath in Paris The power of one THE ONE FEMTO PLATFORM for cornea, presbyopia and cataract. Presenting the unparalleled Ziemer FEMTO LDV Z Models – a technical revolution in ocular surgery. No laser is more Precise, more powerful or more progressive when it comes to meeting all your procedural needs in a single platform. With Ziemer’s FEMTO LDV Z Models, now you can operate with a modular femtosecond system that is easy to configure, designed to grow with your practice – cornea and presbyopia today, cataract tomorrow. www.ziemergroup.com The Ziemer FEMTO LDV Z Models are FDA cleared and CE marked and available for immediate delivery. For some countries, availability may be restricted due to local regulatory requirements; please contact Ziemer for details. The creation of a corneal pocket is part of a presbyopia intervention. Availability of related corneal inlays and implants according to policy of the individual manufacturers and regulatory status in the individual countries. Cataract procedures with the FEMTO LDV Z2, Z4 and Z6 models are not cleared in the United States and in all other countries. An upgrade possibility for these devices is planned once cataract options are available and cleared by the responsible regulatory bodies. Update GLAUCOMA

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24

EUROTIMES | Volume 17 | Issue 7/8

The study of brain changes in glaucoma may provide new insights into the pathobiology of glaucomatous damage and disease

progression and stimulate new detection and therapeutic strategies to prevent blindness, according to Neeru Gupta MD, PhD.

“There is now abundant evidence that glaucoma is a neurodegenerative disease that affects the central visual system. This is borne out by our own research over the last decade as well as work from other laboratories around the world. It is clear that if we want to do something about glaucoma we should be tackling the eye but also remembering that we need to follow up with the connections to the brain, focusing on structures such as the retinal ganglion cell and lateral geniculate nucleus,” Dr Gupta told delegates attending the World Glaucoma Congress.

Dr Gupta, professor and Dorothy Pitts chair of ophthalmology and vision sciences, and laboratory medicine and pathobiology at St Michael’s Hospital, University of Toronto, said that it was important to consider other factors beyond optic disc changes in recognising and treating glaucoma.

“If we want to move forward, it may be worthwhile to explore some of the processes that go into the visual aspects that take place in the brain,” she said.

While a lot of work in glaucoma research and treatment has focused on measures to lower intraocular pressure, Dr Gupta said that the elephant in the room is the fact that many patients will continue to lose sight despite treatment.

One promising avenue of research has been to focus on the target of retinal ganglion cells, the lateral geniculate nucleus (LGN), a structure located in the thalamus of the brain which serves as the primary relay centre for visual information received from the retina.

Dr Gupta described the LGN as a very special structure exquisitely organised into six distinctive layers: the ventral two magnocellular layers and the dorsal four parvocellular layers. An additional set of neurons, known as the koniocellular sublayers, are found ventral to each of the magnocellular and parvocellular layers.

In studies of experimental monkey glaucoma with optic nerve fibre loss, the LGN was shown to undergo significant

degenerative changes, including overall LGN shrinkage and reduced neuron size and number, said Dr Gupta.

There is also evidence that the same process holds true for humans. In 2006, Dr Gupta’s group published the results of a post-mortem human glaucoma case with bilateral visual-field loss in which reduced LGN and neuron size were observed by histomorphometry and ex vivo MRI scans compared with age-matched controls. In the same study, pre-chiasmal optic nerve and visual cortex changes were also seen. In 2009, Dr Gupta and colleagues looked at patients with glaucoma, and evaluated the structure of the LGN by MRI. This work provides evidence of significant LGN atrophy in human disease.

New techniques The use of latest-generation imaging technologies, in particular MRI scanning techniques, is helping to transform understanding of the role of the brain in glaucoma, said Dr Gupta. Functional magnetic resonance imaging (fMRI), a non-invasive means of inferring function-specific neuronal activity, enables researchers to evaluate glaucomatous changes in neuronal activity throughout the visual pathway in vivo.

Recent glaucoma research has focused on the potentially protective effects of memantine, a neuroprotective agent used in neurodegenerative diseases such as Parkinson’s disease and Alzheimer’s disease. In a 2006 study of memantine in monkey glaucoma, Yucel et al showed that memantine attenuates LGN neuron shrinkage.

Following up this work, more recently, Dr Gupta’s group used Sholl analysis to demonstrate that dendrites in monkey LGN have reduced complexity.

“We specifically evaluated dendrite complexity under the microscope and saw a significant increase in dendrite complexity in glaucoma subjects treated with oral memantine compared to those with glaucoma that received only vehicle. This tells us that there is an opportunity to change the wiring in the brain with new treatments as we learn more about visual system degeneration in glaucoma,” she said.

contact Neeru Gupta – [email protected]

NEw STRATEgIESOther factors beyond optic disk changes should be considered when treating glaucomaBy Dermot McGrath in Paris

The power of one

The one FeMTo plaTForM for cornea, presbyopia and cataract.

Presenting the unparalleled Ziemer FEMTO LDV Z Models – a technical revolution in ocular surgery. No laser is more Precise, more powerful or more progressive when it comes to meeting all your procedural needs in a single platform. With Ziemer’s FEMTO LDV Z Models, now you can operate with a modular femtosecond system that is easy to configure, designed to grow with your practice – cornea and presbyopia today, cataract tomorrow.www.ziemergroup.com

The Ziemer FEMTO LDV Z Models are FDA cleared and CE marked and available for immediate delivery. For some countries, availability may be restricted due to local regulatory requirements; please contact Ziemer for details. The creation of a corneal pocket is part of a presbyopia intervention. Availability of related corneal inlays and implants according to policy of the individual manufacturers and regulatory status in the individual countries. Cataract procedures with the FEMTO LDV Z2, Z4 and Z6 models are not cleared in the United States and in all other countries. An upgrade possibility for these devices is planned once cataract options are available and cleared by the responsible regulatory bodies.

eurotimes_junaug2012_FEMTO_LDV_Z_Models_Ad_120x300mm.indd 1 12.06.12 12:01

Update

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