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Genetic influences on outcome following acute neurological insults

Genetic influences on outcome following acute neurological insults
Genetic influences on outcome following acute neurological insults
Purpose of review: To examine the evidence for a genetic influence on clinical outcome after a variety of acute neurologic events.
Recent findings: Clinical outcome after brain injury is variable and cannot easily be predicted. It has been proposed that genetic polymorphisms may have an important role in determining outcome from a number of conditions, including acute neurologic events. Apolipoprotein E, an important mediator of cholesterol and lipid transport in the brain, is coded by a polymorphic gene (APOE). The APOE [varepsilon]4 allele has been associated with unfavorable outcome after traumatic brain injury (TBI), hemorrhagic stroke and subarachnoid hemorrhage (SAH). Genes involved in other pathophysiological processes, such as cytokine genes in neuroinflammation, are now being implicated. For example interleukin-6 (IL-6) promoter polymorphisms are a risk factor for poor outcome after ischemic stroke, and may have an effect after traumatic brain injury. The emerging importance of a number of other gene polymorphisms is outlined in the review.
Summary: There is evidence demonstrating the [varepsilon]4 allele of APOE predisposes to poor outcome after TBI, hemorrhagic stroke and SAH, but not ischemic stroke. The reason for this difference is unclear but it suggests there may be differences in the key mechanisms underlying the response to different types of insult. The role of other gene polymorphisms is being increasingly explored but there is still a need for larger prospective studies looking at larger panels of gene polymorphisms.
1070-5295
105-110
Waters, Ryan J.
088ec072-634a-4444-948d-5b8ae5e9ad19
Nicoll, James A.R.
88c0685f-000e-4eb7-8f72-f36b4985e8ed
Waters, Ryan J.
088ec072-634a-4444-948d-5b8ae5e9ad19
Nicoll, James A.R.
88c0685f-000e-4eb7-8f72-f36b4985e8ed

Waters, Ryan J. and Nicoll, James A.R. (2005) Genetic influences on outcome following acute neurological insults. Current Opinion in Critical Care, 11 (2), 105-110.

Record type: Article

Abstract

Purpose of review: To examine the evidence for a genetic influence on clinical outcome after a variety of acute neurologic events.
Recent findings: Clinical outcome after brain injury is variable and cannot easily be predicted. It has been proposed that genetic polymorphisms may have an important role in determining outcome from a number of conditions, including acute neurologic events. Apolipoprotein E, an important mediator of cholesterol and lipid transport in the brain, is coded by a polymorphic gene (APOE). The APOE [varepsilon]4 allele has been associated with unfavorable outcome after traumatic brain injury (TBI), hemorrhagic stroke and subarachnoid hemorrhage (SAH). Genes involved in other pathophysiological processes, such as cytokine genes in neuroinflammation, are now being implicated. For example interleukin-6 (IL-6) promoter polymorphisms are a risk factor for poor outcome after ischemic stroke, and may have an effect after traumatic brain injury. The emerging importance of a number of other gene polymorphisms is outlined in the review.
Summary: There is evidence demonstrating the [varepsilon]4 allele of APOE predisposes to poor outcome after TBI, hemorrhagic stroke and SAH, but not ischemic stroke. The reason for this difference is unclear but it suggests there may be differences in the key mechanisms underlying the response to different types of insult. The role of other gene polymorphisms is being increasingly explored but there is still a need for larger prospective studies looking at larger panels of gene polymorphisms.

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Published date: 2005

Identifiers

Local EPrints ID: 27735
URI: http://eprints.soton.ac.uk/id/eprint/27735
ISSN: 1070-5295
PURE UUID: 74b82885-d3bd-46f3-a917-5f2d6bc3b31a
ORCID for James A.R. Nicoll: ORCID iD orcid.org/0000-0002-9444-7246

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Date deposited: 25 Apr 2006
Last modified: 09 Jan 2022 03:09

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Contributors

Author: Ryan J. Waters

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