The influence of apolipoprotein E genotype on outcome after spontaneous subarachnoid hemorrhage: a preliminary study
The influence of apolipoprotein E genotype on outcome after spontaneous subarachnoid hemorrhage: a preliminary study
OBJECTIVE: Possession of an apolipoprotein E (APOE)[epsilon]4 allele has been shown to be associated with a poor outcome after closed head injury and spontaneous intracerebral hemorrhage but not after ischemic stroke. This study assessed the influence of the APOE genotype on outcome in patients admitted to a neurosurgical unit with spontaneous subarachnoid hemorrhage.
METHODS: A total of 100 patients with spontaneous subarachnoid hemorrhage were studied. Four patients were excluded because the diagnosis of subarachnoid hemorrhage was not confirmed. The incidence of rehemorrhage and delayed ischemia and the outcome at 6 months were determined using the Glasgow Outcome Scale. APOE genotypes were determined by polymerase chain reaction and restriction enzyme digestion.
RESULTS: Allele frequencies in this patient group were 0.04 for [epsilon]2, 0.86 for [epsilon]3, and 0.1 for [epsilon]4. Of 96 patients, 72 had an aneurysmal hemorrhage and 1 had a hemorrhage from an arteriovenous malformation. In 14 patients, the results of angiography were negative, and in 9, no angiogram was performed. Of the 96 patients, 20 had one or more [epsilon]4 allele. Outcome at 6 months was no worse in patients with one or more [epsilon]4 allele than in those with no [epsilon]4 allele (odds ratio, 0.98; 95% confidence interval, 0.35-2.74). None of the 12 patients who experienced delayed ischemic deterioration had an [epsilon]4 allele. Of the 20 patients with an [epsilon]4 allele, 3 had a rehemorrhage, as compared with 6 of 76 patients without an [epsilon]4 allele.
CONCLUSION: There was underrepresentation of the [epsilon]4 allele in this group when compared with previously studied cases of subarachnoid hemorrhage with a fatal outcome and with the general population. This suggests that patients with the [epsilon]4 allele who have a subarachnoid hemorrhage are less likely to be admitted to a neurosurgical unit. This study does not support an association between possession of an [epsilon]4 allele and poor outcome in patients admitted to a neurosurgical unit with spontaneous subarachnoid hemorrhage, although the wide confidence interval does not preclude a clinically relevant association between APOE genotype and outcome. The findings indicate that an association between genotype and the development of delayed ischemic complications after subarachnoid hemorrhage may be possible
1006-1010
Dunn, Laurence T.
8cbc115e-b8c9-4449-98dd-af388ff545bb
Stewart, Elaine
5a2e7454-2162-4ee2-b39c-359e17319058
Murray, Gordon D.
71d366ae-f424-49b6-854f-91bccbbc0beb
Nicoll, James A.
88c0685f-000e-4eb7-8f72-f36b4985e8ed
Teasdale, Graham M.
84a32691-2b76-4a52-8a11-7745fa97ed51
2001
Dunn, Laurence T.
8cbc115e-b8c9-4449-98dd-af388ff545bb
Stewart, Elaine
5a2e7454-2162-4ee2-b39c-359e17319058
Murray, Gordon D.
71d366ae-f424-49b6-854f-91bccbbc0beb
Nicoll, James A.
88c0685f-000e-4eb7-8f72-f36b4985e8ed
Teasdale, Graham M.
84a32691-2b76-4a52-8a11-7745fa97ed51
Dunn, Laurence T., Stewart, Elaine, Murray, Gordon D., Nicoll, James A. and Teasdale, Graham M.
(2001)
The influence of apolipoprotein E genotype on outcome after spontaneous subarachnoid hemorrhage: a preliminary study.
Neurosurgery, 48 (5), .
Abstract
OBJECTIVE: Possession of an apolipoprotein E (APOE)[epsilon]4 allele has been shown to be associated with a poor outcome after closed head injury and spontaneous intracerebral hemorrhage but not after ischemic stroke. This study assessed the influence of the APOE genotype on outcome in patients admitted to a neurosurgical unit with spontaneous subarachnoid hemorrhage.
METHODS: A total of 100 patients with spontaneous subarachnoid hemorrhage were studied. Four patients were excluded because the diagnosis of subarachnoid hemorrhage was not confirmed. The incidence of rehemorrhage and delayed ischemia and the outcome at 6 months were determined using the Glasgow Outcome Scale. APOE genotypes were determined by polymerase chain reaction and restriction enzyme digestion.
RESULTS: Allele frequencies in this patient group were 0.04 for [epsilon]2, 0.86 for [epsilon]3, and 0.1 for [epsilon]4. Of 96 patients, 72 had an aneurysmal hemorrhage and 1 had a hemorrhage from an arteriovenous malformation. In 14 patients, the results of angiography were negative, and in 9, no angiogram was performed. Of the 96 patients, 20 had one or more [epsilon]4 allele. Outcome at 6 months was no worse in patients with one or more [epsilon]4 allele than in those with no [epsilon]4 allele (odds ratio, 0.98; 95% confidence interval, 0.35-2.74). None of the 12 patients who experienced delayed ischemic deterioration had an [epsilon]4 allele. Of the 20 patients with an [epsilon]4 allele, 3 had a rehemorrhage, as compared with 6 of 76 patients without an [epsilon]4 allele.
CONCLUSION: There was underrepresentation of the [epsilon]4 allele in this group when compared with previously studied cases of subarachnoid hemorrhage with a fatal outcome and with the general population. This suggests that patients with the [epsilon]4 allele who have a subarachnoid hemorrhage are less likely to be admitted to a neurosurgical unit. This study does not support an association between possession of an [epsilon]4 allele and poor outcome in patients admitted to a neurosurgical unit with spontaneous subarachnoid hemorrhage, although the wide confidence interval does not preclude a clinically relevant association between APOE genotype and outcome. The findings indicate that an association between genotype and the development of delayed ischemic complications after subarachnoid hemorrhage may be possible
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Published date: 2001
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Local EPrints ID: 27566
URI: http://eprints.soton.ac.uk/id/eprint/27566
ISSN: 0148-396X
PURE UUID: 42ae4f68-1dd6-4461-b28b-9035077c5b3d
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Date deposited: 28 Apr 2006
Last modified: 10 Jan 2022 02:46
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Author:
Laurence T. Dunn
Author:
Elaine Stewart
Author:
Gordon D. Murray
Author:
Graham M. Teasdale
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