Skip Navigation


Brain Advance Access originally published online on April 7, 2005
Brain 2005 128(7):1677-1685; doi:10.1093/brain/awh497
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
128/7/1677    most recent
awh497v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (12)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Teasdale, G. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Teasdale, G. M.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author (2005). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For Permissions, please email: journals.permissions@oupjournals.org

The familial risk of subarachnoid haemorrhage

Graham M. Teasdale1, Joanna M. Wardlaw3, Philip M. White1,3, Gordon Murray4, Evelyn M. Teasdale2, Valerie Easton3 on behalf of the Davie Cooper Scottish Aneurysm Study Group

1 University Department of Neurosurgery and 2 Department of Neuroradiology, Institute of Neurological Sciences, Southern General Hospital, Glasgow, 3 University of Edinburgh, Division of Clinical Neurosciences, Western General Hospital and 4 University of Edinburgh, Public Health Sciences, Medical School, Edinburgh, UK

Correspondence to: Professor J. M. Wardlaw, Division of Clinical Neurosciences, Western General Hospital, Crewe Rd, Edinburgh EH4 2XU, UK E-mail: joanna.wardlaw{at}ed.ac.uk

Relatives of people with aneurysmal subarachnoid haemorrhage (SAH) may be at increased risk of SAH, but precise data on the level of risk and which relatives are most likely to be affected are lacking. We studied two samples: 5478 relatives of patients from the whole of Scotland who had a SAH in one year and 3213 relatives of patients with a SAH admitted to the West of Scotland regional neurosurgical unit 10 years previously. Overall, 2% of all relatives in each sample had a SAH. In the Scotland-wide sample, the absolute lifetime risk of SAH (from birth to 70 years) was higher for first-degree relatives [4.7%; 95% confidence interval (CI): 3.1–6.3%] than for second-degree (1.9%; 95% CI: 1.0–2.9%). In the West of Scotland sample, the lifetime risks were very similar to the Scotland-wide sample. The 10-year prospective risk for first-degree relatives alive at the time of the index patient's SAH was 1.2% (95% CI: 0.4–2%) and for second-degree was 0.5% (95% CI: 0.1–0.8%). There was a trend for risk to be highest in families with two first-degree relatives affected and lowest with only one second-degree affected. Most living relatives of patients who suffer a SAH are at low absolute risk of a future haemorrhage; screening is inappropriate except for the few families in whom two or more first-degree relatives, i.e. index case plus one extra have been affected.

Key Words: subarachnoid haemorrhage; intracranial aneurysm; familial risk; epidemiology; screening

Abbreviations: CHI = Community Health Index; CI = confidence interval; ISD = Scottish Office Information and Statistics Division; MRA = magnetic resonance angiography; SAH = subarachnoid haemorrhage

Received July 15, 2004. Revised December 8, 2004. Accepted March 7, 2005.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
StrokeHome page
Y. M. Ruigrok, C. Wijmenga, G. J.E. Rinkel, R. v. Slot, F. Baas, M. Wolfs, A. Westerveld, and Y. B.W.E.M. Roos
Genomewide Linkage in a Large Dutch Family With Intracranial Aneurysms: Replication of 2 Loci for Intracranial Aneurysms to Chromosome 1p36.11-p36.13 and Xp22.2-p22.32
Stroke, April 1, 2008; 39(4): 1096 - 1102.
[Abstract] [Full Text] [PDF]


Home page
Physiol. GenomicsHome page
S. Weinsheimer, G. M. Lenk, M. van der Voet, S. Land, A. Ronkainen, I. Alafuzoff, H. Kuivaniemi, and G. Tromp
Integration of expression profiles and genetic mapping data to identify candidate genes in intracranial aneurysm
Physiol Genomics, December 19, 2007; 32(1): 45 - 57.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
S. Weinsheimer, K. A.B. Goddard, A. R. Parrado, Q. Lu, M. Sinha, E. R. Lebedeva, A. Ronkainen, M. Niemela, E. K. Khusnutdinova, R. I. Khusainova, et al.
Association of Kallikrein Gene Polymorphisms With Intracranial Aneurysms
Stroke, October 1, 2007; 38(10): 2670 - 2676.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
Y. M. Ruigrok, G. J.E. Rinkel, R. van't Slot, M. Wolfs, S. Tang, and C. Wijmenga
Evidence in favor of the contribution of genes involved in the maintenance of the extracellular matrix of the arterial wall to the development of intracranial aneurysms
Hum. Mol. Genet., November 15, 2006; 15(22): 3361 - 3368.
[Abstract] [Full Text] [PDF]


Home page
BMJHome page
R. Al-Shahi, P. M White, R. J Davenport, and K. W Lindsay
Subarachnoid haemorrhage
BMJ, July 29, 2006; 333(7561): 235 - 240.
[Full Text] [PDF]


Home page
StrokeHome page
H. S. Markus and M. J. Alberts
Update on Genetics of Stroke and Cerebrovascular Disease 2005
Stroke, February 1, 2006; 37(2): 288 - 290.
[Full Text] [PDF]


Home page
JWatch NeurologyHome page
Familial Risk for Subarachnoid Hemorrhage
Journal Watch Neurology, October 6, 2005; 2005(1006): 3 - 3.
[Full Text]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.