Literature DB >> 22540404

Unruptured intracranial aneurysms in the Familial Intracranial Aneurysm and International Study of Unruptured Intracranial Aneurysms cohorts: differences in multiplicity and location.

Jason Mackey1, Robert D Brown, Charles J Moomaw, Laura Sauerbeck, Richard Hornung, Dheeraj Gandhi, Daniel Woo, Dawn Kleindorfer, Matthew L Flaherty, Irene Meissner, Craig Anderson, E Sander Connolly, Guy Rouleau, David F Kallmes, James Torner, John Huston, Joseph P Broderick.   

Abstract

OBJECT: Familial predisposition is a recognized nonmodifiable risk factor for the formation and rupture of intracranial aneurysms (IAs). However, data regarding the characteristics of familial IAs are limited. The authors sought to describe familial IAs more fully, and to compare their characteristics with a large cohort of nonfamilial IAs.
METHODS: The Familial Intracranial Aneurysm (FIA) study is a multicenter international study with the goal of identifying genetic and other risk factors for formation and rupture of IAs in a highly enriched population. The authors compared the FIA study cohort with the International Study of Unruptured Intracranial Aneurysms (ISUIA) cohort with regard to patient demographic data, IA location, and IA multiplicity. To improve comparability, all patients in the ISUIA who had a family history of IAs or subarachnoid hemorrhage were excluded, as well as all patients in both cohorts who had a ruptured IA prior to study entry.
RESULTS: Of 983 patients enrolled in the FIA study with definite or probable IAs, 511 met the inclusion criteria for this analysis. Of the 4059 patients in the ISUIA study, 983 had a previous IA rupture and 657 of the remainder had a positive family history, leaving 2419 individuals in the analysis. Multiplicity was more common in the FIA patients (35.6% vs 27.9%, p<0.001). The FIA patients had a higher proportion of IAs located in the middle cerebral artery (28.6% vs 24.9%), whereas ISUIA patients had a higher proportion of posterior communicating artery IAs (13.7% vs 8.2%, p=0.016).
CONCLUSIONS: Heritable structural vulnerability may account for differences in IA multiplicity and location. Important investigations into the underlying genetic mechanisms of IA formation are ongoing.

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Year:  2012        PMID: 22540404      PMCID: PMC3914137          DOI: 10.3171/2012.4.JNS111822

Source DB:  PubMed          Journal:  J Neurosurg        ISSN: 0022-3085            Impact factor:   5.115


  16 in total

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3.  Unruptured intracranial aneurysms--risk of rupture and risks of surgical intervention.

Authors: 
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4.  Stroke incidence is decreasing in whites but not in blacks: a population-based estimate of temporal trends in stroke incidence from the Greater Cincinnati/Northern Kentucky Stroke Study.

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5.  Prevalence and risk of rupture of intracranial aneurysms: a systematic review.

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6.  Unruptured intracranial aneurysms: natural history, clinical outcome, and risks of surgical and endovascular treatment.

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7.  Genome-wide association study of intracranial aneurysm identifies three new risk loci.

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8.  Familial intracranial aneurysms.

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Journal:  J Neurosurg       Date:  1987-04       Impact factor: 5.115

9.  Greater rupture risk for familial as compared to sporadic unruptured intracranial aneurysms.

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Journal:  Stroke       Date:  2009-02-19       Impact factor: 7.914

Review 10.  Genetics of intracranial aneurysms.

Authors:  Ynte M Ruigrok; Gabriel J E Rinkel
Journal:  Stroke       Date:  2008-02-07       Impact factor: 7.914

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2.  Comparative effectiveness research.

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3.  PCNT point mutations and familial intracranial aneurysms.

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6.  A 54-year-old man with 12 intracranial aneurysms and familial subarachnoid hemorrhage: case report.

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Review 7.  Factors affecting formation and rupture of intracranial saccular aneurysms.

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8.  Incidence of Aneurysmal Subarachnoid Hemorrhage with Procedures Requiring General Anesthesia in Patients with Unruptured Intracranial Aneurysms.

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Review 9.  Genetic factors involves in intracranial aneurysms--actualities.

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10.  High risk population isolate reveals low frequency variants predisposing to intracranial aneurysms.

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