Risk of Intracranial Aneurysms in Families with Subarachnoid
Hemorrhage
Mark J Alberts, Ana Quinones, Carmelo Graffagnino, Allan
Friedman and Allen D Roses

Abstract:
Background: Genetic factors may be important
in the etiology of subarachnoid hemorrhage (SAH) and intracranial
aneurysm (IA) formation. Several studies have reported the familial
occurrence of SAH and IA, although in most cases asymptomatic
family members were not studied with elective angiography. The
examination of data from large sibships could provide important
information about the frequency of IA occurrence in at-risk
individuals and the mode of inheritance for familial SAH/IA.
Methods: We reviewed published case series of
sibships with SAH and at least four siblings, in which at least
one sibling underwent elective angiography. Data were collected
on age-of-onset, clinical events, presence of hypertension,
angiographic findings, and outcome. Patients were classified
as "affected" if they had a SAH or if an IA was detected by
elective angiography, and "unaffected" if they were asymptomatic
and had a negative angiogram. Results: Seven case
series with 52 individuals (26 men and 26 women) met our inclusion
criteria. The sibships ranged from 6 to 13 members. Most of
the siblings (32 of 52, 61%) were asymptomatic, 18 (35%) had
a SAH, and 2 (4%) had focal symptoms but no SAH. Elective angiography
of 34 siblings showed an IA in 11 (32%) and was negative in
23 (68%). The overall rate of affecteds (SAH or IA) was 56%.
Conclusions: Based on data from these sibships,
angiography of asymptomatic at-risk siblings demonstrated an
IA in almost one-third of cases. Familial SAH/IA segregated
with a pattern that was consistent with an autosomal dominant
trait in this selected series of sibships, although other factors
could produce these findings.
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Can.
J. Neurol. Sci. 1995; 22: 121-125
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