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Genetic investigations on intracranial aneurysm: Update and perspectives
被引:23
作者:
Bourcier, Romain
[1
,2
]
Redon, Richard
[2
]
Desal, Hubert
[1
,2
]
机构:
[1] CHU Nantes, Dept Neuroradiol, F-44000 Nantes, France
[2] Inst Thorax, Inserm Unit 1087, F-44000 Nantes, France
关键词:
Genetics;
Intracranial;
Aneurysm;
GENOME-WIDE ASSOCIATION;
RISK-FACTORS;
SUBARACHNOID HEMORRHAGE;
EXPRESSION PROFILES;
SUSCEPTIBILITY LOCI;
CEREBRAL ANEURYSMS;
BLOOD-PRESSURE;
LINKAGE SCANS;
METAANALYSIS;
MUTATIONS;
D O I:
10.1016/j.neurad.2015.01.002
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Detection of an intracranial aneurysm (IA) is a common finding in MRI practice. Nowadays, the incidence of unruptured IA seems to be increasing with the continuous evolution of imaging techniques. Important modifiable risk factors for SAH are well defined, but familial history of IA is the best risk marker for the presence of IA. Numerous heritable conditions are associated with IA formation but these syndromes account for less than 1% of all As in the population. No diagnostic test based on genetic knowledge is currently available to identify theses mutations and patients who are at higher risk for developing IAs. In the longer term, a more comprehensive understanding of independent and interdependent molecular pathways germane to IA formation and rupture may guide the physician in developing targeted therapies and optimizing prognostic risk assessment. (C) 2015 Elsevier Masson SAS. All rights reserved.
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页码:67 / 71
页数:5
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