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A Murine Model of Carotid Aneurysm Formation
Published on: September 9, 2025
Familial intracranial aneurysms
Jin Soo Lee1, In Sung Park, Kyung Bum Park
1Department of Neurosurgery, Gyeongsang National University, School of Medicine, Jinju, Korea.
Insights
Familial intracranial aneurysms rupture at younger ages and are often found in the middle cerebral artery. Screening for subarachnoid hemorrhage (SAH) is recommended for relatives in their fifth or sixth decade.
Area of Science:
- Neurology
- Genetics
- Vascular Surgery
Background:
- Familial intracranial aneurysms (IAs) present distinct characteristics compared to non-familial cases.
- Understanding the genetic and clinical patterns of familial subarachnoid hemorrhage (SAH) is crucial for effective management.
Purpose of the Study:
- To investigate the clinical features of patients with familial SAH.
- To compare the characteristics of familial IAs with non-familial IAs.
Main Methods:
- Retrospective analysis of patients treated for SAH between 1993 and 2006.
- Identification of patients with at least one first-degree relative with SAH.
- Data collection on family history, aneurysm location, and age at rupture.
Main Results:
- Twelve patients from six families with familial SAH were identified.
- Mean age at rupture was 49.75 years, with similar ages among affected relatives.
- Middle cerebral artery aneurysms were common (42%), while anterior communicating artery aneurysms were rare.
Conclusions:
- Familial aneurysms rupture earlier and at smaller sizes than non-familial ones.
- High incidence in the middle cerebral artery and underrepresentation in the anterior communicating artery noted.
- Screening for SAH is advised for individuals with a sibling history of SAH, particularly in the fifth or sixth decade of life.
Objective:
Numerous studies have compared the characteristics of familial intracranial aneurysms with those of non-familial aneurysms. To better understand familial subarachnoid hemorrhage (SAH), we studied a series of patients with SAH who had at least one first-degree relative with SAH, and compared our results with those of previous studies.
Methods:
We identified patients treated for SAH at our hospital between January 1993 and October 2006 and analyzed those patients with one or more first-degree relatives with SAH. We retrospectively collected data from patients with a family history and searched for patients who had relatives with aneurysms or who had been treated at other hospitals for SAH.
Results:
We identified 12 patients from six families with at least two first-degree relatives with SAH. All patients had affected first-degree relatives; in five families, they were siblings. The mean age at the time of rupture was 49.75 years; in four families, the age difference was within 5 years. In five patients (42%), the aneurysm was located in the middle cerebral artery. Only one patient had an aneurysm in the anterior communicating artery.
Conclusion:
In agreement with previous studies, our results showed that familial aneurysms, in comparison with non-familiar aneurysms, ruptured at a younger age and smaller size, had a high incidence in the middle cerebral artery, and were underrepresented in the anterior communicating artery. Interestingly, the age at the time of rupture was similar between relatives. Screening should be considered in the fifth or sixth decade for those who have a sibling with SAH.
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