Ronkainen A, Miettinen H, Karkola K, Papinaho S, Vanninen R, Puranen M, Hernesniemi J
Department of Neurosurgery, Kuopio University Hospital, Finland.
Stroke. 1998 Feb;29(2):359-62. doi: 10.1161/01.str.29.2.359.
The purpose of the present study was to calculate the prevalence and relative risk of unruptured incidental intracranial aneurysms (IAs) among families with IA case(s) compared with the general population in one geographically defined area in East Finland and to identify the risk group that could benefit most from screening for IAs. We compared these results with our earlier study results of familial IA (FIA) cases, with two or more known IA cases in the same family.
The study groups were collected from the catchment area of the University Hospital of Kuopio in East Finland. The inclusion criteria were age 30 to 70 years and unruptured incidental IAs > or =3 mm. Patients with previous subarachnoid hemorrhage or in whom a ruptured IA was found to be the cause of death were excluded from all study groups. During routine forensic autopsies the circle of Willis was studied for IAs to estimate the number of IAs in the general population. In the families with one known IA case and in FIA families, MR angiography was used as a preliminary screening method for IAs, followed by intra-arterial angiography to verify suspected IAs. Study populations were age and sex adjusted for the statistical calculations.
The relative risk for IAs among first-degree relatives in FIA families was 4.2 (95% confidence interval, 2.2 to 8.0) and among first-degree relatives in families with only one affected family member was 1.8 (95% confidence interval, 0.7 to 4.8) compared with the general population in East Finland.
First-degree relatives in FIA families constitute a high-risk group for incidental IAs, and this group would benefit from screening studies for IAs. Screening for IAs in families with only one affected member or in the general population is not recommended.
本研究旨在计算与芬兰东部一个地理区域的普通人群相比,颅内动脉瘤(IA)病例家庭中未破裂偶然发现的颅内动脉瘤的患病率和相对风险,并确定最能从IA筛查中获益的风险组。我们将这些结果与我们早期关于家族性IA(FIA)病例的研究结果进行了比较,FIA病例是指在同一家族中有两个或更多已知IA病例。
研究组来自芬兰东部库奥皮奥大学医院的服务区域。纳入标准为年龄30至70岁且未破裂偶然发现的IA≥3mm。既往有蛛网膜下腔出血或发现破裂IA是死亡原因的患者被排除在所有研究组之外。在常规法医尸检期间,研究Willis环以估计普通人群中IA的数量。在有一个已知IA病例的家庭和FIA家庭中,磁共振血管造影用作IA的初步筛查方法,随后进行动脉内血管造影以验证疑似IA。研究人群在统计计算时进行了年龄和性别调整。
与芬兰东部的普通人群相比,FIA家庭中一级亲属患IA的相对风险为4.2(95%置信区间,2.2至8.0),而在只有一名受影响家庭成员的家庭中一级亲属患IA的相对风险为1.8(95%置信区间,0.7至4.8)。
FIA家庭中的一级亲属构成偶然发现IA的高危组,该组将从IA筛查研究中获益。不建议对只有一名受影响成员的家庭或普通人群进行IA筛查。