Woo D, Hornung R, Sauerbeck L, Brown R, Meissner I, Huston J, Foroud T, Broderick J
Departments of Neurology, Environmental Health, and Center for Environmental Genetics, University of Cincinnati, Cincinnati, OH 45267-0525, USA.
Neurology. 2009 Feb 24;72(8):695-8. doi: 10.1212/01.wnl.0000342999.99907.fd.
Previous studies have reported intracranial aneurysm (IA) occurring at young ages in subsequent generations. These studies did not correct for duration of follow-up. Second-generation members who would have their ruptured IA late in life may not be detected due to shorter follow-up time than the first generation. We examined families in which ruptured IA occurred in two consecutive generations for the hypothesis that the second generation (F1) was more likely to have a rupture at a younger age than the older generation (F0).
The Familial Intracranial Aneurysm (FIA) Study is a multicenter, international study recruiting families of ruptured and unruptured IA. All available family members are interviewed. Cox proportional hazards regression models and Kaplan-Meier curves were used to examine differences by generation.
Although we found that the F1 generation was more likely to have an aneurysm rupture at a younger age than the F0 generation, we found that this was largely because of a lack of follow-up time in the F1 generation. The F1 generation had 50% the rupture rate of the prior generation. When analyzed by Kaplan-Meier curves, we found a tendency to have a slightly later rupture rate in the F1 generation once time to follow-up was included in the analysis model.
Families of ruptured intracranial aneurysm (IA) do not appear to demonstrate "anticipation." Our finding suggests that genetic epidemiology of ruptured IA should examine all types of variations such as single base-pair changes, deletions, insertions, and other variations that do not demonstrate anticipation.
既往研究报道了颅内动脉瘤(IA)在后代中发生于年轻时。这些研究未对随访时间进行校正。由于随访时间比第一代短,那些颅内动脉瘤破裂较晚的第二代成员可能未被检测到。我们研究了连续两代发生颅内动脉瘤破裂的家族,以验证第二代(F1)比第一代(F0)在年轻时更易发生破裂的假设。
家族性颅内动脉瘤(FIA)研究是一项多中心国际研究,招募颅内动脉瘤破裂和未破裂患者的家族。对所有可用的家庭成员进行访谈。使用Cox比例风险回归模型和Kaplan-Meier曲线按代来检验差异。
尽管我们发现F1代比F0代在年轻时更易发生动脉瘤破裂,但我们发现这很大程度上是由于F1代随访时间不足。F1代的破裂率是上一代的50%。通过Kaplan-Meier曲线分析,当将随访时间纳入分析模型时,我们发现F1代的破裂率有稍晚出现的趋势。
颅内动脉瘤(IA)破裂的家族似乎未表现出“遗传早现”。我们的发现表明,颅内动脉瘤破裂的遗传流行病学应研究所有类型的变异,如单碱基对变化、缺失、插入以及其他未表现出遗传早现的变异。