Struycken P M, Pals G, Limburg M, Pronk J C, Wijmenga C, Pearson P L, Luijten J A F M, van den Berg J S P, Vermeulen M, Rinkel G J E, Westerveld A
Department of Human Genetics, Academic Medical Center, Universiteit van Amsterdam, The Netherlands.
Eur J Hum Genet. 2003 Oct;11(10):737-43. doi: 10.1038/sj.ejhg.5201039.
Intracranial aneurysms (IA) are the major cause of subarachnoid haemorrhages (SAH). A positive family history for SAH is reported in 5-10% of the patients. The mode of inheritance is not unambiguously established; both autosomal dominant and recessive modes have been reported. In sporadic as well as in familial SAH, approximately 60% of the SAH patients are female. Recently, anticipation has been described in familial SAH. Since up to 15% of the SAHs are not caused by an IA, we have analysed anticipation, sex ratio and mode of inheritance only in families with patients with a proven IA in two consecutive generations. A total of 10 families were studied in which at least two persons in consecutive generations were affected by SAH, a symptomatic IA (SIA) or a presymptomatic IA (PIA). We also analysed published data from families with a proven IA in two consecutive generations on age of SIA onset and sex ratios among affected family members (both SIA and PIA). The age of SIA onset in the parental generation (mean 55.5 years) differed significantly from the age of onset in their children (mean 32.4 years). In the parental generation 11 men and 37 women were affected (both SIA and PIA), in the consecutive generation these numbers were 28 men and 32 women. There is a significant difference in sex ratio of affected family members when the generations are compared (P<0.02). No family could be found in which three consecutive generations were affected by an IA (SIA or PIA).
颅内动脉瘤(IA)是蛛网膜下腔出血(SAH)的主要病因。据报道,5% - 10%的患者有SAH的阳性家族史。遗传模式尚未明确确定;常染色体显性和隐性模式均有报道。在散发性以及家族性SAH中,约60%的SAH患者为女性。最近,家族性SAH中出现了遗传早现现象。由于高达15%的SAH并非由IA引起,我们仅在连续两代有确诊IA患者的家庭中分析了遗传早现、性别比例和遗传模式。总共研究了10个家庭,其中连续两代至少有两人受SAH、症状性IA(SIA)或症状前IA(PIA)影响。我们还分析了已发表的连续两代有确诊IA的家庭中SIA发病年龄和受影响家庭成员(SIA和PIA)性别比例的数据。亲代的SIA发病年龄(平均55.5岁)与他们子女的发病年龄(平均32.4岁)有显著差异。亲代中有11名男性和37名女性受影响(SIA和PIA),在连续的一代中,这些数字分别为28名男性和32名女性。比较各代时,受影响家庭成员的性别比例有显著差异(P<0.02)。未发现有连续三代受IA(SIA或PIA)影响的家庭。