Mackey Jason, Brown Robert D, Sauerbeck Laura, Hornung Richard, Moomaw Charles J, Koller Daniel L, Foroud Tatiana, Deka Ranjan, Woo Daniel, Kleindorfer Dawn, Flaherty Matthew L, Meissner Irene, Anderson Craig, Rouleau Guy, Connolly E Sander, Huston John, Broderick Joseph P
Department of Neurology, Indiana University, Indianapolis, Ind., USA.
Cerebrovasc Dis. 2015;39(2):82-6. doi: 10.1159/000369961. Epub 2015 Jan 8.
Very few cases of intracranial aneurysms (IAs) in twins have been reported. Previous work has suggested that vulnerability to IA formation is heritable. Twin studies provide an opportunity to evaluate the impact of genetics on IA characteristics, including IA location. We therefore sought to examine IA location concordance, multiplicity, and rupture status within affected twin-pairs.
The Familial Intracranial Aneurysm study was a multicenter study whose goal was to identify genetic and other risk factors for formation and rupture of IAs. The study required at least three affected family members or an affected sibling pair for inclusion. Subjects with fusiform aneurysms, an IA associated with an AVM, or a family history of conditions known to predispose to IA formation, such as polycystic kidney disease, Ehlers-Danlos syndrome, Marfan syndrome, fibromuscular dysplasia, or moyamoya syndrome were excluded. Twin-pairs were identified by birth date and were classified as monozygotic (MZ) or dizygotic (DZ) through DNA marker genotypes. In addition to zygosity, we evaluated twin-pairs by smoking status, major arterial territory of IAs, and rupture status. Location concordance was defined as the presence of an IA in the same arterial distribution (ICA, MCA, ACA, and vertebrobasilar), irrespective of laterality, in both members of a twin-pair. The Fisher exact test was used for comparisons between MZ and DZ twin-pairs.
A total of 16 affected twin-pairs were identified. Location concordance was observed in 8 of 11 MZ twin-pairs but in only 1 of 5 DZ twin-pairs (p = 0.08). Three MZ subjects had unknown IA locations and comprised the three instances of MZ discordance. Six of the 11 MZ twin-pairs and none of the 5 DZ twin-pairs had IAs in the ICA distribution (p = 0.03). Multiple IAs were observed in 11 of 22 MZ and 5 of 10 DZ twin-pairs. Thirteen (13) of the 32 subjects had an IA rupture, including 10 of 22 MZ twins.
We found that arterial location concordance was greater in MZ than DZ twins, which suggests a genetic influence upon aneurysm location. The 16 twin-pairs in the present study are nearly the total of affected twin-pairs that have been reported in the literature to date. Further studies are needed to determine the impact of genetics in the formation and rupture of IAs.
双胞胎颅内动脉瘤(IA)的病例报道极少。此前的研究表明,IA形成的易感性具有遗传性。双胞胎研究为评估遗传学对IA特征(包括IA位置)的影响提供了契机。因此,我们试图研究受影响双胞胎对中IA的位置一致性、多发性和破裂状态。
家族性颅内动脉瘤研究是一项多中心研究,其目的是确定IA形成和破裂的遗传及其他危险因素。该研究要求至少有三名受影响的家庭成员或一对受影响的兄弟姐妹才能纳入。排除患有梭形动脉瘤、与动静脉畸形相关的IA或有已知易患IA形成疾病家族史的受试者,如多囊肾病、埃勒斯-当洛综合征、马凡综合征、纤维肌发育不良或烟雾病综合征。通过出生日期确定双胞胎对,并通过DNA标记基因型将其分类为同卵双胞胎(MZ)或异卵双胞胎(DZ)。除了合子性,我们还根据吸烟状况、IA的主要动脉区域和破裂状态对双胞胎对进行评估。位置一致性定义为双胞胎对的两名成员在相同动脉分布(颈内动脉、大脑中动脉、大脑前动脉和椎基底动脉)中存在IA,无论其侧别如何。采用Fisher精确检验对MZ和DZ双胞胎对进行比较。
共确定了16对受影响的双胞胎对。在11对MZ双胞胎对中有8对观察到位置一致性,而在5对DZ双胞胎对中只有1对观察到位置一致性(p = 0.08)。3名MZ受试者的IA位置未知,构成了3例MZ不一致的情况。11对MZ双胞胎对中有6对在颈内动脉分布中有IA,而5对DZ双胞胎对中均无(p = 0.03)。在22对MZ双胞胎对中的11对和10对DZ双胞胎对中的5对中观察到多发性IA。32名受试者中有13名发生了IA破裂,其中22名MZ双胞胎中有10名。
我们发现MZ双胞胎的动脉位置一致性高于DZ双胞胎,这表明遗传学对动脉瘤位置有影响。本研究中的16对双胞胎对几乎是迄今为止文献中报道的受影响双胞胎对的总数。需要进一步研究以确定遗传学在IA形成和破裂中的作用。