Mineharu Y, Takenaka K, Yamakawa H, Inoue K, Ikeda H, Kikuta K-I, Takagi Y, Nozaki K, Hashimoto N, Koizumi A
Department of Health and Environmental Sciences, Kyoto University Graduate School of Medicine, Yoshida, Kyoto 606-8501, Japan.
J Neurol Neurosurg Psychiatry. 2006 Sep;77(9):1025-9. doi: 10.1136/jnnp.2006.096040. Epub 2006 Jun 20.
Although the aetiology of moyamoya disease (MMD) has not been fully clarified, genetic analysis of familial MMD (F-MMD) has considerable potential to disclose it.
To determine the inheritance pattern and clinical characteristics of F-MMD to enable precise genetic analyses of the disease.
15 highly aggregated Japanese families (52 patients; 38 women and 14 men) with three or more affected members were examined. The difference in categories of age at onset (child onset, adult onset and asymptomatic) between paternal and maternal transmission was compared by chi2 statistics.
In all families there had been three or more generations without consanguinity, and all types of transmission, including father-to-son, were observed. Among a total of 135 offspring of affected people, 59 (43.7%) were patients with MMD or obligatory carriers. Affected mothers were more likely to produce late-onset (adult-onset or asymptomatic) female offspring (p = 0.007).
The mode of inheritance of F-MMD is autosomal dominant with incomplete penetrance. Thus, in future genetic studies on F-MMD, parametric linkage analyses using large families with an autosomal dominant mode of inheritance are recommended. Genomic imprinting may be associated with the disease.
尽管烟雾病(MMD)的病因尚未完全阐明,但对家族性烟雾病(F-MMD)进行基因分析有很大潜力揭示其病因。
确定F-MMD的遗传模式和临床特征,以便对该疾病进行精确的基因分析。
对15个高度聚集的日本家族(52例患者;38名女性和14名男性)进行检查,这些家族中有三名或更多受影响成员。采用卡方检验比较父系和母系遗传在发病年龄类别(儿童期发病、成年期发病和无症状)上的差异。
所有家族中均有三代或三代以上无血缘关系,且观察到包括父子遗传在内的所有遗传类型。在受影响者的135名后代中,59名(43.7%)为MMD患者或必然携带者。受影响的母亲更有可能生育晚发型(成年期发病或无症状)的女性后代(p = 0.007)。
F-MMD的遗传模式为常染色体显性遗传且具有不完全外显率。因此,在未来对F-MMD的基因研究中,建议使用具有常染色体显性遗传模式的大家庭进行参数连锁分析。基因组印记可能与该疾病有关。