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[特发性正常压力脑积水(iNPH)和无症状性脑室扩大且磁共振成像(MRI)具有iNPH特征(AVIM)]

[iNPH (Idiopathic normal pressure hydrocephalus) and AVIM (asymptomatic ventriculomegaly with features of iNPH on MRI)].

作者信息

Kato Takeo, Iseki Chifumi, Takahashi Yoshimi, Wada Manabu, Kawanami Toru, Sato Hidenori, Emi Mitsuru

机构信息

Department of Neurology, Hematology, Metabolism, Endocrinology and Diabetology, Yamagata University Faculty of Medicine, Yamagata, Japan.

出版信息

Rinsho Shinkeigaku. 2010 Nov;50(11):963-5.

Abstract

We investigated if there are individuals at a preclinical stage of idiopathic normal pressure hydrocephalus (iNPH) in a general population. All the residents aged 61 years and 70-72 years in the two communities of Japan (n=1142) were requested to take brain MRI examination. 790 residents (69.2%) participated in this study. Among them, 51 individuals (6.46%) had the enlarged ventricles (Evans index of >0.3), 12 (1.52%) of which showed the iNPH features on MRI. Of the 12 individuals, 8 were asymptomatic, while 4 had gait disturbance and/or dementia (possible iNPH). During a follow-up period of 4-8 years, two of the 8 asymptomatic subjects developed dementia and/or gait disturbance. The prevalence of possible iNPH was 0.51% (4/790) among Japanese elderly (>61 years of age). Asymptomatic ventriculomegaly with the iNPH features on MRI (AVIM) may represent a preclinical stage of iNPH. To identify a possible genetic change of AVIM and possible iNPH, we performed a genome-wide screening for copy number variations (CNV), and found that a segmental copy number loss of the SFMBT1 gene may be a genetic risk for the disease.

摘要

我们调查了普通人群中是否存在处于特发性正常压力脑积水(iNPH)临床前期的个体。要求日本两个社区所有年龄在61岁以及70 - 72岁的居民进行脑部MRI检查。790名居民(69.2%)参与了本研究。其中,51人(6.46%)脑室扩大(Evans指数>0.3),其中12人(1.52%)在MRI上表现出iNPH特征。在这12人中,8人无症状,4人有步态障碍和/或痴呆(可能为iNPH)。在4至8年的随访期内,8名无症状受试者中有2人出现痴呆和/或步态障碍。在日本老年人(>61岁)中,可能的iNPH患病率为0.51%(4/790)。MRI上具有iNPH特征的无症状脑室扩大(AVIM)可能代表iNPH的临床前期。为了确定AVIM和可能的iNPH的潜在基因变化,我们进行了全基因组拷贝数变异(CNV)筛查,发现SFMBT1基因的片段性拷贝数缺失可能是该疾病的遗传风险因素。

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