University of Kansas School of Medicine, Department of Neurology, 2100 West 36th Ave., Suite 110, Kansas City, KS 66160, USA.
Neurology. 2010 Jan 12;74(2):113-20. doi: 10.1212/WNL.0b013e3181c918cb.
A consistently identified risk factor for Alzheimer disease (AD) is family history of dementia, with maternal transmission significantly more frequent than paternal transmission. A history of maternal AD may be related to AD-like glucose consumption in cognitively healthy subjects. In this cross-sectional study, we tested whether cognitively healthy people with a family history of AD have less gray matter volume (GMV), an endophenotype for late-onset AD, than individuals with no family history, and whether decreases in GMV are different in subjects with a maternal family history.
As part of the Kansas University Brain Aging Project, 67 cognitively intact individuals with a maternal history of late-onset AD (FHm, n = 16), a paternal history of AD (FHp, n = 8), or no parental history of AD (FH-, n = 43), similar in age, gender, education, and Mini-Mental State Examination score, were scanned at 3 T. We used voxel-based morphometry to examine GMV differences between groups, controlling for age, gender, and apoE4.
Cognitively healthy individuals with a family history of late-onset AD had significantly decreased GMV in the precuneus, middle frontal, inferior frontal, and superior frontal gyri compared with FH- individuals. FHm subjects had significantly smaller inferior frontal, middle frontal, precuneus, and lingual gyri compared with FH- and FHp subjects.
Overall, maternal family history of Alzheimer disease (AD) in cognitively normal individuals is associated with lower gray matter volume in AD-vulnerable brain regions. These data complement and extend reports of cerebral metabolic differences in subjects with a maternal family history.
阿尔茨海默病(AD)的一个明确的危险因素是痴呆家族史,其中母系遗传比父系遗传更为常见。AD 的家族史可能与认知正常的个体中 AD 样葡萄糖消耗有关。在这项横断面研究中,我们测试了是否有 AD 家族史的认知正常个体的灰质体积(GMV)减少,GMV 是迟发性 AD 的一个内表型,其 GMV 减少程度是否与有母系家族史的个体不同。
作为堪萨斯大学大脑老化项目的一部分,67 名认知正常的个体有晚发性 AD 的母系家族史(FHm,n = 16)、父系家族史(FHp,n = 8)或无 AD 家族史(FH-,n = 43),年龄、性别、教育程度和 Mini-Mental State 考试成绩相似,在 3T 下进行扫描。我们使用基于体素的形态测量学来检查组间 GMV 的差异,同时控制年龄、性别和 apoE4。
与 FH-个体相比,有晚发性 AD 家族史的认知正常个体的扣带回、额中回、额下回和额上回的 GMV 明显减少。FHm 个体的额下回、额中回、扣带回和舌回的 GMV 明显小于 FH-和 FHp 个体。
总体而言,认知正常个体的 AD 母系家族史与 AD 易损脑区的 GMV 减少有关。这些数据补充和扩展了母系家族史个体脑代谢差异的报告。