Department of Epidemiology, Erasmus MC University Medical Center Rotterdam, PO Box 2040, Rotterdam, CA, 3000, The Netherlands.
The Generation R Study Group, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.
Eur J Epidemiol. 2024 Oct;39(10):1151-1160. doi: 10.1007/s10654-024-01160-2. Epub 2024 Oct 10.
We aimed to determine the association of family history of dementia with structural brain measures and cognitive performance in childhood and mid-life adulthood. We studied 1,259 parents (mean age: 47.3 years, range 31.9-67.4) and 866 of their children (mean age [range] at brain MRI: 9.9 years [8.8-11.9], and for cognition: 13.5 years [12.6-15.8]) of the population-based Generation R Study. Parents filled in a questionnaire on family history, and both parents and children underwent cognitive assessment and neuroimaging. Of all participants, 109 parents (8.6%) reported a parental family history of dementia and 73 children (8.4%) had a grandparental history of dementia with mean age of dementia diagnosis in those affected 75 years (± 7.3). We observed no associations of dementia family history with cognitive ability in either parents or their children, except for worse Purdue pegboard in parents with a parental history of dementia, compared to those without (mean difference [95%CI]: -1.23 [-2.15; -0.31], test range: 21-52). In parents and children, neuroimaging measures did not differ significantly by family history. Results did not depend on age, sex, and APOE genotype. Family history of dementia was associated with worse manual dexterity in mid-life adulthood, but not with any other measures of cognitive ability or subclinical brain health in childhood and mid-life. These findings suggest that the association of family history with dementia risk is due chiefly to neurodegenerative rather than neurodevelopmental processes, and might first present with reduced motor skills.
我们旨在确定痴呆症家族史与儿童和中年期成年期的结构性大脑测量和认知表现之间的关联。我们研究了 1259 名父母(平均年龄:47.3 岁,范围 31.9-67.4)和他们的 866 名孩子(脑 MRI 的平均年龄[范围]:9.9 岁[8.8-11.9],认知评估年龄:13.5 岁[12.6-15.8]),他们都来自基于人群的 Generation R 研究。父母填写了一份关于家族史的问卷,父母和孩子都接受了认知评估和神经影像学检查。在所有参与者中,有 109 名父母(8.6%)报告了父母痴呆症家族史,73 名孩子(8.4%)有祖辈痴呆症家族史,受影响者的痴呆症平均诊断年龄为 75 岁(±7.3)。我们没有观察到痴呆症家族史与父母或其子女的认知能力之间存在任何关联,除了父母中痴呆症家族史与父母痴呆症家族史的父母相比,普渡钉板测试成绩更差(平均差异[95%CI]:-1.23[-2.15;-0.31],测试范围:21-52)。在父母和孩子中,神经影像学测量结果与家族史无显著差异。结果不依赖于年龄、性别和 APOE 基因型。痴呆症家族史与中年期手动灵巧度降低有关,但与儿童和中年期的任何其他认知能力或亚临床大脑健康指标无关。这些发现表明,家族史与痴呆症风险的关联主要归因于神经退行性过程,而不是神经发育过程,并且可能首先表现为运动技能下降。