From the Department of Psychiatry and Legal Medicine, Universidade Federal do Rio Grande do Sul, Hospital de Clínicas de Porto Alegre, Section on Negative Affect and Social Processes, Porto Alegre, Brazil; the National Institute of Developmental Psychiatry, São Paulo, Brazil; the Department of Morphology and Genetics and the Department of Psychiatry, Universidade Federal de São Paulo, São Paulo, Brazil; the Emotion and Development Branch, NIMH, Bethesda, Md.; the Graduate Program in Pediatric and Child Health, Pontificial Catholic University of Rio Grande do Sul, Developmental Cognitive Neuroscience Lab, Porto Alegre, Brazil; the Department of Psychiatry, Universidade de São Paulo, São Paulo, Brazil; the Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia; the Rotman Research Institute, Baycrest, Toronto; the Departments of Psychology and Psychiatry, University of Toronto, Toronto; the Child Mind Institute, New York; and the Hospital for Sick Children, University of Toronto, Toronto.
Am J Psychiatry. 2018 Jun 1;175(6):555-563. doi: 10.1176/appi.ajp.2017.17050529. Epub 2018 Mar 2.
Alzheimer's disease is a heritable neurodegenerative disorder in which early-life precursors may manifest in cognition and brain structure. The authors evaluate this possibility by examining, in youths, associations among polygenic risk score for Alzheimer's disease, cognitive abilities, and hippocampal volume.
Participants were children 6-14 years of age in two Brazilian cities, constituting the discovery (N=364) and replication samples (N=352). As an additional replication, data from a Canadian sample (N=1,029), with distinct tasks, MRI protocol, and genetic risk, were included. Cognitive tests quantified memory and executive function. Reading and writing abilities were assessed by standardized tests. Hippocampal volumes were derived from the Multiple Automatically Generated Templates (MAGeT) multi-atlas segmentation brain algorithm. Genetic risk for Alzheimer's disease was quantified using summary statistics from the International Genomics of Alzheimer's Project.
Analyses showed that for the Brazilian discovery sample, each one-unit increase in z-score for Alzheimer's polygenic risk score significantly predicted a 0.185 decrement in z-score for immediate recall and a 0.282 decrement for delayed recall. Findings were similar for the Brazilian replication sample (immediate and delayed recall, β=-0.259 and β=-0.232, both significant). Quantile regressions showed lower hippocampal volumes bilaterally for individuals with high polygenic risk scores. Associations fell short of significance for the Canadian sample.
Genetic risk for Alzheimer's disease may affect early-life cognition and hippocampal volumes, as shown in two independent samples. These data support previous evidence that some forms of late-life dementia may represent developmental conditions with roots in childhood. This result may vary depending on a sample's genetic risk and may be specific to some types of memory tasks.
阿尔茨海默病是一种遗传性神经退行性疾病,其早期前体可能表现在认知和大脑结构上。作者通过研究年轻人中阿尔茨海默病多基因风险评分与认知能力和海马体积之间的关系来评估这种可能性。
研究对象为来自巴西两个城市的 6-14 岁儿童,构成了发现(N=364)和复制样本(N=352)。作为额外的复制,还包括了来自加拿大样本(N=1029)的数据,该样本具有不同的任务、MRI 方案和遗传风险。认知测试量化了记忆和执行功能。阅读和写作能力通过标准化测试进行评估。海马体积是从多自动生成模板(MAGeT)多图谱分割脑算法中得出的。阿尔茨海默病的遗传风险是使用国际阿尔茨海默病基因组学项目的汇总统计数据来量化的。
分析表明,对于巴西发现样本,阿尔茨海默病多基因风险评分每增加一个 z 分数单位,即时回忆的 z 分数就会显著下降 0.185,延迟回忆的 z 分数就会下降 0.282。巴西复制样本的结果相似(即时和延迟回忆,β=-0.259 和β=-0.232,均有统计学意义)。分位数回归显示,高多基因风险评分个体的双侧海马体积较低。加拿大样本的关联未达到统计学意义。
阿尔茨海默病的遗传风险可能会影响儿童期的认知和海马体积,这在两个独立的样本中得到了证实。这些数据支持了先前的证据,即某些类型的迟发性痴呆可能代表具有儿童期根源的发育性疾病。这一结果可能因样本的遗传风险而异,并且可能特定于某些类型的记忆任务。