Lupton Michelle K, Strike Lachlan, Hansell Narelle K, Wen Wei, Mather Karen A, Armstrong Nicola J, Thalamuthu Anbupalam, McMahon Katie L, de Zubicaray Greig I, Assareh Amelia A, Simmons Andrew, Proitsi Petroula, Powell John F, Montgomery Grant W, Hibar Derrek P, Westman Eric, Tsolaki Magda, Kloszewska Iwona, Soininen Hilkka, Mecocci Patrizia, Velas Bruno, Lovestone Simon, Brodaty Henry, Ames David, Trollor Julian N, Martin Nicholas G, Thompson Paul M, Sachdev Perminder S, Wright Margaret J
Genetic Epidemiology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Genetic Epidemiology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia; Queensland Brain Institute, The University of Queensland, St Lucia, Queensland, Australia.
Neurobiol Aging. 2016 Apr;40:68-77. doi: 10.1016/j.neurobiolaging.2015.12.023. Epub 2016 Jan 11.
Reduction in hippocampal and amygdala volume measured via structural magnetic resonance imaging is an early marker of Alzheimer's disease (AD). Whether genetic risk factors for AD exert an effect on these subcortical structures independent of clinical status has not been fully investigated. We examine whether increased genetic risk for AD influences hippocampal and amygdala volumes in case-control and population cohorts at different ages, in 1674 older (aged >53 years; 17% AD, 39% mild cognitive impairment [MCI]) and 467 young (16-30 years) adults. An AD polygenic risk score combining common risk variants excluding apolipoprotein E (APOE), and a single nucleotide polymorphism in TREM2, were both associated with reduced hippocampal volume in healthy older adults and those with MCI. APOE ε4 was associated with hippocampal and amygdala volume in those with AD and MCI but was not associated in healthy older adults. No associations were found in young adults. Genetic risk for AD affects the hippocampus before the clinical symptoms of AD, reflecting a neurodegenerative effect before clinical manifestations in older adults.
通过结构磁共振成像测量发现,海马体和杏仁核体积减小是阿尔茨海默病(AD)的早期标志。AD的遗传风险因素是否独立于临床状态对这些皮质下结构产生影响,尚未得到充分研究。我们在1674名老年人(年龄>53岁;17%为AD,39%为轻度认知障碍[MCI])和467名年轻人(16 - 30岁)的病例对照和人群队列中,研究AD遗传风险增加是否会影响海马体和杏仁核体积。一个结合了排除载脂蛋白E(APOE)的常见风险变异和TREM2中的一个单核苷酸多态性的AD多基因风险评分,与健康老年人和患有MCI的人的海马体体积减小均相关。APOE ε4与患有AD和MCI的人的海马体和杏仁核体积相关,但在健康老年人中无相关性。在年轻人中未发现关联。AD的遗传风险在AD临床症状出现之前就影响海马体,这反映了在老年人临床表现之前的神经退行性作用。