Huentelman Matthew J, Piras Ignazio S, Siniard Ashley L, De Both Matthew D, Richholt Ryan F, Balak Chris D, Jamshidi Pouya, Bigio Eileen H, Weintraub Sandra, Loyer Emmaleigh T, Mesulam M-Marsel, Geula Changiz, Rogalski Emily J
Neurogenomics Division, Translational Genomics Research Institute, Phoenix, AZ, United States.
Cognitive Neurology & Alzheimer's Disease Center, Northwestern University Feinberg School of Medicine (NU FSM), Chicago, IL, United States.
Front Aging Neurosci. 2018 May 29;10:155. doi: 10.3389/fnagi.2018.00155. eCollection 2018.
: SuperAgers are adults age 80+ with episodic memory performance that is as good as that of average middle-aged adults. Understanding the biological determinants of SuperAging may have relevance to preventing age-related cognitive decline and dementia. This study aimed to identify associations between genetic variations and the SuperAging phenotype using Whole Exome Sequencing (WES). : Sequence Kernel Association Combined (SKAT-C) test was conducted at the gene level including both rare and common variants in 56 SuperAgers and 22 cognitively-average controls from the Alzheimer's disease Neuroimaging Initiative (ADNI). : The SuperAging phenotype was associated with variants in the Mitogen-Activated Protein Kinase Kinase 3 gene. Three single nucleotide polymorphisms (SNPs) contributed to the significance (rs2363221 [intron 1], rs2230435 [exon 5], rs736103 [intron 7]). : MAP2K3 resides in a biological pathway linked to memory. It is in a signaling cascade associated with beta-amyloid mediated apoptosis and has enriched expression in microglia. This preliminary work suggests MAP2K3 may represent a novel therapeutic target for age-related memory decline and perhaps Alzheimer's disease (AD).
超级老人是指年龄在80岁及以上且情景记忆表现与普通中年成年人相当的成年人。了解超级老龄化的生物学决定因素可能与预防与年龄相关的认知衰退和痴呆症有关。本研究旨在通过全外显子组测序(WES)确定基因变异与超级老龄化表型之间的关联。:在基因水平上进行了序列核关联组合(SKAT-C)测试,包括来自阿尔茨海默病神经影像学倡议(ADNI)的56名超级老人和22名认知正常的对照中的罕见和常见变异。:超级老龄化表型与丝裂原活化蛋白激酶激酶3基因的变异有关。三个单核苷酸多态性(SNP)对此显著性有贡献(rs2363221[内含子1]、rs2230435[外显子5]、rs736103[内含子7])。:MAP2K3存在于与记忆相关的生物学途径中。它处于与β-淀粉样蛋白介导的细胞凋亡相关的信号级联中,并且在小胶质细胞中表达丰富。这项初步工作表明,MAP2K3可能代表了与年龄相关的记忆衰退以及可能的阿尔茨海默病(AD)的一个新的治疗靶点。