Laboratory of Neurobiology and Pathological Physiology, Institute of Animal Physiology and Genetics, Czech Academy of Sciences, Veveří 97, 602 00, Brno 2, Czech Republic.
Laboratory of Neurobiology and Molecular Psychiatry, Department of Biochemistry, Faculty of Science, Masaryk University, Brno, Czech Republic.
Sci Rep. 2022 Jun 29;12(1):10994. doi: 10.1038/s41598-022-15299-z.
The risk of Alzheimer's disease (AD) has a strong genetic component, also in the case of late-onset AD (LOAD). Attempts to sequence whole genome in large populations of subjects have identified only a few mutations common to most of the patients with AD. Targeting smaller well-characterized groups of subjects where specific genetic variations in selected genes could be related to precisely defined psychological traits typical of dementia is needed to better understand the heritability of AD. More than one thousand participants, categorized according to cognitive deficits, were assessed using 14 psychometric tests evaluating performance in five cognitive domains (attention/working memory, memory, language, executive functions, visuospatial functions). CD36 was selected as a gene previously shown to be implicated in the etiology of AD. A total of 174 polymorphisms were tested for associations with cognition-related traits and other AD-relevant data using the next generation sequencing. Several associations between single nucleotide polymorphisms (SNP's) and the cognitive deficits have been found (rs12667404 with language performance, rs3211827 and rs41272372 with executive functions, rs137984792 with visuospatial performance). The most prominent association was found between a group of genotypes in six genetically linked and the age at which the AD patients presented with, or developed, a full-blown dementia. The identified alleles appear to be associated with a delay in the onset of LOAD. In silico studies suggested that the SNP's alter the expression of CD36 thus potentially affecting CD36-related neuroinflammation and other molecular and cellular mechanisms known to be involved in the neuronal loss leading to AD. The main outcome of the study is an identification of a set of six new mutations apparently conferring a distinct protection against AD and delaying the onset by about 8 years. Additional mutations in CD36 associated with certain traits characteristic of the cognitive decline in AD have also been found.
阿尔茨海默病(AD)的风险具有很强的遗传成分,即使是在迟发性 AD(LOAD)中也是如此。尝试对大量受试者的全基因组进行测序,仅发现了少数几种常见于大多数 AD 患者的突变。需要针对特定遗传变异与特定基因相关的较小、特征明确的受试者群体进行靶向研究,这些特定基因的遗传变异与痴呆症的特定心理特征有关,以便更好地理解 AD 的遗传性。将 1000 多名参与者根据认知缺陷进行分类,使用 14 项心理测试评估 5 个认知领域(注意力/工作记忆、记忆、语言、执行功能、视空间功能)的表现。CD36 被选为先前显示与 AD 病因学相关的基因。使用下一代测序技术,共测试了 174 种与认知相关的特征和其他 AD 相关数据的多态性。在一些单核苷酸多态性(SNP)与认知缺陷之间发现了一些关联(与语言表现相关的 rs12667404、与执行功能相关的 rs3211827 和 rs41272372、与视空间表现相关的 rs137984792)。发现与一组在六个遗传相关的基因型与 AD 患者出现或发展为全面痴呆的年龄之间存在最显著的关联。鉴定的等位基因似乎与 LOAD 发病的延迟有关。计算机模拟研究表明,SNP 改变了 CD36 的表达,从而可能影响与 CD36 相关的神经炎症和其他已知参与导致 AD 的神经元丧失的分子和细胞机制。研究的主要结果是确定了一组六个新的突变,这些突变显然赋予了对 AD 的明显保护作用,并将发病时间延迟了大约 8 年。还发现了与 AD 认知衰退的某些特征相关的 CD36 相关的其他突变。