Bellou Eftychia, Escott-Price Valentina
UK Dementia Research Institute, School of Medicine, Cardiff University, Cardiff, United Kingdom.
Division of Neuroscience and Mental Health, School of Medicine, Cardiff University, Cardiff, United Kingdom.
Front Psychiatry. 2023 Jan 6;13:1102347. doi: 10.3389/fpsyt.2022.1102347. eCollection 2022.
In the last decade researchers have attempted to investigate the shared genetic architecture of longevity and age-related diseases and assess whether the increased longevity in certain people is due to protective alleles in the risk genes for a particular condition or whether there are specific "longevity" genes increasing the lifespan independently of age-related conditions' risk genes. The aim of this study was to investigate the shared genetic component between longevity and two age-related conditions.
We performed a cross-trait meta-analysis of publicly available genome-wide data for Alzheimer's disease, coronary artery disease and longevity using a subset-based approach provided by the R package ASSET.
Despite the lack of strong genetic correlation between longevity and the two diseases, we identified 38 genome-wide significant lead SNPs across 22 independent genomic loci. Of them 6 were found to be potentially shared among the three traits mapping to genes including , and . We also identified 19 novel genome-wide associations for the individual traits in this study. Functional annotations and biological pathway enrichment analyses suggested that pleiotropic variants are involved in clathrin-mediated endocytosis and plasma lipoprotein and neurotransmitter clearance processes.
In summary, we have been able to advance in the knowledge of the genetic overlap existing among longevity and the two most common age-related disorders.
在过去十年中,研究人员试图探究长寿与年龄相关疾病的共同遗传结构,并评估某些人寿命延长是由于特定疾病风险基因中的保护性等位基因,还是存在独立于年龄相关疾病风险基因的特定“长寿”基因来延长寿命。本研究的目的是探究长寿与两种年龄相关疾病之间的共同遗传成分。
我们使用R包ASSET提供的基于子集的方法,对公开可用的阿尔茨海默病、冠状动脉疾病和长寿的全基因组数据进行了跨性状荟萃分析。
尽管长寿与这两种疾病之间缺乏强遗传相关性,但我们在22个独立基因组位点上鉴定出38个全基因组显著的先导单核苷酸多态性(SNP)。其中6个被发现可能在这三个性状之间共享,定位到的基因包括 、 和 。我们还在本研究中为个体性状鉴定出19个新的全基因组关联。功能注释和生物通路富集分析表明,多效性变异参与网格蛋白介导的内吞作用以及血浆脂蛋白和神经递质清除过程。
总之,我们在长寿与两种最常见的年龄相关疾病之间存在的遗传重叠知识方面取得了进展。