Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, London, UK.
Department of Hygiene and Epidemiology, University of Ioannina Medical School, Ioannina, Greece.
Nat Commun. 2024 Nov 13;15(1):9827. doi: 10.1038/s41467-024-53452-6.
Several cardiovascular traits and diseases co-occur with Alzheimer's disease. We mapped their shared genetic architecture using multi-trait genome-wide association studies. Subsequent fine-mapping and colocalisation highlighted 16 genetic loci associated with both Alzheimer's and cardiovascular diseases. We prioritised rs11786896, which colocalised with Alzheimer's disease, atrial fibrillation and expression of PLEC in the heart left ventricle, and rs7529220, which colocalised with Alzheimer's disease, atrial fibrillation and expression of C1Q family genes. Single-cell RNA-sequencing data, co-expression network and protein-protein interaction analyses provided evidence for different mechanisms of PLEC, which is upregulated in left ventricular endothelium and cardiomyocytes with heart failure and in brain astrocytes with Alzheimer's disease. Similar common mechanisms are implicated for C1Q in heart macrophages with heart failure and in brain microglia with Alzheimer's disease. These findings highlight inflammatory and pleomorphic risk determinants for the co-occurrence of Alzheimer's and cardiovascular diseases and suggest PLEC, C1Q and their interacting proteins as potential therapeutic targets.
几种心血管特征和疾病与阿尔茨海默病同时发生。我们使用多性状全基因组关联研究来绘制它们共同的遗传结构。随后的精细映射和共定位突出了与阿尔茨海默病和心血管疾病都相关的 16 个遗传位点。我们优先考虑 rs11786896,它与阿尔茨海默病、心房颤动和左心室心脏中 PLEC 的表达共定位,以及 rs7529220,它与阿尔茨海默病、心房颤动和 C1Q 家族基因的表达共定位。单细胞 RNA 测序数据、共表达网络和蛋白质-蛋白质相互作用分析为 PLEC 的不同机制提供了证据,PLEC 在心力衰竭时左心室内皮细胞和心肌细胞以及阿尔茨海默病时大脑星形胶质细胞中上调。类似的共同机制涉及心力衰竭时心脏巨噬细胞中的 C1Q 和阿尔茨海默病时大脑小神经胶质细胞中的 C1Q。这些发现强调了阿尔茨海默病和心血管疾病同时发生的炎症和多态风险决定因素,并表明 PLEC、C1Q 及其相互作用蛋白可能是潜在的治疗靶点。