| Title: |
Genome-wide association neural networks identify genes linked to family history of Alzheimer's disease. |
| Authors: |
Ghose, Upamanyu1,2 (AUTHOR), Sproviero, William1 (AUTHOR), Winchester, Laura1 (AUTHOR), Amin, Najaf3 (AUTHOR), Zhu, Taiyu1 (AUTHOR), Newby, Danielle1,4 (AUTHOR), Ulm, Brittany S2,3 (AUTHOR), Papathanasiou, Angeliki1 (AUTHOR), Shi, Liu1,5 (AUTHOR), Liu, Qiang1,6 (AUTHOR), Fernandes, Marco1,7 (AUTHOR), Adams, Cassandra2,8 (AUTHOR), Albukhari, Ashwag2,9 (AUTHOR), Almansouri, Majid2,10 (AUTHOR), Choudhry, Hani2,9 (AUTHOR), Duijn, Cornelia van2,3 (AUTHOR), Nevado-Holgado, Alejo1,2 (AUTHOR) |
| Source: |
Briefings in Bioinformatics. Jan2025, Vol. 26 Issue 1, p1-10. 10p. |
| Subject Terms: |
Hippo signaling pathway, Family history (Genealogy), Alzheimer's disease, Genome-wide association studies, Focal adhesions |
| Abstract: |
Augmenting traditional genome-wide association studies (GWAS) with advanced machine learning algorithms can allow the detection of novel signals in available cohorts. We introduce "genome-wide association neural networks (GWANN)" a novel approach that uses neural networks (NNs) to perform a gene-level association study with family history of Alzheimer's disease (AD). In UK Biobank, we defined cases (n = 42 110) as those with AD or family history of AD and sampled an equal number of controls. The data was split into an 80:20 ratio of training and testing samples, and GWANN was trained on the former followed by identifying associated genes using its performance on the latter. Our method identified 18 genes to be associated with family history of AD. APOE , BIN1 , SORL1 , ADAM10 , APH1B , and SPI1 have been identified by previous AD GWAS. Among the 12 new genes, PCDH9 , NRG3 , ROR1 , LINGO2 , SMYD3 , and LRRC7 have been associated with neurofibrillary tangles or phosphorylated tau in previous studies. Furthermore, there is evidence for differential transcriptomic or proteomic expression between AD and healthy brains for 10 of the 12 new genes. A series of post hoc analyses resulted in a significantly enriched protein–protein interaction network (P -value < 1 × 10−16), and enrichment of relevant disease and biological pathways such as focal adhesion (P -value = 1 × 10−4), extracellular matrix organization (P -value = 1 × 10−4), Hippo signaling (P -value = 7 × 10−4), Alzheimer's disease (P -value = 3 × 10−4) , and impaired cognition (P -value = 4 × 10−3). Applying NNs for GWAS illustrates their potential to complement existing algorithms and methods and enable the discovery of new associations without the need to expand existing cohorts. [ABSTRACT FROM AUTHOR] |
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| Database: |
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