Autosomal Dominantly Inherited Alzheimer Disease: Analysis of genetic subgroups by Machine Learning.

dc.contributor.authorCastillo-Barnes, Diego
dc.contributor.authorSu, Li
dc.contributor.authorRamírez, Javier
dc.contributor.authorSalas-Gonzalez, Diego
dc.contributor.authorMartinez-Murcia, Francisco J
dc.contributor.authorIllan, Ignacio A
dc.contributor.authorSegovia, Fermin
dc.contributor.authorOrtiz, Andres
dc.contributor.authorCruchaga, Carlos
dc.contributor.authorFarlow, Martin R
dc.contributor.authorXiong, Chengjie
dc.contributor.authorGraff-Radford, Neil R
dc.contributor.authorSchofield, Peter R
dc.contributor.authorMasters, Colin L
dc.contributor.authorSalloway, Stephen
dc.contributor.authorJucker, Mathias
dc.contributor.authorMori, Hiroshi
dc.contributor.authorLevin, Johannes
dc.contributor.authorGorriz, Juan M
dc.contributor.authorDominantly Inherited Alzheimer Network (DIAN)
dc.date.accessioned2025-01-07T14:40:43Z
dc.date.available2025-01-07T14:40:43Z
dc.date.issued2020-01-07
dc.description.abstractDespite subjects with Dominantly-Inherited Alzheimer's Disease (DIAD) represent less than 1% of all Alzheimer's Disease (AD) cases, the Dominantly Inherited Alzheimer Network (DIAN) initiative constitutes a strong impact in the understanding of AD disease course with special emphasis on the presyptomatic disease phase. Until now, the 3 genes involved in DIAD pathogenesis (PSEN1, PSEN2 and APP) have been commonly merged into one group (Mutation Carriers, MC) and studied using conventional statistical analysis. Comparisons between groups using null-hypothesis testing or longitudinal regression procedures, such as the linear-mixed-effects models, have been assessed in the extant literature. Within this context, the work presented here performs a comparison between different groups of subjects by considering the 3 genes, either jointly or separately, and using tools based on Machine Learning (ML). This involves a feature selection step which makes use of ANOVA followed by Principal Component Analysis (PCA) to determine which features would be realiable for further comparison purposes. Then, the selected predictors are classified using a Support-Vector-Machine (SVM) in a nested k-Fold cross-validation resulting in maximum classification rates of 72-74% using PiB PET features, specially when comparing asymptomatic Non-Carriers (NC) subjects with asymptomatic PSEN1 Mutation-Carriers (PSEN1-MC). Results obtained from these experiments led to the idea that PSEN1-MC might be considered as a mixture of two different subgroups including: a first group whose patterns were very close to NC subjects, and a second group much more different in terms of imaging patterns. Thus, using a k-Means clustering algorithm it was determined both subgroups and a new classification scenario was conducted to validate this process. The comparison between each subgroup vs. NC subjects resulted in classification rates around 80% underscoring the importance of considering DIAN as an heterogeneous entity.
dc.identifier.doi10.1016/j.inffus.2020.01.001
dc.identifier.issn1566-2535
dc.identifier.pmcPMC7153760
dc.identifier.pmid32284705
dc.identifier.pubmedURLhttps://pmc.ncbi.nlm.nih.gov/articles/PMC7153760/pdf
dc.identifier.unpaywallURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7153760
dc.identifier.urihttps://hdl.handle.net/10668/26584
dc.journal.titleAn international journal on information fusion
dc.journal.titleabbreviationInf Fusion
dc.language.isoen
dc.organizationSAS - Hospital Universitario de Jaén
dc.page.number153-167
dc.pubmedtypeJournal Article
dc.rights.accessRightsopen access
dc.subjectAlzheimer’s Disease (AD)
dc.subjectDIAN
dc.subjectDominantly-Inherited Alzheimer’s Disease (DIAD)
dc.subjectMachine Learning
dc.subjectNeuroimaging
dc.titleAutosomal Dominantly Inherited Alzheimer Disease: Analysis of genetic subgroups by Machine Learning.
dc.typeresearch article
dc.type.hasVersionAM
dc.volume.number58

Files

Original bundle

Now showing 1 - 1 of 1
No Thumbnail Available
Name:
PMC7153760.pdf
Size:
2.31 MB
Format:
Adobe Portable Document Format