Wiki source code of Neurodiagnoses
Version 22.1 by manuelmenendez on 2025/01/29 18:44
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17.1 | 5 | = //A new tridimensional diagnostic framework for neurodegenerative diseases// = |
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19.1 | 7 | This project is focused on developing a novel nosological and diagnostic framework for neurodegenerative diseases by using advanced AI techniques and integrating data from neuroimaging, biomarkers, and biomedical ontologies. |
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6.1 | 8 | We aim to create a structured, interpretable, and scalable diagnostic tool. |
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6.1 | 16 | = What is this about and what can I find here? = |
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9.1 | 18 | == **Overview** == |
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6.1 | 19 | |
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17.1 | 20 | The //Tridimensional Diagnostic Framework// redefines how neurodegenerative diseases (NDD) are classified by focusing on: |
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6.1 | 21 | |
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16.1 | 22 | * **Axis 1**: Etiology (genetic or other causes of diseases). |
23 | * **Axis 2**: Molecular Markers (biomarkers). | ||
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6.1 | 24 | * **Axis 3**: Neuroanatomoclinical correlations (linking clinical symptoms to structural changes in the nervous system). |
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14.1 | 26 | [[Neurodegenerative diseases can be studied and classified in a tridimensional scheme with three axes: anatomic–clinical, molecular, and etiologic. CSF, cerebrospinal fluid; FDG, fluorodeoxyglucose; MRI, magnetic resonance imaging; PET, positron emission tomography.>>image:tridimensional.png||alt="tridimensional view of neurodegenerative diseases"]] |
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6.1 | 29 | This methodology enables: |
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31 | * Greater precision in diagnosis. | ||
32 | * Integration of incomplete datasets using AI-driven probabilistic modeling. | ||
33 | * Stratification of patients for personalized treatment. | ||
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9.1 | 35 | == **Diagnostic Axes** == |
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6.1 | 36 | |
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38 | **Axis 1: Etiology** | ||
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40 | * //Description//: Focuses on genetic and sporadic causes, identifying risk factors and potential triggers. | ||
41 | * //Examples//: APOE ε4 as a genetic risk factor, or cardiovascular health affecting NDD progression. | ||
42 | * //Tests//: Genetic testing, lifestyle and cardiovascular screening. | ||
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45 | **Axis 2: Molecular Markers** | ||
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47 | * //Description//: Analyzes primary (amyloid-beta, tau) and secondary biomarkers (NFL, GFAP) for tracking disease progression. | ||
48 | * //Examples//: CSF amyloid-beta concentrations to confirm Alzheimer’s pathology. | ||
49 | * //Tests//: Blood/CSF biomarkers, PET imaging (Tau-PET, Amyloid-PET). | ||
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52 | **Axis 3: Neuroanatomoclinical** | ||
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54 | * //Description//: Links clinical symptoms to neuroanatomical changes, such as atrophy or functional impairments. | ||
55 | * //Examples//: Hippocampal atrophy correlating with memory deficits. | ||
56 | * //Tests//: MRI volumetrics, FDG-PET, neuropsychological evaluations. | ||
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9.1 | 59 | == **Applications** == |
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6.1 | 60 | |
61 | This system enhances: | ||
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7.2 | 63 | * **Research**: By stratifying patients, reduces cohort heterogeneity in clinical trials. |
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6.1 | 64 | * **Clinical Practice**: Provides dynamic diagnostic annotations with timestamps for longitudinal tracking. |
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5.1 | 66 | == Who has access? == |
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4.2 | 68 | We welcome contributions from the global community. Let’s build the future of neurological diagnostics together! |
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4.4 | 69 | |
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10.1 | 70 | == How to Contribute == |
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4.4 | 71 | |
72 | * Access the `/docs` folder for guidelines. | ||
73 | * Use `/code` for the latest AI pipelines. | ||
74 | * Share feedback and ideas in the wiki discussion pages. | ||
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5.1 | 75 | |
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10.1 | 76 | == Key Objectives == |
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5.1 | 77 | |
78 | * Develop interpretable AI models for diagnosis and progression tracking. | ||
79 | * Integrate data from Human Phenotype Ontology (HPO), Gene Ontology (GO), and other biomedical resources. | ||
80 | * Foster collaboration among neuroscientists, AI researchers, and clinicians. | ||
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86 | {{box title="**Contents**"}} | ||
87 | {{toc/}} | ||
88 | {{/box}} | ||
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10.1 | 90 | == Main contents == |
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4.4 | 91 | |
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5.1 | 92 | * `/docs`: Documentation and contribution guidelines. |
93 | * `/code`: Machine learning pipelines and scripts. | ||
94 | * `/data`: Sample datasets for testing. | ||
95 | * `/outputs`: Generated models, visualizations, and reports. | ||
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21.1 | 96 | * [[Methodology>>url:https://wiki.ebrains.eu/bin/view/Collabs/neurodiagnoses/Methodology/]] |
97 | * [[Results>>url:https://wiki.ebrains.eu/bin/view/Collabs/neurodiagnoses/Results/]] | ||
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22.1 | 98 | * [[to-do-list>>to-do-list]] |
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