Wiki source code of Neurodiagnoses
Version 9.1 by manuelmenendez on 2025/01/27 23:23
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| 5 | = //A new tridimensional diagnostic framework for CNS conditions// = | ||
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| 7 | This project is focused on developing a novel nosological and diagnostic framework for neurological diseases by using advanced AI techniques and integrating data from neuroimaging, biomarkers, and biomedical ontologies. | ||
| 8 | We aim to create a structured, interpretable, and scalable diagnostic tool. | ||
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| 16 | = What is this about and what can I find here? = | ||
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| 18 | == **Overview** == | ||
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| 20 | The //Tridimensional Diagnostic Framework// redefines how neurodegenerative diseases (NDDs) are classified by focusing on: | ||
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| 22 | * **Axis 1**: Etiology (genetic/sporadic and environmental factors). | ||
| 23 | * **Axis 2**: Molecular Markers (biomarkers and proteinopathies). | ||
| 24 | * **Axis 3**: Neuroanatomoclinical correlations (linking clinical symptoms to structural changes in the nervous system). | ||
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| 26 | This methodology enables: | ||
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| 28 | * Greater precision in diagnosis. | ||
| 29 | * Integration of incomplete datasets using AI-driven probabilistic modeling. | ||
| 30 | * Stratification of patients for personalized treatment. | ||
| 31 | |||
| 32 | == **Diagnostic Axes** == | ||
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| 34 | * ((( | ||
| 35 | **Axis 1: Etiology** | ||
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| 37 | * //Description//: Focuses on genetic and sporadic causes, identifying risk factors and potential triggers. | ||
| 38 | * //Examples//: APOE ε4 as a genetic risk factor, or cardiovascular health affecting NDD progression. | ||
| 39 | * //Tests//: Genetic testing, lifestyle and cardiovascular screening. | ||
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| 42 | **Axis 2: Molecular Markers** | ||
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| 44 | * //Description//: Analyzes primary (amyloid-beta, tau) and secondary biomarkers (NFL, GFAP) for tracking disease progression. | ||
| 45 | * //Examples//: CSF amyloid-beta concentrations to confirm Alzheimer’s pathology. | ||
| 46 | * //Tests//: Blood/CSF biomarkers, PET imaging (Tau-PET, Amyloid-PET). | ||
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| 49 | **Axis 3: Neuroanatomoclinical** | ||
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| 51 | * //Description//: Links clinical symptoms to neuroanatomical changes, such as atrophy or functional impairments. | ||
| 52 | * //Examples//: Hippocampal atrophy correlating with memory deficits. | ||
| 53 | * //Tests//: MRI volumetrics, FDG-PET, neuropsychological evaluations. | ||
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| 56 | == **Applications** == | ||
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| 58 | This system enhances: | ||
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| 60 | * **Research**: By stratifying patients, reduces cohort heterogeneity in clinical trials. | ||
| 61 | * **Clinical Practice**: Provides dynamic diagnostic annotations with timestamps for longitudinal tracking. | ||
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| 63 | == Who has access? == | ||
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| 65 | We welcome contributions from the global community. Let’s build the future of neurological diagnostics together! | ||
| 66 | |||
| 67 | == How to Contribute: == | ||
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| 69 | * Access the `/docs` folder for guidelines. | ||
| 70 | * Use `/code` for the latest AI pipelines. | ||
| 71 | * Share feedback and ideas in the wiki discussion pages. | ||
| 72 | |||
| 73 | == Key Objectives: == | ||
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| 75 | * Develop interpretable AI models for diagnosis and progression tracking. | ||
| 76 | * Integrate data from Human Phenotype Ontology (HPO), Gene Ontology (GO), and other biomedical resources. | ||
| 77 | * Foster collaboration among neuroscientists, AI researchers, and clinicians. | ||
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| 83 | {{box title="**Contents**"}} | ||
| 84 | {{toc/}} | ||
| 85 | {{/box}} | ||
| 86 | |||
| 87 | == Main contents: == | ||
| 88 | |||
| 89 | * `/docs`: Documentation and contribution guidelines. | ||
| 90 | * `/code`: Machine learning pipelines and scripts. | ||
| 91 | * `/data`: Sample datasets for testing. | ||
| 92 | * `/outputs`: Generated models, visualizations, and reports. | ||
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