Changes for page Neurodiagnoses
Last modified by manuelmenendez on 2025/03/03 22:46
From version 24.1
edited by manuelmenendez
on 2025/01/29 18:46
on 2025/01/29 18:46
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To version 5.1
edited by manuelmenendez
on 2025/01/27 23:04
on 2025/01/27 23:04
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... ... @@ -2,10 +2,9 @@ 2 2 ((( 3 3 (% class="container" %) 4 4 ((( 5 -= //A new tridimensionaldiagnostic framework for CNS diseases//=5 += Neurodiagnoses = 6 6 7 -This project is focused on developing a novel nosological and diagnostic framework for CNS 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. 7 +This project is focused on developing a novel nosological and diagnostic framework for neurological diseases. Using advanced AI techniques and integrating data from neuroimaging, biomarkers, and biomedical ontologies, we aim to create a structured, interpretable, and scalable diagnostic tool. 9 9 ))) 10 10 ))) 11 11 ... ... @@ -13,70 +13,19 @@ 13 13 ((( 14 14 (% class="col-xs-12 col-sm-8" %) 15 15 ((( 16 -= What is this about and whatcan I find here? =15 += What can I find here? = 17 17 18 -== **Overview** == 19 - 20 -The //Tridimensional Diagnostic Framework// redefines CNS diseases can be classified and diagnosed by focusing on: 21 - 22 -* **Axis 1**: Etiology (genetic or other causes of diseases). 23 -* **Axis 2**: Molecular Markers (biomarkers). 24 -* **Axis 3**: Neuroanatomoclinical correlations (linking clinical symptoms to structural changes in the nervous system). 25 - 26 - 27 -[[For instance, 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"]] 28 - 29 - 30 -This methodology enables: 31 - 32 -* Greater precision in diagnosis. 33 -* Integration of incomplete datasets using AI-driven probabilistic modeling. 34 -* Stratification of patients for personalized treatment. 35 - 36 -== **The case of neurodegenerative diseases** == 37 - 38 -There have been described these 3 diagnostic axes: 39 - 40 -* ((( 41 -**Axis 1: Etiology** 42 - 43 -* //Description//: Focuses on genetic and sporadic causes, identifying risk factors and potential triggers. 44 -* //Examples//: APOE ε4 as a genetic risk factor, or cardiovascular health affecting NDD progression. 45 -* //Tests//: Genetic testing, lifestyle, and cardiovascular screening. 46 -))) 47 -* ((( 48 -**Axis 2: Molecular Markers** 49 - 50 -* //Description//: Analyzes primary (amyloid-beta, tau) and secondary biomarkers (NFL, GFAP) for tracking disease progression. 51 -* //Examples//: CSF amyloid-beta concentrations to confirm Alzheimer’s pathology. 52 -* //Tests//: Blood/CSF biomarkers, PET imaging (Tau-PET, Amyloid-PET). 53 -))) 54 -* ((( 55 -**Axis 3: Neuroanatomoclinical** 56 - 57 -* //Description//: Links clinical symptoms to neuroanatomical changes, such as atrophy or functional impairments. 58 -* //Examples//: Hippocampal atrophy correlating with memory deficits. 59 -* //Tests//: MRI volumetrics, FDG-PET, neuropsychological evaluations. 60 -))) 61 - 62 -== **Applications** == 63 - 64 -This system enhances: 65 - 66 -* **Research**: By stratifying patients, reduces cohort heterogeneity in clinical trials. 67 -* **Clinical Practice**: Provides dynamic diagnostic annotations with timestamps for longitudinal tracking. 68 - 69 69 == Who has access? == 70 70 71 71 We welcome contributions from the global community. Let’s build the future of neurological diagnostics together! 72 72 73 -== How to Contribute == 21 +== How to Contribute: == 74 74 75 75 * Access the `/docs` folder for guidelines. 76 76 * Use `/code` for the latest AI pipelines. 77 77 * Share feedback and ideas in the wiki discussion pages. 78 78 79 -== Key Objectives == 27 +== Key Objectives: == 80 80 81 81 * Develop interpretable AI models for diagnosis and progression tracking. 82 82 * Integrate data from Human Phenotype Ontology (HPO), Gene Ontology (GO), and other biomedical resources. ... ... @@ -90,14 +90,11 @@ 90 90 {{toc/}} 91 91 {{/box}} 92 92 93 -== Main contents == 41 +== Main contents: == 94 94 95 95 * `/docs`: Documentation and contribution guidelines. 96 96 * `/code`: Machine learning pipelines and scripts. 97 97 * `/data`: Sample datasets for testing. 98 98 * `/outputs`: Generated models, visualizations, and reports. 99 -* [[Methodology>>url:https://wiki.ebrains.eu/bin/view/Collabs/neurodiagnoses/Methodology/]] 100 -* [[Results>>url:https://wiki.ebrains.eu/bin/view/Collabs/neurodiagnoses/Results/]] 101 -* [[to-do-list>>to-do-list]] 102 102 ))) 103 103 )))
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