Changes for page Neurodiagnoses
Last modified by manuelmenendez on 2025/03/03 22:46
From version 13.1
edited by manuelmenendez
on 2025/01/27 23:54
on 2025/01/27 23:54
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To version 40.1
edited by manuelmenendez
on 2025/02/02 15:12
on 2025/02/02 15:12
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... ... @@ -2,9 +2,9 @@ 2 2 ((( 3 3 (% class="container" %) 4 4 ((( 5 -= //A new tridimensional diagnostic framework for CNS conditions// =5 += //A new tridimensional diagnostic framework for complex CNS diseases// = 6 6 7 -This project is focused on developing a novel nosological and diagnostic framework for neurologicaldiseases by using advanced AI techniques and integrating data from neuroimaging, biomarkers, and biomedical ontologies.7 +This project is focused on developing a novel nosological and diagnostic framework for complex CNS diseases by using advanced AI techniques and integrating data from neuroimaging, biomarkers, and biomedical ontologies. 8 8 We aim to create a structured, interpretable, and scalable diagnostic tool. 9 9 ))) 10 10 ))) ... ... @@ -15,12 +15,17 @@ 15 15 ((( 16 16 = What is this about and what can I find here? = 17 17 18 -= =**Overview** ==18 += **Overview** = 19 19 20 -The //Tridimensional Diagnostic Framework// redefines how neurodegenerative diseases (NDDs) are classified by focusing on: 21 21 22 -* **Axis 1**: Etiology (genetic/sporadic and environmental factors). 23 -* **Axis 2**: Molecular Markers (biomarkers and proteinopathies). 21 +The classification and diagnosis of central nervous system (CNS) diseases have long been constrained by traditional phenotype-based approaches, which often fail to capture the complex pathophysiological mechanisms, molecular biomarkers, and neuroanatomical changes that drive disease progression. 22 + 23 +Neurodiagnoses is an open-source AI-powered diagnostic system designed for complex CNS disorders, including neurodegenerative diseases, autoimmune encephalopathies, prion disorders, and genetic syndromes. The project aims to develop a tridimensional diagnostic framework with an AI-powered annotation system, integrating etiology, molecular biomarkers, and neuroanatomoclinical correlations for precise, standardized, and scalable CNS disease diagnostics. 24 + 25 +The //Tridimensional Diagnostic Framework// redefines CNS diseases can be classified and diagnosed by focusing on: 26 + 27 +* **Axis 1**: Etiology (genetic or other causes of diseases). 28 +* **Axis 2**: Molecular Markers (biomarkers). 24 24 * **Axis 3**: Neuroanatomoclinical correlations (linking clinical symptoms to structural changes in the nervous system). 25 25 26 26 This methodology enables: ... ... @@ -29,14 +29,52 @@ 29 29 * Integration of incomplete datasets using AI-driven probabilistic modeling. 30 30 * Stratification of patients for personalized treatment. 31 31 32 -== ** DiagnosticAxes** ==37 +== **The Role of AI-Powered Annotation** == 33 33 39 +To enhance standardization, interpretability, and clinical application, the framework integrates an AI-powered annotation system, which: 40 + 41 +* Assigns structured metadata tags to diagnostic features. 42 +* Provides real-time contextual explanations for AI-based classifications. 43 +* Tracks longitudinal disease progression using timestamped AI annotations. 44 +* Improves AI model transparency through interpretability tools (e.g., SHAP analysis). 45 +* Facilitates decision-making for clinicians by linking annotations to standardized biomedical ontologies (SNOMED, HPO). 46 + 47 +Neurodiagnoses provides two complementary AI-driven diagnostic approaches: 48 + 49 +1. Traditional Probabilistic Diagnosis 50 + 51 +* AI provides multiple possible diagnoses, each assigned a probability percentage based on biomarker, imaging, and clinical data. 52 +* Example Output: 53 +** 75% Alzheimer's Disease 54 +** 20% Lewy Body Dementia 55 +** 5% Vascular Dementia 56 +* Useful for differential diagnosis and treatment decision-making. 57 + 58 +2. Tridimensional Diagnosis 59 + 60 +* Diagnoses are structured based on: 61 +(1) Etiology (genetic, autoimmune, metabolic, infectious) 62 +(2) Molecular Biomarkers (amyloid-beta, tau, inflammatory markers, EEG patterns) 63 +(3) Neuroanatomoclinical Correlations (brain atrophy, connectivity alterations) 64 +* This approach enables precise disease subtyping and biologically meaningful classification, particularly useful to track progression over time. 65 + 66 +For every patient case, both systems will be offered, allowing clinicians to compare AI-generated probabilistic diagnosis with a structured tridimensional classification. 67 + 68 + 69 +== **The case of neurodegenerative diseases** == 70 + 71 +There have been described these 3 diagnostic axes: 72 + 73 +[[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"]] 74 + 34 34 * ((( 35 35 **Axis 1: Etiology** 36 36 37 37 * //Description//: Focuses on genetic and sporadic causes, identifying risk factors and potential triggers. 38 38 * //Examples//: APOE ε4 as a genetic risk factor, or cardiovascular health affecting NDD progression. 39 -* //Tests//: Genetic testing, lifestyle and cardiovascular screening. 80 +* //Tests//: Genetic testing, lifestyle, and cardiovascular screening. 81 + 82 + 40 40 ))) 41 41 * ((( 42 42 **Axis 2: Molecular Markers** ... ... @@ -44,6 +44,8 @@ 44 44 * //Description//: Analyzes primary (amyloid-beta, tau) and secondary biomarkers (NFL, GFAP) for tracking disease progression. 45 45 * //Examples//: CSF amyloid-beta concentrations to confirm Alzheimer’s pathology. 46 46 * //Tests//: Blood/CSF biomarkers, PET imaging (Tau-PET, Amyloid-PET). 90 + 91 + 47 47 ))) 48 48 * ((( 49 49 **Axis 3: Neuroanatomoclinical** ... ... @@ -60,10 +60,6 @@ 60 60 * **Research**: By stratifying patients, reduces cohort heterogeneity in clinical trials. 61 61 * **Clinical Practice**: Provides dynamic diagnostic annotations with timestamps for longitudinal tracking. 62 62 63 -== Who has access? == 64 - 65 -We welcome contributions from the global community. Let’s build the future of neurological diagnostics together! 66 - 67 67 == How to Contribute == 68 68 69 69 * Access the `/docs` folder for guidelines. ... ... @@ -75,9 +75,17 @@ 75 75 * Develop interpretable AI models for diagnosis and progression tracking. 76 76 * Integrate data from Human Phenotype Ontology (HPO), Gene Ontology (GO), and other biomedical resources. 77 77 * Foster collaboration among neuroscientists, AI researchers, and clinicians. 119 + 120 +== Who has access? == 121 + 122 +We welcome contributions from the global community. Let’s build the future of neurological diagnostics together! 78 78 ))) 79 79 80 80 126 + 127 + 128 + 129 + 81 81 (% class="col-xs-12 col-sm-4" %) 82 82 ((( 83 83 {{box title="**Contents**"}} ... ... @@ -90,5 +90,9 @@ 90 90 * `/code`: Machine learning pipelines and scripts. 91 91 * `/data`: Sample datasets for testing. 92 92 * `/outputs`: Generated models, visualizations, and reports. 142 +* [[Methodology>>url:https://wiki.ebrains.eu/bin/view/Collabs/neurodiagnoses/Methodology/]] 143 +* [[Notebooks>>Notebooks]] 144 +* [[Results>>url:https://wiki.ebrains.eu/bin/view/Collabs/neurodiagnoses/Results/]] 145 +* [[to-do-list>>to-do-list]] 93 93 ))) 94 94 )))
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