Changes for page Neurodiagnoses
Last modified by manuelmenendez on 2025/03/03 22:46
From version 19.1
edited by manuelmenendez
on 2025/01/28 00:02
on 2025/01/28 00:02
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To version 47.1
edited by manuelmenendez
on 2025/03/03 22:46
on 2025/03/03 22:46
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... ... @@ -2,9 +2,9 @@ 2 2 ((( 3 3 (% class="container" %) 4 4 ((( 5 -= //A new tridimensional diagnostic framework for neurodegenerativediseases// =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 neurodegenerativediseases 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 ))) ... ... @@ -15,35 +15,73 @@ 15 15 ((( 16 16 = What is this about and what can I find here? = 17 17 18 -= =**Overview** ==18 += **Overview** = 19 19 20 -The //TridimensionalDiagnosticFramework//redefines how neurodegenerative diseases(NDD)are classifiedby focusingon:20 +The classification and diagnosis of central nervous system (CNS) diseases have long been constrained by traditional, phenotype-based approaches that often fail to capture the complex interplay of pathophysiological mechanisms, molecular biomarkers, and neuroanatomical changes. 21 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). 22 +**Neurodiagnoses** redefines this landscape by integrating advanced AI with multi-modal data—including genetics, neuroimaging, biomarkers, and digital health records—to create a more precise, scalable, and data-driven diagnostic system. 25 25 26 - [[Neurodegenerativediseasescanbestudiedandclassifiedin atridimensionalscheme with threeaxes: anatomic–clinical,molecular,and etiologic.CSF, cerebrospinalfluid;FDG, fluorodeoxyglucose;MRI, magneticresonanceimaging; PET,positronemissiontomography.>>image:tridimensional.png||alt="tridimensionalview ofneurodegenerativediseases"]]24 +Additionally, **Neurodiagnoses is now expanding into disease prediction and biomarker estimation**, integrating state-of-the-art machine learning models to enhance precision diagnostics and disease progression forecasting. 27 27 26 +On this page, you will find: 28 28 29 -This methodology enables: 28 +* Detailed descriptions of both the clinical diagnostic tools and the research framework. 29 +* Access to our AI models, data processing pipelines, and digital twin simulations. 30 +* Collaborative resources for researchers, clinicians, and AI developers. 31 +* Guidelines and instructions on how to contribute to and expand the project. 30 30 31 -* Greater precision in diagnosis. 32 -* Integration of incomplete datasets using AI-driven probabilistic modeling. 33 -* Stratification of patients for personalized treatment. 33 +== **The role of AI-powered annotation** == 34 34 35 - ==**Diagnostic Axes**==35 +To enhance standardization, interpretability, and clinical application, the framework integrates an AI-powered annotation system, which: 36 36 37 +* Assigns structured metadata tags to diagnostic features. 38 +* Provides real-time contextual explanations for AI-based classifications. 39 +* Tracks longitudinal disease progression using timestamped AI annotations. 40 +* Improves AI model transparency through interpretability tools (e.g., SHAP analysis). 41 +* Facilitates decision-making for clinicians by linking annotations to standardized biomedical ontologies (SNOMED, HPO). 42 + 43 +Neurodiagnoses provides **two complementary AI-driven diagnostic approaches**: 44 + 45 +1. **Probabilistic Diagnosis** 46 + * AI assigns probability scores to multiple possible diagnoses based on biomarker, imaging, and clinical data. 47 + * Useful for differential diagnosis and treatment decision-making. 48 + 49 +2. **Tridimensional Diagnosis** 50 + * Diagnoses are structured based on: 51 + - **(1) Etiology** (genetic, autoimmune, metabolic, infectious). 52 + - **(2) Molecular Biomarkers** (amyloid-beta, tau, inflammatory markers, EEG patterns). 53 + - **(3) Neuroanatomoclinical Correlations** (brain atrophy, connectivity alterations). 54 + * This approach enables precise disease subtyping and biologically meaningful classification, particularly useful for tracking progression over time. 55 + 56 +Both systems will be offered for every patient case, allowing clinicians to compare AI-generated probabilistic diagnosis with a structured tridimensional classification. 57 + 58 +== **Disease Prediction and Biomarker Estimation** == 59 + 60 +Neurodiagnoses is also implementing **biomarker prediction and disease progression modeling**, using advanced machine learning techniques: 61 + 62 +* **Biomarker Prediction:** 63 + - Estimation of fluid-based and neuroimaging biomarkers without invasive testing. 64 + - Multi-modal machine learning models for predicting molecular and clinical markers. 65 + 66 +* **Disease Progression Modeling:** 67 + - AI-driven forecasts for neurodegenerative disease evolution. 68 + - Probabilistic disease conversion models (e.g., MCI to AD, Parkinson's prodromal phases). 69 + - Survival models and risk stratification for precision medicine applications. 70 + 71 +== **The case of neurodegenerative diseases** == 72 + 73 +There have been described these 3 diagnostic axes: 74 + 75 +[[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"]] 76 + 37 37 * ((( 38 38 **Axis 1: Etiology** 39 - 40 40 * //Description//: Focuses on genetic and sporadic causes, identifying risk factors and potential triggers. 41 41 * //Examples//: APOE ε4 as a genetic risk factor, or cardiovascular health affecting NDD progression. 42 -* //Tests//: Genetic testing, lifestyle and cardiovascular screening. 81 +* //Tests//: Genetic testing, lifestyle, and cardiovascular screening. 43 43 ))) 44 44 * ((( 45 45 **Axis 2: Molecular Markers** 46 - 47 47 * //Description//: Analyzes primary (amyloid-beta, tau) and secondary biomarkers (NFL, GFAP) for tracking disease progression. 48 48 * //Examples//: CSF amyloid-beta concentrations to confirm Alzheimer’s pathology. 49 49 * //Tests//: Blood/CSF biomarkers, PET imaging (Tau-PET, Amyloid-PET). ... ... @@ -50,7 +50,6 @@ 50 50 ))) 51 51 * ((( 52 52 **Axis 3: Neuroanatomoclinical** 53 - 54 54 * //Description//: Links clinical symptoms to neuroanatomical changes, such as atrophy or functional impairments. 55 55 * //Examples//: Hippocampal atrophy correlating with memory deficits. 56 56 * //Tests//: MRI volumetrics, FDG-PET, neuropsychological evaluations. ... ... @@ -60,18 +60,16 @@ 60 60 61 61 This system enhances: 62 62 63 -* **Research**: By stratifying patients, reduc escohort heterogeneity in clinical trials.100 +* **Research**: By stratifying patients, reducing cohort heterogeneity in clinical trials. 64 64 * **Clinical Practice**: Provides dynamic diagnostic annotations with timestamps for longitudinal tracking. 65 65 66 -== Who has access? == 67 - 68 -We welcome contributions from the global community. Let’s build the future of neurological diagnostics together! 69 - 70 70 == How to Contribute == 71 71 72 72 * Access the `/docs` folder for guidelines. 73 73 * Use `/code` for the latest AI pipelines. 74 74 * Share feedback and ideas in the wiki discussion pages. 108 +* Join our [[Community on EBRAINS>>https://community.ebrains.eu/_ideas/-OJHTZrpKrrrkx-u0djj/about]] 109 +* Join the [[Discussion Forum at GitHub>>https://github.com/Fundacion-de-Neurociencias/neurodiagnoses/discussions]] 75 75 76 76 == Key Objectives == 77 77 ... ... @@ -78,9 +78,17 @@ 78 78 * Develop interpretable AI models for diagnosis and progression tracking. 79 79 * Integrate data from Human Phenotype Ontology (HPO), Gene Ontology (GO), and other biomedical resources. 80 80 * Foster collaboration among neuroscientists, AI researchers, and clinicians. 81 -))) 116 +* Provide a dual diagnostic system: 117 + ** Probabilistic Diagnosis – AI assigns multiple traditional possible diagnoses with probability percentages. 118 + ** Tridimensional Diagnosis – AI structures diagnoses based on etiology, biomarkers, and neuroanatomical correlations. 119 +* Implement disease prediction models for neurodegenerative conditions. 120 +* Predict biomarkers from non-invasive data sources. 82 82 122 +== Who has access? == 83 83 124 +We welcome contributions from the global community. Join us as we transform CNS diagnostics and drive precision medicine forward through a collaborative, open-source approach. Let’s build the future of neurological diagnostics together! 125 +))) 126 + 84 84 (% class="col-xs-12 col-sm-4" %) 85 85 ((( 86 86 {{box title="**Contents**"}} ... ... @@ -93,5 +93,10 @@ 93 93 * `/code`: Machine learning pipelines and scripts. 94 94 * `/data`: Sample datasets for testing. 95 95 * `/outputs`: Generated models, visualizations, and reports. 139 +* [[Methodology>>url:https://wiki.ebrains.eu/bin/view/Collabs/neurodiagnoses/Methodology/]] 140 +* [[Notebooks>>Notebooks]] 141 +* [[Results>>url:https://wiki.ebrains.eu/bin/view/Collabs/neurodiagnoses/Results/]] 142 +* [[to-do-list>>to-do-list]] 96 96 ))) 97 97 ))) 145 +