Changes for page Neurodiagnoses

Last modified by manuelmenendez on 2025/03/03 22:46

From version 20.1
edited by manuelmenendez
on 2025/01/28 00:03
Change comment: There is no comment for this version
To version 47.1
edited by manuelmenendez
on 2025/03/03 22:46
Change comment: There is no comment for this version

Summary

Details

Page properties
Content
... ... @@ -2,9 +2,9 @@
2 2  (((
3 3  (% class="container" %)
4 4  (((
5 -= //A new tridimensional diagnostic framework for neurodegenerative diseases// =
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 neurodegenerative diseases 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  )))
... ... @@ -15,36 +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 //Tridimensional Diagnostic Framework// redefines how neurodegenerative diseases (NDD) are classified by focusing on:
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  
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.
26 26  
27 -[[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"]]
26 +On this page, you will find:
28 28  
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.
29 29  
30 -This methodology enables:
33 +== **The role of AI-powered annotation** ==
31 31  
32 -* Greater precision in diagnosis.
33 -* Integration of incomplete datasets using AI-driven probabilistic modeling.
34 -* Stratification of patients for personalized treatment.
35 +To enhance standardization, interpretability, and clinical application, the framework integrates an AI-powered annotation system, which:
35 35  
36 -== **Diagnostic Axes** ==
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).
37 37  
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 +
38 38  * (((
39 39  **Axis 1: Etiology**
40 -
41 41  * //Description//: Focuses on genetic and sporadic causes, identifying risk factors and potential triggers.
42 42  * //Examples//: APOE ε4 as a genetic risk factor, or cardiovascular health affecting NDD progression.
43 -* //Tests//: Genetic testing, lifestyle and cardiovascular screening.
81 +* //Tests//: Genetic testing, lifestyle, and cardiovascular screening.
44 44  )))
45 45  * (((
46 46  **Axis 2: Molecular Markers**
47 -
48 48  * //Description//: Analyzes primary (amyloid-beta, tau) and secondary biomarkers (NFL, GFAP) for tracking disease progression.
49 49  * //Examples//: CSF amyloid-beta concentrations to confirm Alzheimer’s pathology.
50 50  * //Tests//: Blood/CSF biomarkers, PET imaging (Tau-PET, Amyloid-PET).
... ... @@ -51,7 +51,6 @@
51 51  )))
52 52  * (((
53 53  **Axis 3: Neuroanatomoclinical**
54 -
55 55  * //Description//: Links clinical symptoms to neuroanatomical changes, such as atrophy or functional impairments.
56 56  * //Examples//: Hippocampal atrophy correlating with memory deficits.
57 57  * //Tests//: MRI volumetrics, FDG-PET, neuropsychological evaluations.
... ... @@ -61,18 +61,16 @@
61 61  
62 62  This system enhances:
63 63  
64 -* **Research**: By stratifying patients, reduces cohort heterogeneity in clinical trials.
100 +* **Research**: By stratifying patients, reducing cohort heterogeneity in clinical trials.
65 65  * **Clinical Practice**: Provides dynamic diagnostic annotations with timestamps for longitudinal tracking.
66 66  
67 -== Who has access? ==
68 -
69 -We welcome contributions from the global community. Let’s build the future of neurological diagnostics together!
70 -
71 71  == How to Contribute ==
72 72  
73 73  * Access the `/docs` folder for guidelines.
74 74  * Use `/code` for the latest AI pipelines.
75 75  * 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]]
76 76  
77 77  == Key Objectives ==
78 78  
... ... @@ -79,9 +79,17 @@
79 79  * Develop interpretable AI models for diagnosis and progression tracking.
80 80  * Integrate data from Human Phenotype Ontology (HPO), Gene Ontology (GO), and other biomedical resources.
81 81  * Foster collaboration among neuroscientists, AI researchers, and clinicians.
82 -)))
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.
83 83  
122 +== Who has access? ==
84 84  
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 +
85 85  (% class="col-xs-12 col-sm-4" %)
86 86  (((
87 87  {{box title="**Contents**"}}
... ... @@ -94,5 +94,10 @@
94 94  * `/code`: Machine learning pipelines and scripts.
95 95  * `/data`: Sample datasets for testing.
96 96  * `/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]]
97 97  )))
98 98  )))
145 +