Changes for page Neurodiagnoses
Last modified by manuelmenendez on 2025/03/03 22:46
From version 5.1
edited by manuelmenendez
on 2025/01/27 23:04
on 2025/01/27 23:04
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To version 7.2
edited by manuelmenendez
on 2025/01/27 23:22
on 2025/01/27 23:22
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... ... @@ -2,9 +2,10 @@ 2 2 ((( 3 3 (% class="container" %) 4 4 ((( 5 -= Neurodiagnoses =5 += //A new tridimensional diagnostic framework for CNS conditions// = 6 6 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. 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. 8 8 ))) 9 9 ))) 10 10 ... ... @@ -12,8 +12,53 @@ 12 12 ((( 13 13 (% class="col-xs-12 col-sm-8" %) 14 14 ((( 15 -= What can I find here? = 16 += What is this about and what can I find here? = 16 16 18 +==== **Overview** ==== 19 + 20 +The //Tridimensional Diagnostic Framework// redefines how neurodegenerative diseases (NDDs) are classified by focusing on: 21 + 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). 25 + 26 +This methodology enables: 27 + 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** ==== 33 + 34 +* ((( 35 +**Axis 1: Etiology** 36 + 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. 40 +))) 41 +* ((( 42 +**Axis 2: Molecular Markers** 43 + 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). 47 +))) 48 +* ((( 49 +**Axis 3: Neuroanatomoclinical** 50 + 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. 54 +))) 55 + 56 +==== **Applications** ==== 57 + 58 +This system enhances: 59 + 60 +* **Research**: By stratifying patients, reduces cohort heterogeneity in clinical trials. 61 +* **Clinical Practice**: Provides dynamic diagnostic annotations with timestamps for longitudinal tracking. 62 + 17 17 == Who has access? == 18 18 19 19 We welcome contributions from the global community. Let’s build the future of neurological diagnostics together!