Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Neural Regulation01:37

Neural Regulation

45.1K
Digestion begins with a cephalic phase that prepares the digestive system to receive food. When our brain processes visual or olfactory information about food, it triggers impulses in the cranial nerves innervating the salivary glands and stomach to prepare for food.
45.1K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Risk of epilepsy in people with adult-onset hydrocephalus: insights from the UK Biobank.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology·2026
Same author

Reduced Mitochondrial DNA Copy Number and Telomere Length in Essential Tremor Patients: Evidence from an Age- and Sex-Adjusted Cross-Sectional Case-Control Study.

International journal of molecular sciences·2026
Same author

Planimetric and Linear MRI Markers for Progressive Supranuclear Palsy Classification: A Large Multicohort International Study.

Radiology·2026
Same author

The bidirectional association of epilepsy with Alzheimer's disease and other neurodegenerative dementias: A longitudinal observational study on the UK Biobank.

Journal of Alzheimer's disease : JAD·2026
Same author

Cytoskeletal Imbalance and Axonal Vulnerability in Sporadic PSP-RS: Early Changes in a Human iPSC-Derived Neuronal Model with Altered mTOR Signaling.

Cells·2026
Same author

Serum Neurofilament Light Chain and GFAP Levels Are Associated with Structural Brain Connectivity in Parkinson's Disease.

International journal of molecular sciences·2026

Related Experiment Video

Updated: Apr 12, 2026

Identification of Disease-related Spatial Covariance Patterns using Neuroimaging Data
14:27

Identification of Disease-related Spatial Covariance Patterns using Neuroimaging Data

Published on: June 26, 2013

16.5K

Subregional thalamic atrophy in Progressive Supranuclear Palsy: A machine learning study.

Camilla Calomino1, Maria Giovanna Bianco2, Chiara Camastra2

  • 1Azienda Ospedaliero Universitaria "Renato Dulbecco", Catanzaro, Italy; Neuroscience Research Center, Magna Graecia University of Catanzaro, Italy.

Neuroimage. Clinical
|April 10, 2026
PubMed
Summary

Subregional thalamic atrophy, particularly in specific nuclei, can accurately distinguish Progressive Supranuclear Palsy (PSP) from Parkinson's disease (PD). This finding highlights thalamic nuclei volumes as a potential diagnostic biomarker for PSP.

Keywords:
MRIMachine learningParkinson’s diseaseProgressive Supranuclear PalsyThalamic nuclei

More Related Videos

Whole-brain Segmentation and Change-point Analysis of Anatomical Brain MRI—Application in Premanifest Huntington's Disease
09:06

Whole-brain Segmentation and Change-point Analysis of Anatomical Brain MRI—Application in Premanifest Huntington's Disease

Published on: June 9, 2018

12.7K
Translational Brain Mapping at the University of Rochester Medical Center: Preserving the Mind Through Personalized Brain Mapping
13:12

Translational Brain Mapping at the University of Rochester Medical Center: Preserving the Mind Through Personalized Brain Mapping

Published on: August 12, 2019

46.8K

Related Experiment Videos

Last Updated: Apr 12, 2026

Identification of Disease-related Spatial Covariance Patterns using Neuroimaging Data
14:27

Identification of Disease-related Spatial Covariance Patterns using Neuroimaging Data

Published on: June 26, 2013

16.5K
Whole-brain Segmentation and Change-point Analysis of Anatomical Brain MRI—Application in Premanifest Huntington's Disease
09:06

Whole-brain Segmentation and Change-point Analysis of Anatomical Brain MRI—Application in Premanifest Huntington's Disease

Published on: June 9, 2018

12.7K
Translational Brain Mapping at the University of Rochester Medical Center: Preserving the Mind Through Personalized Brain Mapping
13:12

Translational Brain Mapping at the University of Rochester Medical Center: Preserving the Mind Through Personalized Brain Mapping

Published on: August 12, 2019

46.8K

Area of Science:

  • Neuroimaging
  • Neurology
  • Machine Learning

Background:

  • Previous MRI studies show whole thalamus atrophy in Progressive Supranuclear Palsy (PSP).
  • These studies did not evaluate specific thalamic substructures.
  • This research investigates thalamic subregional atrophy in PSP for diagnostic potential.

Purpose of the Study:

  • To assess atrophy in thalamic substructures in PSP patients.
  • To determine if thalamic subregional atrophy can aid in differentiating PSP from Parkinson's disease (PD).
  • To validate the diagnostic potential of thalamic nuclei volumes.

Main Methods:

  • Utilized T1-weighted MRI scans from 398 subjects (164 PSP, 180 PD, 64 controls).
  • Employed automatic probabilistic segmentation of thalamic nuclei to analyze subregional atrophy.
  • Applied machine learning (XGBoost) to distinguish PSP from PD, validated on an independent cohort.

Main Results:

  • PSP patients exhibited significant atrophy in lateral, paraventricular, and pulvinar thalamic nuclei compared to controls.
  • No significant thalamic differences were found between PD patients and controls.
  • The machine learning model accurately differentiated PSP from PD (AUC: 0.96), outperforming whole thalamus volume analysis.

Conclusions:

  • Subregional thalamic atrophy is prominent in PSP, affecting specific nuclei.
  • Machine learning models using thalamic nuclei volumes effectively distinguish PSP from PD.
  • Thalamic subregional atrophy shows promise as a diagnostic biomarker for PSP.