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

Multiple Sclerosis l: Introduction01:19

Multiple Sclerosis l: Introduction

32
Multiple sclerosis is a chronic autoimmune disease of the central nervous system (CNS) that affects the brain, spinal cord, and optic nerves. It is an inflammatory demyelinating disorder and a leading cause of neurological disability in young adults.EpidemiologyMS commonly begins between 20 and 40 years of age and is twice as common in women. Its exact cause remains unclear, but genetic susceptibility contributes, with higher risk in first-degree relatives and identical twins. A greater...
32
Nervous Tissue: Myelin01:25

Nervous Tissue: Myelin

12.2K
The myelin sheath is a multilayered lipid and protein covering that insulates the axon of a neuron, enhancing the speed of nerve impulse conduction. Axons without this sheath are referred to as unmyelinated. Two types of neuroglia, Schwann cells in the peripheral nervous system (PNS) and oligodendrocytes in the central nervous system (CNS) are responsible for producing myelin sheaths.
Schwann cells begin to form myelin sheaths around axons during fetal development. They wrap around a small...
12.2K
Alzheimer Disease ll: Pathophysiology01:23

Alzheimer Disease ll: Pathophysiology

44
Alzheimer disease involves structural changes in the brain that begin long before symptoms appear. The most distinctive features are extracellular neuritic plaques and intracellular neurofibrillary tangles.Neuritic plaques form in the cerebral cortex and around blood vessels. These plaques contain a dense core of beta-amyloid (Aβ)—a toxic protein fragment that clumps outside neurons. The core is surrounded by damaged neuronal extensions, as well as reactive astrocytes and...
44

You might also read

Related Articles

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

Sort by
Same author

Impact of depression and anxiety on health-related quality of life changes over time within individuals with rheumatoid arthritis or inflammatory bowel disease: A prospective Canadian cohort study.

PloS one·2026
Same author

Physical, cognitive, and psychosocial fatigue are differently related to cortical complexity of superior temporal and frontal brain regions in Crohn's disease.

Frontiers in neuroimaging·2026
Same author

Sex differences in cerebrovascular function across an aerobic exercise intervention in older adults using MRI: Results from the Brain in Motion study.

Physiological reports·2026
Same author

White Matter Damage in Multiple Sclerosis Disproportionately Targets Default Mode, Executive Control, and Salience Networks.

The Journal of neuroscience : the official journal of the Society for Neuroscience·2026
Same author

Sex differences in the rate and factors for elevated depressive symptoms in multiple sclerosis, inflammatory bowel disease, and rheumatoid arthritis.

Journal of health psychology·2026
Same author

Basic Science and Pathogenesis.

Alzheimer's & dementia : the journal of the Alzheimer's Association·2025

Related Experiment Video

Updated: May 6, 2026

Comprehensive Autopsy Program for Individuals with Multiple Sclerosis
09:41

Comprehensive Autopsy Program for Individuals with Multiple Sclerosis

Published on: July 19, 2019

12.4K

Intra-individual variability in information processing speed reflects white matter microstructure in multiple

Erin L Mazerolle1, Magdalena A Wojtowicz, Antonina Omisade

  • 1McConnell Brain Imaging Centre, Montreal Neurological Institute, McGill University, Room WB325, 3801 University St, Montreal, Quebec H3A 2B4, Canada ; Department of Psychology and Neuroscience, Dalhousie University, Life Sciences Centre, P.O. Box 15000, Halifax, Nova Scotia B3H 4R2, Canada.

Neuroimage. Clinical
|November 2, 2013
PubMed
Summary

Intra-individual variability (IIV) in information processing speed, not just average speed, is a more sensitive indicator of neurological status in multiple sclerosis (MS). Increased IIV in MS patients correlates with reduced white matter integrity, highlighting its importance in understanding cognitive dysfunction.

Keywords:
CTIP, Computerized Test of Information ProcessingDiffusion tensor imagingIIV, intra-individual variabilityInformation processing speedIntra-individual variabilityMultiple sclerosisTract-based spatial statistics

More Related Videos

Magnetic Resonance Imaging of Multiple Sclerosis at 7.0 Tesla
08:51

Magnetic Resonance Imaging of Multiple Sclerosis at 7.0 Tesla

Published on: February 19, 2021

9.7K
Diffusion Tensor Magnetic Resonance Imaging in the Analysis of Neurodegenerative Diseases
09:33

Diffusion Tensor Magnetic Resonance Imaging in the Analysis of Neurodegenerative Diseases

Published on: July 28, 2013

27.9K

Related Experiment Videos

Last Updated: May 6, 2026

Comprehensive Autopsy Program for Individuals with Multiple Sclerosis
09:41

Comprehensive Autopsy Program for Individuals with Multiple Sclerosis

Published on: July 19, 2019

12.4K
Magnetic Resonance Imaging of Multiple Sclerosis at 7.0 Tesla
08:51

Magnetic Resonance Imaging of Multiple Sclerosis at 7.0 Tesla

Published on: February 19, 2021

9.7K
Diffusion Tensor Magnetic Resonance Imaging in the Analysis of Neurodegenerative Diseases
09:33

Diffusion Tensor Magnetic Resonance Imaging in the Analysis of Neurodegenerative Diseases

Published on: July 28, 2013

27.9K

Area of Science:

  • Neuroscience
  • Cognitive Psychology
  • Radiology

Background:

  • Slowed information processing speed is a common symptom in multiple sclerosis (MS).
  • Intra-individual variability (IIV) in processing speed may be a more sensitive marker of neurological impairment than mean-level performance.
  • Understanding the neural basis of IIV in MS is crucial for accurate diagnosis and treatment.

Purpose of the Study:

  • To investigate the neural underpinnings of increased IIV in information processing speed in individuals with relapsing-remitting MS.
  • To examine the relationship between IIV, mean processing speed, and white matter integrity using diffusion tensor imaging (DTI).

Main Methods:

  • Twenty women with relapsing-remitting MS and 20 controls completed the Computerized Test of Information Processing (CTIP) to measure mean response time and IIV.
  • Diffusion tensor imaging (DTI) and tract-based spatial statistics were used to assess white matter microstructure.
  • Clinical measures of information processing speed were also collected for comparison.

Main Results:

  • MS patients exhibited slower and more variable responses on the CTIP compared to controls.
  • Significant associations were found between white matter microstructure and IIV in MS patients.
  • Increased IIV was linked to reduced integrity in a greater number of white matter tracts than mean processing speed measures.

Conclusions:

  • Intra-individual variability (IIV) in information processing speed is a more sensitive indicator of white matter disease burden in MS than mean-level performance.
  • Assessing within-person fluctuations in cognitive function, alongside average performance, is valuable for understanding brain-behavior relationships in neurological disorders with white matter pathology.