The influence of posterior visual pathway damage on visual information processing speed in multiple sclerosis

Iñigo Gabilondo1, Oiane Rilo2, Natalia Ojeda2

  • 1Department of Methods and Experimental Psychology, Faculty of Psychology and Education, Universidad de Deusto, Bilbao, Spain/Neurodegenerative Diseases Group, BioCruces Health Research Institute, Barakaldo, Spain.

Multiple Sclerosis (Houndmills, Basingstoke, England)
|March 10, 2017
PubMed
Abstract

Insights

Visual processing speed (VPS) in multiple sclerosis (MS) is linked to the posterior visual pathway. Structural integrity (V2 thickness, optic radiation fractional anisotropy) and functional connectivity (medial visual component) significantly impact VPS in MS patients.

Area of Science:

  • Neuroscience
  • Ophthalmology
  • Radiology

Background:

  • Multiple Sclerosis (MS) frequently involves visual pathway damage and altered visual processing speed (VPS).
  • The direct association between posterior visual pathway integrity and VPS in MS remains largely unexplored.

Purpose of the Study:

  • To investigate the relationship between the structural and functional integrity of the posterior visual pathway and VPS in patients with MS.
  • To determine how specific MRI-derived measures correlate with impaired visual processing speed.

Main Methods:

  • A cross-sectional study included 30 MS patients and 28 controls.
  • Visual processing speed (VPS) was assessed using a composite of standardized tests.
  • 3T MRI was used to evaluate visual cortex thickness, optic radiations (OR) diffusion tensor imaging (DTI) indices, and medial visual component (MVC) functional connectivity (FC).

Main Results:

  • V2 atrophy, reduced OR fractional anisotropy (FA), and altered MVC functional connectivity (FC) were significantly associated with slower VPS in MS patients.
  • These associations remained significant after controlling for factors like Expanded Disability Status Scale and prior optic neuritis.
  • Specific findings included V2 atrophy (r²=0.210), OR FA (r²=0.243), and MVC iFC (r²=0.450) influencing VPS.

Conclusions:

  • Posterior visual pathway structural integrity, specifically V2 thickness and OR FA, can explain up to 24% of VPS variability in MS.
  • Functional integrity of the medial visual component (MVC FC) may account for up to 45% of VPS variability in MS patients.
  • These findings highlight the importance of the posterior visual pathway in MS-related visual processing deficits.