Mapping face encoding using functional MRI in multiple sclerosis across disease phenotypes

Maria A Rocca1,2, Laura Vacchi1, Mariaemma Rodegher2

  • 1Neuroimaging Research Unit, Institute of Experimental Neurology, Division of Neuroscience, San Raffaele Scientific Institute, Vita-Salute San Raffaele University, Via Olgettina, 60, 20132, Milan, Italy.

Insights

Multiple sclerosis (MS) patients show altered brain activity during face encoding (FE). Early MS stages involve increased visual area recruitment, while later stages show frontal lobe involvement, correlating with disease severity.

Area of Science:

  • Neuroimaging
  • Neurology
  • Cognitive Neuroscience

Background:

  • Multiple sclerosis (MS) is a demyelinating disease affecting the central nervous system.
  • Understanding the neural underpinnings of cognitive deficits in MS is crucial for patient management.
  • Face encoding (FE) performance and its neural correlates may be altered in MS.

Purpose of the Study:

  • To investigate the behavioral and functional magnetic resonance imaging (fMRI) correlates of face encoding (FE) in multiple sclerosis (MS) patients.
  • To examine how FE-related brain activity varies across different MS clinical phenotypes (clinically isolated syndromes - CIS, relapsing-remitting MS - RRMS, and secondary progressive MS - SPMS).
  • To correlate fMRI findings with clinical, cognitive-executive performance, and structural MRI measures of disease-related damage.

Main Methods:

  • fMRI during a face encoding (FE) task was administered to 75 MS patients (CIS, RRMS, SPMS) and 22 healthy controls (HC).
  • Analysis correlated fMRI activity during FE with behavioral, clinical, neuropsychological, and structural MRI data.
  • Brain activation and deactivation patterns were compared across patient groups and HC.

Main Results:

  • All participants activated face perception/encoding networks and deactivated default-mode network areas.
  • MS patients exhibited abnormal patterns of increased/decreased activation and deactivation compared to HC.
  • CIS patients showed increased recruitment of posterior-visual areas; RRMS patients showed greater activation in thalami, para-hippocampal gyri, and anterior cingulum compared to CIS/SPMS; SPMS patients demonstrated increased frontal lobe recruitment.
  • Abnormal activation patterns correlated significantly with clinical, cognitive, and structural MRI measures.

Conclusions:

  • Face encoding network abnormalities are present in MS and differ across clinical phenotypes.
  • Early MS stages (CIS) are characterized by compensatory hyperactivation in visual processing areas.
  • Later MS stages (SPMS) show aberrant functional recruitment in frontal regions, potentially contributing to clinical symptom severity.

Related Concept Videos