Impaired processing of 3D motion-defined faces in mild cognitive impairment and healthy aging: an fMRI study

Britta Graewe1, Raquel Lemos, Carlos Ferreira

  • 1Department of Cognitive Neuroscience, Faculty of Psychology & Neuroscience, Maastricht University, PO Box 616, 6200 MD Maastricht, the Netherlands.

Insights

Mild cognitive impairment (MCI) disrupts visual processing, with MCI patients showing altered brain activity in face-sensitive areas. This visual impairment may indicate early Alzheimer's disease (AD) risk.

Area of Science:

  • Neuroscience
  • Cognitive Science
  • Medical Imaging

Background:

  • Mild cognitive impairment (MCI) is a precursor to Alzheimer's disease (AD) and is associated with poorly understood visual declines.
  • Understanding these visual changes may offer insights into early AD detection.

Purpose of the Study:

  • To investigate functional magnetic resonance imaging (fMRI) differences in visual processing between individuals with amnestic MCI, healthy elderly, and young participants.
  • To explore the relationship between visual perception deficits and brain activity in the dorsal and ventral visual streams during face categorization.

Main Methods:

  • Compared fMRI activity in dorsal and ventral visual streams of amnestic MCI, healthy elderly, and young adults.
  • Utilized structure-from-motion (SFM) face categorization tasks with varying stimulus depth and duration.
  • Analyzed activation patterns in the fusiform face area (FFA) and occipital face area (OFA).

Main Results:

  • Healthy elderly showed reduced face sensitivity compared to young adults in right FFA/OFA.
  • MCI patients exhibited reversed face sensitivity (scrambled faces > faces) in right FFA/OFA.
  • MCI patients displayed heightened depth sensitivity in left FFA/OFA, suggesting impaired face perception due to overemphasis on low-level features.
  • Discriminant function analysis accurately classified MCI and healthy elderly (88.2%) using FFA/OFA sensitivity indices.
  • Altered activation was observed in dorsal-ventral stream integration and attention networks in MCI patients.

Conclusions:

  • Aberrant visual processing and compensatory mechanisms in MCI patients may signify preclinical AD.
  • Face and depth sensitivity in FFA/OFA can distinguish MCI from healthy elderly, offering potential biomarkers for early AD detection.
  • Visual stream alterations provide critical insights into the neurobiological underpinnings of MCI and its progression to AD.