White matter alterations in the internal capsule and psychomotor impairment in melancholic depression

Matthew P Hyett1,2, Alistair Perry1,2,3, Michael Breakspear2,4,5

  • 1School of Psychiatry, University of New South Wales, Sydney, New South Wales, Australia.

Plos One
|April 20, 2018
PubMed

Insights

Melancholic depression shows distinct white matter changes in the right anterior internal capsule, linked to psychomotor disturbances. These findings in brain structure may help subtype depression.

Area of Science:

  • Neuroimaging
  • Psychiatry
  • Neuroscience

Background:

  • Structural brain abnormalities are increasingly implicated in the pathophysiology of melancholic depression.
  • Specific white matter disruptions may underlie the psychomotor dysfunction characteristic of melancholia.

Purpose of the Study:

  • To investigate white matter integrity in the internal capsule subdivisions using diffusion magnetic resonance imaging (dMRI) in individuals with melancholic depression.
  • To correlate white matter measures with psychomotor functioning in melancholia.

Main Methods:

  • dMRI data were analyzed for fractional anisotropy (FA), radial diffusivity (RD), and axial diffusivity (AD) in anterior, posterior, and retrolenticular internal capsule limbs.
  • Participants included 22 melancholic depressed, 23 non-melancholic depressed, and 29 healthy controls.
  • Neuropsychological and psychomotor assessments were performed and correlated with dMRI metrics.

Main Results:

  • Individuals with melancholia exhibited increased FA and decreased RD in the right anterior internal capsule compared to controls.
  • The right anterior internal capsule's FA correlated with psychomotor disturbance ratings.
  • Reduced psychomotor speed in melancholia was associated with increased FA in the right retrolenticular limb.

Conclusions:

  • This study reveals specific white matter disturbances within the internal capsule in melancholia, directly associated with psychomotor dysfunction.
  • These findings contribute to understanding the neurobiological underpinnings of melancholic depression and may aid in developing neurobiological markers for depression subtyping.

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