Increased rates of white matter hyperintensities in late-onset bipolar disorder

Jaqueline Hatsuko Tamashiro1, Stevin Zung, Marcus Vinicius Zanetti

  • 1Department of Psychiatry, University of São Paulo Medical School, São Paulo, Brazil. jhatsu@gmail.com

Bipolar Disorders
|November 27, 2008
PubMed
Abstract

Insights

Late-onset bipolar disorder (LO-BD) shows higher rates of white matter hyperintensities (WMH) compared to early-onset BD and healthy controls. This suggests vascular factors are involved in LO-BD, differentiating it from early-onset forms.

Area of Science:

  • Neuroimaging and Psychiatry
  • Cerebrovascular Disease and Mental Health

Background:

  • Late-onset depression is associated with increased white matter hyperintensities (WMH), suggesting vascular mechanisms in late-onset mood disorders.
  • Emerging evidence links late-onset bipolar disorder (LO-BD) to cerebrovascular risk factors, but neuroimaging data remain limited.
  • Understanding WMH in LO-BD is crucial for differentiating its pathophysiology from early-onset bipolar disorder (EO-BD).

Purpose of the Study:

  • To investigate the association between white matter hyperintensities (WMH) and late-onset bipolar disorder (LO-BD).
  • To compare WMH prevalence in LO-BD patients versus early-onset BD (EO-BD) patients and elderly healthy volunteers.
  • To explore neuroimaging evidence for vascular contributions to LO-BD.

Main Methods:

  • Acquisition of T2-weighted MRI data from three groups: LO-BD (n=10), EO-BD (n=49), and healthy controls (n=24).
  • Assessment of white matter hyperintensities (WMH) using the Scheltens scale.
  • Statistical comparison of WMH rates and scores between groups, with adjustments for age.

Main Results:

  • Late-onset bipolar disorder (LO-BD) patients exhibited a significantly higher prevalence of WMH in the deep parietal region and basal ganglia compared to EO-BD and healthy controls.
  • After adjusting for age, LO-BD patients showed more severe WMH scores in deep frontal and parietal regions, and the putamen.
  • These findings indicate a distinct pattern of WMH in LO-BD.

Conclusions:

  • The study provides empirical support for a link between vascular risk factors and late-onset bipolar disorder (LO-BD).
  • The observed WMH patterns may help distinguish the pathophysiology of LO-BD from early-onset bipolar disorder (EO-BD).
  • Larger sample studies are needed to confirm these findings and elucidate the role of vascular mechanisms in LO-BD.

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