Related Experiment Video
Updated: Jun 27, 2026

Brain Morphology of Cannabis Users With or Without Psychosis: A Pilot MRI Study
Published on: August 18, 2020
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
Objectives:
Magnetic resonance imaging (MRI) studies have reported an increased frequency of white matter hyperintensities (WMH) in association with late-onset (LO) depression, and this has supported the notion that vascular-related mechanisms may be implicated in the pathophysiology of LO mood disorders. Recent clinical studies have also suggested a link between LO bipolar disorder (LO-BD) and cerebrovascular risk factors, but this has been little investigated with neuroimaging techniques. In order to ascertain whether there could be a specific association between WMH and LO-BD, we directly compared WMH rates between LO-BD subjects (illness onset >or= 60 years), early-onset BD subjects (EO-BD, illness onset <60 years), and elderly healthy volunteers.
Methods:
T2-weighted MRI data were acquired in LO-BD subjects (n = 10, age = 73.60 +/- 4.09), EO-BD patients (n = 49, age = 67.78 +/- 4.44), and healthy subjects (n = 24, age = 69.00 +/- 7.22). WMH rates were assessed using the Scheltens scale.
Results:
There was a greater prevalence of WMH in LO-BD patients relative to the two other groups in the deep parietal region (p = 0.018) and basal ganglia (p < 0.045). When between-group comparisons of mean WMH scores were conducted taking account of age differences (ANCOVA), there were more severe scores in LO-BD patients relative to the two other groups in deep frontal and parietal regions, as well as in the putamen (p < 0.05).
Conclusions:
Our results provide empirical support to the proposed link between vascular risk factors and LO-BD. If extended in future studies with larger samples, these findings may help to clarify the pathophysiological distinctions between bipolar disorder emerging at early and late stages of life.
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.
Related Concept Videos
Bipolar Disorder
Mania and Antimanic Drugs: Overview
Biological Causes of Schizophrenia
Genetic Factors in Schizophrenia
The genetic basis of schizophrenia is strongly supported by family and twin studies.
Attention-Deficit/Hyperactivity Disorder
Diagnostic Criteria and Symptoms
To diagnose ADHD, symptoms must manifest before age 12 and be evident across multiple settings.
Depressive Disorders: Etiology
Biological Factors in Depression
Biological predispositions significantly influence the risk of developing depressive disorders. Genetic studies highlight the role of variations in the serotonin transporter...
Depression: Overview
