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Assessment of Age-related Changes in Cognitive Functions Using EmoCogMeter, a Novel Tablet-computer Based Approach
Published on: February 14, 2014
Homocysteine, rather than age of onset, is a better predictor for cognitive function in older adults with bipolar
Pao-Huan Chen1,2, Hsing-Cheng Liu2,3, Mong-Liang Lu2,4
1Department of Psychiatry, Taipei Medical University Hospital, Taipei, Taiwan.
Insights
Late-onset bipolar disorder (LOBD) in older adults shows no cognitive decline compared to early-onset bipolar disorder (EOBD). However, elevated homocysteine levels are linked to poorer cognitive function in this population.
Area of Science:
- Neuroscience
- Gerontology
- Psychiatry
Background:
- Bipolar disorder in older adults may be linked to cognitive impairments, potentially influenced by vascular factors.
- Distinguishing between late-onset bipolar disorder (LOBD) and early-onset bipolar disorder (EOBD) is crucial for understanding cognitive trajectories.
Purpose of the Study:
- To compare cognitive function between older individuals with LOBD and EOBD.
- To investigate the role of vascular risk burden and biochemical markers in cognitive performance.
Main Methods:
- 95 outpatients over 55 with bipolar I disorder were assessed.
- Cognitive function was evaluated using a comprehensive test battery.
- Vascular risk factors, cardiovascular risk scores, and serum biomarkers (homocysteine, B12, folate, T3) were assessed.
Main Results:
- No significant cognitive differences were found between LOBD and EOBD groups after adjusting for confounders.
- Higher serum homocysteine levels were negatively associated with cognitive performance in attention, psychomotor speed, verbal memory, and executive function.
Conclusions:
- Late-onset bipolar disorder is not associated with greater cognitive dysfunction compared to early-onset bipolar disorder in older adults.
- Elevated serum homocysteine levels correlate with worse cognitive function in older bipolar disorder patients, warranting clinical attention.
Objectives:
The association between older-age bipolar disorder and cognitive impairments may be mediated by vascular burden. The aim of the study was to examine the difference of cognitive function between older people with late-onset bipolar disorder (LOBD) and early-onset bipolar disorder (EOBD) by considering rigorous vascular risk burden evaluation, comprehensive cognitive tests, and relevant biochemistry data.
Methods:
We recruited 95 outpatients aged over 55 with a DSM-IV-TR diagnosis of bipolar I disorder. Fifty had LOBD, defined by age of onset after 40. Cognitive function was evaluated through a battery of tests assessing verbal memory, attention/speed, visuospatial function, verbal fluency, and cognitive flexibility. Vascular risk assessments included individual disorders, 10-year Framingham cardiovascular risk scores, and serum levels of homocysteine, vitamin B12, folate, and triiodothyronine.
Results:
No differences were observed between LOBD and EOBD on any cognitive test after adjusting for potential confounders. In addition to age and educational years, multiple linear regression analyses indicated significantly negative associations between serum homocysteine levels and cognitive performances in attention, psychomotor speed, verbal memory, and executive function.
Conclusions:
Among older people with bipolar disorder, LOBD is not associated with more cognitive dysfunction in this study. However, higher serum homocysteine levels were significantly associated with worse cognitive performance in this particular group. Clinicians therefore have to pay attention to the cognitive function in older bipolar patients with higher levels of homocysteine.
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