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Published on: May 22, 2019
BDNF genotype potentially modifying the association between incident stroke and depression
Jae-Min Kim1, Robert Stewart, Sung-Wan Kim
1Department of Psychiatry and Depression Clinical Research Center, Chonnam National University Medical School, Kwangju, Republic of Korea.
The brain-derived neurotrophic factor (BDNF) val66met polymorphism may increase depression risk after stroke. This genetic variant, particularly the met/met genotype, significantly linked stroke incidence to depression in older adults.
Area of Science:
- Neuroscience
- Genetics
- Psychiatry
Background:
- Stroke is a leading cause of disability and can precipitate depression.
- The brain-derived neurotrophic factor (BDNF) gene plays a crucial role in neuronal plasticity and mood regulation.
- Previous research suggests a link between BDNF and depression, but its role in post-stroke depression is less understood.
Purpose of the Study:
- To examine the influence of the brain-derived neurotrophic factor (BDNF) val66met gene polymorphism on the relationship between stroke and subsequent depression.
- To determine if specific BDNF genotypes modify the risk of developing depression after a stroke.
Main Methods:
- A longitudinal study of 500 community-dwelling older adults (>65 years) without prior stroke or depression.
- Assessment of disability (WHODAS II), cognitive function (MMSE), and BDNF genotype (val66met) at baseline.
- Follow-up evaluation after 2 years to identify incident stroke and depression.
Main Results:
- The association between stroke and depression risk increased with the number of 'met' alleles.
- This association was statistically significant only in individuals with the met/met BDNF genotype, even after accounting for disability and cognitive function.
- The val/val and val/met genotypes did not show a significant association between stroke and depression.
Conclusions:
- The BDNF val66met polymorphism appears to be a significant modifier in the development of depression following a stroke.
- Individuals with the met/met genotype may be at a higher risk for post-stroke depression.
- Further research is warranted to elucidate the precise mechanisms underlying this genetic influence.
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