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The Val66Met polymorphism of the brain-derived neurotrophic-factor gene is associated with geriatric depression

pmid: 16343697
The Val66Met polymorphism of the brain-derived neurotrophic-factor gene is associated with geriatric depression
Brain-derived neurotrophic-factor (BDNF), the most abundant of the neurotrophins in the brain, has been implicated in both major depression and cognitive function. This study examines the association between the BDNF-gene Val66Met polymorphism and depression susceptibility and severity, age-of-onset, cognitive function and suicidal attempt history in an elderly Chinese sample population. We genotyped the BDNF-gene Val66Met polymorphism in 110 elderly inpatients diagnosed with major depression and 171 age- and sex-similar control subjects. All patients were assessed with the Hamilton Rating Scale for Depression (HAM-D) for depression severity and the Mini-Mental Status Examination (MMSE) for cognitive function after admission. Suicide attempt history and age-of-onset of depression were evaluated by interview and medical record. The BDNF Val66Met genotype distribution was significantly different between depressed patients and control subjects (P=0.003) and there was a significant excess of Met allele in the depressed patients compared to the control group (P=0.001). The BDNF polymorphism did not affect age-of-onset, depression severity, cognitive function or suicidal attempt history. The results suggest that the BDNF Val66Met polymorphism is a relevant risk factor for geriatric depression.
- National Yang Ming University Taiwan
- Taipei Veterans General Hospital Taiwan
- National Chiao Tung University Taiwan
Aged, 80 and over, Genetic Markers, Male, Depressive Disorder, Polymorphism, Genetic, Brain-Derived Neurotrophic Factor, Mutation, Missense, Valine, Severity of Illness Index, Methionine, Amino Acid Substitution, Humans, Female, Genetic Predisposition to Disease, Aged
Aged, 80 and over, Genetic Markers, Male, Depressive Disorder, Polymorphism, Genetic, Brain-Derived Neurotrophic Factor, Mutation, Missense, Valine, Severity of Illness Index, Methionine, Amino Acid Substitution, Humans, Female, Genetic Predisposition to Disease, Aged
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