Epigenetic Regulation of Brain-Derived Neurotropic Factor (BDNF) in Patients With Major Depression
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Major Depressive Disorder
- Sponsor
- Chang Gung Memorial Hospital
- Enrollment
- 110
- Locations
- 1
- Primary Endpoint
- Brain-derived Neurotrophic Factor (BDNF) DNA Methylation of Major Depressive Disorder (MDD) Patients and Healthy Controls
- Status
- Completed
- Last Updated
- 11 years ago
Overview
Brief Summary
The investigators will (1) detect the associations between brain-derived neurotrophic factor (BDNF) DNA methylation, histone modification, depressive symptoms, suicidal behavior and antidepressant responses in major depressive disorder (MDD) patients, (2) check the correlation between blood BDNF protein and RNA and BDNF rs6265 gene, and (3) discuss the possible mechanisms of epigenetic regulation of BDNF in Taiwanese major depressive patients.
Detailed Description
Brain-derived neurotrophic factor (BDNF) had been chosen as a candidate gene for a development of major depressive disorder (MDD). BDNF had been reported to have an important role on neuronal plasticity, axonal growth and connectivity, and participating in the local response to various types of neuronal stressors. BDNF also influences the differentiation of neurons. In the past studies, the investigators had found that major depressive women had lower serum BDNF protein levels than healthy controls, and their BDNF levels became significantly increased after antidepressant treatments. In addition, some authors had found that reduced expression of BDNF was noted in postmortem brain of completed suicide subjects. Suicidal major depressive patients also had lower plasma BDNF levels than non-suicidal major depressive patients. These findings suggested that BDNF might play an important role in the suicidal behavior. However, in past studies, the results did not fully explain why major depressive patients with same genotypes had different clinical expression, including the severity of depression, with/without suicide, and the treatment response. Recently, some papers found that there were relationships between epigenetic regulation, including DNA methylation and histone modification, and psychopathology of major depression. Therefore, we try to investigate the relationships between epigenetic regulation of BDNF and major depression.
Investigators
Tiao-Lai Huang
Head of Department of Psychiatry
Chang Gung Memorial Hospital
Eligibility Criteria
Inclusion Criteria
- •The clinical screening and assessment in patients with major depression：
- •40 major depression will be recruited in psychiatric inpatients according to DSM-IV criteria by a semi-structured interview. The assessment will be done by two senior psychiatrists. The intra-rater and inter-rater reliability will be done before this project started.
- •The patients had the ability to complete the written inform consent.
- •The choice of antidepressant drugs depended on the need of patients in natural treatment procedure. They included selective serotonin reuptake inhibitors (SSRI), eg. fluoxetine or paroxetine.
- •The 17-item Hamilton Depression Rating Scale (HAM-D) was used to assess severity of depression. The minimum baseline score of the 17-item HAM-D was 18.
Exclusion Criteria
- •The patients had systemic diseases, including metabolic, heart, and liver diseases。
- •The patients had received any drugs before entering this protocol.
- •The patients were heavy smokers or dependent on alcohol.
- •The use of secondary generation anti-psychotic drugs and mood stabilizers.
Outcomes
Primary Outcomes
Brain-derived Neurotrophic Factor (BDNF) DNA Methylation of Major Depressive Disorder (MDD) Patients and Healthy Controls
Time Frame: 2 years
averaged percentage of methylation at each CpG site listed
Histone Modification of MDD Patients Before and After Treatment and With Healthy Controls
Time Frame: 2 years
Chromatin immunoprecipitation (ChIP) was used to measure histone modification. The unit of our given machine is relative quantification, and a higher value indicated increased histone modification. The detailed method could be found in: Huebert DJ, Kamal M, O'Donovan A, Bernstein BE: Genome-wide analysis of histone modifications by ChIP-on-chip. Methods 2006; 40: 365-369.
Secondary Outcomes
- BDNF Levels of MDD Patients Before and After Treatment and Healthy Controls(2 years)