Effect of Oxcarbazepine on Serum Brain Derived Neurotrophic Factor (BDNF) in Bipolar Disorder
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- Change in Serum Brain Derived Neurotrophic Factor (BDNF)
研究概览
简要总结
The present study has been designed to evaluate the change in serum BDNF level with oxcarbazepine monotherapy in bipolar disorder and to explore the possibility of its neuroprotective effect.
详细描述
Bipolar disorder (BD) is a chronic psychiatric illness of partially unknown pathophysiology. BD likely involves, at a molecular and cellular level, dysfunctions of critical neurotrophic, cellular plasticity and resilience pathways and neuroprotective processes. Abnormalities of neurotrophins (NTs) and other trophic factors orchestrate important alterations which could be implicated in the etiology of BD. As consistently reported in post-mortem studies, these modifications are generally associated with the disruption of distinct subregions and functions of the brain, one of which is the deregulation of neurotrophins.
NTs are capable of signaling neurons, glial cells and other cellular systems to enable survival, differentiation and growth. BDNF is one of the most studied and abundant NTs in the brain, which plays an important role in a variety of neural processes during the development of both animals and humans. Initially, BDNF is important for neurogenesis, neuronal survival, and normal maturation of neural development pathways. In the adult, BDNF is not only important for synaptic plasticity and dendritic growth, but also for long-term memory consolidation. Several studies have proved that BDNF is significantly reduced in manic, hypomanic or depressive stages of BD, whereas euthymic patients exhibit BDNF levels similar to healthy controls.
Rafael T. de Sousa et al have observed a significant increase in serum BDNF levels after 28 days of lithium monotherapy in patients with BD and suggested neuroprotective role of lithium due to its direct regulatory effect on BDNF. Oxcarbazepine is a commonly used mood stabilizer which has demonstrated comparable efficacy to divalproate sodium and better tolerability profile but till date there is no study on its effect on BDNF. The aim of the present study is to evaluate the change in serum BDNF level with oxcarbazepine monotherapy in bipolar disorder and to explore the possibility of its neuroprotective effect.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 45 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •All patients with the diagnosis of bipolar affective disorder (by ICD-10 DCR) current episode mania without psychotic symptoms
- •Patients aged 18-45 years, of either sex.
- •Patients with baseline score > 20 on the Young Mania Rating Scale (YMRS).
- •Patients who had not taken any treatment for at least 4 weeks before inclusion.
排除标准
- •Patients with bipolar disorder (by ICD-10 DCR) presenting during depressive/euthymic/mixed episode.
- •Patients who are already under treatment for the presenting conditions.
- •Rapid cycling in the past 12 months.
- •Previous history of refractoriness to carbazepine or oxcarbazepine.
- •Patients with comorbid substance abuse or history of organicity
- •Pregnant and nursing women, patients with history of major medical or neurological illness.
研究组 & 干预措施
Oxcarbazepine
Twenty five (25) patients of bipolar mania will be prescribed oxcarbazepine for 4 weeks.
干预措施: Oxcarbazepine (Drug)
结局指标
主要结局
Change in Serum Brain Derived Neurotrophic Factor (BDNF)
时间窗: Baseline and 4 weeks
Serum BDNF was estimated by ELISA using human BDNF ELISA kit from Boster Biological Technology Co. Ltd., Pleasanton, CA.
次要结局
- Correlation Between Young Mania Rating Scale (YMRS) and Serum Brain Derived Neurotrophic Factor (BDNF)(At baseline)
研究者
RITUPARNA MAITI
Associate Professor
All India Institute of Medical Sciences, Bhubaneswar