跳至主要内容
临床试验/NCT00969930
NCT00969930Unknown不适用

Genetic Association Study Between Single Nucleotide Polymorphisms (SNPs) and Cognitive Performance in Young Bipolar Type I Patients: LICAVALGENE

University of Sao Paulo1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2009年8月最近更新:
适应症

试验速览

阶段
不适用
入组人数
80
试验地点
1
主要终点
Cognitive deficits in BD patients are associated with COMT, ApoE and BDNF polymorphisms

研究概览

简要总结

This is a genetic association study of cognitive impairment in young bipolar disease type I patients without medications in mania, depression, hypomania or mixed states.

详细描述

Introduction

Cognitive impairment in bipolar disease (BD) patients is common and recent data suggests that it may be an endophenotype of the disease as it differs individually, persists during periods of euthymia and co segregates in families of BD patients. Cognition is a complex trait and is therefore likely to be underpinned by many genes, each with a relatively small effect. Performance in each domain of the neuropsychological assessment can be statistically linked to the functional activity of particular protein and by extension to the genetic variants accounting for theses functional differences.

Methods:

80 patients with BD type I (SCID DSM-IV), age from 18 to 35 years old, currently on mania, depression, hypomania or mixed state after medication wash out will be submitted to complete neuropsychological evaluation and genotyped for COMT (val158met, rs165599, -287, rs737865), ApoE (epsilon 4) and BDNF (val66met)and 80 healthy controls.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • BD type 1
  • non euthymia
  • 18-35 y.o.

排除标准

  • pregnancy
  • organic disease
  • use of drugs
  • schizophrenia
  • mental retardation
  • illiterate

结局指标

主要结局

Cognitive deficits in BD patients are associated with COMT, ApoE and BDNF polymorphisms

时间窗: 18 months

次要结局

未报告次要终点

研究者

申办方类型
Other

研究点 (1)

Loading locations...

相似试验