Bipolar Disorders Clinical Trial
The aim of this study is to explore relation between the comorbidity of different bipolar disorders with alcoholism and neuropsychiatric function and candidate genes. The investigators plan to establish genetic validity for this subtype of alcoholism. In addition, by comparing this subtyped alcoholism to normal control, the investigators plan to examine the genetic validity of such comorbidity. The investigators plan to find specific clinical characteristic from neuropsychiatric aspects of such subtype for future early diagnosis, prediction and prevention.
From family, twin and adoption studies supported a strong hereditary component in unsubtyped
alcohol dependency (Cloninger et al., 1981; Reich et al., 1999; Huang et al., 2004).
Dopamine, serotonin related genes and ADH, ALDH genes have been considered as candidate
genes for alcohol dependency (Goldman, 1995; Reich et al., 1999; Noble et al., 2000).
However, both in simple or family-base association studies have generated controversy about
the relationship between candidate genes and alcoholism (Edenberg et al., 1998; Reich et
al., 1999; Noble et al., 2000). One of the possible explanations may be due to that those
studies did not subtype alcohol dependency, even though alcoholism is a complex phenotype
with a heterogeneous etiology (Huang et al., 2004; Lu et al., 2005a).
Our previous research results had already categorized AD among Han Chinese in Taiwan into
four subtypes, pure alcoholism (Pure ALC), anxiety-depression alcoholism (ANX/DEP ALC),
antisocial alcoholism (Antisocial ALC) and mixed type alcoholism (Mixed ALC) (Huang et al.,
2004; Lu et al., 2005; Wang et al., 2007). Except for Mixed ALC, we have established
fundamental genetic validity, and confirmed several candidate genes including
MAOA、ADH、ALDH、DRD2.
Mixed ALC is categorized by alcoholism comorbid with other psychiatric disorders including
schizophrenia and bipolar disorder. Among them all, bipolar disorders most frequently
comorbid with alcohol and substance dependence. The high comorbidity between alcohol
dependence among patients with bipolar disorder worsens the treatment effect and prognosis.
Bipolar disorders are divided into several categories, including bipolar I disorder (BP-I),
bipolar II disorder (BP-II), and cyclothymic disorder. Previous literatures have documented
that BP-I and BP-II might have different etiology, phenomenology, characteristics and
neuropsychiatric functional impairments in the course of the illness (APA, 1994).
The aim of this study is to explore relation between the comorbidity of different bipolar
disorders with alcoholism and neuropsychiatric function and candidate genes. We plan to
establish genetic validity for this subtype of alcoholism. In addition, by comparing this
subtyped alcoholism to normal control, we plan to examine the genetic validity of such
comorbidity. We plan to find specific clinical characteristic from neuropsychiatric aspects
of such subtype for future early diagnosis, prediction and prevention.
;
Observational Model: Ecologic or Community, Time Perspective: Cross-Sectional
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