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首页> 外文期刊>Bipolar disorders. >Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis shows genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31.
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Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis shows genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31.

机译:双相情感障碍中的情绪不一致精神病:条件连锁分析显示,全基因组暗示性连锁在1q32.3、7p13和20q13.31。

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OBJECTIVE: The majority of research into functional psychosis has proceeded under the assumption that schizophrenia and bipolar disorder are distinct entities with separate underlying disease processes and treatments. This view has been increasingly challenged in both clinical and genetic studies. Findings in recent association studies at two specific genes suggest that the occurrence of mood-incongruent psychotic features may indicate a relatively homogeneous subset of the bipolar phenotype. We examined this hypothesis. METHODS: Caucasian affected individuals were ascertained from Europe (the United Kingdom, the Republic of Ireland, Germany, Italy and Andalusia). Consensus best-estimate diagnoses were assigned by two independent raters according to all available information. There was no cross-site evaluation of inter-rater reliability. Families multiply affected by bipolar spectrum mood disorder were selected, comprising 383 affected relative pairs. Individuals were considered to be affected if they were diagnosed with DSM-IV bipolar I disorder or schizoaffective disorder, bipolar type. Multipoint, affected relative pair covariate linkage analysis was performed. RESULTS: Significant familiality of incongruent psychosis was observed [intra-class correlation coefficient (ICC) = 0.309; p = 0.001, one-tail]. Covariate linkage analysis provided three regions with genome-wide suggestive evidence for linkage on chromosomes 1q32.3 (LOD = 4.15, expected 0.12 times per genome scan), 7p13 (LOD = 3.32) and 20q13.31 (LOD = 2.98). No region in our analysis met criteria for genome-wide significance. CONCLUSION: Our results provide molecular support for the hypothesis that genes may exist for specific forms of bipolar illness, dependent on the presence or absence of incongruent psychosis. Our findings suggest that researchers should take account of mood-congruence/incongruence of psychotic features in studies of bipolar disorder.
机译:目的:大多数功能性精神病学的研究假设是精神分裂症和躁郁症是不同的实体,具有独立的基础疾病过程和治疗方法。这种观点在临床和遗传研究中都受到越来越多的挑战。最近在两个特定基因的关联研究中的发现表明,与情绪无关的精神病特征的出现可能表明双极性表型的相对同质子集。我们检查了这个假设。方法:从欧洲(英国,爱尔兰共和国,德国,意大利和安大路西亚)确定白种人受影响的个体。共识最佳估计诊断由两个独立的评估者根据所有可用信息进行分配。没有评估者之间可靠性的跨站点评估。选择了受双相性谱系情绪障碍影响的多重家庭,包括383个受影响的相对对。如果被诊断患有DSM-IV双相I型障碍或精神分裂性情感障碍(双相型),则认为个体受到影响。进行了多点受影响的相对对协变量连锁分析。结果:观察到显着的家族性精神病[类内相关系数(ICC)= 0.309; p = 0.001,单尾]。协变量连锁分析为三个区域提供了在染色体1q32.3(LOD = 4.15,预期每个基因组扫描为0.12次),7p13(LOD = 3.32)和20q13.31(LOD = 2.98)上连锁的全基因组证据。我们的分析中没有区域符合全基因组意义的标准。结论:我们的研究结果为分子假说可能存在某种特定形式的双相情感障碍这一假说提供了分子支持,取决于是否存在不一致的精神病。我们的发现表明,在躁郁症的研究中,研究人员应考虑到精神病特征的情绪一致性/不一致。

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