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Heritability estimates for psychotic symptom dimensions in twins with psychotic disorders.

机译:患有精神病的双胞胎的精神病症状维度的遗传力估计。

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Factor analysis of psychotic symptoms frequently results in positive, negative, and disorganized dimensions, but heritability estimates have not yet been reported. Symptom dimensions are usually only measured in individuals with psychotic disorders. Here, it is valuable to assess influences acting via liability to psychosis and independent modifying effects. We estimated heritability for psychotic symptom dimensions, taking account of these issues. Two-hundred-and-twenty-four probandwise twin pairs (106 monozygotic, 118 same-sex dizygotic), where probands had psychoses, were ascertained from the Maudsley Twin Register in London (1948-1993). Lifetime history of DSM-III-R psychotic disorder and psychotic symptom dimensions was assessed from clinical records and research interviews and rated using the Operational Criteria Checklist. Estimates of heritability and environmental components of variance in liability were made with structural equation modeling using a causal-contingent common pathway model adapted for ascertainment from a clinical register. Significant heritability was found for DSM-III-R psychotic disorder (h(2) = 90%, 95%CI 68-94%) and the disorganized symptom dimension (h(2) = 84%, 95%CI 18-93%). The heritability for the disorganized dimension remained significant when influences acting through liability to psychosis were set to zero, suggesting that some influences on disorganization are modifying factors independent of psychosis liability. However, the relative extent of modifying factors versus influences acting through psychosis liability could not be clearly determined. To our knowledge, this study provides the first formal evidence of substantive heritability for the disorganized symptom dimension, and suggests that genetic loci influencing disorganization in individuals with psychoses are in some cases different from loci that influence risk of psychotic disorders themselves.
机译:精神病症状的因素分析通常会导致正面,负面和混乱的维度,但尚未报道遗传估计。通常仅在患有精神病的患者中测量症状的大小。在这里,评估通过对精神病的责任和独立的改变作用而起作用的影响是有价值的。考虑到这些问题,我们估计了精神病症状维度的遗传力。从伦敦的Maudsley Twin Register(1948-1993)确定了244个先证者双胞胎对(106个单卵双胞胎,118个同性双卵双胞胎),其中先证者患有精神病。从临床记录和研究访谈中评估了DSM-III-R精神病的终生病史和精神症状征兆,并使用《手术标准清单》进行了评估。使用适合于从临床登记册确定的因果偶然通用路径模型的结构方程模型,对赔偿责任中的可遗传性和环境成分进行估算。发现DSM-III-R精神病具有显着遗传力(h(2)= 90%,95%CI 68-94%)和症状紊乱(h(2)= 84%,95%CI 18-93%) )。当通过对精神病责任承担的影响设为零时,对无组织维度的遗传力仍然很重要,这表明对组织混乱的某些影响正在改变独立于精神病责任的因素。但是,尚不清楚因精神病责任引起的影响因素与影响因素的相对范围。据我们所知,该研究为症状紊乱维度的实质性遗传力提供了第一个正式证据,并表明影响精神病患者个体混乱的遗传基因座在某些情况下与影响精神病风险本身的基因座不同。

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