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首页> 外文期刊>Twin research and human genetics : >Strong genetic correlation between interview-assessed internalizing disorders and a brief self-report symptom scale.
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Strong genetic correlation between interview-assessed internalizing disorders and a brief self-report symptom scale.

机译:访谈评估的内在障碍与简短的自我报告症状量表之间具有很强的遗传相关性。

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摘要

Self-report scales for symptoms of anxiety and depression are frequently used for screening and research purposes. A moderate phenotypic association between disorders measured by diagnostic interviews and symptoms of anxiety and depression measured by self-report scales has been shown, but little is known about the overlap in these phenotypes' genetic and environmental variance. In the present study, we used twin modeling to identify common genetic and environmental liabilities underlying the phenotypic association between the self-report Symptom Checklist-5 (SCL-5) and lifetime internalizing disorders derived from the Composite International Diagnostic Interview (CIDI). The sample consisted of 7,992 young adult twins from the Norwegian Institute of Public Health Twin Panel (NIPHT), who all responded to a questionnaire. A subset of 2,793 individuals later underwent structured interviews. The best fitting model showed a strong genetic correlation of 0.82 (95% confidence interval; 0.61-1.0) between current self-report symptoms of anxiety and depression, and lifetime internalizing disorders, which suggests an almost complete overlap in genetic liability. The correlation between environmental factors was much lower: 0.16 (0.00-0.34, 95% CI). This implies that brief self-report scales capture genetic variance that is highly overlapping with the genetic variance common to internalizing disorder diagnoses. It thus follows that SCL-5 and similar instruments may be used as screening instruments for genetic risk factors that influence liability to internalizing disorders. In addition, existing data on self-report symptoms of anxiety and depression can be used with increased confidence to specify models including effects from genes coding for internalizing disorders.
机译:焦虑和抑郁症状的自我报告量表通常用于筛查和研究目的。已经显示出通过诊断性访谈测得的疾病与通过自我报告量表测得的焦虑和抑郁症状之间存在中等程度的表型关联,但对于这些表型的遗传和环境差异的重叠知之甚少。在本研究中,我们使用双胞胎模型来识别自我报告症状清单5(SCL-5)与源自综合国际诊断访谈(CIDI)的终身内在失调之间的表型关联的常见遗传和环境责任。样本由来自挪威公共卫生学院双生子小组(NIPHT)的7,992名成年双胞胎组成,他们都对问卷进行了回复。随后,对2,793名个人的一部分进行了结构化访谈。最佳拟合模型显示当前的焦虑和抑郁自我报告症状与终生内在化障碍之间有0.82(95%置信区间; 0.61-1.0)的强遗传相关性,这表明遗传责任几乎完全重叠。环境因素之间的相关性要低得多:0.16(0.00-0.34,95%CI)。这意味着简短的自我报告量表捕获的遗传变异与内部化疾病诊断常见的遗传变异高度重叠。因此,可以得出结论,SCL-5和类似的仪器可以用作筛选遗传风险因素的筛选工具,这些因素会影响内在化疾病的发生。此外,关于焦虑和抑郁自我报告症状的现有数据可以更有把握地用于确定模型,包括编码内在化疾病的基因的作用。

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