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A population-based heritability estimate of bipolar disorder - In a Swedish twin sample

机译:一种基于人口的遗传性估算双相障碍 - 在瑞典双胞胎样本中

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Twin- and family studies have shown variations in the heritability estimates of bipolar disorder (BPD). The current study uses an updated statistical methodology for heritability estimation in BPD by taking available time of follow-up into account while controlling for co-variates. We identified monozygotic and dizygotic same and different sex twins with BPD (n = 804) or unaffected from BPD (n = 91,604) from the Swedish Twin Register and the National Patient Register. We applied structural equational modeling with inversed probability weighting to estimate the heritability, taking into account censoring and truncation of data. Sex-limitation models were constructed to analyze qualitative or quantitative sex-differences in BPD. Heritability for BPD was 60.4% (95% Confidence Interval: 50.3-70.5) after age, sex, left-hand truncation and censoring of the data was taken into account. A larger proportion of females were affected from BPD (females 62.2%; males 37.8%, p < 0.001), but no sex-difference in BPD heritability was found, nor any sex-specific genetic effects. We demonstrated a robust 60% heritability for BPD with no evidence of sex-specific genetic effects on disease liability.
机译:双胞胎和家庭研究表明了双相障碍(BPD)的可遗传性估计的变化。目前的研究通过在控制共变体的同时考虑到可用的随访时间来使用更新的统计方法来进行BPD中的可遗传性估计。我们鉴定了单卵和Dizygotic,与BPD(n = 804)相同和不同的性双胞胎,或者从瑞典双寄存器和全国患者登记册的BPD(n = 91,604)不受影响。我们用反向概率加权应用结构实体建模以估计遗传性,考虑到数据的审查和截断。性限制模型被构建为分析BPD的定性或定量性别差异。迄今为止,BPD的遗传性为60.4%(95%置信区间:50.3-70.5),考虑到数据的年龄,性,左手截断和审查。较大比例的女性受到BPD的影响(女性62.2%;男性37.8%,P <0.001),但发现了BPD遗传性的性别差异,也没有任何性别特异性遗传效应。我们展示了BPD的强大60%遗传性,没有关于疾病责任的性别特异性遗传效应的证据。

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