重度抑郁症的基因变异。

Jonathan Flint, Sagiv Shifman, Marcus Munafo, Richard Mott
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引用次数: 7

摘要

重度抑郁症是世界上最常见、最使人衰弱的疾病之一。大量数据表明,累加性遗传效应至少占重性抑郁症易感性变异的30%,然而,使用标准的基于家族的连锁和遗传关联方法来确定易感性的分子基础的尝试收效甚微。其他方法最近被提倡,如环境相互作用的基因包含和使用内表型。我们自己的数据表明,情感疾病的遗传结构比预期的更复杂。神经质是一种与抑郁症有许多相同易感位点的人格特征,一项对神经质的全基因组关联研究显示,个体效应小于1%。将需要比迄今所采用的更大的样本量和更复杂的分析方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic variants in major depression.

Major depression is one of the most common and most debilitating disorders in the world. A wealth of data indicate that additive genetic effects contribute to at least 30% of the variance in liability to major depression, yet attempts to identify the molecular basis of susceptibility using standard family based linkage and genetic association methodologies have had limited success. Alternative approaches have recently been advocated, such as the inclusion of gene by environment interactions and the use of endophenotypes. Our own data indicate that the genetic architecture of affective illness is more complex than expected. A whole genome association study of neuroticism, a personality trait that shares many of the same susceptibility loci as depression, reveals that the individual effect sizes are less than 1%. Larger sample sizes and more sophisticated analytical approaches will be needed than have hitherto been applied.

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