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Interest, rationale, and potential clinical applications of genetic testing for mood disorders: A survey of stakeholders

机译:情绪障碍基因检测的兴趣,原理和潜在临床应用:利益相关者调查

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摘要

Bipolar disorder (BP) and major depressive disorder (MDD) are among the most severe, persistent, and debilitating illnesses occurring in young people, with an estimated lifetime prevalence of approximately 1-1.5% for BP (Kessler et al., 2005; Kato, 2007; Merikangas et al. 2007; Braff and Freedman, 2008) and 9.2-19.6% for MDD (Kessler et al., 2005). Although genetic testing for psychiatric disorders has been the goal of psychiatrists and geneticists for years (Braff and Freedman, 2008) this goal has been difficult to attain since the impact of individual genes on risk for psychiatric illness is small, often nonspecific and embedded in intricate causal pathways (Kendler, 2005). In contrast to Mende-lian disorders, tests for complex conditions such as MDD and BP may yield only weak estimates of risk, as such conditions appear to be caused by a complicated interplay of multiple genetic and environmental factors, and the associated genetic variants may be common and confer only a small increment of increased or decreased risk (Wright and Kroese, 2010).
机译:双相情感障碍(BP)和重度抑郁症(MDD)是年轻人中最严重,持续和使人衰弱的疾病,据估计,BP的终生患病率约为1-1.5%(Kessler et al。,2005; Kato ,2007; Merikangas等,2007; Braff and Freedman,2008)和MDD的9.2-19.6%(Kessler等,2005)。尽管多年来对精神病患者进行基因检测一直是精神病学家和遗传学家的目标(Braff和Freedman,2008),但由于个体基因对精神疾病风险的影响很小,常常是非特异性的并且错综复杂,因此很难实现这一目标因果路径(肯德勒,2005年)。与Mende-lian疾病相反,对复杂条件(例如MDD和BP)的测试可能只能得出较弱的风险估计,因为这种情况似乎是由多种遗传和环境因素的复杂相互作用所引起的,并且相关的遗传变异可能是常见的风险只是增加或降低的风险很小(Wright and Kroese,2010)。

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