药物遗传学——抗抑郁药物治疗的有用工具?

K. Domschke
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摘要

重度抑郁症(MDD)是一种高度致残的疾病,其特点是终生患病率为5%-25%,女性的发病率约为男性的两倍。家庭和双胞胎研究表明,重度抑郁症的发病机制有很强的遗传作用,估计遗传率为40%-50%。抗抑郁药物治疗药物,如三环抗抑郁药(TCA),选择性5 -羟色胺再摄取抑制剂(SSRI),去甲肾上腺素和5 -羟色胺再摄取抑制剂(SNRI)或去甲肾上腺素和特异性5 -羟色胺能抗抑郁药(NaSSA)已被证明对很大一部分患者治疗重度抑郁症非常有效。然而,在MDD的药物治疗中,有两个主要问题需要解决,即治疗耐药性和治疗不耐受。30%-40%的患者对最初的药物治疗没有充分的反应。由于这些药物在治疗开始后可能需要几周的时间才能发挥抗抑郁作用,患者可能必须忍受这段时间症状没有缓解,然后才知道抗抑郁药无效。因此,对于提供者来说,能够识别对
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Pharmacogenetics—A Useful Tool in Antidepressant Pharmacotherapy?
Major Depressive Disorder (MDD) is a highly disabling disease characterized by a lifetime prevalence of 5%–25%, with women being affected approximately twice as often as men. Family and twin studies indicate a strong genetic contribution to the pathogenesis of MDD with an estimated heritability of 40%–50%. Antidepressive pharmacotherapeutic agents such as tricyclic antidepressants (TCA), selective serotonin reuptake inhibitors (SSRI), norepinephrine and serotonin reuptake inhibitors (SNRI) or noradrenergic and specific serotonergic antidepressants (NaSSA) have proven to be highly effective for a large proportion of patients in the treatment of major depression. However, two major issues need to be addressed in the pharmacotherapy of MDD, treatment resistance and treatment intolerance. Treatment Resistance A full 30%–40% of all patients fail to respond sufficiently to initial pharmacotherapy treatment. Since it can take several weeks after treatment initiation for these agents to exert antidepressant effects, patients might have to endure this period of time without symptom relief before the antidepressant is known to be ineffective. Thus, it would be highly beneficial for providers to be able to identify non–responders to a
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