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METHOD FOR TREATING DEPRESSION AND MAJOR DEPRESSIVE DISORDER.

机译:治疗抑郁症和主要抑郁症的方法。

摘要

The present invention provides methods for treating depression such as major depressive disorder (MDD) in an individual. The invention further provides methods for determining if an individual suffering from depression is likely to respond favorably or experience an enhanced treatment effect in response to treatment with vortioxetine. The present invention also provides methods for treating cognitive impairment in an individual, optionally wherein the individual also suffers from depression and/or MDD. The invention further provides methods for determining if an individual suffering from cognitive impairment is likely to respond favorably or experience an enhanced treatment effect in response to treatment with vortioxetine. The methods comprise determining the presence of polymorphisms in the collagen, type XXVI, alpha 1 (COL26A1) gene and/or the calcium channel, voltage-dependent, L type, alpha 1C subunit (CACNA1C) gene and/or the CUB and Sushi Multiple Domains 1 (CSMD1) gene and/or the Zinc Finger Protein 494 (ZSCAN4) gene and/or the Zinc Finger Protein 551 (ZNF551) gene and/or the dymeclin (DYM) gene and/or the LINC00348 gene and/or the FOXL2NB gene and/or intergenic regions in the individual.
机译:本发明提供了用于治疗个体中的抑郁症例如重度抑郁症(MDD)的方法。本发明进一步提供用于确定患有抑郁症的个体响应于伏替西汀治疗是否可能有利地响应或经历增强的治疗效果的方法。本发明还提供了用于治疗个体的认知障碍的方法,任选地,其中该个体还患有抑郁症和/或MDD。本发明进一步提供了用于确定患有认知障碍的个体是否可能响应于伏替西汀的治疗而响应良好或经历增强的治疗效果的方法。该方法包括确定胶原蛋白,XXVI型,α1(COL26A1)基因和/或钙通道,电压依赖性,L型,α1C亚基(CACNA1C)基因和/或CUB和Sushi Multiple中是否存在多态性域1(CSMD1)基因和/或锌指蛋白494(ZSCAN4)基因和/或锌指蛋白551(ZNF551)基因和/或dymeclin(DYM)基因和/或LINC00348基因和/或FOXL2NB基因和/或个体中的基因间区域。

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