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Correspondence| Volume 61, ISSUE 9, P1113-1115, May 01, 2007

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  • Joan Kaufman
    Affiliations
    Yale University School of Medicine, University Towers-Suite 2H, Child and Adolescent Research, New Haven, CT 06511

    Yale University School of Medicine, Department of Psychiatry
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  • Johari Massey
    Affiliations
    Yale University School of Medicine, University Towers-Suite 2H, Child and Adolescent Research, New Haven, CT 06511

    Yale University School of Medicine, Department of Psychiatry
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  • John Krystal
    Affiliations
    Yale University School of Medicine, University Towers-Suite 2H, Child and Adolescent Research, New Haven, CT 06511

    Yale University School of Medicine, Department of Psychiatry
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  • Joel Gelernter
    Affiliations
    Yale University School of Medicine, University Towers-Suite 2H, Child and Adolescent Research, New Haven, CT 06511

    Yale University School of Medicine, Department of Psychiatry
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Published:September 05, 2006DOI:https://doi.org/10.1016/j.biopsych.2006.07.004
      We appreciate Dr. Kalueff et al’s thoughtful commentary of our paper. They are absolutely correct to note that there are contradictory data on the role of brain-derived neurotrophic factor (BDNF) in depression. As we discussed in our report, prior investigations examining the BDNF val66met polymorphism have reported opposite findings in association with depression and other traits, with the “val” allele associated with vulnerability in some studies (
      • Lang U.E.
      • Hellweg R.
      • Kalus P.
      • et al.
      Association of a functional BDNF polymorphism and anxiety-related personality traits.
      ), and the “met” allele designated as the “risk” allele in others (
      • Jiang X.
      • Xu K.
      • Hoberman J.
      • et al.
      BDNF variation and mood disorders: a novel functional promoter polymorphism and Val66Met are associated with anxiety but have opposing effects.
      ). Inconsistencies in prior investigations might be attributable to sampling and measurement issues or genetic heterogeneity, which can result from many sources, including differences in the ethnic composition of samples across studies. It might also relate to failure to take into account relevant gene × gene and gene × environment interactions.
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      Linked Article

      • Brain-Derived Neurotrophic Factor, Serotonin Transporter, and Depression: Comment on Kaufman et al
        Biological PsychiatryVol. 61Issue 9
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          Brain-derived neurotrophic factor (BDNF) and serotonin transporter (SERT) have recently been implicated in depression (Caspi et al. 2003; Kaufman et al. 2004) and depression-like behavior in animals (Berton et al. 2006). A recent study has examined BDNF/SERT genes interactions in depressed children, reporting that a combination of met-BDNF allele with two short SERT alleles was associated with higher depression in maltreated children (Kaufman et al. 2006). The effect was magnified in children with reduced social support, suggesting its protective role in depression (Kaufman et al.
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