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 et al 2005
), and the “met” allele designated as the “risk” allele in others (
Jiang et al 2005
). 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.To read this article in full you will need to make a payment
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Published online: September 05, 2006
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© 2007 Society of Biological Psychiatry. Published by Elsevier Inc. All rights reserved.
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- Brain-Derived Neurotrophic Factor, Serotonin Transporter, and Depression: Comment on Kaufman et alBiological PsychiatryVol. 61Issue 9
- PreviewBrain-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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