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. 2015 Dec 21;9:329. doi: 10.3389/fnbeh.2015.00329

Table 3.

Outcomes of studies on the relationship between BDNF and dopaminergic pathway and depression in adolescents.

Reference Sample size Main outcomes or conclusion
Stavrakakis et al. (2013) 1196 Adolescents’ depressive symptoms are not modified by BDNF
Comasco et al. (2013) 1393 Depressive symptoms and depression were more common among carriers of either the Val/Val or Met genotypes
Goodyer et al. (2010) 401 BDNF (Val66Met) modify the risk of a new depressive episode associated with elevated morning salivary cortisol
Chen et al. (2012) 780 Interaction between BDNF Val66Met polymorphism and environmental stress on depression was observed
Nederhof et al. (2010) 1096 Depression score was not significantly predicted by interaction between BDNF Val66Met polymorphism and childhood adversities
Mata et al. (2010) 82 BDNF met allele moderate the relation between exercise and depressive symptoms
Duncan et al. (2009) 217 Val/Val genotype correlated with higher levels of depression symptoms
Hilt et al. (2007) 100 Val/Val genotype was associated with more depressive symptoms
Cicchetti and Rogosch (2014) 1096 G × G × E interaction of BDNF, 5-HTTLPR/CRHR1 and maltreatment on depression symptoms
Cruz-Fuentes et al. (2014) 246 Possession of BDNF Met allele was statistically linked with a resilient phenotype of major depression disorder
Buchmann et al. (2013) 259 The carriers of the BDNF Met and 5-HTTLPR s allele are susceptible to depressive symptoms
Chen et al. (2013) 780 BDNF Val allele modulates the influence of environmental stress on depression
Stavrakakis et al. (2013) 1196 Adolescents’ depressive symptoms are not modified by COMT
Guo and Tillman (2009) 2286 DRD2*304/178 and DRD4*379/379 genotype are associated with a level of depressive symptoms
Bobadilla et al. (2013) 1882 DRD4 polymorphism is linked to comorbid marijuana use and depression