Título The risk for major depression conferred by childhood maltreatment is multiplied by BDNF and SERT genetic vulnerability: a replication study
Autores Gutierrez, Blanca , Angel Bellon, Juan , Rivera, Margarita , Molina, Esther , King, Michael , Marston, Louise , Torres-Gonzalez, Francisco , Moreno-Kuestner, Berta , Moreno-Peral, Patricia , MOTRICO MARTINEZ, EMMA, Monton-Franco, Carmen , Josefa GildeGomez-Barragan, Maria , Sanchez-Celaya, Marta , Angel Diaz-Barreiros, Miguel , Vicens, Catalina , de Dios Luna, Juan , Nazareth, Irwin , Cervilla, Jorge
Publicación externa No
Medio J Psychiatry Neurosci
Alcance Article
Naturaleza Científica
Cuartil JCR 1
Cuartil SJR 1
Impacto JCR 5.57000
Impacto SJR 2.69800
Web https://www.scopus.com/inward/record.uri?eid=2-s2.0-84928737124&doi=10.1503%2fjpn.140097&partnerID=40&md5=6d3fb1c73b3454a4ef9dcf61c3464de9
Fecha de publicacion 01/05/2015
ISI 000353901000007
Scopus Id 2-s2.0-84928737124
DOI 10.1503/jpn.140097
Abstract Background There is limited evidence for a moderating role of both serotonin transporter (SERT) and brain-derived neurotrophic factor (BDNF) genes on the risk for major depression (MD) developing after childhood maltreatment. However, research on this topic remains inconclusive, and there is a lack of data from longitudinal studies with large and representative population samples. Our study aimed to clarify whether, in the presence of previous childhood maltreatment, individuals carrying low functional alleles for both SERT 5-HTTLPR and BDNF Val66Met polymorphisms had a higher risk for MD.\n Methods We explored 2- and 3-way gene (SERT and BDNF) x environment (childhood maltreatment) interactions in a large sample of Spanish adults who were followed up over a 3-year period and assessed in person for both DSM-IV MD and exposure to childhood maltreatment.\n Results Our study included 2679 participants. Those with both the 5-HTTLPR s allele and the BDNF Met allele showed the highest risk of MD if they had previously experienced emotional (z = 2.08, p = 0.037), sexual (z = 2.19, p = 0.029) or any kind of childhood abuse (z = 2.37, p = 0.018). These 3-way interactions remained significant regardless of whether the 5-HTTLPR triallelic or the 5-HTTLPR biallelic polymorphisms were included in the analyses.\n Limitations Retrospective assessment of childhood maltreatment may have resulted in a moderate degree of recall bias.\n Conclusion Our results confirm that the risk of depression conferred by childhood maltreatment is modified by variation at both SERT and BDNF genes.
Palabras clave brain derived neurotrophic factor; serotonin transporter; brain derived neurotrophic factor; brain-derived neurotrophic factor, human; serotonin transporter; SLC6A4 protein, human; adult; aged; Articl
Miembros de la Universidad Loyola

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