Genetic epistasis between the brain-derived neurotrophic factor Val66Met polymorphism and the 5-HTT promoter polymorphism moderates the susceptibility to depressive disorders after childhood abuse.
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Genetic epistasis between the brain-derived neurotrophic factor Val66Met polymorphism and the 5-HTT promoter polymorphism moderates the susceptibility to depressive disorders after childhood abuse. / Grabe, Hans Jörgen; Schwahn, Christian; Mahler, Jessie; Appel, Katja; Schulz, Andrea; Spitzer, Carsten; Fenske, Kristin; Barnow, Sven; Freyberger, Harald Jürgen; Teumer, Alexander; Petersmann, Astrid; Biffar, Reiner; Rosskopf, Dieter; John, Ulrich; Völzke, Henry.
in: PROG NEURO-PSYCHOPH, Jahrgang 36, Nr. 2, 2, 2012, S. 264-270.Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung
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TY - JOUR
T1 - Genetic epistasis between the brain-derived neurotrophic factor Val66Met polymorphism and the 5-HTT promoter polymorphism moderates the susceptibility to depressive disorders after childhood abuse.
AU - Grabe, Hans Jörgen
AU - Schwahn, Christian
AU - Mahler, Jessie
AU - Appel, Katja
AU - Schulz, Andrea
AU - Spitzer, Carsten
AU - Fenske, Kristin
AU - Barnow, Sven
AU - Freyberger, Harald Jürgen
AU - Teumer, Alexander
AU - Petersmann, Astrid
AU - Biffar, Reiner
AU - Rosskopf, Dieter
AU - John, Ulrich
AU - Völzke, Henry
PY - 2012
Y1 - 2012
N2 - Based on biological interactions between the serotonergic system and the brain-derived neurotrophic factor (BDNF), BDNF is a plausible candidate for a gene-gene-environment interaction moderating the interaction between the s/l- promoter polymorphism of the serotonin transporter (5-HTTLPR) and childhood abuse. We tested the hypothesis of a three-way interaction with respect to depressive symptoms.
AB - Based on biological interactions between the serotonergic system and the brain-derived neurotrophic factor (BDNF), BDNF is a plausible candidate for a gene-gene-environment interaction moderating the interaction between the s/l- promoter polymorphism of the serotonin transporter (5-HTTLPR) and childhood abuse. We tested the hypothesis of a three-way interaction with respect to depressive symptoms.
KW - Adult
KW - Humans
KW - Male
KW - Aged
KW - Female
KW - Middle Aged
KW - Aged, 80 and over
KW - Child
KW - Genotype
KW - Alleles
KW - Sex Characteristics
KW - Promoter Regions, Genetic/genetics
KW - European Continental Ancestry Group/genetics
KW - Psychiatric Status Rating Scales/statistics & numerical data
KW - Child Abuse/psychology
KW - Serotonin Plasma Membrane Transport Proteins/genetics
KW - Genetic Predisposition to Disease/genetics
KW - Brain-Derived Neurotrophic Factor/genetics
KW - Depressive Disorder/complications/genetics/psychology
KW - Epistasis, Genetic/genetics
KW - Gene-Environment Interaction
KW - Polymorphism, Genetic/genetics
KW - Adult
KW - Humans
KW - Male
KW - Aged
KW - Female
KW - Middle Aged
KW - Aged, 80 and over
KW - Child
KW - Genotype
KW - Alleles
KW - Sex Characteristics
KW - Promoter Regions, Genetic/genetics
KW - European Continental Ancestry Group/genetics
KW - Psychiatric Status Rating Scales/statistics & numerical data
KW - Child Abuse/psychology
KW - Serotonin Plasma Membrane Transport Proteins/genetics
KW - Genetic Predisposition to Disease/genetics
KW - Brain-Derived Neurotrophic Factor/genetics
KW - Depressive Disorder/complications/genetics/psychology
KW - Epistasis, Genetic/genetics
KW - Gene-Environment Interaction
KW - Polymorphism, Genetic/genetics
M3 - SCORING: Journal article
VL - 36
SP - 264
EP - 270
JO - PROG NEURO-PSYCHOPH
JF - PROG NEURO-PSYCHOPH
SN - 0278-5846
IS - 2
M1 - 2
ER -