2014
DOI: 10.1038/tp.2014.85
|View full text |Cite
|
Sign up to set email alerts
|

Association between serotonin transporter genotype, brain structure and adolescent-onset major depressive disorder: a longitudinal prospective study

Abstract: The extent to which brain structural abnormalities might serve as neurobiological endophenotypes that mediate the link between the variation in the promoter of the serotonin transporter gene (5-HTTLPR) and depression is currently unknown. We therefore investigated whether variation in hippocampus, amygdala, orbitofrontal cortex (OFC) and anterior cingulate cortex volumes at age 12 years mediated a putative association between 5-HTTLPR genotype and first onset of major depressive disorder (MDD) between age 13–1… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
16
0
1

Year Published

2015
2015
2022
2022

Publication Types

Select...
7
2
1

Relationship

0
10

Authors

Journals

citations
Cited by 25 publications
(17 citation statements)
references
References 100 publications
0
16
0
1
Order By: Relevance
“…Accordingly, the right hippocampus is important to the curtailment of stress responses (16,34), and fear extinction (35). Furthermore, smaller left hippocampal volume is a risk for the association between recent life stress and the development of anxiety symptoms (36) and onset of major depression (37). Likewise, a recent metaanalysis demonstrates that left hippocampal volume is associated with posttraumatic stress disorder (PTSD) (38).…”
Section: This Article Is a Pnas Direct Submissionmentioning
confidence: 99%
“…Accordingly, the right hippocampus is important to the curtailment of stress responses (16,34), and fear extinction (35). Furthermore, smaller left hippocampal volume is a risk for the association between recent life stress and the development of anxiety symptoms (36) and onset of major depression (37). Likewise, a recent metaanalysis demonstrates that left hippocampal volume is associated with posttraumatic stress disorder (PTSD) (38).…”
Section: This Article Is a Pnas Direct Submissionmentioning
confidence: 99%
“…Furthermore, MDD is associated with atypicalities in the neural circuits that are implicated in ToM decoding and that are heavily innervated by dopamine and serotonin [ 26 ]. For example, MDD patients, and those at risk by virtue of being s-allele carriers of the 5-HTTLPR, show lower amygdala and orbitofrontal cortical volumes than healthy individuals and those not at risk [ 27 , 28 ]. Further, the effect of the s-allele of the 5-HTTLPR on amygdala responses to valenced social stimuli is stronger in MDD patients than controls [ 29 ].…”
Section: Introductionmentioning
confidence: 99%
“…Full-length articles of screening studies, studies in non-adolescents or with a mixed sample with the age beyond the range of 10–19 years for adolescents or 20–25 years for young adults, studies with only the mean age, studies without clearly identified gene expression or polymorphism, or others was excluded from the analysis. Finally, 47 full-length articles (Eley et al, 2004 ; Mamalakis et al, 2004 ; Burcescu et al, 2005 ; Miraglia del Giudice et al, 2006 ; Sjöberg et al, 2006 ; Geng et al, 2007 ; Hilt et al, 2007 ; Pandey et al, 2007 , 2012 ; Feng et al, 2008 ; Aslund et al, 2009 ; Duncan et al, 2009 ; Goodyer et al, 2009 , 2010 ; Guo and Tillman, 2009 ; Laucht et al, 2009 ; Nilsson et al, 2009 ; Nobile et al, 2009 ; Benjet et al, 2010 ; Brent et al, 2010 ; Mata et al, 2010 ; Nederhof et al, 2010 ; Uddin et al, 2010 , 2011 ; Bouma et al, 2011 ; Hankin et al, 2011 ; Jenness et al, 2011 ; Mata and Gotlib, 2011 ; Thompson et al, 2011 ; Chen et al, 2012 , 2013 ; Petersen et al, 2012 ; Buchmann et al, 2013 ; Bobadilla et al, 2013 ; Comasco et al, 2013 ; Cutuli et al, 2013 ; Kohen et al, 2013 ; Otten and Engels, 2013 ; Oppenheimer et al, 2013 ; Priess-Groben and Hyde, 2013 ; Stavrakakis et al, 2013 ; Banducci et al, 2014 ; Cicchetti and Rogosch, 2014 ; Cruz-Fuentes et al, 2014 ; Little et al, 2014 ; Zhang et al, 2015 ) in adolescents and three studies (Hammen et al, 2010 ; Starr et al, 2013 ; Thompson et al, 2014 ) in young adults were included in this study (Figure 1 ). The 47 studies in adolescence included 20 genes or gene families while the three studies in young adults included three genes (Table 1 ).…”
Section: Resultsmentioning
confidence: 99%