Home LiteratureArticle Details
PMID: 15880108 Published · ppublish English Journal Article Research Support, N.I.H., Intramural

5-HTTLPR polymorphism impacts human cingulate-amygdala interactions: a genetic susceptibility mechanism for depression.

Nature neuroscience ·Vol. 8 ·No. 6 ·2005-06-00 ·Pages 828-34

Pezawas L, Meyer-Lindenberg A, Drabant EM, Verchinski BA, Munoz KE, Kolachana BS, Egan MF, Mattay VS, Hariri AR, Weinberger DR

Abstract

Carriers of the short allele of a functional 5' promoter polymorphism of the serotonin transporter gene have increased anxiety-related temperamental traits, increased amygdala reactivity and elevated risk of depression. Here, we used multimodal neuroimaging in a large sample of healthy human subjects to elucidate neural mechanisms underlying this complex genetic association. Morphometrical analyses showed reduced gray matter volume in short-allele carriers in limbic regions critical for processing of negative emotion, particularly perigenual cingulate and amygdala. Functional analysis of those regions during perceptual processing of fearful stimuli demonstrated tight coupling as a feedback circuit implicated in the extinction of negative affect. Short-allele carriers showed relative uncoupling of this circuit. Furthermore, the magnitude of coupling inversely predicted almost 30% of variation in temperamental anxiety. These genotype-related alterations in anatomy and function of an amygdala-cingulate feedback circuit critical for emotion regulation implicate a developmental, systems-level mechanism underlying normal emotional reactivity and genetic susceptibility for depression.

MeSH Terms
Amygdala/metabolism,pathology,physiopathology Anthropometry Anxiety Disorders/genetics,metabolism,pathology Atrophy/genetics,metabolism,pathology Brain Chemistry/genetics Brain Mapping Depressive Disorder/genetics,metabolism,pathology Fear/physiology,psychology Genetic Predisposition to Disease/genetics Gyrus Cinguli/metabolism,pathology,physiopathology Humans Magnetic Resonance Imaging Membrane Glycoproteins/genetics Membrane Transport Proteins/genetics Mutation/genetics Nerve Tissue Proteins/genetics Neural Pathways/metabolism,pathology,physiopathology Neuropsychological Tests Polymorphism, Genetic/genetics Serotonin/metabolism Serotonin Plasma Membrane Transport Proteins Surveys and Questionnaires
Chemicals
Membrane Glycoproteins Membrane Transport Proteins Nerve Tissue Proteins SLC6A4 protein, human Serotonin Plasma Membrane Transport Proteins Serotonin
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Pezawas Lukas
Genes, Cognition and Psychosis Program, National Institute of Mental Health, National Institutes of Health, 10 Center Drive 4S235, Bethesda, Maryland 20892-1379, USA.
Meyer-Lindenberg Andreas
Drabant Emily M
Verchinski Beth A
Munoz Karen E
Kolachana Bhaskar S
Egan Michael F
Mattay Venkata S
Hariri Ahmad R
Weinberger Daniel R
Article Info
Journal
Nature neuroscience
Abbr.
Nat Neurosci
ISSN
1097-6256
Published
2005-06-00
Epub
2005-00-08
Pages
828-34
Language
English
Region
United States
NLM ID
9809671
Subset
IM
Grants
Intramural NIH HHS · United States
Corrections
CommentIn
CommentIn
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com