Evidence map›Paper›PMID 28580622›Full record

ArticleHuman brain mapping2017

Heightened amygdala responsiveness in s-carriers of 5-HTTLPR genetic polymorphism reflects enhanced cortical rather than subcortical inputs: An MEG study.

Qian Luo, Tom Holroyd, Derek Mitchell, Henry Yu, Xi Cheng, Colin Hodgkinson, Gang Chen, Daniel McCaffrey, David Goldman, R James Blair

Open access · bronzeAbstract read
In one paragraph

Article in Human brain mapping, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 53% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 2 countries.

Qian LuoUnit on Affective Cognitive Neuroscience, NIMH/NIMH, Bethesda, MD, USA.ORCID 0000-0003-4669-352X
Tom HolroydMEG Core Facility, NIMH/NIH, Bethesda, MD, USA.
Derek MitchellDepartments of Psychiatry and Anatomy & Cell Biology, Brain and Mind Institute, University of Western Ontario, London, Ontario, Canada.
Henry YuUnit on Affective Cognitive Neuroscience, NIMH/NIMH, Bethesda, MD, USA.
Xi ChengBioinformatics and Computational Biosciences Branch, NIAID/NIH, Rockville, MD, USA.
Colin HodgkinsonLaboratory of Neurogenetics, NIAAA/NIH, Bethesda, MD, USA.
Gang ChenScientific and Statistical Computing Core, NIMH/NIH, Bethesda, MD, USA.
Daniel McCaffreyUnit on Affective Cognitive Neuroscience, NIMH/NIMH, Bethesda, MD, USA.
David GoldmanLaboratory of Neurogenetics, NIAAA/NIH, Bethesda, MD, USA.
R James BlairUnit on Affective Cognitive Neuroscience, NIMH/NIMH, Bethesda, MD, USA.
National Institutes of Health · USNaval Research Laboratory Information Technology DivisionWestern University · CA

Funding

Integrative genetics of behavior with high throughput technologiesZIAAA000301 · NIAAA · NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM · PI GOLDMAN, DAVID · 2009 to 2025
$68.6M
NIMH MEG Core FacilityZICMH002889 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI NUGENT, ALLISON · 2009 to 2025
$31.4M
Acute threat and frustrative non-reward components of irritability and reactive aggressionK22MH109558 · NIMH · FATHER FLANAGAN'S BOYS' HOME · PI BLAIR, JAMES · 2016 to 2018
$972k
NIMH NIH HHS K22 MH109558
6 · The paper itself

Abstract

Short allele carriers (S-carriers) of the serotonin transporter gene (5-HTTLPR) show an elevated amygdala response to emotional stimuli relative to long allele carriers (LL-homozygous). However, whether this reflects increased responsiveness of the amygdala generally or interactions between the amygdala and the specific input systems remains unknown. It is argued that the amygdala receives input via a quick subcortical and a slower cortical pathway. If the elevated amygdala response in S-carriers reflects generally increased amygdala responding, then group differences in amygdala should be seen across the amygdala response time course. However, if the difference is a secondary consequence of enhanced amygdala-cortical interactions, then group differences might only be present later in the amygdala response. Using magnetoencephalography (MEG), we found an enhanced amygdala response to fearful expressions starting 40-50 ms poststimulus. However, group differences in the amygdala were only seen 190-200 ms poststimulus, preceded by increased superior temporal sulcus (STS) responses in S-carriers from 130 to 140 ms poststimulus. An enhanced amygdala response to angry expressions started 260-270 ms poststimulus with group differences in the amygdala starting at 160-170 ms poststimulus onset, preceded by increased STS responses in S-carriers from 150 to 160 ms poststimulus. These suggest that enhanced amygdala responses in S-carriers might reflect enhanced STS-amygdala connectivity in S-carriers. Hum Brain Mapp 38:4313-4321, 2017. © 2017 Wiley Periodicals, Inc.

Indexed as

MagnetoencephalographyPolymorphism, GeneticAdultAmygdalaCerebral CortexEmotionsFacial RecognitionFemaleHeterozygoteHumansMaleNeural PathwaysNeuropsychological TestsReaction TimeSerotonin Plasma Membrane Transport ProteinsSerotonin Plasma Membrane Transport ProteinsSLC6A4 protein, human5-HTTLPRamygdalaemotionmagnetoencephalographyserotonin transporter

Identifiers

PMID28580622
PMCPMC5578743
OpenAlexW2620561337

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.