Evidence map›Paper›PMID 27039701›Full record

ArticleNeuroImage2016

Sex differences in the functional connectivity of the amygdalae in association with cortisol.

Lydia Kogler, Veronika I Müller, Eva-Maria Seidel, Roland Boubela, Klaudius Kalcher, Ewald Moser, Ute Habel, Ruben C Gur, Simon B Eickhoff, Birgit Derntl

Open access · hybridAbstract read
In one paragraph

Article in NeuroImage, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 9% 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

49 citing papers in PubMed, 1 synthesis or guideline pooled it, 77 citations in OpenAlex.

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  13. Sex Differences in the Neurobiology of Fear and Anxiety.Current topics in behavioral neurosciences · 2025
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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 7 institutions in 3 countries.

Lydia KoglerDepartment of Psychiatry and Psychotherapy, Medical School, University of Tübingen, Germany; Jülich-Aachen-Research Alliance, Translational Brain Medicine, Germany; Department of Psychiatry, Psychotherapy and Psychosomatics, RWTH Aachen University, Aachen, Germany. Electronic address: lydia.kogler@med.uni-tuebingen.de.
Veronika I MüllerInstitute of Neuroscience und Medicine, INM-1, Research Centre Jülich, Jülich, Germany; Institute of Clinical Neuroscience and Medical Psychology, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Eva-Maria SeidelDepartment of Basic Psychological Research and Research Methods, Faculty of Psychology, University of Vienna, Vienna, Austria.
Roland BoubelaMR Centre of Excellence, Medical University of Vienna, Vienna, Austria; Centre for Medical Physics and Biomedical Engineering, Medical University, Vienna, Austria.
Klaudius KalcherMR Centre of Excellence, Medical University of Vienna, Vienna, Austria; Centre for Medical Physics and Biomedical Engineering, Medical University, Vienna, Austria.
Ewald MoserMR Centre of Excellence, Medical University of Vienna, Vienna, Austria; Centre for Medical Physics and Biomedical Engineering, Medical University, Vienna, Austria; Neuropsychiatry Division, Department of Psychiatry, Medical School, University of Pennsylvania, Philadelphia, USA.
Ute HabelJülich-Aachen-Research Alliance, Translational Brain Medicine, Germany; Department of Psychiatry, Psychotherapy and Psychosomatics, RWTH Aachen University, Aachen, Germany; Institute of Neuroscience und Medicine, INM-6, Research Centre Jülich, Research Centre Jülich, Jülich, Germany; JARA BRAIN Institute 1: Structure Function Relationship.
Ruben C GurNeuropsychiatry Division, Department of Psychiatry, Medical School, University of Pennsylvania, Philadelphia, USA.
Simon B EickhoffInstitute of Neuroscience und Medicine, INM-1, Research Centre Jülich, Jülich, Germany; Institute of Clinical Neuroscience and Medical Psychology, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Birgit DerntlDepartment of Psychiatry and Psychotherapy, Medical School, University of Tübingen, Germany; Institute of Neuroscience und Medicine, INM-1, Research Centre Jülich, Jülich, Germany; Jülich-Aachen-Research Alliance, Translational Brain Medicine, Germany; Department of Psychiatry, Psychotherapy and Psychosomatics, RWTH Aachen University, Aachen, Germany.
Medical University of Vienna · ATForschungszentrum Jülich · DEJülich Aachen Research Alliance · DERWTH Aachen University · DEUniversity of Pennsylvania · USUniversity of Tübingen · DEUniversity of Vienna · AT

Funding

Meta-anaylsis in human brain mappingR01MH074457 · NIMH · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI FOX, PETER THORNTON · 2006 to 2024
$10.5M
Austrian Science Fund FWF P 23533NIMH NIH HHS R01 MH074457
6 · The paper itself

Abstract

Human amygdalae are involved in various behavioral functions such as affective and stress processing. For these behavioral functions, as well as for psychophysiological arousal including cortisol release, sex differences are reported. Here, we assessed cortisol levels and resting-state functional connectivity (rsFC) of left and right amygdalae in 81 healthy participants (42 women) to investigate potential modulation of amygdala rsFC by sex and cortisol concentration. Our analyses revealed that rsFC of the left amygdala significantly differed between women and men: Women showed stronger rsFC than men between the left amygdala and left middle temporal gyrus, inferior frontal gyrus, postcentral gyrus and hippocampus, regions involved in face processing, inner-speech, fear and pain processing. No stronger connections were detected for men and no sex difference emerged for right amygdala rsFC. Also, an interaction of sex and cortisol appeared: In women, cortisol was negatively associated with rsFC of the amygdalae with striatal regions, mid-orbital frontal gyrus, anterior cingulate gyrus, middle and superior frontal gyri, supplementary motor area and the parietal-occipital sulcus. Contrarily in men, positive associations of cortisol with rsFC of the left amygdala and these structures were observed. Functional decoding analyses revealed an association of the amygdalae and these regions with emotion, reward and memory processing, as well as action execution. Our results suggest that functional connectivity of the amygdalae as well as the regulatory effect of cortisol on brain networks differs between women and men. These sex-differences and the mediating and sex-dependent effect of cortisol on brain communication systems should be taken into account in affective and stress-related neuroimaging research. Thus, more studies including both sexes are required.

Indexed as

Sex FactorsAdultAmygdalaBrain MappingFemaleGonadal Steroid HormonesHumansHydrocortisoneMagnetic Resonance ImagingMaleNerve NetNeural PathwaysSalivaTissue DistributionGonadal Steroid HormonesHydrocortisoneCortisolFrontal cortexHippocampusResting-stateStriatumTask-independent

Identifiers

PMID27039701
PMCPMC6594554
OpenAlexW2327107093

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.