Cited by 772Neural and Behavioral Psychology StudiesMemory and Neural MechanismsAnxiety, Depression, Psychometrics, Treatment, Cognitive Processes

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Predictors of amygdala activation during the processing of emotional stimuli: A meta-analysis of 385 PET and fMRI studies

Costafreda, Sergi G., Brammer, Michael J., David, Anthony S., Fu, Cynthia H.Y.·2008·Brain Research Reviews

DOI 10.1016/j.brainresrev.2007.10.012

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Abstract

Although amygdala activity has been purported to be modulated by affective and non-affective factors, considerable controversy remains on its precise functional nature. We conducted a meta-analysis of 385 functional neuroimaging studies of emotional processing, examining the effects of experimental characteristics on the probability of detecting amygdala activity. All emotional stimuli were associated with higher probability of amygdala activity than neutral stimuli. Comparable effects were observed for most negative and positive emotions, however there was a higher probability of activation for fear and disgust relative to happiness. The level of attentional processing affected amygdala activity, as passive processing was associated with a higher probability of activation than active task instructions. Gustatory-olfactory and visual stimulus modalities increased the probability of activation relative to internal stimuli. Aversive learning increased the probability of amygdala activation as well. There was some evidence of hemispheric specialization with a relative left-lateralization for stimuli containing language and a relative right-lateralization for masked stimuli. Methodological variables, such as type of analysis and magnet strength, were also independent predictors of amygdala activation.

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R: A Language and Environment for Statistical Computing
R Core Team (2000) · doi:10.32614/r.manuals · Cited by 355,893
A new look at the statistical model identification
Akaike, H. (1974) · IEEE Transactions on Automatic Control · doi:10.1109/tac.1974.1100705 · Cited by 51,879
Co-Planar Stereotaxic Atlas of the Human Brain
Talairach, J., & Tournoux, P. (1988) · Medical Entomology and Zoology · Cited by 11,798
Mixed-Effects Models in Sand S-PLUS
Pinheiro, J. C., & Bates, D. M. (2000) · Statistics and Computing · doi:10.1007/978-1-4419-0318-1 · Cited by 11,187
Mixed-Effects Models in S and S-PLUS
(2001) · Technometrics · doi:10.1198/tech.2001.s574 · Cited by 9,278
Emotion circuits in the brain
LeDoux, J. E. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.155 · Cited by 8,444
Co-planar stereotaxic atlas of the human brain
Laitinen, L. (1989) · Clinical Neurology and Neurosurgery · doi:10.1016/0303-8467(89)90128-5 · Cited by 7,565
Emotion regulation: affective, cognitive, and social consequences.
Gross, J. J. (2002) · Psychophysiology · doi:10.1017/s0048577201393198 · Cited by 4,890 · cited 1×
“Studies used two strategies: reappraisal, in which themeaning of the emotional stimulus was manipulated to enhance the emotional experience; and suppression, in which subjects were asked to ‘distance themselves’ emotionally from the stimuli (Gross, 2002).”
Method
The Cognitive neurosciences
(2005) · Choice Reviews Online · doi:10.5860/choice.43-0626 · Cited by 4,726
Approximate Inference in Generalized Linear Mixed Models
Breslow, N. E., & Clayton, D. G. (1993) · Journal of the American Statistical Association · doi:10.1080/01621459.1993.10594284 · Cited by 4,662

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Show all 109 references

Research works printed but not linked: 1

Kapler, 2001, Correlated attenuation of amygdala and autonomic responses: A simultaneous fMRI and SCR study, Soc. Neurosci. Abstr., 645, 3

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Authors: Costafreda, S. G., Brammer, M. J., David, A. S., & Fu, C. H. Y.
Affiliations: King's College London (GB)
ORCID: Costafreda, Sergi G.
Brammer, Michael J.
David, Anthony S.
Fu, Cynthia H.Y.
Venue: Brain Research Reviews
Publisher: Elsevier BV
Published: 2008-06
Volume: 58
Issue: 1
Pages: 57-70
ISSN: 0165-0173 (ISSN-L)
DOI: 10.1016/j.brainresrev.2007.10.012
OpenAlex: W1974635983
Cited by: 772
References: 109
Citations by year: 2026: 10 · 2025: 26 · 2024: 25 · 2023: 29 · 2022: 33 · 2021: 37 · 2020: 48 · 2019: 54 · 2018: 50 · 2017: 46 · 2016: 43 · 2015: 58 · 2014: 71 · 2013: 49 · 2012: 61
FWCI: 2.18
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
www.elsevier.com/legal/tdmrep-license (tdm)
Locations: Brain Research Reviews (publishedVersion)
PubMed (publishedVersion)
UCL Discovery (University College London) (submittedVersion)
Research Portal (King's College London) (submittedVersion)
Funders: Medical Research Council
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Social Sciences › Psychology › Experimental and Cognitive Psychology › Anxiety, Depression, Psychometrics, Treatment, Cognitive Processes
Keywords: amygdala activation, emotional processing, emotional stimuli, fear, disgust, happiness, attentional processes, stimulus modality, aversive learning, hemispheric lateralization, masked stimuli, PET, functional MRI
MeSH terms: Adolescent, Adult, Aged, Amygdala, Emotions, Humans, Magnetic Resonance Imaging, Middle Aged, Positron-Emission Tomography

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Predictors of amygdala activation during the processing of emotional stimuli: A meta-analysis of 385 PET and fMRI studies

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