Literature DB >> 29520882

Sex-related differences in behavioral and amygdalar responses to compound facial threat cues.

Hee Yeon Im1,2, Reginald B Adams3, Cody A Cushing1, Jasmine Boshyan1,2, Noreen Ward1, Kestutis Kveraga1,2.   

Abstract

During face perception, we integrate facial expression and eye gaze to take advantage of their shared signals. For example, fear with averted gaze provides a congruent avoidance cue, signaling both threat presence and its location, whereas fear with direct gaze sends an incongruent cue, leaving threat location ambiguous. It has been proposed that the processing of different combinations of threat cues is mediated by dual processing routes: reflexive processing via magnocellular (M) pathway and reflective processing via parvocellular (P) pathway. Because growing evidence has identified a variety of sex differences in emotional perception, here we also investigated how M and P processing of fear and eye gaze might be modulated by observer's sex, focusing on the amygdala, a structure important to threat perception and affective appraisal. We adjusted luminance and color of face stimuli to selectively engage M or P processing and asked observers to identify emotion of the face. Female observers showed more accurate behavioral responses to faces with averted gaze and greater left amygdala reactivity both to fearful and neutral faces. Conversely, males showed greater right amygdala activation only for M-biased averted-gaze fear faces. In addition to functional reactivity differences, females had proportionately greater bilateral amygdala volumes, which positively correlated with behavioral accuracy for M-biased fear. Conversely, in males only the right amygdala volume was positively correlated with accuracy for M-biased fear faces. Our findings suggest that M and P processing of facial threat cues is modulated by functional and structural differences in the amygdalae associated with observer's sex.
© 2018 Wiley Periodicals, Inc.

Keywords:  amygdala; emotion perception; eye gaze; fMRI; gender; sex differences

Mesh:

Year:  2018        PMID: 29520882      PMCID: PMC6866386          DOI: 10.1002/hbm.24035

Source DB:  PubMed          Journal:  Hum Brain Mapp        ISSN: 1065-9471            Impact factor:   5.038


  96 in total

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Journal:  Neuropsychologia       Date:  2012-03-17       Impact factor: 3.139

8.  Women process multisensory emotion expressions more efficiently than men.

Authors:  O Collignon; S Girard; F Gosselin; D Saint-Amour; F Lepore; M Lassonde
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10.  Sex and age differences in attention-deficit/hyperactivity disorder symptoms and diagnoses: implications for DSM-V and ICD-11.

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  7 in total

1.  Sex-related differences in behavioral and amygdalar responses to compound facial threat cues.

Authors:  Hee Yeon Im; Reginald B Adams; Cody A Cushing; Jasmine Boshyan; Noreen Ward; Kestutis Kveraga
Journal:  Hum Brain Mapp       Date:  2018-03-08       Impact factor: 5.038

2.  Differential magnocellular versus parvocellular pathway contributions to the combinatorial processing of facial threat.

Authors:  Reginald B Adams; Hee Yeon Im; Cody Cushing; Jasmine Boshyan; Noreen Ward; Daniel N Albohn; Kestutis Kveraga
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3.  Sex-specific effects of low-dose hydrocortisone on threat detection in HIV.

Authors:  Asante R Kamkwalala; Pauline M Maki; Scott A Langenecker; K Luan Phan; Kathleen M Weber; Leah H Rubin
Journal:  J Neurovirol       Date:  2021-09-24       Impact factor: 2.643

4.  Observer's anxiety facilitates magnocellular processing of clear facial threat cues, but impairs parvocellular processing of ambiguous facial threat cues.

Authors:  Hee Yeon Im; Reginald B Adams; Jasmine Boshyan; Noreen Ward; Cody A Cushing; Kestutis Kveraga
Journal:  Sci Rep       Date:  2017-11-09       Impact factor: 4.379

5.  Magnocellular and parvocellular pathway contributions to facial threat cue processing.

Authors:  Cody A Cushing; Hee Yeon Im; Reginald B Adams; Noreen Ward; Kestutis Kveraga
Journal:  Soc Cogn Affect Neurosci       Date:  2019-02-13       Impact factor: 3.436

6.  A deep neural network model of the primate superior colliculus for emotion recognition.

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Review 7.  The Neurobiological Correlates of Gaze Perception in Healthy Individuals and Neurologic Patients.

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