236
Views
1
CrossRef citations to date
0
Altmetric
Original Research

Individual Differences in Hemispheric Emotional Valence by Computerized Test Correlate with Lateralized Differences in Nucleus Accumbens, Hippocampal and Amygdala Volumes

ORCID Icon, , , , , & show all
Pages 1371-1384 | Published online: 01 Jun 2022

References

  • Lee GP, Meador KJ, Loring DW, et al. Neural substrates of emotion as revealed by functional magnetic resonance imaging. Cogn Behav Neurol. 2004;17(1):9–17. doi:10.1097/00146965-200403000-00002
  • Roesmann K, Dellert T, Junghoefer M, et al. The causal role of prefrontal hemispheric asymmetry in valence processing of words - Insights from a combined cTBS-MEG study. Neuroimage. 2019;191:367–379. doi:10.1016/j.neuroimage.2019.01.057
  • Gainotti G. Emotions and the right hemisphere: can new data clarify old models? Neuroscientist. 2019;25(3):258–270. doi:10.1177/1073858418785342
  • Packheiser J, Rook N, Dursun Z, et al. Embracing your emotions: affective state impacts lateralisation of human embraces. Psychol Res. 2019;83(1):26–36. doi:10.1007/s00426-018-0985-8
  • Gainotti G. A historical review of investigations on laterality of emotions in the human brain. J Hist Neurosci. 2019;28(1):23–41. doi:10.1080/0964704X.2018.1524683
  • Harmon-Jones E. Early Career Award. Clarifying the emotive functions of asymmetrical frontal cortical activity. Psychophysiology. 2003;40(6):838–848. doi:10.1111/1469-8986.00121
  • Harmon-Jones E. On motivational influences, moving beyond valence, and integrating dimensional and discrete views of emotion. Cogn Emot. 2019;33(1):101–108. doi:10.1080/02699931.2018.1514293
  • Schiffer F. Of Two Minds: Dual-Brain Psychology. 2nd ed. Amazon KDP; 2021.
  • Schiffer F. Of Two Minds: The Revolutionary Science of Dual-Brain Psychology. The Free Press; 1998:243.
  • Schiffer F. Unilateral transcranial photobiomodulation for opioid addiction in a clinical practice: a clinical overview and case series. J Psychiatr Res. 2021;133:134–141. doi:10.1016/j.jpsychires.2020.12.004
  • Schiffer F, Anderson CM, Teicher MH. Electroencephalogram, bilateral ear temperature, and affect changes induced by lateral visual field stimulation. Compr Psychiatry. 1999;40(3):221–225. doi:10.1016/S0010-440X(99)90007-X
  • Schiffer F, Glass I, Lord J, Teicher MH. Prediction of clinical outcomes from rTMS in depressed patients with lateral visual field stimulation: a replication. J Neuropsychiatry Clin Neurosci. 2008;20(2):194–200. doi:10.1176/jnp.2008.20.2.194
  • Schiffer F, Khan A, Bolger E, Flynn E, Seltzer WP, Teicher MH. An effective and safe novel treatment of opioid use disorder: unilateral transcranial photobiomodulation. Front Psychiatry. 2021;12:713686. doi:10.3389/fpsyt.2021.713686
  • Schiffer F, Mottaghy FM, Pandey Vimal RL, et al. Lateral visual field stimulation reveals extrastriate cortical activation in the contralateral hemisphere: an fMRI study. Psychiatry Res. 2004;131(1):1–9. doi:10.1016/j.pscychresns.2004.01.002
  • Schiffer F, Teicher MH, Anderson C, et al. Determination of hemispheric emotional valence in individual subjects: a new approach with research and therapeutic implications. Behav Brain Funct. 2007;3(1):13. doi:10.1186/1744-9081-3-13
  • Schiffer F, Teicher MH, Papanicolaou AC. Evoked potential evidence for right brain activity during the recall of traumatic memories. J Neuropsychiatry Clin Neurosci. 1995;7:169–175.
  • Schiffer F, Zaidel E, Bogen J, Chasan-Taber S. Different psychological status in the two hemispheres of two split-brain patients. Neuropsychiatry Neuropsychol Behav Neurol. 1998;11(3):151–156.
  • Schiffer F, Reichmann W, Flynn E, Hamblin MR, McCormack H. A novel treatment of opioid cravings with an effect size of 73 for unilateral transcranial photobiomodulation over sham. Front Psychiatry. 2020;11:827. doi:10.3389/fpsyt.2020.00827
  • Schiffer F, Stinchfield Z, Pascual-Leone A. Prediction of clinical response to transcranial magnetic stimulation for depression by baseline lateral visual-field stimulation. Neuropsychiatry Neuropsychol Behav Neurol. 2002;15(1):18–27.
  • Wittling W, Roschmann R. Emotion-related hemisphere asymmetry: subjective emotional responses to laterally presented films. Cortex. 1993;29(3):431–448. doi:10.1016/s0010-9452(13)80252-3
  • Wittling W, Schweiger E. Neuroendocrine brain asymmetry and physical complaints. Neuropsychologia. 1993;31(6):591–608. doi:10.1016/0028-3932(93)90054-4
  • Sperry RW, Zaidel E, Zaidel D. Self recognition and social awareness in the deconnected minor hemisphere. Neuropsychologia. 1979;17(2):153–166. doi:10.1016/0028-3932(79)90006-X
  • Zaidel E, Zaidel DW, Sperry RW. Left and right intelligence: case studies of Raven’s progressive matrices following brain bisection and hemidecortication. Cortex. 1981;17(2):167–185. doi:10.1016/S0010-9452(81)80039-1
  • Schiffer F, Zaidel E, Bogen J, Chasan-Taber S. Different psychological status in the two hemispheres of two split brain patients. Neuropsychiatry Neuropsychol Behav Neurol. 1998;11(3):151–156.
  • Schiffer F. Can the different cerebral hemispheres have distinct personalities? Evidence and its implications for theory and treatment of PTSD and other disorders. J Trauma Dissociation. 2000;1(2):83–104. doi:10.1300/J229v01n02_06
  • Pascual-Leone A, Rubio B, Pallardo F, Catala MD. Rapid-rate transcranial magnetic stimulation of left dorsolateral prefrontal cortex in drug-resistant depression. Lancet. 1996;348(9022):233–237. doi:10.1016/S0140-6736(96)01219-6
  • Oathes DJ, Patenaude B, Schatzberg AF, Etkin A. Neurobiological signatures of anxiety and depression in resting-state functional magnetic resonance imaging. Biol Psychiatry. 2015;77(4):385–393. doi:10.1016/j.biopsych.2014.08.006
  • Teicher MH, Samson JA, Anderson CM, Ohashi K. The effects of childhood maltreatment on brain structure, function and connectivity. Nat Rev Neurosci. 2016;17(10):652–666. doi:10.1038/nrn.2016.111
  • Gong L, Yin Y, He C, et al. Disrupted reward circuits is associated with cognitive deficits and depression severity in major depressive disorder. J Psychiatr Res. 2017;84:9–17. doi:10.1016/j.jpsychires.2016.09.016
  • Ohashi K, Anderson CM, Bolger EA, Khan A, McGreenery CE, Teicher MH. Susceptibility or resilience to maltreatment can be explained by specific differences in brain network architecture. Biol Psychiatry. 2019;85(8):690–702. doi:10.1016/j.biopsych.2018.10.016
  • Schiffer F, Teicher M, Anderson C, et al. Determination of hemispheric emotional valence in individual subjects: a new approach with research and therapeutic implications. Behav Brain Funct. 2007;3(1):13. doi:10.1186/1744-9081-3-13
  • Teicher MH, Anderson CM, Ohashi K, Polcari A. Childhood maltreatment: altered network centrality of cingulate, precuneus, temporal pole and insula. Biol Psychiatry. 2014;76(4):297–305. doi:10.1016/j.biopsych.2013.09.016
  • Teicher MH, Anderson CM, Polcari A. Childhood maltreatment is associated with reduced volume in the hippocampal subfields CA3, dentate gyrus, and subiculum. Proc Natl Acad Sci U S A. 2012;109(9):E563–72. doi:10.1073/pnas.1115396109
  • Peirce JW. PsychoPy–psychophysics software in python. J Neurosci Methods. 2007;162(1–2):8–13. doi:10.1016/j.jneumeth.2006.11.017
  • Peirce JW. Generating stimuli for neuroscience using psychopy. Front Neuroinform. 2008;2:10. doi:10.3389/neuro.11.010.2008
  • Teicher MH, Parigger A. The ‘Maltreatment and Abuse Chronology of Exposure’ (MACE) scale for the retrospective assessment of abuse and neglect during development. PLoS One. 2015;10(2):e0117423. doi:10.1371/journal.pone.0117423
  • Felitti VJ, Anda RF, Nordenberg D, et al. Relationship of childhood abuse and household dysfunction to many of the leading causes of death in adults. The Adverse Childhood Experiences (ACE) Study. Am J Prev Med. 1998;14(4):245–258. doi:10.1016/S0749-3797(98)00017-8
  • Bernstein DP, Fink L. Childhood Trauma Questionnaire Manual. The Psychological Corporation; 1998.
  • First MB, Gibbon M, Spitzer RL, Williams JBW, Benjamin LS. Structured Clinical Interview for DSM–IV Axis II Personality Disorders. American Psychiatric Association; 1997.
  • First MB, Spitzer RL, Gibbon M, Williams JBW. Structured Clinical Interview for DSM-IV Axis I Disorders - Clinician Version (SCID-CV). American Psychiatric Press; 1997.
  • Costa PTJ, McCrae RR. Revised NEO Personality Inventory (NEO-PI-R) and NEO Five-Factor Inventory (NEO-FF1) Professional Manual. Psychological Assessment Resources; 1992.
  • McCrae RR, Costa PT Jr. NEO Inventories: Professional Manual. Psychological Assessment Resources, Inc.; 2010.
  • Fischl B, Dale AM. Measuring the thickness of the human cerebral cortex from magnetic resonance images. Proc Natl Acad Sci U S A. 2000;97(20):11050–11055. doi:10.1073/pnas.200033797
  • Dale AM, Fischl B, Sereno MI. Cortical surface-based analysis. I. Segmentation and surface reconstruction. Neuroimage. 1999;9(2):179–194. doi:10.1006/nimg.1998.0395
  • Fischl B, Salat DH, van der Kouwe AJ, et al. Sequence-independent segmentation of magnetic resonance images. Neuroimage. 2004;23(Suppl 1):S69–84. doi:10.1016/j.neuroimage.2004.07.016
  • Segonne F, Dale AM, Busa E, et al. A hybrid approach to the skull stripping problem in MRI. Neuroimage. 2004;22(3):1060–1075. doi:10.1016/j.neuroimage.2004.03.032
  • Fischl B, van der Kouwe A, Destrieux C, et al. Automatically parcellating the human cerebral cortex. Cereb Cortex. 2004;14(1):11–22. doi:10.1093/cercor/bhg087
  • Fischl B, Salat DH, Busa E, et al. Whole brain segmentation: automated labeling of neuroanatomical structures in the human brain. Neuron. 2002;33(3):341–355. doi:10.1016/S0896-6273(02)00569-X
  • Fischl B, Liu A, Dale AM. Automated manifold surgery: constructing geometrically accurate and topologically correct models of the human cerebral cortex. IEEE Trans Med Imaging. 2001;20(1):70–80. doi:10.1109/42.906426
  • Dale AM, Sereno MI. Improved localization of cortical activity by combining EEG and MEG with MRI cortical surface reconstruction: a linear approach. J Cogn Neurosci. 1993;5(2):162–176. doi:10.1162/jocn.1993.5.2.162
  • Sled JG, Zijdenbos AP, Evans AC. A nonparametric method for automatic correction of intensity nonuniformity in MRI data. IEEE Trans Med Imaging. 1998;17(1):87–97. doi:10.1109/42.668698
  • Segonne F, Pacheco J, Fischl B. Geometrically accurate topology-correction of cortical surfaces using nonseparating loops. IEEE Trans Med Imaging. 2007;26(4):518–529. doi:10.1109/TMI.2006.887364
  • Ohashi K, Anderson CM, Bolger EA, Khan A, McGreenery CE, Teicher MH. Childhood maltreatment is associated with alteration in global network fiber-tract architecture independent of history of depression and anxiety. Neuroimage. 2017;150:50–59. doi:10.1016/j.neuroimage.2017.02.037
  • Gong G, He Y, Concha L, et al. Mapping anatomical connectivity patterns of human cerebral cortex using in vivo diffusion tensor imaging tractography. Cereb Cortex. 2009;19(3):524–536. doi:10.1093/cercor/bhn102
  • Li Y, Liu Y, Li J, et al. Brain anatomical network and intelligence. PLoS Comput Biol. 2009;5(5):e1000395. doi:10.1371/journal.pcbi.1000395
  • Tzourio-Mazoyer N, Landeau B, Papathanassiou D, et al. Automated anatomical labeling of activations in SPM using a macroscopic anatomical parcellation of the MNI MRI single-subject brain. Neuroimage. 2002;15(1):273–289. doi:10.1006/nimg.2001.0978
  • Wang R, Benner T, Sorensen AG, Wedeen V. Diffusion toolkit: a software package for diffusion imaging data processing and tractography. ISMRM Abstract Proc Intl Soc Mag Reson Med. 2007;15:3720.
  • Csardi G, Nepusz T. The igraph software package for complex network research. Int J Complex Syst. 2006;1695:1–9.
  • Grömping U. Estimators of relative importance in linear regression based on variance decomposition. Am Stat. 2007;61(2):139–147. doi:10.1198/000313007X188252
  • Lindeman RH, Merenda PF, Gold RZ. Introduction to Bivariate and Multivariate Analysis. Scott, Foresman; 1980.
  • Strobl C, Boulesteix AL, Zeileis A, Hothorn T. Bias in random forest variable importance measures: illustrations, sources and a solution. BMC Bioinform. 2007;8(1):25. doi:10.1186/1471-2105-8-25
  • Khan A, McCormack HC, Bolger EA, et al. Childhood maltreatment, depression, and suicidal ideation: critical importance of parental and peer emotional abuse during developmental sensitive periods in males and females. Front Psychiatry. 2015;6:42. doi:10.3389/fpsyt.2015.00042
  • Teicher MH, Anderson CM, Ohashi K, et al. Differential effects of childhood neglect and abuse during sensitive exposure periods on male and female hippocampus. Neuroimage. 2018;169:443–452. doi:10.1016/j.neuroimage.2017.12.055
  • Pechtel P, Lyons-Ruth K, Anderson CM, Teicher MH. Sensitive periods of amygdala development: the role of maltreatment in preadolescence. Neuroimage. 2014;97:236–244. doi:10.1016/j.neuroimage.2014.04.025
  • Breiman L. Random Forests. Mach Learn. 2001;45:5–32.
  • Liaw A, Wiener M. Classification and Regression by randomForest. R News. 2002;2/3:18–22.
  • Widiger TA, Crego C. The five factor model of personality structure: an update. World Psychiatry. 2019;18(3):271–272. doi:10.1002/wps.20658
  • Jenkins LM, Stange JP, Barba A, et al. Integrated cross-network connectivity of amygdala, insula, and subgenual cingulate associated with facial emotion perception in healthy controls and remitted major depressive disorder. Cogn Affect Behav Neurosci. 2017;17(6):1242–1254. doi:10.3758/s13415-017-0547-3
  • Forbes EE, Hariri AR, Martin SL, et al. Altered striatal activation predicting real-world positive affect in adolescent major depressive disorder. Am J Psychiatry. 2009;166(1):64–73. doi:10.1176/appi.ajp.2008.07081336
  • Berridge KC, Kringelbach ML. Neuroscience of affect: brain mechanisms of pleasure and displeasure. Curr Opin Neurobiol. 2013;23(3):294–303. doi:10.1016/j.conb.2013.01.017
  • Redlich R, Grotegerd D, Opel N, et al. Are you gonna leave me? Separation anxiety is associated with increased amygdala responsiveness and volume. Soc Cogn Affect Neurosci. 2015;10(2):278–284. doi:10.1093/scan/nsu055
  • Soares JM, Marques P, Alves V, Sousa N. A hitchhiker’s guide to diffusion tensor imaging. Front Neurosci. 2013;7:31. doi:10.3389/fnins.2013.00031
  • Luders E, Narr KL, Bilder RM, et al. Positive correlations between corpus callosum thickness and intelligence. Neuroimage. 2007;37(4):1457–1464. doi:10.1016/j.neuroimage.2007.06.028
  • Schiffer F, Stinchfield Z, Pascual-Leone A. Prediction of clinical response to transcranial magnetic stimulation for depression by baseline lateral visual stimulation. Neuropsychiatry Neuropsychol Behav Neurol. 2002;15(1):18–27.
  • Schiffer F. A dual mind approach to understanding the conscious self and its treatment. Neuroscience. 2021;2(2):224–234. doi:10.3390/neurosci2020016