Emotional Awareness in Schizophrenia Is Associated With Gray Matter Volume of Right Precuneus

. 2021 ; 12 () : 601742. [epub] 20210401

Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic-ecollection

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid33868042

Grantová podpora
R01 HD090641 NICHD NIH HHS - United States
R01 MH112748 NIMH NIH HHS - United States
R01 MH074794 NIMH NIH HHS - United States
P41 EB015902 NIBIB NIH HHS - United States
R21 MH106793 NIMH NIH HHS - United States

Objectives: We assessed the relationship between emotional awareness (e.g., the ability to identify and differentiate our own feelings and feelings of others) and regional brain volumes in healthy and in schizophrenia groups. Methods: Magnetic resonance images of 29 subjects with schizophrenia and 33 matched healthy controls were acquired. Brain gray matter was parcellated using FreeSurfer and 28 regions of interest associated with emotional awareness were analyzed. All participants were assessed using the Levels of Emotional Awareness Scale (LEAS) of Self and of Other. LEAS scores were correlated with gray matter volume for each hemisphere on the 14 brain regions of the emotional awareness network. Results: Individuals with schizophrenia showed decreased emotional awareness on both LEAS Self and LEAS Other compared to healthy controls. There were no statistically significant between-group differences in gray matter volumes of the emotional awareness network. The performance on LEAS Other correlated negatively with right precuneus gray matter volume only in the schizophrenia group. Conclusion: Our findings suggest a relationship between gray matter volume of the right precuneus and deficits in understanding of emotional states of others in schizophrenia.

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Fett A-KJ, Viechtbauer W, Dominguez M-G, Penn DL, van Os J, Krabbendam L. The relationship between neurocognition and social cognition with functional outcomes in schizophrenia: a meta-analysis. Neurosci Biobehav Rev. (2011) 35:573–88. 10.1016/j.neubiorev.2010.07.001 PubMed DOI

Green MF, Horan WP, Lee J. Social cognition in schizophrenia. Nat Rev Neurosci. (2015) 16:620–31. 10.1038/nrn4005 PubMed DOI

Baslet G, Termini L, Herbener E. Deficits in emotional awareness in schizophrenia and their relationship with other measures of functioning. J Nerv Ment Dis. (2009) 197:655–60. 10.1097/NMD.0b013e3181b3b20f PubMed DOI PMC

Kimhy D, Vakhrusheva J, Jobson-Ahmed L, Tarrier N, Malaspina D, Gross JJ. Emotion awareness and regulation in individuals with schizophrenia: implications for social functioning. Psychiatry Res. (2012) 200:193–201. 10.1016/j.psychres.2012.05.029 PubMed DOI PMC

Larsen JK, Brand N, Bermond B, Hijman R. Cognitive and emotional characteristics of Alexithymia: a review of neurobiological studies. J Psychosom Res. (2003) 54:533–41. 10.1016/S0022-3999(02)00466-X PubMed DOI

Sifneos PE. Alexithymia: past and present. Am J Psychiatry. (1996) 153:137–42. 10.1176/ajp.153.7.137 PubMed DOI

Goerlich KS. The multifaceted nature of alexithymia – a neuroscientific perspective. Front Psychol. (2018) 9:1614. 10.3389/fpsyg.2018.01614 PubMed DOI PMC

Zech E, Luminet O, Rimé B, Wagner H. Alexithymia and its measurement: confirmatory factor analyses of the 20-item Toronto Alexithymia Scale and the Bermond-Vorst Alexithymia Questionnaire. Eur J Pers. (1999) 13:511–32. 10.1002/(SICI)1099-0984(199911/12)13:6<511::AID-PER347>3.0.CO;2-0 DOI

Vorst HC, Bermond B. Validity and reliability of the Bermond–Vorst Alexithymia Questionnaire. Pers Individ Dif. (2001) 30:413–34. 10.1016/S0191-8869(00)00033-7 PubMed DOI

O'Driscoll C, Laing J, Mason O. Cognitive emotion regulation strategies, alexithymia and dissociation in schizophrenia, a review and meta-analysis. Clin Psychol Rev. (2014) 34:482–95. 10.1016/j.cpr.2014.07.002 PubMed DOI

Smith R, Quinlan D, Schwartz GE, Sanova A, Alkozei A, Lane RD. Developmental contributions to emotional awareness. J Pers Assess. (2019) 101:150–8. 10.1080/00223891.2017.1411917 PubMed DOI

Mancini G, Agnoli S, Trombini E, Baldaro B, Surcinelli P. Predictors of emotional awareness during childhood. Health (Irvine Calif). (2013) 05:375–80. 10.4236/health.2013.53050 DOI

Ciarrochi J, Caputi P, Mayer JD. The distinctiveness and utility of a measure of trait emotional awareness. Pers Individ Dif. (2003) 34:1477–90. 10.1016/S0191-8869(02)00129-0 DOI

Kubota M, Miyata J, Hirao K, Fujiwara H, Kawada R, Fujimoto S, et al. . Alexithymia and regional gray matter alterations in schizophrenia. Neurosci Res. (2011) 70:206–13. 10.1016/j.neures.2011.01.019 PubMed DOI

Terasawa Y, Fukushima H, Umeda S. How does interoceptive awareness interact with the subjective experience of emotion? An fMRI study. Hum Brain Mapp. (2013) 34:598–612. 10.1002/hbm.21458 PubMed DOI PMC

van der Velde J, Servaas MN, Goerlich KS, Bruggeman R, Horton P, Costafreda SG, et al. . Neural correlates of alexithymia: a meta-analysis of emotion processing studies. Neurosci Biobehav Rev. (2013) 37:1774–85. 10.1016/j.neubiorev.2013.07.008 PubMed DOI

Xu P, Opmeer EM, van Tol MJ, Goerlich KS, Aleman A. Structure of the alexithymic brain: a parametric coordinate-based meta-analysis. Neurosci Biobehav Rev. (2018) 87:50–5. 10.1016/j.neubiorev.2018.01.004 PubMed DOI

Lane RD, Quinlan DM, Schwartz GE, Walker PA, Zeitlin SB. The levels of emotional awareness scale: a cognitive-developmental measure of emotion. J Pers Assess. (1990) 55:124–34. 10.1207/s15327752jpa5501&amp;2_12 PubMed DOI

Lane RD, Hsu CH, Locke DEC, Ritenbaugh C, Stonnington CM. Role of theory of mind in emotional awareness and alexithymia: Implications for conceptualization and measurement. Conscious Cogn. (2015) 33:398–405. 10.1016/j.concog.2015.02.004 PubMed DOI

Harrison BJ, Yücel M, Pujol J, Pantelis C. Task-induced deactivation of midline cortical regions in schizophrenia assessed with fMRI. Schizophr Res. (2007) 91:82–6. 10.1016/j.schres.2006.12.027 PubMed DOI

Henry JD, Bailey PE, von Hippel C, Rendell PG, Lane A. Alexithymia in schizophrenia. J Clin Exp Neuropsychol. (2010) 32:890–7. 10.1080/13803391003596462 PubMed DOI

First MB. Structured Clinical Interview for the DSM (SCID). In: The Encyclopedia of Clinical Psychology. Hoboken, NJ, USA: John Wiley & Sons, Inc. (2015). p. 1–6. 10.1002/9781118625392.wbecp351 DOI

Kay SR, Fiszbein A, Opler LA. The Positive and Negative Syndrome Scale (PANSS) for Schizophrenia. Schizophr Bull. (1987) 13:261–76. 10.1093/schbul/13.2.261 PubMed DOI

Sheehan DV, Lecrubier Y, Sheehan KH, Amorim P, Janavs J, Weiller E, et al. . The Mini-International Neuropsychiatric Interview (M.I.N.I.): the development and validation of a structured diagnostic psychiatric interview for DSM-IV and ICD-10. J Clin Psychiatry. (1998) 59:22–33. PubMed

Sloan DM, Kring AM. Measuring changes in emotion during psychotherapy: conceptual and methodological issues. Clin Psychol Sci Pract. (2007) 14:307–22. 10.1111/j.1468-2850.2007.00092.x DOI

Bezdicek O, Michalec J, Kališová L, Kufa T, Děchtěrenko F, Chlebovcová M, et al. . Profile of cognitive deficits in schizophrenia and factor structure of the Czech MATRICS Consensus Cognitive Battery. Schizophr Res. (2020) 218:85–92. 10.1016/j.schres.2020.02.004 PubMed DOI

Green MF, Penn DL, Bentall R, Carpenter WT, Gaebel W, Gur RC, et al. . Social cognition in schizophrenia: an NIMH workshop on definitions, assessment, and research opportunities. Schizophr Bull. (2008) 34:1211–20. 10.1093/schbul/sbm145 PubMed DOI PMC

Green MF, Harris JG, Nuechterlein KH. The MATRICS consensus cognitive battery: what we know 6 years later. Am J Psychiatry. (2014) 171:1151–4. 10.1176/appi.ajp.2014.14070936 PubMed DOI

Desikan RS, Ségonne F, Fischl B, Quinn BT, Dickerson BC, Blacker D, et al. . An automated labeling system for subdividing the human cerebral cortex on MRI scans into gyral based regions of interest. Neuroimage. (2006) 31:968–80. 10.1016/j.neuroimage.2006.01.021 PubMed DOI

Bora E, Fornito A, Radua J, Walterfang M, Seal M, Wood SJ, et al. . Neuroanatomical abnormalities in schizophrenia: a multimodal voxelwise meta-analysis and meta-regression analysis. Schizophr Res. (2011) 127:46–57. 10.1016/j.schres.2010.12.020 PubMed DOI

Haijma SV, Van Haren N, Cahn W, Koolschijn PCMPP, Hulshoff Pol HE, Kahn RS. Brain volumes in schizophrenia: a meta-analysis in over 18 000 subjects. Schizophr Bull. (2013) 39:1129–38. 10.1093/schbul/sbs118 PubMed DOI PMC

Vita A, De Peri L, Deste G, Sacchetti E. Progressive loss of cortical gray matter in schizophrenia: a meta-analysis and meta-regression of longitudinal MRI studies. Transl Psychiatry. (2012) 2:e190. 10.1038/tp.2012.116 PubMed DOI PMC

Olabi B, Ellison-Wright I, McIntosh AM, Wood SJ, Bullmore E, Lawrie SM. Are there progressive brain changes in schizophrenia? A meta-analysis of structural magnetic resonance imaging studies. Biol Psychiatry. (2011) 70:88–96. 10.1016/j.biopsych.2011.01.032 PubMed DOI

Cavanna AE, Trimble MR. The precuneus: a review of its functional anatomy and behavioural correlates. Brain. (2006) 129:564–83. 10.1093/brain/awl004 PubMed DOI

Ochsner KN, Knierim K, Ludlow DH, Hanelin J, Ramachandran T, Glover G, et al. . Reflecting upon feelings: an fmri study of neural systems supporting the attribution of emotion to self and other. J Cogn Neurosci. (2004) 16:1746–72. 10.1162/0898929042947829 PubMed DOI

Jáni M, Kašpárek T. Emotion recognition and theory of mind in schizophrenia: a meta-analysis of neuroimaging studies. World J Biol Psychiatry. (2017) 113:1–11. 10.1080/15622975.2017.1324176 PubMed DOI

Vogeley K, Fink GR. Neural correlates of the first-person-perspective. Trends Cogn Sci. (2003) 7:38–42. 10.1016/S1364-6613(02)00003-7 PubMed DOI

Vogeley K, May M, Ritzl A, Falkai P, Zilles K, Fink GR. Neural correlates of first-person perspective as one constituent of human self-consciousness. J Cogn Neurosci. (2004) 16:817–27. 10.1162/089892904970799 PubMed DOI

Freton M, Lemogne C, Bergouignan L, Delaveau P, Lehéricy S, Fossati P. The eye of the self: precuneus volume and visual perspective during autobiographical memory retrieval. Brain Struct Funct. (2014) 219:959–68. 10.1007/s00429-013-0546-2 PubMed DOI

Hebscher M, Levine B, Gilboa A. The precuneus and hippocampus contribute to individual differences in the unfolding of spatial representations during episodic autobiographical memory. Neuropsychologia. (2018) 110:123–33. 10.1016/j.neuropsychologia.2017.03.029 PubMed DOI

Pronin E. How we see ourselves and how we see others. Science. (2008) 320:1177–80. 10.1126/science.1154199 PubMed DOI

Mattila AK, Salminen JK, Nummi T, Joukamaa M. Age is strongly associated with alexithymia in the general population. J Psychosom Res. (2006) 61:629–35. 10.1016/j.jpsychores.2006.04.013 PubMed DOI

Bora E, Murray RM. Meta-analysis of cognitive deficits in ultra-high risk to psychosis and first-episode psychosis: do the cognitive deficits progress over, or after, the onset of psychosis? Schizophr Bull. (2014) 40:744–55. 10.1093/schbul/sbt085 PubMed DOI PMC

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