Brain structural correlates of alexithymia in patients with major depressive disorder

BACKGROUND: Alexithymia is a risk factor for major depressive disorder (MDD) and has been associated with diminished treatment response. Neuroimaging studies have revealed structural aberrations of the anterior cingulate cortex and the fusiform gyrus in healthy controls with high levels of alexithym...

Verfasser: Förster, Katharina
Enneking, Verena
Dohm, Katharina
Redlich, Ronny
Meinert, Susanne L.
Geisler, Adina Isabel
Leehr, Elisabeth Johanna
Kugel, Harald
Baune, Bernhard Th.
Arolt, Volker
Zwitserlood, Pienie
Grotegerd, Dominik
Dannlowski, Udo
FB/Einrichtung:FB 05: Medizinische Fakultät
FB 07: Psychologie und Sportwissenschaft
Dokumenttypen:Artikel
Medientypen:Text
Erscheinungsdatum:2019
Publikation in MIAMI:07.07.2020
Datum der letzten Änderung:21.08.2020
Angaben zur Ausgabe:[Electronic ed.]
Quelle:Journal of Psychiatry & Neuroscience 45 (2020) 2, 117-124
Fachgebiet (DDC):610: Medizin und Gesundheit
Lizenz:InC 1.0
Sprache:English
Förderung:Finanziert durch den Open-Access-Publikationsfonds der Westfälischen Wilhelms-Universität Münster (WWU Münster).
This work was funded by the German Research Foundation (DFG, grant FOR2107 DA1151/5-1 and DA1151/5-2 to U. Dannlowski; SFB-TRR58, Projects C09 and Z02 to U. Dannlowski) and the Interdisciplinary Centre for Clinical Research (IZKF) of the medical faculty of Münster (grant Dan3/012/17 to U. Dannlowski).
Format:PDF-Dokument
URN:urn:nbn:de:hbz:6-90179615726
Weitere Identifikatoren:DOI: 10.1503/jpn.190044
Permalink:https://nbn-resolving.de/urn:nbn:de:hbz:6-90179615726
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Onlinezugriff:artikel_dannlowski_2019.pdf

BACKGROUND: Alexithymia is a risk factor for major depressive disorder (MDD) and has been associated with diminished treatment response. Neuroimaging studies have revealed structural aberrations of the anterior cingulate cortex and the fusiform gyrus in healthy controls with high levels of alexithymia. The present study tried to corroborate and extend these results to patients with MDD compared with healthy controls. METHODS: We investigated the relationship between alexithymia, depression and grey matter volume in 63 patients with MDD (mean age ± standard deviation = 42.43 yr ± 11.91; 33 female) and 46 healthy controls (45.35 yr ± 8.37; 22 female). We assessed alexithymia using the Toronto Alexithymia Scale. We conducted an alexithymia × group analysis of covariance; we used a region-of-interest approach, including the fusiform gyrus and anterior cingulate cortex, and conducted whole brain analysis using voxelbased morphometry. RESULTS: Our analysis revealed a significant alexithymia × group interaction in the fusiform gyrus (left, pFWE = 0.031; right, pFWE = 0.010). Higher alexithymia scores were associated with decreased grey matter volume in patients with MDD (pFWE = 0.009), but with increased grey matter volume of the fusiform gyrus in healthy controls (pFWE = 0.044). We found no significant main effects in the region-of-interest analysis. LIMITATIONS: Owing to the naturalistic nature of our study, patients with MDD and healthy controls differed significantly in their alexithymia scores. CONCLUSION: Our results showed the fusiform gyrus as a correlate of alexithymia. We also found differences related to alexithymia between patients with MDD and healthy controls in the fusiform gyrus. Our study encourages research related to the transition from risk to MDD in people with alexithymia.