An fMRI study of cognitive reappraisal in major depressive disorder and borderline personality disorder. Issue 1 (1st September 2021)

• Record Type: Journal Article
• Authors: De la Peña-Arteaga, Víctor; Berruga-Sánchez, Mercedes; Steward, Trevor; Martínez-Zalacaín, Ignacio; Goldberg, Ximena; Wainsztein, Agustina; Abulafia, Carolina; Cardoner, Narcís; Castro, Mariana N.; Villarreal, Mirta; Menchón, José M.; Guinjoan, Salvador M.; Soriano-Mas, Carles
• Is Part Of: European psychiatry. Volume 64:Issue 1(2021)
• Publication Date: 2021-09-01
• Subjects: Borderline personality disorder -- emotion regulation -- fMRI -- major depressive disorder -- neuroimaging; Psychiatry -- Periodicals; Mental illness -- Periodicals; Electronic journals; 616.89
• DOI: 10.1192/j.eurpsy.2021.2231
• Languages: English
• ISSNs: 0924-9338

Abstract

Abstract: Background: One common denominator to the clinical phenotypes of borderline personality disorder (BPD) and major depressive disorder (MDD) is emotion regulation impairment. Although these two conditions have been extensively studied separately, it remains unclear whether their emotion regulation impairments are underpinned by shared or distinct neurobiological alterations. Methods: We contrasted the neural correlates of negative emotion regulation across an adult sample of BPD patients ( n = 19), MDD patients ( n = 20), and healthy controls (HCs; n = 19). Emotion regulation was assessed using an established functional magnetic resonance imaging cognitive reappraisal paradigm. We assessed both task-related activations and modulations of interregional connectivity. Results: When compared to HCs, patients with BPD and MDD displayed homologous decreased activation in the right ventrolateral prefrontal cortex (vlPFC) during cognitive reappraisal. In addition, the MDD group presented decreased activations in other prefrontal areas (i.e., left dorsolateral and bilateral orbitofrontal cortices), while the BPD group was characterized by a more extended pattern of alteration in the connectivity between the vlPFC and cortices of the visual ventral stream during reappraisal. Conclusions: This study identified, for the first time, a shared neurobiological contributor to emotion regulation deficits in MDD and BPD characterized by decreased vlPFC activity, although we also observed disorder-specific alterations. In MDD, results suggest a primary deficit in the strength of prefrontal activations, while BPD is better defined by connectivity disruptions between the vlPFC and temporal emotion processing regions. These findings substantiate, in neurobiological terms, the different profiles of emotion regulation alterations observed in these disorders.