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Abstract
Affective experience colours everyday perception and cognition, yet its fundamental and neurobiological basis is poorly understood. The current debate essentially centers around the communalities and specificities across individuals, events, and emotional categories like anger, sadness, and happiness. Using fMRI during the experience of these emotions, we critically compare the two dominant conflicting theories on human affect. Basic emotion theory posits emotions as discrete universal entities generated by dedicated emotion category-specific neural circuits, while psychological construction theory claims emotional events as unique, idiosyncratic, and constructed by psychological primitives like core affect and conceptualization, which underlie each emotional event and operate in a predictive framework. Based on the findings of 8 a priori-defined model-specific prediction tests on the neural response amplitudes and patterns, we conclude that the neurobiological basis of affect is primarily characterized by idiosyncratic mechanisms and a common neural basis shared across emotion categories, consistent with psychological construction theory. The findings provide further insight into the organizational principles of the neural basis of affect and brain function in general. Future studies in clinical populations with affective symptoms may reveal the corresponding underlying neural changes from a psychological construction perspective.
Analysis of fMRI recordings from an autobiographical memory recall tasks suggests that neural activation during emotional experiences can be better predicted by psychological construction theory, rather than classic basic emotions theory.
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Details
; Potočnik, Jure 1 ; De Winter, François-Laurent 2 ; El Kaddouri, Amal 1 ; Stam, Daphne 1
; Peeters, Ronald 3 ; Emsell, Louise 4
; Sunaert, Stefan 5 ; Van Oudenhove, Lukas 6
; Vandenbulcke, Mathieu 2 ; Feldman Barrett, Lisa 7
; Van den Stock, Jan 2
1 KU Leuven, Neuropsychiatry, Department of Neurosciences, Leuven Brain Institute, Leuven, Belgium (GRID:grid.5596.f) (ISNI:0000 0001 0668 7884)
2 KU Leuven, Neuropsychiatry, Department of Neurosciences, Leuven Brain Institute, Leuven, Belgium (GRID:grid.5596.f) (ISNI:0000 0001 0668 7884); University Psychiatric Center KU Leuven, Geriatric Psychiatry, Leuven, Belgium (GRID:grid.5596.f) (ISNI:0000 0001 0668 7884)
3 University Hospitals Leuven, Department of Radiology, Leuven, Belgium (GRID:grid.410569.f) (ISNI:0000 0004 0626 3338)
4 KU Leuven, Neuropsychiatry, Department of Neurosciences, Leuven Brain Institute, Leuven, Belgium (GRID:grid.5596.f) (ISNI:0000 0001 0668 7884); University Hospitals Leuven, Department of Radiology, Leuven, Belgium (GRID:grid.410569.f) (ISNI:0000 0004 0626 3338); KU Leuven, Department of Imaging and Pathology, Leuven, Belgium (GRID:grid.5596.f) (ISNI:0000 0001 0668 7884)
5 University Hospitals Leuven, Department of Radiology, Leuven, Belgium (GRID:grid.410569.f) (ISNI:0000 0004 0626 3338); KU Leuven, Department of Imaging and Pathology, Leuven, Belgium (GRID:grid.5596.f) (ISNI:0000 0001 0668 7884)
6 KU Leuven, Laboratory for Brain-Gut Axis Studies (LaBGAS), Translational Research in Gastrointestinal Disorders (TARGID), Department of Chronic Diseases and Metabolism, Leuven Brain Institute, Leuven, Belgium (GRID:grid.5596.f) (ISNI:0000 0001 0668 7884); Dartmouth College, Cognitive and Affective Neuroscience Lab, Department of Psychological and Brain Sciences, Hanover, USA (GRID:grid.254880.3) (ISNI:0000 0001 2179 2404)
7 Northeastern University, Department of Psychology, Boston, USA (GRID:grid.261112.7) (ISNI:0000 0001 2173 3359); Massachusetts General Hospital, Harvard Medical School, Department of Psychiatry, Boston, USA (GRID:grid.38142.3c) (ISNI:000000041936754X); Massachusetts General Hospital, Athinoula A. Martinos Center for Biomedical Imaging, Charlestown, USA (GRID:grid.32224.35) (ISNI:0000 0004 0386 9924)




