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Pupillary response in reward processing in adults with major depressive disorder in remission.
Guath, Mona; Willfors, Charlotte; Björlin Avdic, Hanna; Nordgren, Ann; Kleberg, Johan Lundin.
  • Guath M; Uppsala University, Uppsala, Sweden.
  • Willfors C; Department of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden.
  • Björlin Avdic H; Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden.
  • Nordgren A; Centre for Psychiatry Research, Department of Clinical Neuroscience, Karolinska Institute, Stockholm Health Care Services, Region Stockholm, Stockholm, Sweden.
  • Kleberg JL; Department of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden.
J Int Neuropsychol Soc ; 29(3): 306-315, 2023 03.
Article en En | MEDLINE | ID: mdl-35545874
ABSTRACT

OBJECTIVE:

Major depressive disorder (MDD) is associated with impaired reward processing and reward learning. The literature is inconclusive regarding whether these impairments persist after remission. The current study examined reward processing during a probabilistic learning task in individuals in remission from MDD (n = 19) and never depressed healthy controls (n = 31) matched for age and sex. The outcome measures were pupil dilation (an indirect index of noradrenergic activity and arousal) and computational modeling parameters.

METHOD:

Participants completed two versions (facial/nonfacial feedback) of probabilistic reward learning task with changing contingencies. Pupil dilation was measured with a corneal reflection eye tracker. The hypotheses and analysis plan were preregistered.

RESULT:

Healthy controls had larger pupil dilation following losses than gains (p <.001), whereas no significant difference between outcomes was found in individuals with a history of MDD, resulting in an interaction between group and outcome (ß = 0.81, SE = 0.34, t = 2.37, p = .018). The rMDD group also achieved lower mean score at the last trial (t[46.77] = 2.12, p = .040) as well as a smaller proportion of correct choices (t[46.70] = 2.09, p = .041) compared with healthy controls.

CONCLUSION:

Impaired reward processing may persist after remission from MDD and could constitute a latent risk factor for relapse. Measuring pupil dilation in a reward learning task is a promising method for identifying reward processing abnormalities linked to MDD. The task is simple and noninvasive, which makes it feasible for clinical research.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trastorno Depresivo Mayor Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Adult / Humans Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trastorno Depresivo Mayor Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Adult / Humans Idioma: En Año: 2023 Tipo del documento: Article