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Resting-state dynamics as a neuromarker of dopamine administration in healthy female adults.
Bellucci, Gabriele; Münte, Thomas F; Park, Soyoung Q.
Affiliation
  • Bellucci G; 1 Department of Psychology I, University of Lübeck, Lübeck, Germany.
  • Münte TF; 2 Decision Neuroscience and Nutrition, German Institute of Human Nutrition (DIfE), Nuthetal, Germany.
  • Park SQ; 3 Department of Neurology, Universitätsklinikum Schleswig-Holstein, Lübeck, Germany.
J Psychopharmacol ; 33(8): 955-964, 2019 08.
Article in En | MEDLINE | ID: mdl-31246145
ABSTRACT

BACKGROUND:

Different neuromarkers of people's emotions, personality traits and behavioural performance have recently been identified. However, not much attention has been devoted to neuromarkers of neural responsiveness to drug administration.

AIMS:

We investigated the predictive neuromarkers of acute dopamine (DA) administration.

METHODS:

In a double-blind, within-subject study, we administrated a DA agonist (pramipexole) or placebo to 27 healthy female subjects. Using multivariate classification and prediction analyses, we examined whether dopaminergic modulations of task-free resting-state brain dynamics predict individual differences in pramipexole's modulation of facial attractiveness evaluations.

RESULTS:

Our results demonstrate that pramipexole's effects on brain dynamics could be successfully discriminated from resting-state functional connectivity (accuracy 78.9%; p < 0.0001). On the behavioural level, pramipexole increased facial attractiveness evaluations (t(39) = 4.44; p < 0.0001). In particular, pramipexole administration enhanced connectivity strength of the cinguloopercular network (t(23) = 3.29; p = 0.003) and increased brain signal variability in subcortical and prefrontal brain areas (t(13) = 3.05, p = 0.009). Importantly, multivariate predictive models reveal that pramipexole-dependent modulation of resting-state dynamics predicted the increase of facial attractiveness evaluations after pramipexole (connectivity strength standardized mean squared error, smse = 0.65; p = 0.0007; brain signal variability smse = 0.94, p = 0.015).

CONCLUSION:

These results demonstrate that modulations of resting-state brain dynamics induced by a DA agonist predict drug-related effects on evaluation processes, providing a neuromarker of the neural responsiveness of specific brain networks to DA administration.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rest / Dopamine Type of study: Clinical_trials / Prognostic_studies Limits: Adult / Female / Humans Language: En Journal: J Psychopharmacol Journal subject: PSICOFARMACOLOGIA Year: 2019 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rest / Dopamine Type of study: Clinical_trials / Prognostic_studies Limits: Adult / Female / Humans Language: En Journal: J Psychopharmacol Journal subject: PSICOFARMACOLOGIA Year: 2019 Document type: Article Affiliation country: