Aberrant striatal dopamine links topographically with cortico-thalamic dysconnectivity in schizophrenia

Author:

Avram Mihai123ORCID,Brandl Felix124,Knolle Franziska125,Cabello Jorge3,Leucht Claudia4,Scherr Martin4,Mustafa Mona3,Koutsouleris Nikolaos67,Leucht Stefan48,Ziegler Sibylle39,Sorg Christian124

Affiliation:

1. Department of Neuroradiology, Klinikum rechts der Isar, Technische Universität München, Munich, 81675, Germany

2. TUM-NIC Neuroimaging Center, Klinikum rechts der Isar, Technische Universität München, Munich, 81675, Germany

3. Department of Nuclear Medicine, Klinikum rechts der Isar, Technische Universität München, Munich, 81675, Germany

4. Department of Psychiatry, Klinikum rechts der Isar, Technische Universität München, Munich, 81675, Germany

5. Department of Psychiatry, University of Cambridge, Cambridge, UK

6. Department of Psychiatry, University Hospital, LMU Munich, Munich, 81377, Germany

7. Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE5 8AB, UK

8. Department of Psychosis studies, King’s College London, UK

9. Department of Nuclear Medicine, University Hospital, LMU Munich, Munich, 81377, Germany

Abstract

Abstract Aberrant dopamine function in the dorsal striatum and aberrant intrinsic functional connectivity (iFC) between distinct cortical networks and thalamic nuclei are among the most consistent large-scale brain imaging findings in schizophrenia. A pathophysiological link between these two alterations is suggested by theoretical models based on striatal dopamine’s topographic modulation of cortico-thalamic connectivity within cortico-basal-ganglia-thalamic circuits. We hypothesized that aberrant striatal dopamine links topographically with aberrant cortico-thalamic iFC, i.e. aberrant associative striatum dopamine is associated with aberrant iFC between the salience network and thalamus, and aberrant sensorimotor striatum dopamine with aberrant iFC between the auditory-sensorimotor network and thalamus. Nineteen patients with schizophrenia during remission of psychotic symptoms and 19 age- and sex-comparable control subjects underwent simultaneous fluorodihydroxyphenyl-l-alanine PET (18F-DOPA-PET) and resting state functional MRI (rs-fMRI). The influx constant kicer based on 18F-DOPA-PET was used to measure striatal dopamine synthesis capacity; correlation coefficients between rs-fMRI time series of cortical networks and thalamic regions of interest were used to measure iFC. In the salience network-centred system, patients had reduced associative striatum dopamine synthesis capacity, which correlated positively with decreased salience network-mediodorsal-thalamus iFC. This correlation was present in both patients and healthy controls. In the auditory-sensorimotor network-centred system, patients had reduced sensorimotor striatum dopamine synthesis capacity, which correlated positively with increased auditory-sensorimotor network-ventrolateral-thalamus iFC. This correlation was present in patients only. Results demonstrate that reduced striatal dopamine synthesis capacity links topographically with cortico-thalamic intrinsic dysconnectivity in schizophrenia. Data suggest that aberrant striatal dopamine and cortico-thalamic dysconnectivity are pathophysiologically related within dopamine-modulated cortico-basal ganglia-thalamic circuits in schizophrenia.

Funder

European Union 7th Framework Programme

Hans und Klementia Langmatz Stiftung

European Union’s Horizon 2020

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

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