4.8 Article

Mapping dopaminergic projections in the human brain with resting-state fMRI

Journal

ELIFE
Volume 11, Issue -, Pages -

Publisher

eLIFE SCIENCES PUBL LTD
DOI: 10.7554/eLife.71846

Keywords

dopaminergic projections; striatum; Parkinson's disease; connectopic mapping; resting-state fMRI; Human

Categories

Funding

  1. Nederlandse Organisatie voor Wetenschappelijk Onderzoek [864-12-004, 17854, 016.156.415, 016.171.068, 91617077, 012200-013]
  2. ZonMw Rubicon [452172019]
  3. Dutch Brain Foundation [F2013(10-15)]

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This study uses connectopic mapping to investigate the striatum and finds that the functional connectivity within the striatum corresponds to dopaminergic projections. It also shows that this connectivity pattern is associated with Parkinson's disease symptoms, sensitivity to dopamine replacement therapy, and levels of nicotine and alcohol use.
The striatum receives dense dopaminergic projections, making it a key region of the dopaminergic system. Its dysfunction has been implicated in various conditions including Parkinson's disease (PD) and substance use disorder. However, the investigation of dopamine-specific functioning in humans is problematic as current MRI approaches are unable to differentiate between dopaminergic and other projections. Here, we demonstrate that 'connectopic mapping' - a novel approach for characterizing fine-grained, overlapping modes of functional connectivity - can be used to map dopaminergic projections in striatum. We applied connectopic mapping to resting-state functional MRI data of the Human Connectome Project (population cohort; N = 839) and selected the second-order striatal connectivity mode for further analyses. We first validated its specificity to dopaminergic projections by demonstrating a high spatial correlation (r = 0.884) with dopamine transporter availability - a marker of dopaminergic projections - derived from DaT SPECT scans of 209 healthy controls. Next, we obtained the subject-specific second-order modes from 20 controls and 39 PD patients scanned under placebo and under dopamine replacement therapy (L-DOPA), and show that our proposed dopaminergic marker tracks PD diagnosis, symptom severity, and sensitivity to L-DOPA. Finally, across 30 daily alcohol users and 38 daily smokers, we establish strong associations with self-reported alcohol and nicotine use. Our findings provide evidence that the second-order mode of functional connectivity in striatum maps onto dopaminergic projections, tracks inter-individual differences in PD symptom severity and L-DOPA sensitivity, and exhibits strong associations with levels of nicotine and alcohol use, thereby offering a new biomarker for dopamine-related (dys)function in the human brain.

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