Resting state functional connectivity modifications in monoaminergic circuits underpin fatigue development in patients with multiple sclerosis

Mol Psychiatry. 2024 Sep;29(9):2647-2656. doi: 10.1038/s41380-024-02532-6. Epub 2024 Mar 25.

Abstract

Dysregulation of monoaminergic networks might have a role in the pathogenesis of fatigue in multiple sclerosis (MS). We investigated longitudinal changes of resting state (RS) functional connectivity (FC) in monoaminergic networks and their association with the development of fatigue in MS. Eighty-nine MS patients and 49 age- and sex-matched healthy controls (HC) underwent neurological, fatigue, and RS functional MRI assessment at baseline and after a median follow-up of 1.3 years (interquartile range = 1.01-2.01 years). Monoaminergic-related RS FC was estimated with an independent component analysis constrained to PET atlases for dopamine (DA), noradrenaline (NA), and serotonin (5-HT) transporters. At baseline, 24 (27%) MS patients were fatigued (F) and 65 were not fatigued (NF). Of these, 22 (34%) developed fatigue (DEV-FAT) at follow-up and 43 remained not fatigued (NO-FAT). At baseline, F-MS patients showed increased monoaminergic-related RS FC in the caudate nucleus vs NF-MS and in the hippocampal, postcentral, temporal, and occipital cortices vs NF-MS and HC. Moreover, F-MS patients exhibited decreased RS FC in the frontal cortex vs NF-MS and HC, and in the thalamus vs NF-MS. During the follow-up, no RS FC changes were observed in HC. NO-FAT patients showed limited DA-related RS FC modifications, whereas DEV-FAT MS patients showed increased DA-related RS FC in the left hippocampus, significant at time-by-group interaction analysis. In the NA-related network, NO-FAT patients showed decreased RS FC over time in the left superior frontal gyrus. This region showed increased RS FC in both DEV-FAT and F-MS patients; this divergent behavior was significant at time-by-group interaction analysis. Finally, DEV-FAT MS patients presented increased 5-HT-related RS FC in the angular and middle occipital gyri, while this latter region showed decreased 5-HT-related RS FC during the follow-up in F-MS patients. In MS patients, distinct patterns of alterations were observed in monoaminergic networks based on their fatigue status. Fatigue was closely linked to specific changes in the basal ganglia and hippocampal, superior frontal, and middle occipital cortices.

MeSH terms

  • Adult
  • Biogenic Monoamines / metabolism
  • Brain Mapping / methods
  • Brain* / metabolism
  • Brain* / physiopathology
  • Dopamine Plasma Membrane Transport Proteins / metabolism
  • Fatigue* / etiology
  • Fatigue* / metabolism
  • Fatigue* / physiopathology
  • Female
  • Humans
  • Longitudinal Studies
  • Magnetic Resonance Imaging* / methods
  • Male
  • Middle Aged
  • Multiple Sclerosis* / complications
  • Multiple Sclerosis* / metabolism
  • Multiple Sclerosis* / physiopathology
  • Nerve Net / diagnostic imaging
  • Nerve Net / metabolism
  • Nerve Net / physiopathology
  • Neural Pathways / physiopathology
  • Norepinephrine Plasma Membrane Transport Proteins / metabolism
  • Positron-Emission Tomography / methods
  • Rest / physiology
  • Serotonin Plasma Membrane Transport Proteins / metabolism

Substances

  • Serotonin Plasma Membrane Transport Proteins
  • Biogenic Monoamines
  • Norepinephrine Plasma Membrane Transport Proteins
  • Dopamine Plasma Membrane Transport Proteins