4.4 Article

Gender-Related Vulnerability of Dopaminergic Neural Networks in Parkinson's Disease

Journal

BRAIN CONNECTIVITY
Volume 11, Issue 1, Pages 3-11

Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/brain.2020.0781

Keywords

dopaminergic networks; FDG-PET; gender; metabolic connectivity; Parkinson's disease

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Funding

  1. CARIPLO Project Evaluation of autonomic, genetic, imaging, and biochemical markers for Parkinson-related dementia [2014-0832]

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This study found that male PD patients exhibited widespread connectivity alterations in the nigro-striato-cortical network and preservation of the mesolimbic pathway, while female PD patients showed severe connectivity abnormalities in the mesolimbic network and only partial reconfiguration of the nigro-striato-cortical network.
Background: In Parkinson's disease (PD), neurodegeneration of dopaminergic systems leads to motor and non-motor abnormalities. Sex might influence the clinical PD phenotypes and progression. Previous molecular imaging data focused only on the nigro-striato-cortical dopamine system that appeared more preserved in women. There is still a lack of evidence on gender/sex differences in the mesolimbic dopaminergic system. We aimed at assessing PD gender differences in both the dopaminergic pathways, by using a brain metabolic connectivity approach. This is based on the evidence of a significant coupling between the neurotransmission and metabolic impairments. Methods: We included 34 idiopathic PD patients (Female/Male: 16/18) and 34 healthy controls for comparison. The molecular architecture of both the dopaminergic networks was estimated throughout partial correlation analyses using brain metabolism data obtained by fluorine-18-fluorodeoxyglucose positron emission tomography (threshold set at p < 0.01, corrected for Bonferroni multiple comparisons). Results: Male patients were characterized by a widespread altered connectivity in the nigro-striato-cortical network and a sparing of the mesolimbic pathway. On the contrary, PD females showed a severe altered connectivity in the mesolimbic network and only a partial reconfiguration of the nigro-striato-cortical network. Discussion: Our findings add remarkable knowledge on the neurobiology of gender differences in PD, with the identification of specific neural vulnerabilities. The gender differences here revealed might be due to the combination of both biological and sociodemographic life factors. Gender differences in PD should be considered also for treatments and the targeting of modifiable risk factors.

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