Frontiers in Neuroscience (Mar 2022)

Dysautonomia in Parkinson’s Disease: Impact of Glucocerebrosidase Gene Mutations on Cardiovascular Autonomic Control

  • Angelica Carandina,
  • Giulia Lazzeri,
  • Giulia Lazzeri,
  • Gabriel Dias Rodrigues,
  • Gabriel Dias Rodrigues,
  • Giulia Franco,
  • Edoardo Monfrini,
  • Edoardo Monfrini,
  • Federica Arienti,
  • Federica Arienti,
  • Emanuele Frattini,
  • Emanuele Frattini,
  • Ilaria Trezzi,
  • Ilaria Trezzi,
  • Pedro Paulo da Silva Soares,
  • Chiara Bellocchi,
  • Chiara Bellocchi,
  • Ludovico Furlan,
  • Ludovico Furlan,
  • Nicola Montano,
  • Nicola Montano,
  • Alessio Di Fonzo,
  • Alessio Di Fonzo,
  • Eleonora Tobaldini,
  • Eleonora Tobaldini

DOI
https://doi.org/10.3389/fnins.2022.842498
Journal volume & issue
Vol. 16

Abstract

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Evidence from clinical practice suggests that PD patients with the Glucocerebrosidase gene mutations (GBA-PD) are characterized by more severe dysautonomic symptoms than patients with idiopathic PD (iPD). Therefore, an accurate assessment of cardiovascular autonomic control (CAC) is necessary to clarify the role of GBA mutations in the pathophysiology of PD. We evaluated the CAC at rest and during orthostatic challenge of 15 iPD, 15 GBA-PD and 15 healthy controls (CTR). ECG and respiration were recorded in supine position and during active standing. The analysis of Heart Rate Variability (HRV) was performed on ECG recordings using two different approaches, linear spectral analysis and non-linear symbolic analysis. GBA-PD patients presented more frequently an akinetic-rigid phenotype and cognitive dysfunction than iPD patients. Both iPD and GBA-PD group were characterized by a lower spectral HRV than CTR group. At rest, the GBA-PD group was characterized by a lower parasympathetic modulation and a shift of the sympathovagal balance toward a sympathetic predominance compared to the CTR group. Moreover, the GBA-PD patients presented a lower HR increment and a lower or absent reduction of the vagal modulation in response to the active standing than iPD patients. Lastly, the cardiovascular autonomic dysfunction in PD patients was associated with longer disease duration, and with the occurrence of REM sleep behavior disorder and constipation. Our findings suggest a more severe impairment of the CAC in PD patients with GBA mutations. These results and further studies on the role of GBA mutations could allow a stratification based on cardiovascular risk in PD patients and the implementation of specific prevention programs.

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