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Subthalamic Peak Beta Ratio Is Asymmetric in Glucocerebrosidase Mutation Carriers With Parkinson's Disease: A Pilot Study.
David, Fabian J; Munoz, Miranda J; Shils, Jay L; Pauciulo, Michael W; Hale, Philip T; Nichols, William C; Afshari, Mitra; Sani, Sepehr; Verhagen Metman, Leo; Corcos, Daniel M; Pal, Gian D.
Afiliação
  • David FJ; Department of Physical Therapy and Human Movement Sciences, Northwestern University, Chicago, IL, United States.
  • Munoz MJ; Department of Physical Therapy and Human Movement Sciences, Northwestern University, Chicago, IL, United States.
  • Shils JL; Department of Anesthesiology, Rush University Medical Center, Chicago, IL, United States.
  • Pauciulo MW; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
  • Hale PT; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
  • Nichols WC; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
  • Afshari M; Department of Neurological Science, Rush University Medical Center, Chicago, IL, United States.
  • Sani S; Department of Neurosurgery, Rush University Medical Center, Chicago, IL, United States.
  • Verhagen Metman L; Department of Neurological Science, Rush University Medical Center, Chicago, IL, United States.
  • Corcos DM; Department of Physical Therapy and Human Movement Sciences, Northwestern University, Chicago, IL, United States.
  • Pal GD; Department of Neurological Science, Rush University Medical Center, Chicago, IL, United States.
Front Neurol ; 12: 723476, 2021.
Article em En | MEDLINE | ID: mdl-34659089
ABSTRACT

Introduction:

Up to 27% of individuals undergoing subthalamic nucleus deep brain stimulation (STN-DBS) have a genetic form of Parkinson's disease (PD). Glucocerebrosidase (GBA) mutation carriers, compared to sporadic PD, present with a more aggressive disease, less asymmetry, and fare worse on cognitive outcomes with STN-DBS. Evaluating STN intra-operative local field potentials provide the opportunity to assess and compare symmetry between GBA and non-GBA mutation carriers with PD; thus, providing insight into genotype and STN physiology, and eligibility for and programming of STN-DBS. The purpose of this pilot study was to test differences in left and right STN resting state beta power in non-GBA and GBA mutation carriers with PD. Materials and

Methods:

STN (left and right) resting state local field potentials were recorded intraoperatively from 4 GBA and 5 non-GBA patients with PD while off medication. Peak beta power expressed as a ratio to total beta power (peak beta ratio) was compared between STN hemispheres and groups while co-varying for age, age of disease onset, and disease severity.

Results:

Peak beta ratio was significantly different between the left and the right STN for the GBA group (p < 0.01) but not the non-GBA group (p = 0.56) after co-varying for age, age of disease onset, and disease severity.

Discussion:

Peak beta ratio in GBA mutation carriers was more asymmetric compared with non-mutation carriers and this corresponded with the degree of clinical asymmetry as measured by rating scales. This finding suggests that GBA mutation carriers have a physiologic signature that is distinct from that found in sporadic PD.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Neurol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Neurol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos