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Whole body-electromyostimulation effects on serum biomarkers, physical performances and fatigue in Parkinson's patients: A randomized controlled trial.
di Cagno, Alessandra; Buonsenso, Andrea; Centorbi, Marco; Manni, Luigi; Di Costanzo, Alfonso; Casazza, Giusy; Parisi, Attilio; Guerra, Germano; Calcagno, Giuseppe; Iuliano, Enzo; Soligo, Marzia; Fiorilli, Giovanni.
Affiliation
  • di Cagno A; Department of Movement, Human and Health Sciences, University of Rome "Foro Italico", Rome, Italy.
  • Buonsenso A; Department of Medicine and Health Sciences, University of Molise, Campobasso, Italy.
  • Centorbi M; Department of Medicine and Health Sciences, University of Molise, Campobasso, Italy.
  • Manni L; Institute of Translational Pharmacology and Cellular Biology and Neurobiology Institute (CNR), National Research Council (CNR), Rome, Italy.
  • Di Costanzo A; Centre for Research and Training in Medicine of Aging, Department of Medicine and Health Sciences, University of Molise, Campobasso, Italy.
  • Casazza G; Department of Medicine and Health Sciences, University of Molise, Campobasso, Italy.
  • Parisi A; Department of Movement, Human and Health Sciences, University of Rome "Foro Italico", Rome, Italy.
  • Guerra G; Department of Medicine and Health Sciences, University of Molise, Campobasso, Italy.
  • Calcagno G; Department of Medicine and Health Sciences, University of Molise, Campobasso, Italy.
  • Iuliano E; Faculty of Psychology, eCampus University, Novedrate, Italy.
  • Soligo M; Institute of Translational Pharmacology and Cellular Biology and Neurobiology Institute (CNR), National Research Council (CNR), Rome, Italy.
  • Fiorilli G; Department of Medicine and Health Sciences, University of Molise, Campobasso, Italy.
Front Aging Neurosci ; 15: 1086487, 2023.
Article in En | MEDLINE | ID: mdl-36845654
Background: Whole-body electromyostimulation (WB-EMS) was never previously applied to Parkinson's disease (PD) patients. This randomized controlled study aimed to find the most effective and safe WB-EMS training protocol for this population. Methods: Twenty-four subjects (age: 72.13 ± 6.20 years), were randomly assigned to three groups: a high-frequency WB-EMS strength training group (HFG) (rectangular stimulation at 85 Hz, 350 µs, 4 s stimulation/4 s rest), a low-frequency WB-EMS aerobic training group (LFG) (rectangular stimulation 7 Hz, 350 µs, with a continuous pulse duration), and an inactive control group (CG). Participants of the two experimental groups underwent 24 controlled WB-EMS training sessions, with a duration of 20 min each, during 12-week intervention. Serum growth factors (BDNF, FGF-21, NGF and proNGF), α-synuclein, physical performance and Parkinson's Disease Fatigue Scale (PFS-16) responses were analyzed to evaluate the pre-post variation and differences among groups. Results: Significant interactions of Time*Groups were detected for BDNF (Time*Groups p = 0.024; Time*CG, b = -628, IC95% = -1,082/-174, p = 0.008), FGF-21 (Time*Groups p = 0.009; Time*LFG b = 1,346, IC95% = 423/2268, p = 0.005), and α-synuclein (Time*Groups p = 0.019; Time*LFG b = -1,572, IC95% = -2,952/-192, p = 0.026). Post hoc analyses and comparisons of ΔS (post-pre), performed independently for each group, showed that LFG increased serum BDNF levels (+ 203 pg/ml) and decreased α-synuclein levels (-1,703 pg/ml), while HFG showed the opposite effects (BDNF: -500 pg/ml; α-synuclein: + 1,413 pg/ml). CG showed a significant BDNF reduction over time. Both LFG and HFG showed significant improvements in several physical performance outcomes and the LFG showed better results than HFG. Concerning PFS-16, significant differences over time (b = -0.4, IC95% = -0.8/-0.0, p = 0.046) and among groups (among all groups p < 0.001) were found, and the LFG exhibited better results than the HFG (b = -1.0, IC95% = -1.3/-0.7, p < 0.001), and CG (b = -1.7, IC95% = -2.0/-1.4, p < 0.001) with this last one that worsened over time. Conclusion: LFG training was the best choice for improving or maintaining physical performance, fatigue perception and variation in serum biomarkers. Clinical trial registration: https://www.clinicaltrials.gov/ct2/show/NCT04878679, identifier NCT04878679.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Guideline / Prognostic_studies Language: En Journal: Front Aging Neurosci Year: 2023 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Guideline / Prognostic_studies Language: En Journal: Front Aging Neurosci Year: 2023 Document type: Article Affiliation country: Country of publication: