12-Week Aerobic Interval Training Boosts Neuroplasticity and Motor Function in Parkinson’s Disease: Insights From BDNF, [ <sup>18</sup> F]Fluorodopa PET/CT, and EEG

BackgroundAnimal models suggest that intensive physical training may promote neuroplasticity in Parkinson's disease (PD), but its effects in humans remain underexplored.ObjectivesTo investigate the effects of aerobic interval training (AIT) on brain-derived neurotrophic factor (BDNF) levels, striatal [<sup>18</sup>F]fluorodopa positron emission tomography/computed tomography (PET/CT) uptake ([<sup>18</sup>F]DOPA<sub>PET/CT</sub>), electroencephalography (EEG), and motor function, and to explore their interrelations.MethodsThirty PD patients were randomly assigned to a 12-week moderate-intensity AIT group (PD Training Group [PD-TR], n = 15) or a non-training group (PD Non-Training Group, n = 15). Pre- and post-intervention assessments included BDNF levels, striatal [<sup>18</sup>F]DOPA<sub>PET/CT</sub>, EEG during motor task-evoked desynchronization (ERD<sub>MT</sub>) and rest-evoked synchronization (ERS<sub>REST</sub>) in primary motor cortex (M1) and supplementary motor area (SMA), and motor function assessed using the Unified PD Rating Scale (UPDRS) Part III and the Manual Bradykinesia Score for the Affected Upper Extremity (MBS-AUE) calculated as the sum of UPDRS items 3.4 to 3.6.ResultsThe PD-TR group showed increased BDNF levels (<i>P</i> < .001) and improved motor scores (UPDRS III and MBS-AUE; <i>P</i> < .05). Both groups exhibited increased EEG-ERS<sub>REST</sub> M1 (<i>P</i> < .05) over time, with no changes in striatal [<sup>18</sup>F]DOPA<sub>PET/CT</sub> uptake. Significant group differences were observed in correlations between changes (Δ = POST minus PRE) in: ΔBDNF with Δ[<sup>18</sup>F] DOPA<sub>PET/CT</sub> uptake in the putamen and ΔEEG-ERD<sub>MT</sub> M1 (<i>P</i> < .001); Δ[<sup>18</sup>F]DOPA<sub>PET/CT</sub> uptake in the putamen with Δ[<sup>18</sup>F]DOPA<sub>PET/CT</sub> uptake in the caudate and ΔEEG-ERS<sub>REST</sub> SMA (<i>P</i> < .05); ΔMBS-AUE scores with ΔEEG-ERS<sub>REST</sub> SMA (<i>P</i> < .001).ConclusionsTwelve-week AIT enhanced BDNF levels and motor function in PD-TR, with central nervous system neuroplasticity supporting motor recovery.

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Journal
Neurorehabilitation and neural repair
Published
2025-08-12
DOI
https://doi.org/10.1177/15459683251360729
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1
Primary Topic
Muscle activation and electromyography studies
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article
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article

12-Week Aerobic Interval Training Boosts Neuroplasticity and Motor Function in Parkinson’s Disease: Insights From BDNF, [ 18 F]Fluorodopa PET/CT, and EEG

Katarzyna Markowska, Leszek Królicki, Magdalena Koszewicz, Joanna Mączewska et al.
1 citations
Neurorehabilitation and neural repair
Muscle activation and electromyography studies
0.67
article

12-Week Aerobic Interval Training Boosts Neuroplasticity and Motor Function in Parkinson’s Disease: Insights From BDNF, [ 18 F]Fluorodopa PET/CT, and EEG

Katarzyna Markowska, Leszek Królicki, Magdalena Koszewicz, Joanna Mączewska, Józef Langfort, Jarosław Marusiak, Karolina Lorek, Zbigniew Wroński, Sławomir Budrewićz, Małgorzata Chalimoniuk
article en
1 citations

Abstract

BackgroundAnimal models suggest that intensive physical training may promote neuroplasticity in Parkinson's disease (PD), but its effects in humans remain underexplored.ObjectivesTo investigate the effects of aerobic interval training (AIT) on brain-derived neurotrophic factor (BDNF) levels, striatal [<sup>18</sup>F]fluorodopa positron emission tomography/computed tomography (PET/CT) uptake ([<sup>18</sup>F]DOPA<sub>PET/CT</sub>), electroencephalography (EEG), and motor function, and to explore their interrelations.MethodsThirty PD patients were randomly assigned to a 12-week moderate-intensity AIT group (PD Training Group [PD-TR], n = 15) or a non-training group (PD Non-Training Group, n = 15). Pre- and post-intervention assessments included BDNF levels, striatal [<sup>18</sup>F]DOPA<sub>PET/CT</sub>, EEG during motor task-evoked desynchronization (ERD<sub>MT</sub>) and rest-evoked synchronization (ERS<sub>REST</sub>) in primary motor cortex (M1) and supplementary motor area (SMA), and motor function assessed using the Unified PD Rating Scale (UPDRS) Part III and the Manual Bradykinesia Score for the Affected Upper Extremity (MBS-AUE) calculated as the sum of UPDRS items 3.4 to 3.6.ResultsThe PD-TR group showed increased BDNF levels (<i>P</i> < .001) and improved motor scores (UPDRS III and MBS-AUE; <i>P</i> < .05). Both groups exhibited increased EEG-ERS<sub>REST</sub> M1 (<i>P</i> < .05) over time, with no changes in striatal [<sup>18</sup>F]DOPA<sub>PET/CT</sub> uptake. Significant group differences were observed in correlations between changes (Δ = POST minus PRE) in: ΔBDNF with Δ[<sup>18</sup>F] DOPA<sub>PET/CT</sub> uptake in the putamen and ΔEEG-ERD<sub>MT</sub> M1 (<i>P</i> < .001); Δ[<sup>18</sup>F]DOPA<sub>PET/CT</sub> uptake in the putamen with Δ[<sup>18</sup>F]DOPA<sub>PET/CT</sub> uptake in the caudate and ΔEEG-ERS<sub>REST</sub> SMA (<i>P</i> < .05); ΔMBS-AUE scores with ΔEEG-ERS<sub>REST</sub> SMA (<i>P</i> < .001).ConclusionsTwelve-week AIT enhanced BDNF levels and motor function in PD-TR, with central nervous system neuroplasticity supporting motor recovery.

Neurorehabilitation and neural repairVol. 39(11)
Medical University of Warsaw (PL), Wroclaw Medical University (PL), Wroclaw University of Health and Sport Sciences (PL), Akademii Wychowania Fizycznego im. Jerzego Kukuczki w Katowicach (PL), Józef Piłsudski University of Physical Education in Warsaw (PL)
Openalex Percentile: Top 28%
Muscle activation and electromyography studies
0.67
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