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Parkinson's disease (PD) is the most common neurodegenerative dyskinesia, with motor and non-motor features, caused by dopamine deficiency in the striatum, attributed to the degenerative nature of dopaminergic nerves in the substantia nigra
.
Current treatment for Parkinson's disease is primarily symptomatic, but treatments to change the condition are underway
.
However, some of the therapies under study have limited penetration into the blood-brain barrier (BBB) (e.
g.
, antibodies against α-synuclein) or use invasive neurosurgical delivery strategies (e.
g.
, convection-enhanced administration of growth factors [CED]
).
Gauccher Disease (GD) is an autosomal recessive lysosomal storage disorder attributed to the GBA1 mutation, and the risk of PD increases
in patients with Gauccher disease.
Magnetic resonance-guided focused ultrasound (MRgFUS), combined with microvesicles, is an emerging technique that enables transient permeability of the BBB and provides anatomically targeted drug delivery
to the brain.
With this, Ying Meng et al.
They explored the safety and feasibility
of MRgFUS intravenous GCase at increasing doses (15 to 30 to 60 IU/kg) every 2 weeks in four PD patients with GBA1 mutations.
BBB permeability was achieved in all patients and was quantified
by dynamic contrast-enhanced magnetic resonance imaging after treatment.
No serious adverse events
occurred.
Two patients developed transient dyskinesias
after treatment.
The Blind Movement Disorders Association-Unified Parkinson's Disease Rating Scale Exercise Score decreased by 12% from baseline at 6 months (from 26±9 to 22±6).
The normalized uptake value ratio for fluorodeoxyglucose positron emission tomography of the treated shell nucleus decreased from 1.
66±0.
14 to 1.
27±0.
08
.
The significance of this study lies in the discovery of the safety and feasibility of MRgFUS GCase delivery in PD and to support further research
into this approach.
Meng Y, Pople CB, Huang Y, et al.