First-in-human trial of blood–brain barrier opening in amyotrophic lateral sclerosis using MR-guided focused ultrasound

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作者
Agessandro Abrahao
Ying Meng
Maheleth Llinas
Yuexi Huang
Clement Hamani
Todd Mainprize
Isabelle Aubert
Chinthaka Heyn
Sandra E. Black
Kullervo Hynynen
Nir Lipsman
Lorne Zinman
机构
[1] University of Toronto,Division of Neurology, Department of Medicine, Sunnybrook Health Sciences Centre
[2] University of Toronto,Hurvitz Brain Sciences Research Program, Sunnybrook Research Institute, Sunnybrook Health Sciences Centre
[3] Sunnybrook Research Institute,Harquail Centre for Neuromodulation
[4] University of Toronto,Division of Neurosurgery, Sunnybrook Health Sciences Centre
[5] University of Toronto,Sunnybrook Research Institute, Sunnybrook Health Sciences Centre
[6] University of Toronto,Department of Laboratory Medicine and Pathobiology
[7] University of Toronto,Department of Medical Imaging, Sunnybrook Health Sciences Centre
[8] University of Toronto,Odette Cancer Research, Sunnybrook Research Institute, Sunnybrook Health Sciences Centre
[9] University of Toronto,Institute of Biomaterials and Biomedical Engineering
[10] University of Toronto,Department of Medical Biophysics
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摘要
MR-guided focused ultrasound (MRgFUS) is an emerging technology that can accurately and transiently permeabilize the blood-brain barrier (BBB) for targeted drug delivery to the central nervous system. We conducted a single-arm, first-in-human trial to investigate the safety and feasibility of MRgFUS-induced BBB opening in eloquent primary motor cortex in four volunteers with amyotrophic lateral sclerosis (ALS). Here, we show successful BBB opening using MRgFUS as demonstrated by gadolinium leakage at the target site immediately after sonication in all subjects, which normalized 24 hours later. The procedure was well-tolerated with no serious clinical, radiologic or electroencephalographic adverse events. This study demonstrates that non-invasive BBB permeabilization over the motor cortex using MRgFUS is safe, feasible, and reversible in ALS subjects. In future, MRgFUS can be coupled with promising therapeutics providing a targeted delivery platform in ALS.
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