Gene therapy reduces Parkinson's disease symptoms by reorganizing functional brain connectivity

被引:70
作者
Niethammer, Martin [1 ]
Tang, Chris C. [1 ]
Vo, An [1 ]
Nguyen, Nha [2 ]
Spetsieris, Phoebe [1 ]
Dhawan, Vijay [1 ]
Ma, Yilong [1 ]
Small, Michael [1 ]
Feigin, Andrew [1 ,5 ]
During, Matthew J. [3 ]
Kaplitt, Michael G. [4 ]
Eidelberg, David [1 ]
机构
[1] Feinstein Inst Med Res, Ctr Neurosci, Manhasset, NY 10030 USA
[2] Univ Penn, Perelman Sch Med, Inst Diabet Obes & Metab, Philadelphia, PA 19104 USA
[3] Ovid Therapeut, New York, NY 10036 USA
[4] Weill Cornell Med Coll, Dept Neurol Surg, New York, NY 10065 USA
[5] NYU Langone Hlth, Dept Neurol, New York, NY 10016 USA
关键词
SUBTHALAMIC NUCLEUS; NETWORK MODULATION; METABOLIC NETWORK; SHAM-SURGERY; DOUBLE-BLIND; GAD GENE; LEVODOPA; STIMULATION; PROGRESSION; TRIALS;
D O I
10.1126/scitranslmed.aau0713
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Gene therapy is emerging as a promising approach for treating neurological disorders, including Parkinson's disease (PD). A phase 2 clinical trial showed that delivering glutamic acid decarboxylase (GAD) into the subthalamic nucleus (STN) of patients with PD had therapeutic effects. To determine the mechanism underlying this response, we analyzed metabolic imaging data from patients who received gene therapy and those randomized to sham surgery, all of whom had been scanned preoperatively and at 6 and 12 months after surgery. Those who received GAD gene therapy developed a unique treatment-dependent polysynaptic brain circuit that we termed as the GAD-related pattern (GADRP), which reflected the formation of new polysynaptic functional pathways linking the STN to motor cortical regions. Patients in both the treatment group and the sham group expressed the previously reported placebo network (the sham surgery-related pattern or SSRP) when blinded to the treatment received. However, only the appearance of the GADRP correlated with clinical improvement in the gene therapy-treated subjects. Treatment-induced brain circuits can thus be useful in clinical trials for isolating true treatment responses and providing insight into their underlying biological mechanisms.
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页数:11
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