Authors Patients | Product | Observ. time (months) | Characteristics/ Dosages/Application | Outcome (* = p < 0.05 / ** = p < 0.01) |
---|---|---|---|---|
Venkataramana, Pal et al. [65] | Allogenic | 3, 6, 12 | 1. PD patients with bilateral subventricular intracerebral application of 2×106 /kg bodyweight MSCs in 2 ml (n = 8) | UPDRS in ON/OFF: |
PD patients | MSCs |  | 2. MSA + PSP patients with bilateral subventricular intracerebral application of 2×106 /kg bodyweight MSCs in 2 ml (n = 4) | a. In PD patients: permanently improved* compared with baseline during both ON (18%: 51.2 versus 62.3) and OFF (31.2%: 59.5 versus 86.5). Effect stronger in patients with disease duration < 5 years (ON 45.5%/ OFF 56.7%) as compared to patients with a duration > 10 years (ON 6.3% OFF 12.4%). |
MSA patients | b. Some MSA/PSP patients temporarily improved. The effect was not correlated with disease severity and disease duration. MR-tractography: | |||
PSP patients | a. PD patients, after implantation, did show a trend of steadily improvement in tractographical images in genu and peduncles. | |||
Open Label | b. MSA/PSP patients showed further reduction of tractographical images after stem cell implantation. | |||
Venkataramana, Kumar et al. [64] | Autologous MSCs | 10-36 | PD patients (n = 7) with an UPDRS ON/OFF score 50.6/65.0 and a mean disease duration of 14.7 yr treated with 106 MSCs/kg bodyweight in the subventricular zone | UPDRS in ON/OFF: |
PD patients | Â | Â | a. In 3/7 patients there was a stable improvement of ON/OFF scores of 38% respect 22.9% with unchanged anti-parkinsonian medication. | |
Open Label | Â | Â | b. In 3/7 patients after treatment, only marginal clinical effects were observed | |
Anti-parkinsonian medication significantly reduced in 2 patients. | ||||
Lee, kim et al. [63] | Autologous MSCs | 1, 2, 3, 4, 5, 6, 8, 10, 12 | Patients with Cognitive intact MSA-C (with UMSARS scores between 30 to 50) | UMSARS score |
a. MSCs-treated patients showed a reduced* increase of UMSARS score compared to placebo treated patients. | ||||
MSA patients | 1. Placebo group: Intravenous or intra-arterial placebo (n = 17) | b. Intra-arterial application of MSCs was complicated with some MRI-detectable ischemic lesions | ||
Cognitive functions: | ||||
Significantly* worsened in the placebo, but not in the MSCs-treated patients | ||||
Placebo controlled | 2. MSCs group: 4×106 MSCs intravenously or intra-arterial (n = 14) | MRI and FDG PET: | ||
Showed significantly increased* gray cerebral cortical areas respectively more decreased cortical and cerebellar glucose metabolism in placebo-treated, as compared to MSCs-treated patients. |