Neuroprotection of Granulocyte Colony-Stimulating Factor for Early Stage Parkinson's Disease
Author(s) -
ShengTzung Tsai,
Sung-Chao Chu,
ShuHsin Liu,
ChengYoong Pang,
Ting-Wen Hou,
ShinnZong Lin,
Shin-Yuan Chen
Publication year - 2017
Publication title -
cell transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.043
H-Index - 100
eISSN - 1555-3892
pISSN - 0963-6897
DOI - 10.3727/096368916x694247
Subject(s) - medicine , neuroprotection , parkinson's disease , granulocyte colony stimulating factor , nausea , gastroenterology , dopaminergic , adverse effect , pathology , disease , dopamine , chemotherapy
Parkinson's disease (PD) is a slowly progressive neurodegenerative disease. Both medical and surgical choices provide symptomatic treatment. Granulocyte colony-stimulating factor (G-CSF), a conventional treatment for hematological diseases, has demonstrated its effectiveness in acute and chronic neurological diseases through its anti-inflammatory and antiapoptosis mechanisms. Based on previous in vitro and in vivo studies, we administered a lower dose (3.3 μg/kg) G-CSF injection for 5 days and six courses for 1 year in early-stage PD patients as a phase I trial. The four PD patient's mean unified PD rating scale motor scores in medication off status remained stable from 23 before the first G-CSF injection to 22 during the 2-year follow-up. 3,4-Dihydroxy-6- 18 F-fluoro-L-phenylalanine ( 18 F-DOPA) positron emission tomography (PET) studies also revealed an annual 3.5% decrease in radiotracer uptake over the caudate nucleus and 7% in the putamen, both slower than those of previous reports of PD. Adverse effects included transient muscular–skeletal pain, nausea, vomiting, and elevated liver enzymes. Based on this preliminary report, G-CSF seems to alleviate disease deterioration for early stage PD patients. The effectiveness of G-CSF was possibly due to its amelioration of progressive dopaminergic neuron degeneration.
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