Polyunsaturated fatty acid levels in the cerebrospinal fluid of patients with Parkinson's disease and multiple system atrophy

2007 ◽  
Vol 23 (2) ◽  
pp. 309-310 ◽  
Author(s):  
Phil Hyu Lee ◽  
Gwang Lee ◽  
Man-Jeong Paik
2010 ◽  
Vol 411 (19-20) ◽  
pp. 1532-1535 ◽  
Author(s):  
Man-Jeong Paik ◽  
Young-Hwan Ahn ◽  
Phil Hyu Lee ◽  
Hyunseung Kang ◽  
Chan Bae Park ◽  
...  

2004 ◽  
Vol 19 (5) ◽  
pp. 571-579 ◽  
Author(s):  
W. Farid Abdo ◽  
Dani�lle De Jong ◽  
Jan C.M. Hendriks ◽  
Martin W.I.M. Horstink ◽  
Berry P.H. Kremer ◽  
...  

2012 ◽  
Vol 27 (7) ◽  
pp. 851-857 ◽  
Author(s):  
Noriko Ishigami ◽  
Takahiko Tokuda ◽  
Masaya Ikegawa ◽  
Mika Komori ◽  
Takashi Kasai ◽  
...  

2021 ◽  
Vol 2021 ◽  
pp. 1-9
Author(s):  
Dan Xie ◽  
Ling Feng ◽  
Hongyan Huang ◽  
Quanzhen Zhao ◽  
Pingping Ning ◽  
...  

Objective. To investigate the differences of candidate cerebrospinal fluid (CSF) biomarkers associated with multiple system atrophy (MSA) and Parkinson’s disease (PD). Method. Here, a systematic review and meta-analysis were conducted on studies related to CSF biomarkers associated with MSA and PD obtained from PubMed, Web of Science, Embase, and Cochrane databases. Data were pooled where appropriate and used to calculate standardized mean differences (SMDs) with 95% confidence intervals (CI). Heterogeneity was assessed using the I 2 statistic while Egger’s test was used to test for existing publication bias. Results. MSA patients had higher CSF t-tau ( SMD = 0.41 , 95% CI: 0.10 to 0.72) and YKL-40 ( SMD = 0.63 , 95% CI 0.12 to1.15) as well as DJ-1 ( SMD = 1.05 , 95% CI 0.67 to 1.42) levels than PD patients, while CSF p-tau ( SMD = − 0.17 , 95% CI, -0.31 to -0.02) and Aβ-42 ( SMD = − 0.33 , 95% CI, -0.55 to -0.12) levels in MSA patients were lower than those in PD patients. There were no differences in CSF’s GFAP and Flt3 ligand levels in both MSA and PD patients. Conclusion. The study revealed the differences in CSF biomarker levels between MSA and PD cohorts that can be further explored to clinically distinguish MSA from PD.


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