The association between the C-reactive protein gene +1444C/T polymorphism and Parkinson's disease susceptibility in a Chinese population

Gene ◽  
2020 ◽  
Vol 753 ◽  
pp. 144808
Author(s):  
Xiong Wang ◽  
Yawei Fan ◽  
Lu Wang ◽  
Bo Chen ◽  
Yanjun Lu ◽  
...  
2018 ◽  
Vol 40 (1) ◽  
pp. 167-173 ◽  
Author(s):  
Aslıhan Baran ◽  
Mahmut Bulut ◽  
Mehmet Cemal Kaya ◽  
Özlem Demirpençe ◽  
Bünyamin Sevim ◽  
...  

2020 ◽  
Vol 2 (2) ◽  
Author(s):  
Can Cui ◽  
Jiangwei Sun ◽  
Yudi Pawitan ◽  
Fredrik Piehl ◽  
Honglei Chen ◽  
...  

Abstract Serum creatinine and C-reactive protein have been proposed as potential biomarkers for neurodegenerative diseases, including amyotrophic lateral sclerosis, multiple sclerosis and Parkinson’s disease. However, longitudinal studies investigating temporal patterns of these biomarkers, including the phase before diagnosis, are rare. We performed a case–control study including all newly diagnosed patients with amyotrophic lateral sclerosis (N = 525), multiple sclerosis (N = 1815) or Parkinson’s disease (N = 3797) during 2006–2013 in Stockholm, Sweden, who participated in the Stockholm CREAtinine Measurements (SCREAM) project. For each case, we randomly selected up to five controls from SCREAM that were individually matched to the case by age, sex and county of residence (N = 2625 for amyotrophic lateral sclerosis, N = 9063 for multiple sclerosis and 18 960 for Parkinson’s disease). We collected for both the cases and the controls testing results of serum creatinine and C-reactive protein performed by healthcare providers in Stockholm during the study period. Median levels of creatinine and C-reactive protein were visualized using locally weighted smoothing curves among cases and controls. A linear mixed model was also applied to explore temporal changes within an individual. Compared to controls, patients with amyotrophic lateral sclerosis had lower levels of creatinine from 2 years before diagnosis onwards. In contrast, patients with amyotrophic lateral sclerosis had lower levels of C-reactive protein before diagnosis but higher levels after diagnosis, compared to controls. Focusing the 2 years before to 2 years after diagnosis, patients with amyotrophic lateral sclerosis displayed statistically significantly decreasing level of creatinine from 1 year before diagnosis until 2 years after diagnosis, whereas increasing level of C-reactive protein from diagnosis until 2 years after diagnosis. There were no similar patterns noted among patients with multiple sclerosis or Parkinson’s disease, or the controls of the three patient groups. Patients with amyotrophic lateral sclerosis display distinct temporal patterns of creatinine and C-reactive protein before and after diagnosis, compared to amyotrophic lateral sclerosis-free controls or patients with multiple sclerosis and Parkinson’s disease.


PLoS ONE ◽  
2014 ◽  
Vol 9 (1) ◽  
pp. e85886 ◽  
Author(s):  
Hideyuki Sawada ◽  
Tomoko Oeda ◽  
Atsushi Umemura ◽  
Satoshi Tomita ◽  
Ryutaro Hayashi ◽  
...  

2011 ◽  
Vol 119 (1) ◽  
pp. 53-57 ◽  
Author(s):  
Uwe Walter ◽  
Rike Witt ◽  
Alexander Wolters ◽  
Matthias Wittstock ◽  
Reiner Benecke

2021 ◽  
pp. 1-12
Author(s):  
Lisanne J. Dommershuijsen ◽  
Rikje Ruiter ◽  
Nicole S. Erler ◽  
Dimitris Rizopoulos ◽  
M. Arfan Ikram ◽  
...  

Background: The immune system is known to be involved in Parkinson’s disease (PD) pathogenesis, but the temporal relationship between peripheral immune responses and PD remains unknown. Objective: We determined the association between peripheral immune cell numbers, C-Reactive protein (CRP), and prevalent as well as incident PD. Methods: This study was embedded in the population-based setting of the Rotterdam Study. We repeatedly measured peripheral immune cell numbers (differential leukocyte count and platelet count, granulocyte-to-lymphocyte ratio [GLR], platelet-to-lymphocyte ratio [PLR], and adapted systemic immune-inflammation index [adapted SII]) and CRP between 1990 and 2016. Participants were continuously followed-up for PD until 2018. We estimated the association of the markers with prevalent and incident PD using logistic regression models and joint models, respectively. Models were adjusted for age, sex, smoking, body mass index, and medication use. Odds ratios (OR) and hazard ratios (HR) are shown per doubling of the marker. Results: A total of 12,642 participants were included in this study. The mean age (standard deviation) was 65.1 (9.8) years and 57.5%were women. Participants with a higher lymphocyte count were less likely to have prevalent PD (adjusted OR: 0.34, 95%CI 0.17–0.68). Participants with a higher GLR, PLR, and adapted SII were more likely to have prevalent PD, but these effects were explained by the lymphocyte count. The peripheral immune cell numbers and CRP were not significantly associated with the risk of incident PD. Conclusion: We found participants with a higher lymphocyte count to be less likely to have prevalent PD, but we did not find an association between peripheral immune cell numbers nor CRP and the risk of incident PD.


2019 ◽  
Vol 126 (12) ◽  
pp. 1599-1608 ◽  
Author(s):  
Diego Santos-García ◽  
◽  
T. de Deus Fonticoba ◽  
E. Suárez Castro ◽  
A. Aneiros Díaz ◽  
...  

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