Chen, Y., Li, J., Hu, Y., Zhang, H., Yang, X., Jiang, Y., Yao, Z., Chen, Y., Gao, Y., Tan, A., Liao, M., Lu, Z., Wu, C., Xian, X., Wei, S., Zhang, Z., Chen, W., Wei, G., Wang, Q., Mo, Z. (2017) Multi-factors including Inflammatory/Immune, Hormones, Tumor-related Proteins and Nutrition associated with Chronic Prostatitis NIH IIIa+b and IV based on FAMHES project. Scientific Reports, 7 (1), doi:10.1038/s41598-017-09751-8
Multi-factors including inflammatory/immune, hormones, tumor-related proteins and nutrition associated with chronic prostatitis NIH IIIa+b and IV based on FAMHES project
|Author:||Chen, Yang1,2,3,4,5; Li, Jie2,6; Hu, Yanling2,3,4,5;|
1Institute of Urology and Nephrology, The First Affiliated Hospital of Guangxi Medical University
2Center for Genomic and Personalized Medicine, Guangxi Medical University
3Guangxi key laboratory for genomic and personalized medicine
4Guangxi collaborative innovation center for genomic and personalized medicine
5Guangxi key laboratory of colleges and universities
6The Guangxi Zhuang Autonomous Region Family Planning Research Center
7Biocenter Oulu, University of Oulu
8Faculty of Biochemistry and Molecular Medicine, University of Oulu
|Online Access:||PDF Full Text (PDF, 2.7 MB)|
|Persistent link:|| http://urn.fi/urn:nbn:fi-fe2017101050006
|Publish Date:|| 2017-10-10
Chronic prostatitis (CP) is a complex disease. Fragmentary evidence suggests that factors such as infection and autoimmunity might be associated with CP. To further elucidate potential risk factors, the current study utilized the Fangchenggang Area Male Health and Examination Survey (FAMHES) project; where 22 inflammatory/immune markers, hormone markers, tumor-related proteins, and nutrition-related variables were investigated. We also performed baseline, regression, discriminant, and receiver operating characteristic (ROC) analyses. According to NIH-Chronic Prostatitis Symptom Index (NIH-CPSI), participants were divided into chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS, pain ≥ 4; divided into IIIa and IIIb sub-groups) and non-CPPS (pain = 0; divided into IV and normal sub-groups). Analyses revealed osteocalcin as a consistent protective factor for CP/CPPS, NIH-IIIb, and NIH-IV prostatitis. Further discriminant analysis revealed that ferritin (p = 0.002) and prostate-specific antigen (PSA) (p = 0.010) were significantly associated with NIH-IIIa and NIH-IV prostatitis, respectively. Moreover, ROC analysis suggested that ferritin was the most valuable independent predictor of NIH-IIIa prostatitis (AUC = 0.639, 95% CI = 0.534–0.745, p = 0.006). Together, our study revealed inflammatory/immune markers [immunoglobulin E, Complement (C3, C4), C-reactive protein, anti-streptolysin, and rheumatoid factors], hormone markers (osteocalcin, testosterone, follicle-stimulating hormone, and insulin), tumor-related proteins (carcinoembryonic and PSA), and a nutrition-related variable (ferritin) were significantly associated with CP or one of its subtypes.
|Type of Publication:||
A1 Journal article – refereed
|Field of Science:||
This study was funded by Guangxi Natural Science Fund for Innovation Research Team (2013GXNSFFA019002), Innovation Project of Guangxi Graduate Education (YCBZ2017037), Guangxi Collaborative Innovation Center for genomic and personalized medicine (201319), The Science and technology development plan of Guangxi (Guikegong 1355005-3-17), National Program on Key Basic Research Project (973 Program) (2012CB518303), Natural Science Foundation of China (81460388).
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