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dc.contributor.authorChiu, Hsien-Yien_US
dc.contributor.authorHuang, Hui-Lingen_US
dc.contributor.authorLi, Chien-Hsunen_US
dc.contributor.authorChen, Hung-Anen_US
dc.contributor.authorYeh, Chia-Lunen_US
dc.contributor.authorChiu, Shih-Hsiangen_US
dc.contributor.authorLin, Wei-Chunen_US
dc.contributor.authorCheng, Yu-Pinen_US
dc.contributor.authorTsai, Tsen-Fangen_US
dc.contributor.authorHo, Shinn-Yingen_US
dc.date.accessioned2019-04-03T06:35:33Z-
dc.date.available2019-04-03T06:35:33Z-
dc.date.issued2015-09-25en_US
dc.identifier.issn1932-6203en_US
dc.identifier.urihttp://dx.doi.org/10.1371/journal.pone.0136508en_US
dc.identifier.urihttp://hdl.handle.net/11536/128272-
dc.description.abstractBackground and Objectives There have been few large population-based studies of the association between rheumatoid arthritis (RA) and chronic kidney disease (CKD) and glomerulonephritis. This nationwide cohort study investigated the risks of developing CKD and glomerulonephritis in patients with RA, and the associated risks for cardiovascular complications. Methods From the Taiwan National Health Insurance Research Database, we identified a study cohort of 12,579 patients with RA and randomly selected 37,737 subjects without RA as a control cohort. Each subject was individually followed for up for 5 years, and the risk of CKD was analyzed using Cox proportional hazards regression models. Results During the follow-up period, after adjusting for traditional cardiovascular risk factors RA was independently associated with a significantly increased risk of CKD (adjusted hazard ratio [aHR] 1.31; 95% confidence interval [CI] 1.23-1.40) and glomerulonephritis (aHR 1.55; 95% CI 1.37-1.76). Increased risk of CKD was also associated with the use of non-steroidal anti-inflammatory drugs, cyclosporine, glucocorticoids, mycophenolate mofetil, and cyclophosphamide. Patients with comorbidities had even greater increased risk of CKD. Moreover, RA patients with concurrent CKD had significantly higher likelihood of developing ischemic heart disease and stroke. Conclusions RA patients had higher risk of developing CKD and glomerulonephritis, independent of traditional cardiovascular risk factors. Their increased risk of CKD may be attributed to glomerulonephritis, chronic inflammation, comorbidities, and renal toxicity of antirheumatic drugs. Careful monitoring of renal function in RA patients and tight control of their comorbid diseases and cardiovascular risk factors are warranted.en_US
dc.language.isoen_USen_US
dc.titleIncreased Risk of Chronic Kidney Disease in Rheumatoid Arthritis Associated with Cardiovascular Complications - A National Population-Based Cohort Studyen_US
dc.typeArticleen_US
dc.identifier.doi10.1371/journal.pone.0136508en_US
dc.identifier.journalPLOS ONEen_US
dc.citation.volume10en_US
dc.citation.issue9en_US
dc.citation.spage0en_US
dc.citation.epage0en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.department生物資訊及系統生物研究所zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.contributor.departmentInstitude of Bioinformatics and Systems Biologyen_US
dc.identifier.wosnumberWOS:000361800700012en_US
dc.citation.woscount37en_US
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