Combination immunosuppressant therapy and lupus nephritis outcome: a hospital-based study

医学 狼疮性肾炎 内科学 危险系数 优势比 胃肠病学 系统性红斑狼疮 终末期肾病 置信区间 肾病科 肌酐 肾活检 回顾性队列研究 尿检 疾病 肾功能 泌尿系统
作者
Y M Chen,Wei Ting Hung,Ying‐Chieh Liao,Chiann‐Yi Hsu,Tsu‐Yi Hsieh,Hsiao‐Huei Chen,Chia‐Wei Hsieh,Ching‐Heng Lin,Kuo-Lung Lai,Kuo‐Tung Tang,Chih‐Wei Tseng,Wen Nan Huang,Y H Chen
出处
期刊:Lupus [SAGE Publishing]
卷期号:28 (5): 658-666 被引量:3
标识
DOI:10.1177/0961203319842663
摘要

Lupus nephritis (LN) is the leading cause of mortality in lupus patients. This study aimed to investigate the treatment outcome and renal histological risk factors of LN in a tertiary referral center. Between 2006 and 2017, a retrospective observational study enrolled 148 biopsy-proven LN patients. After propensity score matching, 75 cases were included for further analysis. The classification and scoring of LN were assessed according to the International Society of Nephrology/Renal Pathology Society. Treatment response was evaluated by daily urine protein and urinalysis at two years after commencing induction treatment and the development of end-stage renal disease (ESRD). In total, 50.7% patients achieved complete remission (CR) or partial remission (PR), while 49.3% patients were categorized as nonresponders. Therapeutic responses in terms of CR/PR rates were associated with Systemic Lupus Erythematosus Disease Activity Index scores (odds ratio (OR): 1.34, 95% confidence interval (CI): 1.12–1.60, p = 0.001). Moreover, higher baseline creatinine levels (hazard ratio (HR): 2.10, 95% CI: 1.29–3.40, p = 0.003), higher renal activity index (HR: 1.30, 95% CI: 1.07–1.58, p = 0.008) and chronicity index (HR: 1.40, 95% CI: 1.06–1.85, p = 0.017) predicted ESRD. Among pathological scores, cellular crescents (HR: 4.42, 95% CI: 1.01–19.38, p = 0.049) and fibrous crescents (HR: 5.93, 95% CI: 1.41–24.92, p = 0.015) were independent risk factors for ESRD. In conclusion, higher lupus activity was a good prognostic marker for renal remission. Renal histology was predictive of ESRD. Large-scale prospective studies are required to verify the efficacy of mycophenolate in combination with azathioprine or cyclosporine in LN patients.

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