Initial serum creatinine concentration affects clinical outcomes in patients with IgA nephropathy treated with mycophenolate mofetil combined with low-dose prednisone

被引:1
|
作者
Song, Haiying [1 ,2 ]
Hu, Haofei [1 ,2 ]
Tang, Fei [1 ,2 ]
Cao, Changchun [1 ,2 ]
Wan, Qijun [1 ,2 ]
He, Yongcheng [1 ,2 ]
机构
[1] Shenzhen Univ, Shenzhen Peoples Hosp 2, Affiliated Hosp 1, Dept Nephrol, 3002 Sungang Rd, Shenzhen 518035, Guangdong, Peoples R China
[2] Shenzhen Univ, Hlth Sci Ctr, Dept Nephrol, Shenzhen 518035, Guangdong, Peoples R China
关键词
IgA nephropathy; mycophenolate mofetil; serum creatinine; clinical outcome; IMMUNOGLOBULIN-A NEPHROPATHY; RANDOMIZED CONTROLLED-TRIAL; CHRONIC KIDNEY-DISEASE; OXFORD CLASSIFICATION; NATURAL-HISTORY; RISK-FACTORS; INTRAVENOUS CYCLOPHOSPHAMIDE; LONG-TERM; THERAPY; METAANALYSIS;
D O I
10.3892/etm.2020.8573
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Indicators for predicting the efficacy of mycophenolate mofetil (MMF) have so far remained elusive. The present study aimed to identify predictive indicators of the efficacy of MMF combined with low-dose prednisone in patients with IgA nephropathy. A total of 598 patients presenting with primary IgA nephropathy at our center were screened. Patients were followed up for 18 months, where the end-point was defined as complete clinical remission. Cox proportional hazards models were performed for analyzing the initial serum creatinine (SCr) concentration to predict incomplete clinical remission. In total, 7 of 71 patients (9.86%) were in complete clinical remission at the final visit. Logistic regression indicated that the hazard ratio (HR) for quartile 4 was significantly higher than the HR for quartile 1 (quartile 4 vs. quartile 1: HR, 2.51; 95% CI, 1.20-5.21; P=0.01). Additional adjustment for the confounding variables, including age, sex, systolic BP, diastolic BP, proteinuria, uric acid, serum triglyceride, hemoglobin, serum albumin, serum total cholesterol and The Oxford classification of the models, did not reduce the HRs for the association between the initial SCr concentration and risk of incomplete clinical remission (quartile 4 vs. quartile 1: HR, 7.27; 95% CI, 1.21-43.63; P=0.03). Each unit increase in the initial SCr concentration was associated with a 67 and 194% increase in the risk of incomplete clinical remission based on model 1 (95% CI, 1.02-2.73; P=0.04) and model 2 (95% CI, 1.01-8.60; P=0.048), respectively. In conclusion, in the present cohort of patients with IgA nephropathy treated with MMF plus low-dose prednisone, the initial SCr concentration was an independent risk factor for incomplete clinical remission.
引用
收藏
页码:3369 / 3376
页数:8
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