Efficacy and safety of calcineurin inhibitor treatment for IgA nephropathy: a meta-analysis

被引:39
作者
Song, Yu-Huan [1 ,2 ]
Cai, Guang-Yan [1 ]
Xiao, Yue-Fei [2 ]
Wang, Yi-Ping [2 ]
Yuan, Bao-Shi [2 ]
Xia, Yuan-Yuan
Wang, Si-Yang [1 ]
Chen, Pu [1 ]
Liu, Shu-Wen [1 ]
Chen, Xiang-Mei [1 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Chinese PLA Inst Nephrol, Natl Clin Res Ctr Kidney Dis, Dept Nephrol,State Key Lab Kidney Dis, 28 Fuxing Rd, Beijing 100853, Peoples R China
[2] Aerosp Cent Hosp, Dept Nephrol, Beijing, Peoples R China
来源
BMC NEPHROLOGY | 2017年 / 18卷
关键词
IgA nephropathy; Calcineurin inhibitor; Cyclosporine A; Tacrolimus; IMMUNOGLOBULIN-A NEPHROPATHY; CYCLOSPORINE-A; IMMUNOSUPPRESSIVE THERAPY; CONTROLLED-TRIAL; NATURAL-HISTORY; CLINICAL-TRIALS; TACROLIMUS; GLOMERULONEPHRITIS; PROTEINURIA; PROGRESSION;
D O I
10.1186/s12882-017-0467-z
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: IgA nephropathy is the most common progressive glomerular disease to end stage renal failure worldwide. Calcineurin inhibitors (CNIs) is a selective immunosuppressant widely used in organ transplantation. The efficacy and safety of calcineurin inhibitors for the treatment of IgA nephropathy remain uncertain. Methods: We performed a systematic literature search using the PubMed, Embase, Science Citation Index, Ovid evidence-based medicine, Chinese Biomedical Literature (CBM) and Chinese science and technology periodicals (CNKI, VIP, and Wan Fang) for randomized, controlled trials of CNIs therapy of IgA nephropathy. Complete remission rate (CR) was defined as proteinuria less than 0.5 or 0.3 g/d. Partial remission rate (PR) was defined as proteinuria reduced to at least half of the baseline measurement and an absolute value of >0.5 or 0.3 g/d. Results: Seven relevant trials were conducted with 374 patients enrolled. CNIs plus medium/low-dose steroid had a higher CR (RR = 2.51 [95% CI, 1.25 to 5.04], P = 0.02) compared to therapy with steroid alone or placebo, but were not significant on PR (RR = 0.87 [95% CI, 0.32 to 2.38]; P = 0.78). Also, significant alterations were observed in proteinuria (weighted mean difference, -0.46 g/d,[95% CI:-0.55 to -0.24], P < 0.01) with no differences were found in serum creatinine (SCr) (weighted mean difference, 0.57,95% CI:-4.05 to 5.19; P = 0.78) and estimated glomerular filtration rate (eGFR) (weighted mean difference, 1.13,95% CI:-4.05 to 6.32; P = 0.34) level between the two groups. CNI therapy was associated with an increased risk for adverse events (RR = 2.21,95% CI: 1.52 to 3.21, P < 0.01), such as gastrointestinal and neurological symptoms or hirsutism. Conclusions: CNIs might provide renal protection in patients with IgAN, but at an increased risk of adverse events. Reliably defining the efficacy and safety of CNIs in IgAN requires a high-quality trial with a large sample size.
引用
收藏
页数:9
相关论文
共 39 条
[1]  
[Anonymous], INT J PHOTOENERGY, DOI DOI 10.1371/J0URNAL.P0NE.0051280
[2]  
Arikan H, 2008, J NEPHROL, V21, P713
[3]   Predicting progression in IgA nephropathy [J].
Bartosik, LP ;
Lajoie, G ;
Sugar, L ;
Cattran, DC .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2001, 38 (04) :728-735
[4]   TOWARD INDIVIDUAL PROGNOSIS OF IGA NEPHROPATHY [J].
BEUKHOF, JR ;
KARDAUN, O ;
SCHAAFSMA, W ;
POORTEMA, K ;
DONKER, AJM ;
HOEDEMAEKER, PJ ;
VANDERHEM, GK .
KIDNEY INTERNATIONAL, 1986, 29 (02) :549-556
[5]   Immunoglobulin A Nephropathy in China: Progress and Challenges [J].
Cai, Guang-Yan ;
Chen, Xiang-Mei .
AMERICAN JOURNAL OF NEPHROLOGY, 2009, 30 (03) :268-273
[6]  
CATTRAN DC, 1991, CLIN NEPHROL, V35, pS43
[7]   Long term treatment of IgA nephropathy with cyclosporine A [J].
Chábová, V ;
Tesar, V ;
Zabka, J ;
Rychlik, I ;
Merta, M ;
Jirsa, M ;
Stejskalová, A .
RENAL FAILURE, 2000, 22 (01) :55-62
[8]   Natural history of idiopathic IgA nephropathy: Role of clinical and histological prognostic factors [J].
D'Amico, G .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2000, 36 (02) :227-237
[9]   Tacrolimus is an alternative therapy option for the treatment of adult steroid-resistant nephrotic syndrome: a prospective, multicenter clinical trial [J].
Fan, Li ;
Liu, Qinghua ;
Liao, Yunhua ;
Li, Zhibin ;
Ji, Yulian ;
Yang, Zhenhua ;
Chen, Jian ;
Fu, Junzhou ;
Zhang, Jinli ;
Kong, Yaozhong ;
Fu, Ping ;
Lou, Tanqi ;
Liu, Zhengrong ;
Yu, Xueqing ;
Chen, Wei .
INTERNATIONAL UROLOGY AND NEPHROLOGY, 2013, 45 (02) :459-468
[10]   Assessing the quality of reports of randomized clinical trials: Is blinding necessary? [J].
Jadad, AR ;
Moore, RA ;
Carroll, D ;
Jenkinson, C ;
Reynolds, DJM ;
Gavaghan, DJ ;
McQuay, HJ .
CONTROLLED CLINICAL TRIALS, 1996, 17 (01) :1-12