Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Safety and efficacy of prednisolone, mizoribine and lisinopril combination therapy for severe childhood IgA Nephropathy

View through CrossRef
Abstract Background Angiotensin-converting enzyme inhibitors such as lisinopril have long been used for childhood IgA Nephropathy (cIgAN). A two-year combined regimen including prednisolone + mizoribine + warfarin + dipyridamole was shown in our previous randomized control trial to be better for severe cIgAN than prednisolone + mizoribine (without warfarin or dipyridamole) in proteinuria remission. However, to avoid warfarin nephropathy and to shorten the duration of prednisolone use, we consider a new two-year combined regimen of prednisolone + mizoribine + lisinopril. Methods Between July 1976 and December 2022, among 567 biopsy-proven cases of cIgAN, there were 93 cases of severe cIgAN treated with prednisolone + mizoribine. We investigated clinicopathological differences between the 77 cases of cIgAN (82.8%) with the previous treatment and the other 16 patients with the new treatment regimen. After 1:1 propensity score matching was performed to account for between-group differences (amount of proteinuria, eGFR, and the percentage of patients with C0, C1, and C2), we analyzed 15 matched pairs. Results Clinicopathological presentations did not significantly differ between the groups. Kaplan-Meier analysis of proteinuria remission showed that the patients with the new treatment achieved significantly higher (90.0 vs. 64.1% at 11 yrs, p = 0.01), and faster (1.0 vs. 4.0 yrs, p = 0.03) proteinuria remission than those with the previous treatment. Proteinuria recurrence was not significantly different between the groups. Conclusions We suggested the superiority of 2-year combined regimen of prednisolone + mizoribine + lisinopril for severe cIgAN in achieving early proteinuria remission and shortening prednisolone use without recurrence of proteinuria.
Title: Safety and efficacy of prednisolone, mizoribine and lisinopril combination therapy for severe childhood IgA Nephropathy
Description:
Abstract Background Angiotensin-converting enzyme inhibitors such as lisinopril have long been used for childhood IgA Nephropathy (cIgAN).
A two-year combined regimen including prednisolone + mizoribine + warfarin + dipyridamole was shown in our previous randomized control trial to be better for severe cIgAN than prednisolone + mizoribine (without warfarin or dipyridamole) in proteinuria remission.
However, to avoid warfarin nephropathy and to shorten the duration of prednisolone use, we consider a new two-year combined regimen of prednisolone + mizoribine + lisinopril.
Methods Between July 1976 and December 2022, among 567 biopsy-proven cases of cIgAN, there were 93 cases of severe cIgAN treated with prednisolone + mizoribine.
We investigated clinicopathological differences between the 77 cases of cIgAN (82.
8%) with the previous treatment and the other 16 patients with the new treatment regimen.
After 1:1 propensity score matching was performed to account for between-group differences (amount of proteinuria, eGFR, and the percentage of patients with C0, C1, and C2), we analyzed 15 matched pairs.
Results Clinicopathological presentations did not significantly differ between the groups.
Kaplan-Meier analysis of proteinuria remission showed that the patients with the new treatment achieved significantly higher (90.
0 vs.
64.
1% at 11 yrs, p = 0.
01), and faster (1.
0 vs.
4.
0 yrs, p = 0.
03) proteinuria remission than those with the previous treatment.
Proteinuria recurrence was not significantly different between the groups.
Conclusions We suggested the superiority of 2-year combined regimen of prednisolone + mizoribine + lisinopril for severe cIgAN in achieving early proteinuria remission and shortening prednisolone use without recurrence of proteinuria.

Related Results

Emerging Evidence of IgG4-Related Disease in Pericarditis: A Systematic Review
Emerging Evidence of IgG4-Related Disease in Pericarditis: A Systematic Review
Abstract Introduction Immunoglobulin G4-related disease (IgG4-RD) is a recently identified immune-mediated condition that is debilitating and often overlooked. While IgG4-RD has be...
Characterization of circulating and cutaneous IgA immune complexes in patients with dermatitis herpetiformis.
Characterization of circulating and cutaneous IgA immune complexes in patients with dermatitis herpetiformis.
Abstract Dermatitis herpetiformis (DH) is a chronic, blistering skin disease characterized in part by deposits of IgA at the dermal-epidermal junction. Eighty-five p...
Mizoribine treatment for childhood IgA nephropathy
Mizoribine treatment for childhood IgA nephropathy
Abstract Background : There is currently no established therapy for childhood IgA nephropathy (IgAN). Mizoribine, a newly developed immunosuppressive agent c...
Murine IgA binding factors (IgA-BF) suppressing IgA production: characterization and target specificity of IgA-BF.
Murine IgA binding factors (IgA-BF) suppressing IgA production: characterization and target specificity of IgA-BF.
Abstract Chemical and functional properties of IgA binding factor(s) (IgA-BF) from both murine Con A-activated spleen cells and Fc gamma R+, Fc alpha R+ T hybridoma ...
Etiology of IgA nephropathy syndrome
Etiology of IgA nephropathy syndrome
Since Berger's original paper on mesangial IgA‐IgG deposition with hematuria, there have been a number of clinical and pathological studies regarding IgA immune complexes, the mech...
Pembrolizumab and Sarcoma: A meta-analysis
Pembrolizumab and Sarcoma: A meta-analysis
Abstract Introduction: Pembrolizumab is a monoclonal antibody that promotes antitumor immunity. This study presents a systematic review and meta-analysis of the efficacy and safety...
An evaluation of the DiaMed assays for immunoglobulin A antibodies (anti‐IgA) and IgA deficiency
An evaluation of the DiaMed assays for immunoglobulin A antibodies (anti‐IgA) and IgA deficiency
BACKGROUND: Immunoglobulin A antibodies (anti‐IgA) are rare but can cause transfusion‐associated anaphylaxis. The detection of anti‐IgA has traditionally been performed using a lab...

Back to Top