Published online Dec 16, 2023. doi: 10.12998/wjcc.v11.i35.8300
Peer-review started: November 3, 2023
First decision: November 16, 2023
Revised: November 27, 2023
Accepted: November 30, 2023
Article in press: November 30, 2023
Published online: December 16, 2023
Processing time: 41 Days and 2.3 Hours
Immunoglobulin A nephropathy (IgAN) accompanied with renal dysfunction is a common disease. There is no standard treatment for IgAN with renal dysfunction, and glucocorticoid therapy is usually administered. However, single glucocorticoid is not a complete response of IgAN with renal dysfunction. IgAN is a disease characterized by abnormal immune system, which may be due to glomerular pathological damage caused by the deposition of IgA or its circulating immune complexes in the glomerulus. Therefore, treatment with glucocorticoid and immunosuppressive drugs may be more effective for patients with IgAN with renal dysfunction.
IgAN is among the most prevalent primary glomerular diseases worldwide. Among primary glomerular diseases in China, IgAN accounts for 45.26%–58.2%. Furthermore, as the most prevalent primary cause of ESRD, IgAN accounts for 26.69% of ESRD cases. Glucocorticoids have been used in IgAN for many years because they have advantageous effects on reducing inflammation and urinary protein excretion. The main feature of IgAN is a change in renal immunopathology, which is often treated with immunosuppressants. Therefore, it is important to research the moderate-to-severe IgAN therapy of glucocorticoids combined with immunosuppressants.
To explore the efficacy and security of prednisone combined with mycophenolate mofetil in IgAN therapy with moderate-to-severe renal dysfunction. We hope that, a safer and more effective treatments will be developed.
This study included 200 patients with moderate-to-severe renal dysfunction and IgAN patients. All patients were divided into the glucocorticoid therapy group (GTG) and immunosuppressive therapy group (ITG) according to different treatment regiments, with 100 patients in each group. The baseline data and follow-up data of patients who underwent kidney biopsy were collected. Finally, the above data were compared and analyzed.
The baseline data before treatment were not significantly different between groups. After treatment, serum creatinine and 24-h urinary protein levels in both groups decreased, but the decrease in the ITG differed from that in the GTGs in the 9th month. In addition, the overall response rate in the ITG was significantly higher than that in the GTG. The GTG had more endpoint events than the ITG, but the adverse reactions were similar between the regimens.
The addition of immunosuppressants on the basis of glucocorticoids is a better treatment option for moderate-to-severe renal dysfunction in patients with IgAN.
Future research will involve large-scale sample-controlled studies and long-term follow-up, and will track outcomes, relapse rates, and side effects of patients in relation to their level of renal impairment or pathological grade of their kidneys.