Possible beneficial association between renin-angiotensin-aldosterone-system blockade usage and graft prognosis in allograft IgA nephropathy: a retrospective cohort study

• Published in: BMC nephrology 2019-09, Vol.20 (1), p.354-354, Article 354
• Main Authors: Park, Sehoon, Baek, Chung Hee, Go, Heounjeong, Kim, Young Hoon, Min, Sang-Il, Ha, Jongwon, Kim, Yong Chul, Lee, Jung Pyo, Kim, Yon Su, Moon, Kyung Chul, Park, Su-Kil, Lee, Hajeong
• Format: Article
• Language: English
• Subjects: ACE inhibitors; Aldosterone; Allograft; Angiotensin; Angiotensin converting enzyme inhibitors; Angiotensin receptor blockade; Angiotensins; Antihypertensive agents; Antihypertensives; Biopsy; Calcium; Calcium channels; Care and treatment; Censorship; Cohort analysis; Death; Diagnosis; Glucocorticoids; Graft rejection; Health aspects; Homografts; Iga glomerulonephritis; IgA nephropathy; Immunoglobulin A; Immunoglobulins; Kidney diseases; Kidney transplantation; Mediation; Medical prognosis; Medical research; Nephrology; Pathology; Patient outcomes; Prognosis; Proteinuria; Regression analysis; Renal failure; Renin; Renin-angiotensin system; Renin-angiotensin-aldosterone system; Risk factors; Statistical analysis; Surgery; Transplantation; Transplants & implants; Variables
• ISSN: 1471-2369; 1471-2369
• DOI: 10.1186/s12882-019-1537-1

Although immunoglobulin A nephropathy (IgAN) is associated with an increased risk of renal allograft failure, evidences for its treatment, including renin-angiotensin-aldosterone system blockade (RAASB) usage, remain limited. In this bi-center retrospective cohort study, we included patients who were recently diagnosed with IgAN through allograft biopsies. We identified their 6-month antihypertensive medication prescriptions and investigated the association between the medication types, albuminuria changes, and risk of 5-year death-censored-graft-failure (DCGF). The mixed effect model and cox regression analysis were used. A total of 464 allograft IgAN patients were included: 272, 38, 33, and 121 patients in the no antihypertensive medication, single agent RAASB, single agent beta blocker (BB)/calcium channel blocker (CCB), and combination therapy groups, respectively. High-degree albuminuria after 6 months of allograft IgAN diagnosis was an important prognostic parameter and a partial mediator for the association between the subgroups and 5-year DCGF. The usage of single RAASB was associated with decrement of albuminuria from allograft IgAN diagnosis (P for interaction = 0.03). The single BB/CCB group demonstrated significantly worse prognosis than the single RAASB group (adjusted hazard ratio, 2.76 [1.09-6.98]; P = 0.03). In conclusion, RAASB may be beneficial for graft prognosis in early allograft IgAN patients who require single antihypertensive medication therapy, by means of reducing albuminuria. Further investigation of treatment strategy in allograft IgAN is warranted.