Initial treatment patterns of primary membranoproliferative glomerulonephritis in Japan (2017–2021): an updated analysis based on nationwide personal clinical records
Naoki Nakagawa, Keiju Hiromura, Yoshitaka Isaka

TL;DR
This study updates treatment patterns for a rare kidney disease in Japan, showing more patients present with severe symptoms and similar treatment approaches across age groups.
Contribution
The study provides an updated analysis of treatment patterns for primary MPGN in Japan using nationwide clinical records from 2017–2021.
Findings
Nephrotic syndrome was present in 83.8% of newly registered primary MPGN patients.
Corticosteroids were used in 63.8% of initial treatments, with increased use of intravenous methylprednisolone pulse therapy.
Cyclosporine and mizoribine were more commonly used in pediatric patients compared to older adults.
Abstract
Primary membranoproliferative glomerulonephritis (MPGN) is a rare progressive kidney disease that often leads to end-stage kidney disease. Our previous nationwide registry study (Report 1, 2015–2018) characterized initial demographics and treatment patterns. In this study (Report 2), we aimed to update these findings, focusing on newly registered cases (2017–2021). Personal clinical records of patients with primary MPGN between 2017 and 2021 were obtained from the national registry organized by the Japanese Ministry of Health, Labour and Welfare. Characteristics of primary MPGN throughout Japan were investigated. A total of 210 patients (median age, 49 years; male, 51%) with newly registered primary MPGN were identified. Nephrotic syndrome was present in 83.8% of patients at enrollment. Initial treatment frequently included corticosteroids (63.8%), with a modest increase in…
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Taxonomy
TopicsRenal Diseases and Glomerulopathies · Vasculitis and related conditions · Complement system in diseases
