Asil Demirezen, Nuri Alperen Malkoç, Veysel Baran Tomar, Taha Enes Çetin, Ömer Faruk Akçay, Sena Türkmen, Özlem Gülbahar, Betül Öğüt, İpek Işık Gönül, Galip Güz, Ülver Derici, Yasemin Erten, Kadriye Altok, Özant Helvacı
Clinical phenotype strongly predicts anti-PLA2R diagnostic yield in nephrotic-range proteinuria. These findings support KDIGO guidelines emphasizing nephrotic syndrome presence for non-invasive anti-PLA2R-positive membranous nephropathy diagnosis and suggest prioritizing anti-PLA2R testing in nephrotic syndrome patients for optimal resource utilization in limited settings.
BACKGROUND: The 2021 KDIGO guidelines permit non-invasive diagnosis of membranous nephropathy using anti-PLA2R antibodies in patients with nephrotic syndrome. However, optimal patient selection for anti-PLA2R testing remains undefined, particularly in patients with nephrotic-range proteinuria without nephrotic syndrome.
METHODS: We conducted a retrospective analysis of 156 consecutive patients with nephrotic-range proteinuria presenting to a tertiary nephrology center between November 2022 and July 2024. Patients were stratified by clinical phenotype: nephrotic syndrome versus nephrotic-range proteinuria without nephrotic syndrome. Primary outcomes were anti-PLA2R positivity rates and anti-PLA2R-positive membranous nephropathy frequency between groups.
RESULTS: Anti-PLA2R positivity was significantly higher in nephrotic syndrome patients compared to those with nephrotic-range proteinuria without nephrotic syndrome (26.5% vs 9.6%, p=0.007). Membranous nephropathy diagnosis was more frequent in the nephrotic syndrome group (43.3% vs 23.2%, p=0.008). Among patients with confirmed anti-PLA2R-positive membranous nephropathy, anti-PLA2R antibody levels were significantly higher in nephrotic syndrome patients (p=0.008).
CONCLUSIONS: Clinical phenotype strongly predicts anti-PLA2R diagnostic yield in nephrotic-range proteinuria. These findings support KDIGO guidelines emphasizing nephrotic syndrome presence for non-invasive anti-PLA2R-positive membranous nephropathy diagnosis and suggest prioritizing anti-PLA2R testing in nephrotic syndrome patients for optimal resource utilization in limited settings.