Clinicopathological features and outcomes of PLA2R-related membranous nephropathy with renal glycosuria

Membranous nephropathy (MN) is an immune complex-mediated disease. Massive proteinuria can lead to Fanconi syndrome, clinically manifesting as renal glycosuria. The prevalence and prognosis of M-type phospholipase A2 receptor (PLA2R)-related MN with renal glycosuria remain unknown. Patients diagnose...

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Veröffentlicht in:Clinical nephrology 2024-11, Vol.102 (5), p.273-284
Hauptverfasser: Zhang, Piao, Xu, Feng, Liu, Xumeng, Hu, Ziyun, Liang, Dandan, Liang, Shaoshan, Zhu, Xiaodong, Yang, Fan, Zeng, Caihong
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Sprache:eng
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Zusammenfassung:Membranous nephropathy (MN) is an immune complex-mediated disease. Massive proteinuria can lead to Fanconi syndrome, clinically manifesting as renal glycosuria. The prevalence and prognosis of M-type phospholipase A2 receptor (PLA2R)-related MN with renal glycosuria remain unknown. Patients diagnosed with PLA2R-related MN with renal glycosuria were reviewed, and the control group comprised patients with MN without renal glycosuria who were randomly selected at a ratio of 1 : 3. 50 patients diagnosed with PLA2R-related MN with renal glycosuria from January 2015 to January 2020 were included, with a prevalence of 2.3%. Compared with patients without renal glycosuria, those with renal glycosuria exhibited greater proteinuria, lower estimated glomerular filtration rate (eGFR), and higher use of diuretics, anticoagulants, antibiotics, traditional Chinese medicine, and tacrolimus within 3 months prior to renal biopsy (all p 
ISSN:0301-0430
DOI:10.5414/CN111362