Fractional excretion of total protein predicts renal prognosis in Japanese patients with primary membranous nephropathy

Author:

Kuno Hideaki1ORCID,Kanzaki Go1ORCID,Sasaki Takaya1ORCID,Okabayashi Yusuke1ORCID,Haruhara Kotaro1ORCID,Yokote Shinya1,Koike Kentaro1,Ueda Hiroyuki1,Tsuboi Nobuo1ORCID,Yokoo Takashi1

Affiliation:

1. Division of Nephrology and Hypertension, The Jikei University School of Medicine , Tokyo , Japan

Abstract

ABSTRACT Background Primary membranous nephropathy (pMN) is one of the most common types of glomerulonephritis, with a third of patients progressing to renal insufficiency. Various prognostic factors have been reported, of which urinary protein and renal function are the most critical parameters. Fractional excretion of total protein (FETP) indicates protein leakage that accounts for creatinine kinetics and serum protein levels. In this study, we investigated the association between FETP and renal prognosis in pMN. Methods We retrospectively identified 150 patients with pMN. FETP was calculated as follows: (serum creatinine × urine protein)/(serum protein × urine creatinine) %. We divided the patients into three groups according to FETP values and compared the clinicopathological findings. The primary outcome was an estimated glomerular filtration rate (eGFR) decrease of ≥30% from the baseline level. Results FETP was associated with urinary protein and renal function, Ehrenreich and Churg stage, and global glomerulosclerosis. The primary outcome was observed in 38 patients (25.3%), and the frequency of the primary outcome was higher in the high FETP group (P = .001). FETP is higher than protein–creatinine ratio (PCR) in the area under the curve. In the multivariate analysis adjusted for age, eGFR, PCR and treatment, FETP was significantly associated with primary outcome (adjusted hazard ratio, 8.19; P = .019). Conclusions FETP is a valuable indicator that can reflect the pathophysiology and is more useful than PCR as a predictor of renal prognosis in patients with Japanese pMN.

Publisher

Oxford University Press (OUP)

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