4.0 Article

Single-Nephron GFR in Different Glomerular Basement Membrane Stages of Membranous Nephropathy

Journal

KIDNEY360
Volume 4, Issue 6, Pages 777-786

Publisher

AMER SOC NEPHROLOGY
DOI: 10.34067/KID.0000000000000142

Keywords

membranous nephropathy; single-nephron GFR; Ehrenreich-Churg stage; kidney biopsy; proteinuria; glomerular filtration rate

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This study applied a new technique to estimate single-nephron parameters in human membranous nephropathy (MN) and found that with advancing stage of the disease, single-nephron glomerular filtration rate (SNGFR) and urinary protein excretion (SNUPE) decreased. The study also revealed that SNGFR was associated with disease progression, while glomerular volume and SNUPE were not.
Background Alterations in single-nephron dynamics have been demonstrated in animal models of membranous nephropathy (MN). This study applied a recently developed technique to estimate single-nephron parameters in human MN. Methods Single-nephron GFR (SNGFR) and single-nephron urinary protein excretion (SNUPE) were calculated by dividing total GFR and UPE by the total estimated number of nonglobally sclerotic glomeruli (NSG). The NSG number per kidney was estimated using cortical volume assessment and biopsy-based stereology. MN staging by electron microscopy was performed using Ehrenreich-Churg (EC) criteria. Single-nephron parameters were analyzed in relation to clinicopathological factors known to associate with disease outcomes. Results The study included 109 patients with MN (mean age 65 years; 73% male; eGFR 62 ml/min, 36% on renin-angiotensin-aldosterone system inhibitors prebiopsy). EC stages were I, 19%; II, 49%; III, 26%; and IV, 6%. There was no difference in glomerular volume among EC stage groups. With advancing EC stage, SNGFR and SNUPE decreased from mean 56-42 nl/min and 5.1-3.8 mu g/d, respectively. In multivariable models, EC stage was associated with SNGFR even after adjustment for key clinicopathological factors, such as reduced GFR, serum albumin, UPE, segmental glomerulosclerosis, chronic tubulointerstitial damage, and prebiopsy use of renin-angiotensin-aldosterone system inhibitors. By contrast, EC stage was not associated with glomerular volume and SNUPE after multivariable adjustment. Conclusions These results provide the first clinical evidence of alterations in single-nephron dynamics with advancing EC stage of human MN and support a role for disease-specific glomerular basement membrane structural lesions as determinants of SNGFR.

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