TY - JOUR
T1 - High incidence of proliferative and membranous nephritis in SLE patients with low proteinuria in the Accelerating Medicines Partnership
AU - the Accelerating Medicines Partnership (AMP) RA/SLE Network
AU - Carlucci, Philip M.
AU - Li, Jessica
AU - Fava, Andrea
AU - Deonaraine, Kristina K.
AU - Wofsy, David
AU - James, Judith A.
AU - Putterman, Chaim
AU - Diamond, Betty
AU - Davidson, Anne
AU - Fine, Derek M.
AU - Monroy-Trujillo, Jose
AU - Atta, Mohamed G.
AU - Dejager, Wade
AU - Guthridge, Joel M.
AU - Haag, Kristin
AU - Rao, Deepak A.
AU - Brenner, Michael B.
AU - Lederer, James A.
AU - Apruzzese, William
AU - Belmont, H. Michael
AU - Izmirly, Peter M.
AU - Zaminski, Devyn
AU - Wu, Ming
AU - Connery, Sean
AU - Payan-Schober, Fernanda
AU - Furie, Richard
AU - Dall'era, Maria
AU - Cho, Kerry
AU - Kamen, Diane
AU - Kalunian, Kenneth
AU - Anolik, Jennifer
AU - Barnas, Jennifer
AU - Ishimori, Mariko
AU - Weisman, Michael H.
AU - Goff, Jennifer
AU - Dunn, Patrick J.
AU - Raychaudhuri, Soumya
AU - Zhang, Fan
AU - Korsunsky, Ilya
AU - Nathan, Aparna
AU - Mears, Joseph
AU - Ishigaki, Kazuyoshi
AU - Xiao, Qian
AU - Millard, Nghia
AU - Weinand, Kathryn
AU - Sakaue, Saori
AU - Utz, P. J.
AU - Mao, Rong
AU - Robinson, Bill
AU - Maecker, Holden
N1 - Publisher Copyright:
© 2022 The Author(s). Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved.
PY - 2022/11/1
Y1 - 2022/11/1
N2 - Objective: Delayed detection of LN associates with worse outcomes. There are conflicting recommendations regarding a threshold level of proteinuria at which biopsy will likely yield actionable management. This study addressed the association of urine protein:creatinine ratios (UPCR) with clinical characteristics and investigated the incidence of proliferative and membranous histology in patients with a UPCR between 0.5 and 1. Methods: A total of 275 SLE patients (113 first biopsy, 162 repeat) were enrolled in the multicentre multi-ethnic/racial Accelerating Medicines Partnership across 15 US sites at the time of a clinically indicated renal biopsy. Patients were followed for 1 year. Results: At biopsy, 54 patients had UPCR <1 and 221 had UPCR ≥1. Independent of UPCR or biopsy number, a majority (92%) of patients had class III, IV, V or mixed histology. Moreover, patients with UPCR <1 and class III, IV, V, or mixed had a median activity index of 4.5 and chronicity index of 3, yet 39% of these patients had an inactive sediment. Neither anti-dsDNA nor low complement distinguished class I or II from III, IV, V or mixed in patients with UPCR <1. Of 29 patients with baseline UPCR <1 and class III, IV, V or mixed, 23 (79%) had a UPCR <0.5 at 1 year. Conclusion: In this prospective study, three-quarters of patients with UPCR <1 had histology showing class III, IV, V or mixed with accompanying activity and chronicity despite an inactive sediment or normal serologies. These data support renal biopsy at thresholds lower than a UPCR of 1.
AB - Objective: Delayed detection of LN associates with worse outcomes. There are conflicting recommendations regarding a threshold level of proteinuria at which biopsy will likely yield actionable management. This study addressed the association of urine protein:creatinine ratios (UPCR) with clinical characteristics and investigated the incidence of proliferative and membranous histology in patients with a UPCR between 0.5 and 1. Methods: A total of 275 SLE patients (113 first biopsy, 162 repeat) were enrolled in the multicentre multi-ethnic/racial Accelerating Medicines Partnership across 15 US sites at the time of a clinically indicated renal biopsy. Patients were followed for 1 year. Results: At biopsy, 54 patients had UPCR <1 and 221 had UPCR ≥1. Independent of UPCR or biopsy number, a majority (92%) of patients had class III, IV, V or mixed histology. Moreover, patients with UPCR <1 and class III, IV, V, or mixed had a median activity index of 4.5 and chronicity index of 3, yet 39% of these patients had an inactive sediment. Neither anti-dsDNA nor low complement distinguished class I or II from III, IV, V or mixed in patients with UPCR <1. Of 29 patients with baseline UPCR <1 and class III, IV, V or mixed, 23 (79%) had a UPCR <0.5 at 1 year. Conclusion: In this prospective study, three-quarters of patients with UPCR <1 had histology showing class III, IV, V or mixed with accompanying activity and chronicity despite an inactive sediment or normal serologies. These data support renal biopsy at thresholds lower than a UPCR of 1.
KW - diagnosis
KW - lupus nephritis
KW - systemic lupus erythematosus
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U2 - 10.1093/rheumatology/keac067
DO - 10.1093/rheumatology/keac067
M3 - Article
C2 - 35212719
AN - SCOPUS:85151124695
SN - 1462-0324
VL - 61
SP - 4335
EP - 4343
JO - Rheumatology (United Kingdom)
JF - Rheumatology (United Kingdom)
IS - 11
ER -