DOES BASELINE NEPHROTIC RANGE PROTEINURIA DETERMINE THE LONG-TERM OUTCOMES OF MEMBRANOUS LUPUS NEPHRITIS PATIENTS?

O037 / #680 Topic: AS15 - Lupus Nephritis-Clinical ABSTRACT CONCURRENT SESSION 06: LUPUS NEPHRITIS – CLINICAL OUTCOMES, PREDICTION AND THERAPY 23-05-2025 1:40 PM - 2:40 PM Background/Purpose Management strategies for membranous lupus nephritis (MLN) are generally based on the severity of proteinuria. However, long-term outcomes comparing subnephrotic and nephrotic range proteinuria remain understudied. We explored whether baseline proteinuria level, subnephrotic or nephrotic, impacts long-term outcomes. Methods We conducted a retrospective study identifying patients with biopsy-proven MLN. Patients were categorized based on baseline proteinuria: subnephrotic (<3.5 g/day) or nephrotic (≥3.5 g/day). Long-term outcomes, including an adverse composite outcome (end-stage kidney disease, sustained ≥30% decline in eGFR, or death) and LN flares, were analyzed. Time-to-event outcomes were assessed using Kaplan-Meier curves, and associations were evaluated using Cox regression. Results Eighty-eight patients were included, with 49 (55.7%) in the subnephrotic group (median 1.5 g/day) and 39 (44.3%) in the nephrotic group (median 4.7 g/day). At baseline, the subnephrotic group had a longer time to LN onset, higher serum albumin, less diffuse podocyte effacement, and less frequent cyclophosphamide treatment (Table 1). No significant differences were noted in kidney function, urine sediment abnormalities, or histopathology. 38 patients (43.2%) experienced the adverse composite outcome, with no difference between groups (40.8% in the subnephrotic group vs. 46.2% in the nephrotic group, p=0.78]. Flares occurred in 35 patients (39.8%), with no difference between groups (38.8% in the subnephrotic group vs. 41.0% in the nephrotic group, p=1.00). Kaplan-Meier curves (Figure) and Cox proportional hazards model further confirmed these findings. Table 1. Patient characteristics at the time of LN onset (baseline). Figure. Conclusions No significant differences in renal disease characteristics or long-term outcomes were found between MLN patients with nephrotic and subnephrotic baseline proteinuria. These findings challenge current practices, suggesting a need for more individualized immunosuppressive treatment in MLN.

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Journal
The Journal of Rheumatology
Published
2025-05-20
DOI
https://doi.org/10.3899/jrheum.2025-0390.o037
Primary Topic
Systemic Lupus Erythematosus Research
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article
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article

DOES BASELINE NEPHROTIC RANGE PROTEINURIA DETERMINE THE LONG-TERM OUTCOMES OF MEMBRANOUS LUPUS NEPHRITIS PATIENTS?

Zahi Touma, Fadi Kharouf, Dafna D. Gladman, Pankti Mehta et al.
The Journal of Rheumatology
Systemic Lupus Erythematosus Research
article

DOES BASELINE NEPHROTIC RANGE PROTEINURIA DETERMINE THE LONG-TERM OUTCOMES OF MEMBRANOUS LUPUS NEPHRITIS PATIENTS?

Zahi Touma, Fadi Kharouf, Dafna D. Gladman, Pankti Mehta, Virginia Carrizo Abarza, Qixuan Li, Laura Whittall-Garcia
article en

Abstract

O037 / #680 Topic: AS15 - Lupus Nephritis-Clinical ABSTRACT CONCURRENT SESSION 06: LUPUS NEPHRITIS – CLINICAL OUTCOMES, PREDICTION AND THERAPY 23-05-2025 1:40 PM - 2:40 PM Background/Purpose Management strategies for membranous lupus nephritis (MLN) are generally based on the severity of proteinuria. However, long-term outcomes comparing subnephrotic and nephrotic range proteinuria remain understudied. We explored whether baseline proteinuria level, subnephrotic or nephrotic, impacts long-term outcomes. Methods We conducted a retrospective study identifying patients with biopsy-proven MLN. Patients were categorized based on baseline proteinuria: subnephrotic (<3.5 g/day) or nephrotic (≥3.5 g/day). Long-term outcomes, including an adverse composite outcome (end-stage kidney disease, sustained ≥30% decline in eGFR, or death) and LN flares, were analyzed. Time-to-event outcomes were assessed using Kaplan-Meier curves, and associations were evaluated using Cox regression. Results Eighty-eight patients were included, with 49 (55.7%) in the subnephrotic group (median 1.5 g/day) and 39 (44.3%) in the nephrotic group (median 4.7 g/day). At baseline, the subnephrotic group had a longer time to LN onset, higher serum albumin, less diffuse podocyte effacement, and less frequent cyclophosphamide treatment (Table 1). No significant differences were noted in kidney function, urine sediment abnormalities, or histopathology. 38 patients (43.2%) experienced the adverse composite outcome, with no difference between groups (40.8% in the subnephrotic group vs. 46.2% in the nephrotic group, p=0.78]. Flares occurred in 35 patients (39.8%), with no difference between groups (38.8% in the subnephrotic group vs. 41.0% in the nephrotic group, p=1.00). Kaplan-Meier curves (Figure) and Cox proportional hazards model further confirmed these findings. Table 1. Patient characteristics at the time of LN onset (baseline). Figure. Conclusions No significant differences in renal disease characteristics or long-term outcomes were found between MLN patients with nephrotic and subnephrotic baseline proteinuria. These findings challenge current practices, suggesting a need for more individualized immunosuppressive treatment in MLN.

The Journal of RheumatologyVol. 52(Suppl 1)
University of Toronto (CA)
Openalex Percentile: Top 82%
Systemic Lupus Erythematosus Research
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