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Analyses of Proteinuria, Renal Infiltration of Leukocytes, and Renal Deposition of Proteins in Lupus-prone MRL/lpr Mice
Published on: June 8, 2022
Efficacy of the Lupus-Cruces Nephritis protocol in different prognostic groups: a propensity score and cluster
Guillermo Ruiz-Irastorza1,2, Beatriz Marín-García1,2, Luis Dueña-Bartolomé2
1Department of Medicine, University of the Basque Country, EHU, Leioa, Spain.
Objective:
To assess the efficacy of the Lupus-Cruces Nephritis (LCN) protocol vs standard of care (SOC) in achieving complete vrenal response (CRR) among different subpopulations and clinical clusters of patients with LN.
Methods:
This was an observational comparative study with clinical care data of patients from the Lupus-Cruces, historic Lupus-Cruces and Lupus-Bordeaux cohorts. Different prognostic factors were obtained from previous studies and analysed in both LCN and SOC groups. Three different clinical clusters of patients were identified using a two-way clustering analysis. A multivariate propensity score (PS) adjusted analysis and Cox proportional hazards analysis were performed comparing both therapeutic schemes in the different identified subpopulations and clusters.
Results:
Within the cohort of 147 patients, those receiving the LCN protocol (40/47, 85%) were more likely to achieve CRR at 12 months than patients receiving the SOC (44/100, 44%). This was consistent across all prognostic subpopulations. The PS-adjusted logistic regression by subgroups confirmed these results. Three different clusters (named C1, C2 and C3) were identified. Both the univariate and the PS-adjusted Cox regression analysis for CRR at any time confirmed the higher likelihood of achieving CRR of patients treated with the LCN protocol in the three clusters: C1, hazard ratio (HR) 10.7 (95% CI 1.65-69.6, P = 0.013); C2, HR 2.2 (95% CI 1.16-4.1, P = 0.016); C3, HR 6.1 (95% CI 2.99-12.51, P < 0.001).
Conclusion:
The LCN protocol was superior to the SOC schemes in achieving CRR in patients with LN across different subpopulations and clinical clusters.
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