# Predictors and long-term impact of sustained complete renal response in lupus nephritis patients over a median 10-year follow-up

**Authors:** Ioannis E Michelakis, Eleni Kapsia, John N Boletis, Smaragdi Marinaki, Petros P Sfikakis, Maria G Tektonidou

PMC · DOI: 10.1093/rheumatology/keaf677 · Rheumatology (Oxford, England) · 2025-12-13

## TL;DR

This study shows that achieving and maintaining complete kidney recovery in lupus nephritis patients for several years significantly reduces long-term kidney damage and disease progression.

## Contribution

The study identifies predictors of sustained kidney recovery and demonstrates its long-term protective effects in lupus nephritis patients.

## Key findings

- 83% of patients achieved sustained complete renal response for at least 12 months.
- Longer duration of sustained response reduced risks of kidney flares and severe kidney function decline.
- sCRR ≥4 years protected against end-stage kidney disease, death, and damage accrual.

## Abstract

Complete renal response (CRR) is a primary goal in lupus nephritis (LN) management. We examined the prevalence and predictors of sustained CRR (sCRR) and long-term outcomes.

We included 142 inception cohort patients with biopsy-proven LN from two academic centres. We assessed the prevalence of sCRR achievement for ≥12 months and the impact of sCRR duration on renal flares, severe kidney function decline (≥30% eGFR decline compared with baseline), a composite end-stage kidney disease (ESKD) or death outcome, and disease damage. We analysed data over a median 121-month follow-up, using linear, logistic and Cox regression models.

A total of 83% of patients achieved sCRR for ≥12 months, 56.3% for ≥5 years and 20.4% for ≥10 years. Persistent hydroxychloroquine use (adjusted HR: 1.86, P = 0.004), non-nephrotic baseline proteinuria (adjusted HR: 1.71, P = 0.016) and class III vs class IV LN (HR: 1.89, P = 0.018) were associated with earlier sCRR achievement. The 5- and 10-year post-sCRR risks for renal flares decreased for every additional year on CRR. sCRR duration rather than its mere achievement reduced the risk of ≥30% eGFR decline (adjusted OR: 0.81/year, P = 0.015) and composite ESKD/death (adjusted HR: 0.75/year, P = 0.001). sCRR ≥ 12 months protected against damage accrual (adjusted β-coef=−1.17, P < 0.001). Among those with ≥100-month follow-up, sCRR ≥ 4 years protected against severe kidney function decline (adjusted OR: 0.10, P = 0.005), ESKD/death (adjusted HR: 0.11, P = 0.043) and damage accrual (adjusted β-coef=–0.81, P = 0.012).

Persistent hydroxychloroquine, non-nephrotic baseline proteinuria and class III vs IV are associated with earlier sCRR. sCRR ≥4 years protects against ≥30% eGFR decline, composite ESKD/death and damage.

## Linked entities

- **Chemicals:** hydroxychloroquine (PubChem CID 3652)
- **Diseases:** lupus nephritis (MONDO:0005556), end-stage kidney disease (MONDO:0004375)

## Full-text entities

- **Diseases:** death (MESH:D003643), kidney function decline (MESH:D007680), proteinuria (MESH:D011507), disease damage (MESH:D004194), renal (MESH:D006030), nephrotic (MESH:D009404), LN (MESH:D008181), ESKD (MESH:D007676)
- **Chemicals:** hydroxychloroquine (MESH:D006886)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13017678/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC13017678/full.md

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Source: https://tomesphere.com/paper/PMC13017678