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Risk of chronic kidney disease in newly diagnosed SLE with preserved renal function: a national study
Iftach Sagy1,2,3,4, Itamar Ben Shitrit3,4, Mahmoud Abu-Shakra2,3
1Lupus and Vasculitis Service, Department of Medicine, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Insights
Patients with systemic lupus erythematosus (SLE) and normal kidney function face higher risks of chronic kidney disease (CKD), cardiovascular events, and mortality. Early monitoring and management of risk factors are crucial for these individuals.
Area of Science:
- Nephrology
- Rheumatology
- Cardiology
Background:
- Systemic lupus erythematosus (SLE) is linked to lupus nephritis (LN), a primary driver of chronic kidney disease (CKD).
- Long-term outcomes for SLE patients with preserved kidney function and no LN are not well understood.
- This study examines CKD development in newly diagnosed SLE patients without baseline LN and with normal kidney function.
Purpose of the Study:
- To investigate the incidence of CKD in SLE patients with preserved kidney function and no concurrent LN at diagnosis.
- To compare CKD development against matched individuals without SLE.
- To assess secondary outcomes including end-stage kidney disease (ESKD), major adverse cardiovascular events (MACE), and all-cause mortality.
Main Methods:
- A national database study analyzed newly diagnosed SLE patients (2015-2023).
- Patients with eGFR >60 mL/min/1.73 m² were matched with non-SLE controls.
- Exclusion criteria included existing LN; primary outcome was incident CKD (eGFR ≤60 mL/min/1.73 m²).
Main Results:
- SLE patients (n=1,145) showed higher risks of CKD (5.2% vs 2.7%), ESKD (HR 3.13), MACE (HR 1.63), and mortality (HR 4.52) compared to controls (n=91,681).
- Median follow-up was 5.77 years with similar baseline eGFR.
- Diabetes and hypertension were significant risk factors for CKD and ESKD.
Conclusions:
- SLE patients with preserved kidney function and no LN face elevated risks for renal complications, cardiovascular events, and mortality.
- These findings underscore the necessity for vigilant long-term monitoring.
- Optimizing modifiable risk factors like diabetes and hypertension is critical for improving patient outcomes.
Objectives:
SLE is strongly associated with LN, a major cause of chronic kidney disease (CKD). However, long-term renal and cardiovascular outcomes in patients with SLE who have preserved kidney function and do not develop LN remain poorly characterized. We sought to investigate the development of CKD among newly diagnosed patients with SLE who had preserved kidney function and no evidence of concomitant LN at baseline, compared with matched control individuals.
Methods:
A national database study of newly diagnosed patients with SLE between 2015 and 2023. Patients with estimated glomerular filtration rate (eGFR) > 60 ml/min/1.73 m2 at diagnosis were matched to non-SLE controls by age, sex and ethnicity. Patients with LN were excluded. The primary outcome was incident CKD, defined as eGFR ≤ 60 ml/min/1.73 m2 after diagnosis. Secondary outcomes included end-stage kidney disease (ESKD), major adverse cardiovascular events (MACE) and all-cause mortality.
Results:
We identified 1145 patients with SLE and 91 681 matched controls, with a median follow-up of 5.77 years and similar baseline eGFR (103 vs 104 ml/min/1.73 m2). SLE was associated with a higher risk of CKD (5.2% vs 2.7%; HR 1.96, 95% CI 1.50-2.54), ESKD (HR 3.13, 95% CI 1.38-7.08), MACE (HR 1.63, 95% CI 1.31-2.04) and all-cause mortality (HR 4.52, 95% CI 3.71-5.50). Mean eGFR trajectories were similar between the groups. Diabetes (HR 1.51, 95% CI 1.39-1.64) and hypertension (HR 2.72, 95% CI 2.42-3.07) were the strongest risk factors for CKD and ESKD.
Conclusion:
Patients with SLE and preserved kidney function at diagnosis, without LN, are at increased risk of adverse renal outcomes, cardiovascular events and mortality, highlighting the importance of long-term monitoring and optimization of modifiable CKD risk factors.
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