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Cystatin C: A Promising Marker of Renal Function in Patients with Systemic Lupus Erythematosus?
Lígia Peixoto1, Patrício Aguiar1, Raquel de Bragança2
1Serviço de Medicina I. Centro Hospitalar Lisboa Norte. Lisboa. Portugal.
Insights
Cystatin C shows promise as a superior marker for detecting kidney function changes in systemic lupus erythematosus patients, potentially identifying chronic kidney disease earlier than creatinine.
Area of Science:
- Nephrology
- Rheumatology
- Clinical Chemistry
Background:
- Serum creatinine is the standard biomarker for assessing kidney function.
- Cystatin C is increasingly recognized for its closer correlation with glomerular filtration rate (GFR) and prognostic value.
- Systemic lupus erythematosus (SLE) is associated with a higher risk of chronic kidney disease (CKD).
Purpose of the Study:
- To evaluate cystatin C as a potential marker of renal function in patients with SLE.
- To compare the performance of cystatin C with creatinine in assessing GFR in this population.
- To determine if cystatin C offers advantages over creatinine for CKD screening in SLE.
Main Methods:
- A cohort of 37 SLE patients was studied.
- Serum cystatin C and creatinine levels were measured.
- GFR was estimated using five different formulas, including CKD-EPI creatinine and CKD-EPI cystatin C, with CKD-EPI creatinine as the reference.
- Multivariate linear regression analyzed factors influencing cystatin C levels.
Main Results:
- Cystatin C was elevated in 10 patients, while creatinine was not elevated in any.
- A trend towards lower GFR estimates with CKD-EPI cystatin C compared to CKD-EPI creatinine was observed, particularly at lower GFRs.
- CKD-EPI cystatin C reclassified 4 patients to having CKD and 1 patient to not having CKD.
- Age was the only significant factor influencing cystatin C levels.
Conclusions:
- Cystatin C demonstrates potential as a superior marker for renal function in SLE patients.
- It may detect GFR changes earlier than creatinine, improving CKD screening.
- Age is a significant confounding factor in cystatin C measurements, necessitating consideration in GFR estimation.
Purpose:
Cystatin C has a higher correlation with glomerular filtration rate and a more significant clinical prognosis than creatinine. We sought to determine whether it is a marker of renal function different from creatinine (cystatin C potentially superior to creatinine), in patients with systemic lupus erythematosus.
Material And Methods:
37 patients with systemic lupus erythematosus were evaluated. Serum cystatin C was determined by nephelometry and creatinine by modified Jaffe method. We compared five formulas: Chronic Kidney Disease â Epidemiology Collaboration cystiatin; Chronic Kidney Disease â Epidemiology Collaboration creatinine-cystatin; Cockcroft-Gault; Modification of Diet in Renal Disease and Chronic Kidney Disease â Epidemiology Collaboration creatinine, using the latter as a reference. We analyzed the influence of clinical and laboratory factors in cystatin C variation, using multivariate linear regression.
Results:
Cystatin C was singly elevated in ten participants, versus none isolated creatinine elevation, and this difference was significant (p = 0.002). There was a difference between the estimated glomerular filtration rate by Chronic Kidney Disease â Epidemiology Collaboration cystatin and by Chronic Kidney Disease â Epidemiology Collaboration creatinine (-6.0541 mL/min/1.73 m², p = 0.07), more pronounced for lower glomerular filtration rate. Consequently, Chronic Kidney Disease â Epidemiology Collaboration cystatin reclassified 4 patients as having chronic kidney disease de novo and 1 patient as not having chronic kidney disease (p = 0.375). Cystatin C was only significantly influenced by age (p < 0.001).
Discussion:
Several reports showed cystatin C as a better marker to define chronic kidney disease, allowing more accurate classification and risk stratification, compared with creatinine. In this study, Cystatin C revealed as a promisor marker of renal function in patient with lupus, mainly in patients with lower glomerular filtration rates. The correlation between age and cystatin C seems to be a confounding factor, as glomerular filtration rate physiologically declines with ageing.
Conclusion:
Cystatin C was potentially superior to creatinine and in this study and cystatin C seems to detect changes in glomerular filtration rate earlier than creatinine and may be a better screening method for chronic kidney disease in systemic lupus erythematosus.
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