Effects of remnant cholesterol on adverse renal outcomes in lupus nephritis
- PMID: 40211319
- PMCID: PMC11984024
- DOI: 10.1186/s12944-025-02503-y
Effects of remnant cholesterol on adverse renal outcomes in lupus nephritis
Abstract
Background: Remnant cholesterol (RC) causes inflammation and promotes kidney diseases development. However, its role in lupus nephritis (LN) remains unclear. The purpose of this study was to investigate the association between RC and LN.
Methods: This observational study was conducted among patients enrolled between 2000 and 2018 in the High Quality Evidence of Guangzhou Lupus Nephritis Cohort. The study outcomes were defined as adverse renal outcomes, including serum creatinine doubled and end-stage renal disease. Patients were stratified into lower and higher RC groups based on the optimal cutoff RC value (86.88 mg/dL) for adverse renal outcomes. To explore the association between renal outcomes and RC, survival analyses, multivariate Cox regression analyses, and subgroup analyses were conducted.
Results: Overall, 909 individuals were enrolled. Over a median follow-up of 8.33 (interquartile range, 3.08-12.83) years, 134(14.74%) of them reached renal endpoints. Kaplan-Meier survival analyses indicated that patients with higher RC levels were more susceptible to adverse renal outcomes in LN (P < 0.001). After adjusting for confounding factors, higher RC levels exhibited significant correlations with adverse renal outcomes in LN [hazard ratio (HR):1.98, 95% confidence interval (CI):1.16-3.39; P = 0.012]. Subgroup analyses revealed a strong relationship between the higher RC and adverse renal outcomes, particularly in patients aged < 40 years, with an estimated glomerular filtration rate < 60 ml/min/1.73m2 or proliferative pathological changes or nephrotic syndrome (P < 0.05).
Conclusions: Higher RC levels were significantly associated with poor renal outcomes in LN, indicating that RC may become a non-invasive prognostic tool in clinical assessment of LN.
Keywords: End-stage renal disease (ESRD); Lipid profile; Lupus nephritis; Remnant cholesterol (RC); Renal outcomes.
© 2025. The Author(s).
Conflict of interest statement
Declarations. Ethics approval and consent to participate: This study was performed in line with the principles of the Declaration of Helsinki and approved by the Human Ethics Committee of Sun Yat-sen University (No. 2016 − 215). Informed consent waivers from 2000 to 2016 were approved due to the retrospective nature of the study. Patients enrolled between 2017 and 2020 all signed written informed consent. Competing interests: The authors declare no competing interests.
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- 2021YFC2501302/the National Key Research and Development Project of China -- Strategy study on lupus nephritis diagnosis and treatment
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