Related Experiment Video
Updated: Dec 30, 2025

The Murine Choline-Deficient, Ethionine-Supplemented CDE Diet Model of Chronic Liver Injury
Published on: October 21, 2017
Complement C3 and Nonalcoholic Fatty Liver Disease in Chronic Kidney Disease Patients: A Pilot Study
Binbin Pan1, Xin Wan1, Mengqing Ma2
1Department of Nephrology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Insights
Complement C3 shows promise as a biomarker for nonalcoholic fatty liver disease (NAFLD) in patients with chronic kidney disease (CKD). This study found C3 levels predict NAFLD in this population.
Area of Science:
- Nephrology
- Hepatology
- Clinical Biochemistry
Background:
- Nonalcoholic fatty liver disease (NAFLD) affects a significant portion of the general population.
- Complement C3 has emerged as a potential biomarker for NAFLD in the general population.
- The utility of C3 as a biomarker in patients with chronic kidney disease (CKD) remains to be fully elucidated.
Purpose of the Study:
- To investigate the predictive value of complement C3 for the presence of NAFLD in patients diagnosed with CKD.
- To assess the association between C3 levels and NAFLD diagnosis in a cohort of CKD patients.
Main Methods:
- A cohort of 648 CKD patients underwent assessment of liver and kidney function, metabolic parameters, and immune markers.
- NAFLD diagnosis was established using established ultrasonographic criteria.
- Statistical analyses, including logistic regression and ROC curve analysis, were employed to evaluate C3's predictive capability.
Main Results:
- Of the 648 CKD patients, 216 (33.3%) were diagnosed with NAFLD.
- Patients with NAFLD exhibited significantly higher levels of complement C3 compared to those without NAFLD (p = 0.001).
- Logistic regression identified complement C3 as a significant predictor of NAFLD in CKD patients (OR = 1.003; p = 0.001), with an optimal cut-off of 993.5 mg/L providing 63.9% sensitivity and 70.1% specificity.
Conclusions:
- Complement C3 demonstrates significant potential as a surrogate biomarker for identifying NAFLD in individuals with CKD.
- These findings suggest that C3 measurement could aid in the non-invasive screening and diagnosis of NAFLD within the CKD population.
Context:
Evidences have suggested complement C3 is a biomarker for nonalcoholic fatty liver disease (NAFLD) in the general population.
Objective:
The present study was conducted to explore the predictive function of C3 for NAFLD in chronic kidney disease (CKD) patients.
Design, Setting, And Participants:
CKD patients were recruited for evaluation of their liver function, kidney function, serum lipids, glycated hemoglobin, blood, and immune function. The glomerular filtration rate was calculated using the CKD-EPI equation. NAFLD was diagnosed according to predefined ultrasonographic criteria.
Results:
A total of 648 consecutive CKD patients were included, with 216 (33.3%) patients diagnosed with NAFLD. The NAFLD group had significant higher levels of serum protein, serum albumin, triglycerides, glycated hemoglobin, complement C3, hemoglobin (p = 0.001), alanine aminotransferase (p = 0.002), estimated glomerular filtration rate (p = 0.007), and C4 (p = 0.043) and lower levels of cystatin C, β2-microglobulin, proteinuria (p = 0.001), and high-density lipoprotein cholesterol (p = 0.008). In a logistic regression model, only complement C3 (OR = 1.003; 95% CI 1.002-1.004, p = 0.001) was associated with a higher likelihood of being diagnosed with NAFLD. Finally, we constructed ROC curves for complement C3 for prediction of having NAFLD. The best cut-off for complement C3 was 993.5 mg/L and it yielded a sensitivity of 63.9% and a specificity of 70.1%.
Conclusion:
Our study revealed that complement C3 can be used as a surrogate biomarker of NAFLD in CKD patients.
More Related Videos
07:03Author Spotlight: Establishing MASLD Cell Models for Investigating Disease Mechanisms and the Lipid-Lowering Effects of Koumiss
Published on: July 19, 2024
04:14Incorporation of a Survivable Liver Biopsy Procedure in Mice to Assess Non-alcoholic Steatohepatitis NASH Resolution
Published on: April 16, 2019
Related Concept Videos
Chronic Kidney Disease II: Clinical Manifestations
Chronic Kidney Disease III: Interprofessional Care
Chronic Kidney Disease I: Introduction
Chronic Pancreatitis II: Collaborative Care
Assessment:
Chronic Kidney Disease IV: Nursing Management
Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test