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Chemerin level and the relation to insulin resistance in chronic kidney disease
Sahier Omar El-Khashab1, Mona Gamil1, Ahmed Yamany Ali1
1Department of Internal Medicine and Nephrology, Kasr Al-Ainy Cairo University, Cairo, Egypt.
Insights
Serum chemerin levels are elevated in chronic kidney disease (CKD) patients and correlate with insulin resistance (IR). Chemerin may serve as a marker for uremic IR in advanced CKD stages.
Area of Science:
- Nephrology
- Endocrinology
- Metabolic Syndrome Research
Background:
- Chemerin is linked to metabolic syndrome components like hypertension, hyperlipidemia, and insulin resistance (IR).
- Understanding chemerin's role in chronic kidney disease (CKD) is crucial for metabolic health assessment.
Purpose of the Study:
- To investigate serum chemerin levels in CKD patients.
- To determine the relationship between serum chemerin and insulin resistance in CKD.
Main Methods:
- Study included 80 participants: 30 CKD patients, 30 end-stage renal disease (ESRD) patients on hemodialysis, and 20 healthy controls.
- Measured serum chemerin, fasting blood sugar, insulin, HOMA-IR index, kidney function markers (urea, creatinine, GFR), lipids, and body composition.
- Statistical analysis included correlation and comparison between groups.
Main Results:
- CKD and ESRD patients exhibited significantly higher serum chemerin levels than controls (P <0.001).
- Serum chemerin strongly correlated positively with HOMA-IR (r = 0.56/0.53, P <0.001) and negatively with GFR (r = -0.51/-0.46, P <0.001).
- In CKD patients, chemerin correlated positively with systolic and diastolic blood pressure and creatinine.
Conclusions:
- Elevated serum chemerin is associated with CKD and ESRD.
- Chemerin may function as a marker for insulin resistance in uremic patients.
- Chemerin shows potential as a biomarker for uremic insulin resistance in CKD Stages 3, 4, and 5.
Abstract:
Chemerin has been associated with different components of the metabolic syndrome, including hypertension, hyperlipidemia, and insulin resistance (IR). The aim of this study was to evaluate serum chemerin level in chronic kidney disease (CKD) patients and its relation to IR. This study was conducted on 80 participants who were classified into three groups: Group I (30 CKD patients with mean age 53 ± 12 years), Group II (30 patients with end-stage renal disease on regular hemodialysis with mean age 48 ± 14.8 years) and Group III having 20 healthy age-and sex-matched controls. Serum chemerin level, fasting blood sugar, fasting insulin, HOMA-IR index calculation, urea, creatinine, estimated glomerular filtration rate, total cholesterol, and triglyceride were measured. Body composition was assessed by dual-energy X-ray absorptiometry. In Groups I and II, we found a significantly higher mean chemerin level compared to healthy controls (P <0.001), a highly significant positive correlation between mean chemerin level and the HOMA-IR index [r = 0.56, P <0.001/(r = 0.53, P <0.001)], and a highly significant negative correlation between mean chemerin level and GFR (r = -0.51, P <0.001/r = -0.46, P <0.001). In Group I, there was also a highly significant positive correlation between mean chemerin and systolic blood pressure (r = 0.31, P <0.05), diastolic blood pressure (r = 0.39, P <0.05 and creatinine (r = 0.34, P <0.05). Chemerin might be considered a uremic IR adipokine marker in CKD Stages 3, 4, and 5.
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