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Updated: Aug 7, 2025

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Relationship between serum CHIP levels with cardiovascular disease in maintenance haemodialysis patients
Taijing Xu1, Mengjun Liu2, Xinhui Zhao3
1Department of Nephrology, the People's Hospital of Huishan District in Wuxi, Jiangsu Province, China.
Insights
Lower serum levels of carboxyl terminus of Hsp70-interacting protein (CHIP) are linked to increased cardiovascular disease (CVD) risk in maintenance hemodialysis (MHD) patients. Reduced CHIP predicts higher risks of cardiovascular events, CVD, and all-cause mortality in this population.
Area of Science:
- Cardiovascular Medicine
- Nephrology
- Biochemistry
Background:
- Preclinical studies suggest cardiovascular protective effects of carboxyl terminus of Hsp70-interacting protein (CHIP).
- The role of CHIP in cardiovascular disease (CVD) among maintenance hemodialysis (MHD) patients remains underexplored.
Purpose of the Study:
- To investigate the association between serum CHIP levels and CVD in MHD patients.
- To determine if CHIP concentration predicts cardiovascular events (CVEs) and mortality in MHD patients.
Main Methods:
- Serum CHIP concentrations were measured in 217 MHD patients and 150 healthy controls.
- MHD patients were followed for 36 months to record CVEs and survival.
- Correlations with clinical characteristics, carotid intima-media thickness (CIMT), and left ventricular septal thickness (LVSTd) were analyzed.
Main Results:
- MHD patients exhibited significantly lower serum CHIP levels compared to controls (31.69 ± 18.2 pg/mL vs 84.53 ± 22.1 pg/mL).
- CHIP negatively correlated with CVD risk factors like age, C-reactive protein, and CIMT, while positively associating with markers of nutritional status and dialysis adequacy (e.g., albumin, Kt/V).
- Lower CHIP levels independently predicted increased risk of CVEs, CVD mortality, and all-cause death (HRs ranging from 0.747 to 0.914).
Conclusions:
- Serum CHIP levels are significantly associated with CVD risk factors in MHD patients.
- Reduced CHIP concentration serves as a potential independent predictor of adverse cardiovascular outcomes and mortality in MHD patients.
- CHIP may represent a novel therapeutic target for mitigating cardiovascular complications in MHD patients.
Abstract:
Many preclinical studies reported that the carboxyl terminus of Hsp70-interacting protein (CHIP) has cardiovascular protective effects. This study was designed to explore whether CHIP is related with cardiovascular disease (CVD) in maintanence haemodialysis (MHD) patients. 217 MHD patients and 150 healthy controls were recruited, serum CHIP concentration and clinical characteristics were measured. MHD patients were followed-up for 36 months and their cardiovascular events (CVEs) and survival conditions were recorded. Here, the data shows that serum CHIP concentrations in MHD patients were lower than those in healthy controls (31.69 ± 18.2 pg/mL vs 84.53 ± 22.1 pg/mL, p < 0.05). CHIP negatively correlated with age, C-reactive protein, B-type brain natriuretic peptide, phosphorus, parathyroid hormone, carotid intima-media thickness (CIMT) and left ventricular septal thickness (LVSTd), whereas it positively associated with albumin, haemoglobin, creatinine, Kt/V and ejection fraction (p < 0.05, respectively). Partial correlation and multiple linear regression analysis verified the negative relationship between CHIP with CIMT or LVSTd (p < 0.05, respectively). Using quartile method and Kaplan-Meier survival function, it indetified that the lower serum CHIP concentration predicted risk of CVEs, CVD and all-cause death (p < 0.001). Cox regression analysis manifested CHIP was negatively associated with CVEs (HR = 0.914, 95%CI 0.880-0.950, p < 0.001), CVD mortality (HR = 0.747, 95%CI 0.651-0.857, p < 0.001) and all-cause death (HR = 0.769, 95%CI 0.696-0.850, p < 0.001). In conclusion, the data of this study revealed that serum CHIP level is significantly correlated with multiple risk factors of CVD and may be one of the predictors of CVD risk and death in MHD patients.
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