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Published on: October 2, 2020
HDL-associated enzymes and proteins in hemodialysis patients
Leonardo D Cacciagiú1, Ana I González, Leonardo Gomez Rosso
1Laboratory of Lipids and Lipoproteins, Department of Clinical Biochemistry, Faculty of Pharmacy and Biochemistry, INFIBIOC, University of Buenos Aires, Junín 954, CP1113AAD, Buenos Aires, Argentina.
Insights
High-density lipoprotein (HDL) functionality, not just concentration, is crucial for hemodialysis patients. HDL-associated proteins and enzymes are altered, impacting lipid profiles and inflammation in chronic kidney disease.
Area of Science:
- Biochemistry
- Nephrology
- Cardiovascular Research
Background:
- Chronic kidney disease (CKD) patients on hemodialysis exhibit dyslipidemia and chronic inflammation.
- High-density lipoprotein (HDL) plays a critical role in reverse cholesterol transport and possesses anti-inflammatory and antioxidant properties.
Purpose of the Study:
- To investigate HDL-associated proteins and enzymes in hemodialysis patients.
- To determine the relationship between these HDL components, lipoprotein profiles, and inflammatory markers.
Main Methods:
- Cross-sectional study comparing 53 hemodialysis patients with 32 healthy controls.
- Assessed plasma lipids, apolipoprotein-AI (Apo-AI), and high-sensitivity C-reactive protein (hs-CRP).
- Measured activities of cholesteryl ester transfer protein (CETP), paraoxonase, lipoprotein lipase A2 (LpPLA2), and postheparin hepatic lipase.
Main Results:
- Hemodialysis patients had higher triglycerides and lower LDL-, HDL-, and total cholesterol compared to controls.
- Apo-AI, paraoxonase, and hepatic lipase levels were significantly lower in patients.
- CETP levels were higher in patients, while LpPLA2 showed no significant difference between groups.
Conclusions:
- Lipoprotein metabolism is significantly altered in hemodialysis patients.
- HDL functionality, influenced by its associated proteins and enzymes, is impaired.
- These alterations may contribute to the pro-oxidative and pro-inflammatory state observed in CKD.
Objectives:
To evaluate HDL-associated proteins and enzymes and their relation with lipoprotein profile and inflammatory markers in chronic renal patients on hemodialysis.
Design And Methods:
We studied 53 patients under hemodialysis and 32 healthy subjects as controls. We compared plasma lipids, Apoprotein-AI and hs-CRP, as a marker of chronic inflammation. We evaluated proteins and enzymes associated to HDL, involved in several points of lipoprotein metabolism: CETP, paraoxonase and LpPLA2 activities. Hepatic lipase was measured in postheparin plasma.
Results:
Patients showed higher triglycerides and lower LDL-, HDL- and total-cholesterol than controls (p<0.05). Also, in comparison with controls, Apoprotein-AI, paraoxonase and hepatic lipase were lower, while CETP was higher (p<0.03). LpPLA2 did not show changes between groups.
Conclusion:
Beyond plasma lipid-lipoprotein profile, other factors could contribute to induce a pro-oxidative and pro-inflammatory status. The protective role of HDL does not only depend on its concentration, but also on its functionality.
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