Kidney and lipids: novel potential therapeutic targets for dyslipidemia in kidney disease?
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Updated: Aug 16, 2025

LDL Cholesterol Uptake Assay Using Live Cell Imaging Analysis with Cell Health Monitoring
Published on: November 17, 2018
Konrad Zuzda1, Wiktoria Grycuk1, Jacek Małyszko2
1Department of Nephrology, Dialysis and Internal Medicine, Medical University of Warsaw, Bialystok, Poland.
Introduction:
Altered lipid distribution and metabolism may lead to the development and/or progression of chronic kidney disease (CKD). Dyslipidemia is a major risk factor for CKD and increases the risk of cardiovascular events and mortality. Therefore, lipid-lowering treatments may decrease cardiovascular risk and prevent death.
Areas Covered:
Key players involved in regulating lipid accumulation in the kidney; contribution of lipids to CKD progression, lipotoxicity, and mitochondrial dysfunction in kidney disease; recent therapeutic approaches for dyslipidemia.
Expert Opinion:
The precise mechanisms for regulating lipid metabolism, particularly in kidney disease, are poorly understood. Guidelines for lipid-lowering therapy for CKD are controversial. Several hypolipemic therapies are available, but compared to others, statin therapy is the most common. No clinical trial has evaluated the efficacy of proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9i) in preventing cardiovascular events or improving kidney function among patients with CKD or kidney transplant recipients. Attractive alternatives, such as PCSK9-small interfering RNA (siRNA) molecules or evinacumab are available. Additionally, several promising agents, such as cyclodextrins and the FXR/TGR5 dual agonist, INT-767, can improve renal lipid metabolism disorders and delay CKD progression. Drugs targeting mitochondrial dysfunction could be an option for the treatment of dyslipidemia and lipotoxicity, particularly in renal diseases.
Insights
Dyslipidemia contributes to chronic kidney disease (CKD) progression and cardiovascular risks. Novel therapies targeting lipid metabolism and mitochondrial dysfunction show promise for managing CKD and reducing associated mortality.
Area of Science:
- Nephrology
- Cardiology
- Metabolic Diseases
Background:
- Altered lipid metabolism and distribution are implicated in chronic kidney disease (CKD) development and progression.
- Dyslipidemia is a significant risk factor for CKD, increasing cardiovascular event risk and mortality.
Purpose of the Study:
- To review the role of lipids in kidney disease progression, lipotoxicity, and mitochondrial dysfunction.
- To discuss current and emerging therapeutic strategies for dyslipidemia in CKD patients.
Main Methods:
- Literature review focusing on lipid metabolism in kidney disease.
- Analysis of current guidelines and clinical trial data for lipid-lowering therapies in CKD.
- Examination of novel therapeutic agents and their mechanisms of action.
Main Results:
- Statin therapy is the most common lipid-lowering treatment for CKD, though guidelines remain controversial.
- Efficacy of proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9i) in CKD patients is not yet established.
- Emerging therapies including PCSK9-small interfering RNA (siRNA), evinacumab, cyclodextrins, and FXR/TGR5 agonists show potential.
Conclusions:
- Understanding lipid metabolism regulation in kidney disease is crucial.
- Targeting mitochondrial dysfunction offers a potential therapeutic avenue for renal lipid disorders.
- Further research is needed to evaluate novel agents for cardiovascular risk reduction and kidney function improvement in CKD.
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