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Updated: May 21, 2026

Differential Effects of Lipid-lowering Drugs in Modulating Morphology of Cholesterol Particles
Published on: November 10, 2017
Statin therapy is associated with decreased small, dense low-density lipoprotein levels in patients undergoing
Insights
Statin therapy may reduce small, dense LDL (sd-LDL) in peritoneal dialysis patients, but not effectively in hemodialysis patients with comorbidities. Further research is needed to understand sd-LDL
Area of Science:
- Nephrology
- Cardiology
- Metabolic Disorders
Background:
- Cardiovascular disease (CVD) is a primary cause of death in dialysis patients.
- Dyslipidemia, particularly small, dense LDL (sd-LDL) particles, is a key CVD risk factor.
- Peritoneal dialysis (PD) patients often have worse lipid profiles than hemodialysis (HD) patients.
Purpose of the Study:
- To compare lipid profiles and sd-LDL proportions in HD and PD patients.
- To investigate the efficacy of statins in altering sd-LDL in these populations.
Main Methods:
- Comparative analysis of lipid profiles.
- Assessment of sd-LDL particle proportion.
- Evaluation of statin therapy effects in HD and PD patients.
Main Results:
- Statin therapy may reduce sd-LDL amount and proportion in PD patients.
- Statins showed limited efficacy in altering sd-LDL in HD patients with hypertension and diabetes.
- PD patients exhibit a more abnormal lipid profile than HD patients.
Conclusions:
- Statin therapy might be beneficial for reducing sd-LDL in PD patients.
- Statin effectiveness on sd-LDL is questionable in HD patients with comorbidities.
- Further large-scale studies are required to confirm findings and elucidate sd-LDL's role in dialysis-associated atherogenesis.
Abstract:
Cardiovascular disease is a major cause of morbidity and mortality among hemodialysis (HD) and peritoneal dialysis (PD) patients, and dyslipidemia plays an important role in its pathogenesis. In particular, small, dense LDL (sd-LDL) particles have been recently highlighted as an emerging cardiovascular risk factor. PD patients exhibit a more overtly abnormal lipid profile than HD patients, probably due to the metabolic interference of the peritoneal dialysis fluid. Statins are the main drugs for the treatment of dyslipidemia and they are able to decrease all LDL subclasses levels, but it remains unclear whether they can influence the proportion of sd-LDL. Only few studies regarding the effect of statins on the proportion of these particles have been performed in HD patients and, to our knowledge, no trials have been carried out in PD patients. Therefore, we compared the lipid profile and the proportion of sd-LDL in two populations of HD and PD patients. Our study suggests that statin therapy may be effective in reducing both the absolute amount and the proportion of sd-LDL in patients with a more overtly abnormal lipid profile, such as patients undergoing peritoneal dialysis. Statins do not seem to be effective in altering sd-LDL levels in patients undergoing hemodialysis with other factors that can influence LDL subtractions generation, such as hypertension and diabetes mellitus. If and when our results prove to be reproducible in large-scale studies, such studies should provide new insights into sd-LDL and its actual role in atherogenesis in patients undergoing hemodialysis or peritoneal dialysis.
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