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Published on: October 2, 2020
Is lipid control necessary in hemodialysis patients?
1Medical Service, Veterans Affairs Salt Lake City Healthcare System and Division of Nephrology and Hypertension and Dialysis Program, University of Utah, Salt Lake City, Utah, USA. alfred.cheung@hsc.utah.edu
Insights
Cardiovascular disease risk in dialysis patients differs from the general population. Research should focus on unique dyslipidemias like hypertriglyceridemia and altered HDL, LDL, and lipoprotein(a) levels, not just LDL cholesterol.
Area of Science:
- Nephrology
- Cardiology
- Lipid Metabolism
Background:
- High LDL cholesterol predicts cardiovascular disease (CVD) in the general population.
- Statins show limited CVD benefit in dialysis patients, reasons unclear.
- Uremic dyslipidemia differs from general population, with high LDL not a hallmark.
Purpose of the Study:
- To explore the complex association between lipid profiles and CVD in dialysis patients.
- To investigate alternative atherogenic lipoproteins in dialysis patients.
- To guide future research on CVD risk factors in this population.
Main Methods:
- Review of recent randomized trials on statin efficacy.
- Analysis of dyslipidemia patterns in dialysis patients.
- In vitro and epidemiologic studies on lipoprotein atherogenicity.
Main Results:
- Statins did not significantly reduce primary CVD outcomes in dialysis patients.
- Dialysis dyslipidemia includes hypertriglyceridemia, low HDL, high Lp(a), and modified LDL.
- These aberrant lipoproteins are suggested to be atherogenic.
Conclusions:
- Standard lipid targets (LDL cholesterol) may not be appropriate for dialysis patients.
- Focus should shift to other dyslipidemic states and risk factors.
- Further research is needed on atherogenic lipoproteins in uremia.
Abstract:
Although high serum total cholesterol and LDL cholesterol levels are predictive of cardiovascular diseases in the general population, this association is more complex in the dialysis patients. Two recent randomized trials failed to show significant beneficial effects of statins on the primary cardiovascular outcomes in these patients. The reasons for this lack of benefits are unclear. The postulates include the possibilities that LDL cholesterol is not important in atherogenesis and that atherosclerosis is not a major contributor to cardiovascular diseases in the dialysis population. It is important to note that high serum LDL cholesterol level is not a prominent feature of uremic dyslipidemia. Instead, the hallmark dyslipidemias in the dialysis population are hypertriglyceridemia as a result of the accumulation of lipoprotein remnant particles, low serum HDL cholesterol levels, high serum levels of lipoprotein(a) [Lp(a)], and the modification of LDL cholesterol by oxidation and carbamylation. In vitro and epidemiologic studies have further suggested that these abnormal lipoproteins or aberrant serum lipoprotein levels are atherogenic. More research efforts should be directed toward these dyslipidemic states and the multitude of other putative cardiovascular risk factors in dialysis patients.
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