Why the study?
Statin treatment reduces cardiovascular events in CKD and erythrocyte membrane oleic acid is higher in acute coronary syndrome, but the effect of pravastatin on erythrocyte membrane fatty acid contents in CKD was unknown.
Does pravastatin alter erythrocyte membrane fatty acid contents in patients with chronic kidney disease?
Does pravastatin alter erythrocyte membrane fatty acid contents in patients with chronic kidney disease?
Pravastatin treatment in CKD patients decreases protective polyunsaturated fatty acids in erythrocyte membranes, suggesting a potential need for omega-3 or linoleic acid supplementation.
Pravastatin may reduce protective fatty acids in CKD; hypothesis-generating for net CV effects, larger trials needed before practice change.
BACKGROUND: Statin treatment has decreased the risk of cardiovascular events in patients with chronic kidney disease (CKD). Erythrocyte membrane oleic acid level is higher in patients with acute coronary syndrome. This study aimed to evaluate the effect of pravastatin on the erythrocyte membrane fatty acid (FA) contents in patients with CKD. METHODS: Sixty-two patients were enrolled from January 2017 to March 2019 (NCT02992548). Pravastatin was initially administered at a dose of 20 mg for 24 weeks. The pravastatin dose was increased to 40 mg after 12 weeks if it was necessary to control dyslipidemia. The primary outcome was change in erythrocyte membrane FA, including oleic acid, after pravastatin treatment for 24 weeks. RESULTS: Forty-five patients finished this study, and there was no adverse effect related to pravastatin. Compared with baseline, total cholesterol and low-density lipoprotein cholesterol levels were significantly decreased after pravastatin treatment. Compared with baseline, saturated FA, oleic acid, and arachidonic acid levels were significantly increased and polyunsaturated FA and linoleic acid (LA) levels were significantly decreased after pravastatin treatment. There was also a decrease in eicosapentaenoic acid after pravastatin treatment in CKD patients with estimated glomerular filtration rate <60 mL/min/1.73 m2. CONCLUSION: Administration of pravastatin in patients with CKD leads to a decrease in FA known to be protective against the risk of CVD. Omega-3 FA or LA supplementation might be necessary to recover changes in erythrocyte membrane FA contents when pravastatin is used for treating dyslipidemia in patients with CKD.
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Lee et al. (2021) studied this question.
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