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Published on: September 20, 2020
Alirocumab in a high cardiovascular risk patient on hemodialysis with liver abnormalities
Periklis Dousdampanis1, Stelios F Assimakopoulos2, Ioulia Syrocosta3
1Hemodialysis Unit Kyanos Stavros Patras, Achaia, Greece.
Insights
Alirocumab offers a safe and effective alternative for lowering cholesterol in hemodialysis patients with high cardiovascular risk and liver issues. This PCSK9 inhibitor presents a promising treatment option for managing hyperlipidemia in this vulnerable population.
Area of Science:
- Cardiology
- Nephrology
- Pharmacology
Background:
- Type 2 diabetes mellitus and hemodialysis (HD) patients often have high cardiovascular disease (CVD) risk and hyperlipidemia.
- Standard lipid-lowering therapies like statins and ezetimibe may be contraindicated due to potential hepatotoxicity, particularly in patients with liver abnormalities such as chronic hepatitis C virus infection.
Observation:
- A male type 2 diabetic patient on hemodialysis with high CVD risk and hyperlipidemia discontinued statin and ezetimibe therapy due to chronic hepatitis C.
- Alirocumab, a PCSK9 inhibitor with no reported hepatotoxic effects, was administered at 150 mg every two weeks for eight weeks as an alternative treatment.
Findings:
- Treatment with alirocumab resulted in a significant decrease in low-density lipoprotein (LDL) levels.
- No adverse side effects were observed during the eight-week treatment period.
Implications:
- Alirocumab is a safe and effective alternative for managing hyperlipidemia and reducing CVD risk in hemodialysis patients with liver abnormalities.
- PCSK9 inhibitors should be considered a first-line treatment option for cholesterol lowering in this specific high-risk patient group.
Abstract:
We present a male diabetic type 2 patient on hemodialysis (HD) with high cardiovascular (CVD) risk and hyperlipidemia. The patient was under cholesterol-lowering therapy with statin and ezetimibe but he was obligated to discontinue due to chronic hepatitis C virus infection. Statins and ezetimibe may exert a potential hepatotoxic effect and for this reason, we attempted to find an alternative treatment to prevent CVD. Given that a potential hepatotoxic effect has not been reported for Abs SPCK9, we administered alirocumab 150 mg every 2 weeks for a total of 8 weeks. Low-density lipoprotein levels have decreased and no side effects have been observed. In conclusion, alirocumab is a safe and efficient alternative therapy approach for HD patients with high CVD risk and liver abnormalities. We suggest that SPCK 9 inhibitors should be considered as a first line treatment for lowering cholesterol in this specific patient group.
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