Copyright
©The Author(s) 2016.
World J Gastroenterol. Mar 28, 2016; 22(12): 3315-3324
Published online Mar 28, 2016. doi: 10.3748/wjg.v22.i12.3315
Published online Mar 28, 2016. doi: 10.3748/wjg.v22.i12.3315
Agent (daily dose) | Interactions | Comment |
HMG-CoA reductase inhibitors (statins) | ||
Lovastatin (20-80 mg) | Lovastatin, Simvastatin, Atorvastatin are mainly catabolized via hepatic CYP3A4: Caution in case of use of CYP3A4-Inhibitors (e.g., Itraconazole, Ketoconazole, HIV-protease-inhibitors Erythromycin, Clarithromycin, Telithromycin, Nefazodon). | Class of drugs with the highest lipid lowering effect |
Pravastatin (20-40 mg) | Contraindications: | |
Simvastatin (20-80 mg) | (1) advanced liver diseases; | |
Fluvastatin (20-80 mg) | (2) Rosuvastatin: simultaneous use of Cyclosporine; | |
Atorvastatin (10-80 mg) | Caution if fibrates or nicotinic acid are simultaneously used: high risk of myopathies. | and (3) Statin intolerance |
Rosuvastatin (5-40 mg) | Caution: serious interactions due to competitive inhibition of CYP450 3A4-metabolism cannot be ruled out: Prefer Fluvastatin or Pravastatin for treatment due to absence of CYP450 3A4 metabolisis. | |
Simultaneous use of calcineurin-inhibiting agents might reduce the elimination of statins: high risk of myopathies and rhabdomyolysis. Monitoring is necessary and low statin doses at the beginning are recommended. | ||
Caution with dose escalation. No interactions have been observed between Sirolimus and | ||
Atorvastatin and between Everolimus and Atorvastatin respectively Pravastatin. | ||
Bile acid binding anion exchange resins | ||
Colestyramine (4-16 g) | Caution: may reduce or retard gastrointestinal absorption of simultaneous orally administered agents. | Lowering of LDL-cholesterol, also used in combination with Statins or Ezetemibe |
Colesevelam (2.5-3.75 g) | ||
If interactions are possible, agents should be taken > 1 before or > 4 h after Colestyramine intake. Colesevelam should be taken 4 h before or after taking other drugs. | Contraindications: | |
Ileus or occlusion of bile ducts | ||
Blood level monitoring is required for agents with a narrow therapeutic window. | ||
Caution with simultaneous use of immunsuppressants or lipid lowering agents. | ||
e.g., bioavailability of mycophenolic acid can be reduced due to the simultaneous use of bile acid binding anion exchange resins (40% in case of MMF + Colestyramine). Intervals of medication intake mentioned above are obligatory. | ||
Nicotinic acid | ||
Sustained-release tablets (Niaspan®) (1-2 g) | In some cases simultaneous use of nicotinic acid and HMG-CoA reductase inhibitors was associated with myopathies/rhabdomyolysis: careful assessment of risks and benefits is required. Tredaptive® (according to medicinal product's professional information use was only evaluated in combination with Simvastatin): small increase of AUC and Cmax of Simvastatin (probably without any clinical relevance). | Lowering of LDL and triglyceride serum concentrations |
Nicotininc acid/Laropiprant (Tredaptive®) (1-2 g) | Contraindications | |
(1) advanced liver diseases; | ||
(2) acute peptic ulcer; | ||
and (3) arterial bleeding | ||
Hot drinks, alcohol and spicy foods may favor flush. Simultaneous use with nicotinic acid should be avoided. | ||
Fibrates | ||
Gemfibrozil (2 × 600 mg) | Caution: Simultaneous treatment with HMG-CoA reductase inhibitors leads to an increased risk for myopathies and rhabdomyolysis. Statin serum concentrations can rise: no combination with statins or monitor patients closely. | Reducing triglycerides. Avoid combination with HMG-CoA reductase inhibitors. |
Fenofibrate (200 mg) | Contraindications | |
Bezafibrate (200-600 mg) | (1) advanced liver dysfunction; | |
and (2) severe renal impairment | ||
Combination with Calcineurin-Inhibitors and mTOR-Inhibitors leads to an increased risk for rhabdomyolysis and other side effects: monitoring is required. | ||
Cholesterol resorption reducing agents | ||
Ezetemibe (Ezetrol®) (10 mg) | Caution: Simultaneous treatment with HMG-CoA reductase inhibitors leads to an increased risk of myopathies and rhabdomyolysis and elevation of liver enzymes: close monitoring of liver function is required. | Lowering of LDL cholesterol: |
(1) advanced liver diseases; | ||
and (2) persistent elevated liver enzymes | ||
Rare interactions (no induction of CYP450 enzymes) | ||
No combination with fibrates: tolerability and effectiveness were not evaluated. | ||
Combination with Fenofibrate leads to an increased risk for cholelithiasis and gall bladder diseases. | ||
Caution with the simultaneous use of Cyclosporine: AUC of Ezetemibe rises, no data concerning changes in Cyclosporine-blood levels available. No clinical effects and interactions with other immunosuppressants have been observed to date. Monitoring of immunosuppressive agents is required[50]. |
- Citation: Hüsing A, Kabar I, Schmidt HH. Lipids in liver transplant recipients. World J Gastroenterol 2016; 22(12): 3315-3324
- URL: https://www.wjgnet.com/1007-9327/full/v22/i12/3315.htm
- DOI: https://dx.doi.org/10.3748/wjg.v22.i12.3315