Safety and Effectiveness of Ezetimibe in Liver Transplant Recipients with Hypercholesterolemia

被引:53
作者
Almutairi, Fawaz [2 ]
Peterson, Theresa C. [2 ,3 ]
Molinari, Michele [4 ]
Walsh, Mark J. [4 ]
Alwayn, Ian [4 ]
Peltekian, Kevork M. [1 ,2 ]
机构
[1] Queen Elizabeth 2 Hlth Sci Ctr, Atlantic Multiorgan Transplantat Program, Liver Team, Halifax, NS B3H 2Y9, Canada
[2] Dalhousie Univ, Dept Med, Halifax, NS, Canada
[3] Dalhousie Univ, Dept Pharmacol, Halifax, NS B3H 4H7, Canada
[4] Dalhousie Univ, Dept Surg, Halifax, NS B3H 4H2, Canada
关键词
SOLID-ORGAN TRANSPLANTATION; HYPERLIPIDEMIA; SIMVASTATIN; EFFICACY; DISEASE; TRIAL; PHARMACOKINETICS; CYCLOSPORINE; CHOLESTEROL; PRAVASTATIN;
D O I
10.1002/lt.21710
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Hypercholesterolemia is a common problem among transplant recipients. Despite package-insert warnings about the potential side effects of the use of statins in patients with chronic liver disease, they are often prescribed for liver transplant recipients. Unlike statins, ezetimibe acts through inhibition of enterohepatic recirculation of lipids. We report the effectiveness and safety of ezetimibe among liver transplant recipients because this has been evaluated previously only in kidney and heart transplant patients. A consecutive cohort of 25 liver graft recipients with serum low-density lipoprotein (LDL) levels > 100 mg/dL (2.5 mmol/L) after a mean (standard deviation) of 55 21 months following liver transplantation received ezetimibe (10 mg orally every day) for at least 6 months. Serum lipid profiles, liver and renal function tests, and dosages and blood levels of the immunosuppression drugs at baseline, 3 months, and 6 months were prospectively collected. The overall mean age was 58 +/- 12 years, and 56% were males. Statin therapy and fibrates were already being used in 32% and 20% of recipients for elevated LDL and/or triglycerides, respectively. The immunosuppression regimen included cyclosporine in 48% of subjects, tacrolimus in 32%, sirolimus in 48%, and mycophenolate mofetil in 44%; only 12% were on oral prednisone with a maximum daily dose of 5 mg. After ezetimibe was started, an 18% reduction in LDL values was observed [at baseline, 147 +/- 35 mg/dL (3.8 +/- 0.9 mmol/L), and at 6 months, 120 +/- 31 mg/dL (3.1 +/- 0.8 mmol/L); P = 0.010]. After 6 months, an additional 32% achieved the target LDL level of <100 mg/dL. None of the remaining variables, including immunosuppression drug levels, varied significantly during ezetimibe therapy. None of the subjects required adjustments in their pharmacological dosages. One discontinued ezetimibe 3 months later because of cost, 2 subjects had minimal nausea, 1 subject had myalgias without a rise in creatine phosphokinase, and 1 subject had a transient elevation (3-5 times) in liver enzymes from baseline with increases in the total and indirect bilirubin levels. In conclusion, among liver transplant recipients, hypercholesterolemia can be effectively treated with ezetimibe with few side effects and no interaction with immunosuppressive regimens. Liver Transpl 15:504-508, 2009. (C) 2009 AASLD.
引用
收藏
页码:504 / 508
页数:5
相关论文
共 31 条
  • [1] Interaction of single-dose ezetimibe and steady-state cyclosporine in renal transplant patients
    Bergman, AJ
    Burke, J
    Larson, P
    Johnson-Levonas, AO
    Reyderman, L
    Statkevich, P
    Maxwell, SE
    Kosoglou, T
    Murphy, G
    Gottesdiener, K
    Robson, R
    Paolini, JF
    [J]. JOURNAL OF CLINICAL PHARMACOLOGY, 2006, 46 (03) : 328 - 336
  • [2] A retrospective analysis of ezetimibe treatment in renal transplant recipients
    Buchanan, C
    Smith, L
    Corbett, J
    Nelson, E
    Shihab, F
    [J]. AMERICAN JOURNAL OF TRANSPLANTATION, 2006, 6 (04) : 770 - 774
  • [3] Serious drug-induced liver disease secondary to ezetimibe
    Castellote, Jose
    Ariza, Javier
    Rota, Rosa
    Girbau, Anna
    Xiol, Xavier
    [J]. WORLD JOURNAL OF GASTROENTEROLOGY, 2008, 14 (32) : 5098 - 5099
  • [4] Efficacy and safety of a potent new selective cholesterol absorption inhibitor, Ezetimibe, in patients with primary hypercholesterolemia
    Dujovne, CA
    Ettinger, MP
    McNeer, JF
    Lipka, LJ
    LeBeaut, AP
    Suresh, R
    Yang, B
    Veltri, EP
    [J]. AMERICAN JOURNAL OF CARDIOLOGY, 2002, 90 (10) : 1092 - 1097
  • [5] Fodor JG, 2000, CAN MED ASSOC J, V162, P1441
  • [6] Statins and solid organ transplantation
    Gazi, I. F.
    Liberopoulos, E. N.
    Athyros, V. G.
    Elisaf, M.
    Mikhailidis, D. P.
    [J]. CURRENT PHARMACEUTICAL DESIGN, 2006, 12 (36) : 4771 - 4783
  • [7] Gisbert C, 1997, Liver Transpl Surg, V3, P416, DOI 10.1002/lt.500030409
  • [8] HARRY DS, 1999, OXFORD TXB CLIN HEPA, P287
  • [9] Hyperlipidemia after liver transplantation - Natural history and treatment with the hydroxy-methylglutaryl-coenzyme a reductase inhibitor pravastatin
    Imagawa, DK
    Dawson, S
    Holt, CD
    Kirk, PS
    Kaldas, FM
    Shackleton, CR
    Seu, P
    Rudich, SM
    Kinkhabwala, MM
    Martin, P
    Goldstein, LI
    Murray, NGB
    Terasaki, PI
    Busuttil, RW
    [J]. TRANSPLANTATION, 1996, 62 (07) : 934 - 942
  • [10] Safety considerations with gastrointestinally active lipid-lowering drugs
    Jacobson, Terry A.
    Armani, Annemarie
    McKenney, James M.
    Guyton, John R.
    [J]. AMERICAN JOURNAL OF CARDIOLOGY, 2007, 99 (6A) : 47C - 55C