Effect of ezetimibe in patients who cannot tolerate statins or cannot get to the low density lipoprotein cholesterol target despite taking a statin

被引:83
作者
Gazi, Irene F. [1 ]
Daskalopoulou, Stella S. [1 ]
Nair, Devaki R. [1 ]
Mikhailidis, Dimitri P. [1 ]
机构
[1] Univ Coll Med, Royal Free Hosp, Dept Clin Biochem, London, England
关键词
creatinine; ezetimibe; high density lipoprotein cholesterol; low density lipoprotein cholesterol; safety; statins; Triglycerides; vascular disease;
D O I
10.1185/030079907X226267
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Recent guidelines underline the need for high-risk patients to reach strict low density lipoprotein cholesterol (LDL-C) targets (1.8-2.6 mmol/L; 70-100 mg/dL), and specifically mention the possible use of combination therapy (e.g. statin + ezetimibe) to achieve these goals. Methods: A retrospective case-note audit was carried out to assess the response to administering ezetimibe in patients unable to tolerate statins (Group 1), or high dose of statins (Group 2) and patients who cannot achieve the LDL-C target (2.6 mmol/L; 100 mg/dL) despite taking a statin (Group 3). Results: Ezetimibe lowered LDL-C levels by 20-29% across the 3 patient groups after 2-3 months of treatment. High density lipoprotein cholesterol (HDL-C) levels tended to remain unchanged, although there was a consistent trend for a fall if baseline values were 'high'. However, the LDLC/HDL-C ratio changed significantly and favourably in all groups. The fall in fasting triglyceride levels in all groups was greater (reaching 19-25%) when baseline levels were >= 1.5 or 1.7 mmol/L (136-150 mg/dL). There were no marked abnormalities in liver function tests or creatine kinase activity. In Group 3 there was a significant trend for a fall in serum creatinine levels across the tertiles of baseline creatinine values. Limitations of the present study include the small sample size (especially in Groups 1 and 2), its short-term duration and the absence of event-based end-points. Therefore, the results are hypothesis-generating rather than conclusive. Conclusions: When used alone or added to a statin, ezetimibe favourably altered the LDL-C/HDL-C ratio and lowered triglyceride levels. Ezetimibe was well tolerated in patients with statin intolerance and was associated with a 26% fall in LDL-C. An additional action may be some degree of improved renal function. Further studies are needed to confirm these findings.
引用
收藏
页码:2183 / 2192
页数:10
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共 51 条
  • [1] The effects of Ezetimibe on the LDL-cholesterol particle number
    Al-Shaer, MH
    [J]. CARDIOVASCULAR DRUGS AND THERAPY, 2004, 18 (04) : 327 - 328
  • [2] Treatment with atorvastatin to the National Cholesterol Educational Program goal versus 'usual' care in secondary coronary heart disease prevention - The GREek Atorvastatin and Coronary-heart-disease Evaluation (GREACE) Study
    Athyros, VG
    Papageorgiou, AA
    Mercouris, BR
    Athyrou, VV
    Symeonidis, AN
    Basayannis, EO
    Demitriadis, DS
    Kontopoulos, AG
    [J]. CURRENT MEDICAL RESEARCH AND OPINION, 2002, 18 (04) : 220 - 228
  • [3] The effect of statins versus untreated dyslipidaemia on renal function in patients with coronary heart disease. A subgroup analysis of the Greek atorvastatin and coronary heart disease evaluation (GREACE) study
    Athyros, VG
    Mikhailidis, DP
    Papageorgiou, AA
    Symeonidis, AN
    Pehlivanidis, AN
    Bouloukos, VI
    Elisaf, M
    [J]. JOURNAL OF CLINICAL PATHOLOGY, 2004, 57 (07) : 728 - 734
  • [4] Pathogenesis and treatment of kidney disease and hypertension - Effect of statins versus untreated dyslipidemia on serum uric acid levels in patients with coronary heart disease: A subgroup analysis of the GREek Atorvastatin and Coronary-heart-disease Evaluation (GREACE) study
    Athyros, VG
    Elisaf, M
    Papageorgiou, AA
    Symeonidis, AN
    Pehlivanidis, AN
    Bouloukos, VI
    Milionis, HJ
    Mikhailidis, DP
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 2004, 43 (04) : 589 - 599
  • [5] Triglyceride, small, dense low-density lipoprotein, and the atherogenic lipoprotein phenotype.
    Austin M.A.
    [J]. Current Atherosclerosis Reports, 2000, 2 (3) : 200 - 207
  • [6] Prevention and Rehabilitation - Dose-comparison study of the combination of ezetimibe and simvastatin (Vytorin) versus atorvastatin in patients with hypercholesterolemia: The Vytorin Versus Atorvastatin (VYVA) Study
    Ballantyne, CM
    Abate, N
    Yuan, Z
    King, TR
    Palmisano, J
    [J]. AMERICAN HEART JOURNAL, 2005, 149 (03) : 464 - 473
  • [7] Effect of ezetimibe coadministered with atorvastatin in 628 patients with primary hypercholesterolemia - A prospective, randomized, double-blind trial
    Ballantyne, CM
    Houri, J
    Notarbartolo, A
    Melani, L
    Lipka, LJ
    Suresh, R
    Sun, S
    LeBeaut, AP
    Sager, PT
    Veltri, EP
    [J]. CIRCULATION, 2003, 107 (19) : 2409 - 2415
  • [8] Effectiveness and tolerability of ezetimibe in patients with primary hypercholesterolemia: Pooled analysis of two phase II studies
    Bays, HE
    Moore, PB
    Drehobl, MA
    Rosenblatt, S
    Toth, PD
    Dujovne, CA
    Knopp, RH
    Lipka, LJ
    LeBeaut, AP
    Yang, B
    Mellars, LE
    Cuffie-Jackson, C
    Veltri, EP
    [J]. CLINICAL THERAPEUTICS, 2001, 23 (08) : 1209 - 1230
  • [9] Efficacy and tolerability of ezetimibe 10 mg/day coadministered with statins in patients with primary hypercholesterolemia who do not achieve target LDL-C while on statin monotherapy:: A Canadian, multicentre, prospective study -: The Ezetrol® Add-On Study
    Bissonnette, Stephane
    Habib, Rafik
    Sampalis, Fotini
    Boukas, Stella
    Sampalis, John S.
    [J]. CANADIAN JOURNAL OF CARDIOLOGY, 2006, 22 (12) : 1035 - 1044
  • [10] 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