Ciprofibrate therapy in patients with hypertriglyceridemia and low high density lipoprotein (HDL)-cholesterol: greater reduction of non-HDL cholesterol in subjects with excess body weight (The CIPROAMLAT study)

Springer Science and Business Media LLC - Tập 3 - Trang 1-6 - 2004
Carlos A Aguilar-Salinas1, Andréia Assis-Luores-Vale2, Benjamín Stockins3, Hector Mario Rengifo4, José Dondici Filho5, Abrahão Afiune Neto6, Lísia Marcílio Rabelo7, Kerginaldo Paulo Torres8, José Egídio Paulo de Oliveira9, Carlos Alberto Machado10, Eliana Reyes11, Victor Saavedra12, Fernando Florenzano13, Ma Victoria Hernández14, Sergio Hernandez Jiménez1, Erika Ramírez1, Cuauhtémoc Vazquez15, Saul Salinas15, Ismael Hernández16, Octavio Medel16, Ricardo Moreno17, Paula Lugo18, Ricardo Alvarado19, Roopa Mehta1, Victor Gutierrez20, Francisco J Gómez Pérez1
1Departamento de Endocrinología y Metabolismo, Instituto Nacional de la Nutrición, México City, Mexico
2Hospital Socor. Dept° de Aterosclerose. Rua Tupis, Brazil
3Universidad De La Frontera. Departamento Medicina Interna. Av, Francisco, Temuco-Chile
4Centro Médico del Pacífico. Departamento de Endocrinología, Calle, Colombia
5CINDI – Centro de Investigações Diagnósticas Ltda. Dept° de Cardiologia. Rua Rei Alberto, Brazil
6Hospital São Salvador. Dept° de Cardiologia. Avenida A, Brazil
7Fundação Baiana de Cardiologia. Dept° de Lípides. Rua Augusto Viana, Brazil
8Prócardio. Dept° de Aterosclerose. Avenida Nascimento de Castro, Brazil
9Hospital Universitário Clementino Fraga Filho. Dept° de Diabetes/Nutrição. Avenida Brigadeiro Trompowiski, Brazil
10Centro de Referência de Hipertensão Arterial Diabetes e Apoio à Saúde do Idoso Dept° de Centro de Referência em Dislipidemia Rua Doutor Clementino, Brazil
11Hospital Dipreca. Unidad de Asistencia Nutricional Intensiva.División Medicina Interna Vital Apoquindo 1200, Las Condes, Chile
12Consulta Privada. Guardia Vieja 181 of. 405, Providencia, Chile
13Hospital Del Salvador. Sección Cardiología. Av. Salvador 364, Providencia, Chile
14Hospital Fuerza Aérea De Chile. Unidad De Cardiología.Av., Las Condes, Chile
15Hospital de Cardiología del Centro Médico Nacional Siglo XXI (IMSS).Depto. de Estudios Metabólicos y Clínica de Lípidos.Av., México, D. F
16Hospital Juárez de México (SSA).Unidad Coronaria.Av. Instituto Politécnico Nacional, México, D. F
17Hospital General Regional No. 72 (IMSS).Terapia Intensiva.Filiberto Gómez, Tlalnepantla, Mexico
18Centro Médico Nacional de Occidente (IMSS).Departamento de Cardiología.Belisario Domínguez sin número Col. Centro., Guadalajara, Mexico
19Hospital Dr. Santiago Ramón y Cajal (ISSSTE). Departamento de Cardiología Predio Canoa S/N Col., Los Angeles, Mexico
20Asociación De Diabéticos De Chile, Quebec, Chile

Tóm tắt

Hypertriglyceridemia in combination with low HDL cholesterol levels is a risk factor for cardiovascular disease. Our objective was to evaluate the efficacy of ciprofibrate for the treatment of this form of dyslipidemia and to identify factors associated with better treatment response. Multicenter, international, open-label study. Four hundred and thirty seven patients were included. The plasma lipid levels at inclusion were fasting triglyceride concentrations between 1.6–3.9 mM/l and HDL cholesterol ≤ 1.05 mM/l for women and ≤ 0.9 mM/l for men. The LDL cholesterol was below 4.2 mM/l. All patients received ciprofibrate 100 mg/d. Efficacy and safety parameters were assessed at baseline and at the end of the treatment. The primary efficacy parameter of the study was percentage change in triglycerides from baseline. After 4 months, plasma triglyceride concentrations were decreased by 44% (p < 0.001). HDL cholesterol concentrations were increased by 10% (p < 0.001). Non-HDL cholesterol was decreased by 19%. A greater HDL cholesterol response was observed in lean patients (body mass index < 25 kg/m2) compared to the rest of the population (8.2 vs 19.7%, p < 0.001). In contrast, cases with excess body weight had a larger decrease in non-HDL cholesterol levels (-20.8 vs -10.8%, p < 0.001). There were no significant complications resulting from treatment with ciprofibrate. Ciprofibrate is efficacious for the correction of hypertriglyceridemia / low HDL cholesterol. A greater decrease in non-HDL cholesterol was found among cases with excess body weight. The mechanism of action of ciprofibrate may be influenced by the pathophysiology of the disorder being treated.

Tài liệu tham khảo

Jeppesen J, Hein HO, Suadicani P, Gyntelberg F: High triglycerides/low high density lipoprotein cholesterol, ischemic electrocardiogram changes, and risk of ischemic heart disease. Am Heart J. 2002, 145: 103-108. 10.1067/mhj.2003.45. Assmann G, Schulte H, Cullen P: New and classical risk factors – The Munster heart study (PROCAM). Eur J Med Res. 1997, 2: 237-242. Stong K, Bonita R, the SuRF Report1: Surveillance of risk factors related to non-communicable diseases: Current status of global data. 2003, Geneva, World Health Organization Aguilar-Salinas CA, Olaiz G, Valles V, Ríos JM, Gómez Pérez FJ, Rull JA, Rojas R, Franco A, Sepúlveda J: High prevalence of low HDL cholesterol concentrations and mixed hyperlipidemia in a Mexican nation wide survey. J Lipid Res. 2001, 42: 1298-1307. Groop L, Orho-Melander M: The dysmetabolic syndrome. J Intern Med. 2001, 250: 105-120. 10.1046/j.1365-2796.2001.00864.x. Bloomfield Rubins H, Robins SJ, Collins D, Fye CL, Anderson JW, Elam MB, Faas F, Linares E, Schaefer EJ, Schectman G, Wilt T, Wittes J, for the Veterans Affairs High-Density Lipoprotein Cholesterol Intervention Trial Study Group: Gemfibrozil for the secondary prevention of coronary heart disease in men with low levels of high density lipoprotein cholesterol. Veterans Affairs High – Density Lipoprotein Cholesterol Intervention Trial Study Group. N Engl J Med. 1999, 341: 410-418. 10.1056/NEJM199908053410604. Robins S, Bloomfield Rubins H, Faas F, Schaefer E, Elam M, Anderson J, Collin D, on behalf of the VA-HIT Study Group: Insulin resistance and cardiovascular events with low HDL cholesterol. Diabetes Care. 2003, 26: 1513-1517. Faergeman O: Hypertriglyceridemia and the fibrate trials. Curr Opin Lipidol. 2000, 11: 609-614. 10.1097/00041433-200012000-00007. Betteridge DJ, Khan M: Review of the guidelines for management of dislipidemia. Baillieres Clin Endocrinol Metab. 1995, 9: 867-890. Expert panel on detection, evaluation and treatment of high blood cholesterol in adults: Executive summary of the third report of the National Cholesterol Education Program (NCEP) Expert panel on detection, evaluation and treatment of high cholesterol in adults (adult treatment panel III). JAMA. 2001, 285: 2486-2497. Cattin L, Da Col PG, Feruglio FS, Finazzo L, Rimondi S, Descovich G, Manzato E, Zambon S, Crepaldi G, Siepi D: Efficacy of ciprofibrate in primary type II and IV hyperlipidemia: the Italian Multicenter Study. Clin Ther. 1990, 12: 482-488. Betteridge DJ: Ciprofibrate: a profile. Postgrad Med J. 1993, 69: S42-S47. Bruckert E, Dejager S, Chapman MJ: Ciprofibrate therapy normalizes the atherogenic low density lipoprotein subspecies profile in combined hyperlipidemia. Atherosclerosis. 1993, 100: 91-102. Goa K, Barradell L, Plosker G: Bezafibrate. Drugs. 1996, 52: 725-753. Knipscheer H, de Valois C, van den Ende B, Wouter J, Kastelin J: Ciprofibrate versus gemfibrozil in the treatment of primary hyperlipidemia. Atherosclerosis. 1996, 124 (Suppl): S75-S81. Ferrannini E, Natali A, Bell P, Cavallo-Perin P, Lalic N, Mingrone G: Insulin resistance and hypersecretion in obesity. J Clin Invest. 1997, 100: 1166-1173. Schmidt MI, Duncan BB, Watson RL, Sharrett AR, Brancati FL, Heiss G: A metabolic syndrome in whites and African-Americans: the Atherosclerosis Risk in Communities baseline study. Diabetes Care. 1996, 19: 414-418. Aguilar Salinas CA, Barrett H, Schonfeld G: Metabolic modes of action of statins in hyperlipoproteinemias. Atherosclerosis. 1998, 141: 203-207. 10.1016/S0021-9150(98)00198-1. Hugh P, Barrett R, Watts GF: Kinetic studies of lipoprotein metabolism in the metabolic syndrome including effects of nutritional interventions. Curr Opin Lipidol. 2003, 14: 61-68. 10.1097/00041433-200302000-00011. Shachter N: Apolipoproteins C-I and C-III as important modulators of lipoprotein metabolism. Curr Opin Lipidol. 2001, 12: 297-304. 10.1097/00041433-200106000-00009. Fu T, Mukhopadhyay D, Davidson NO, Borensztajn J: The PPAR alpha agonist ciprofibrate inhibits apolipoprotein B mRNA editing in LDL receptor-deficient mice: Effects on plasma lipoproteins and the development of atherosclerotic lesions. J Biol Chem. 2004, Apr 27. Guerin M, Le Goff W, Frisdal E, Schneider S, Milosavljevic D, Bruckert E, Chapman MJ: Action of ciprofibrate in type IIb hyperlipoproteinemia: modulation of the atherogenic lipoprotein phenotype and stimulation of high-density lipoprotein-mediated cellular cholesterol efflux. J Clin Endocrinol Metab. 2003, 88: 3738-46. 10.1210/jc.2003-030191. Gaw A: Evidence based approach for the management of mixed hyperlipidemia. Atherosclerosis. 1998, 137 (Suppl): S97-S100. Barbier O, Torra IP, Duguay Y, Blanquart C, Fruchart JC, Glineur C, Staels B: Pleiotropic actions of peroxisome proliferator-activated receptors in lipid metabolism and atherosclerosis. Arterioscler Thromb Vasc Biol. 2002, 22: 717-26. 10.1161/01.ATV.0000015598.86369.04. Tsuyuki RT, Bungard TJ: Poor adherence with hypolipidemic drugs: a lost opportunity. Pharmacotherapy. 2001, 21: 576-582. 10.1592/phco.21.6.576.34541.