The Effect of Prescription Omega-3 Fatty Acids on Body Weight After 8 to 16 Weeks of Treatment for Very High Triglyceride Levels

被引:18
作者
Bays, Harold E. [1 ]
Maki, Kevin C. [2 ]
Doyle, Ralph T. [3 ]
Stein, Evan [4 ]
机构
[1] Louisville Metab & Atherosclerosis Res Ctr, Louisville, KY 40213 USA
[2] Provident Clinical Res & Consulting Inc, Bloomington, IN USA
[3] GlaxoSmithKline, Res Triangle Pk, NC USA
[4] Metab & Atherosclerosis Res Ctr, Cincinnati, OH USA
关键词
Lovaza (R); prescription omega-3 fatty acids; triglycerides; fatty acids; body weight; POLYUNSATURATED FATTY-ACIDS; ETHYL-ESTERS; SIMVASTATIN; 20; DIET;
D O I
10.3810/pgm.2009.09.2061
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Background: Prescription omega-3-acid ethyl ester (P-OM3; Lovaza (R)) therapy is indicated for treating very high triglyceride levels (>= 500 mg/dL) at a dose of 4 g/day. The caloric content associated with each 1-g capsule of P-OM3 is similar to 11 Cal (Cal = kilocalories) - similar to 9 Cal from the oil in the capsule that contains omega-3 fat and similar to 2 Cal attributed to the components of the capsule shell. Thus, the 4-g/day dose contributes similar to 44 Cal/day, with similar to 36 Cal/day derived from the oil. Methods: This analysis evaluated 167 dyslipidemic (triglycerides: >= 500 mg/dL and < 1300 mg/dL), overweight/obese (body mass index [BMI] >= 25 kg/m(2) and <= 43 kg/m(2)) patients aged 18 to 79 years. Data were derived from an 8-week, randomized, double-blinded, placebo-controlled, parallel-group trial comparing P-OM3 4 g/day + fenofibrate 130 mg/day (n = 84) versus placebo (4 g/day of corn oil) + fenofibrate 130 mg/day (n = 83), and an 8-week open-label extension (n = 117), during which all subjects received P-OM3 + fenofibrate. Subjects who received P-OM3 + fenofibrate continued the same treatment in the extension phase (non-switchers; n = 59). Those who initially received corn oil placebo + fenofibrate received P-OM3 + fenofibrate in the extension phase (switchers; n = 58). Results: During the 8-week double-blind phase in subjects receiving fenofibrate, the addition of P-OM3 (versus placebo) did not significantly change median (minimum, maximum) body weight (P-OM3 = 0 [-4.6, +4.2] kg, placebo = 0 [-3.6, +5.5] kg; P = 0.088) or waist circumference (P-OM3 = +0.1 [-12.1, +17.5] cm, placebo = +0.5 [-9.9, +12.2] cm; P = 0.162). In the 8-week extension phase, non-switchers and switchers did not differ in median change from the end of the double-blind phase in body weight (non-switchers = +0.2 [-3.2, +5.6] kg, switchers = +0.1 [-6.9, +7.9] kg; P = 0.982), or waist circumference (non-switchers = +0.1 [-9.8, +41.8] cm, switchers = +0.2 [-12.0, +7.0] cm; P = 0.685). Conclusion: When coadministered with fenofibrate for up to 16 weeks, the modest daily caloric contribution of P-OM3 (4 g/day) did not alter body weight or waist circumference compared with baseline or compared with fenofibrate plus placebo in patients with very high triglyceride levels.
引用
收藏
页码:145 / 150
页数:6
相关论文
共 20 条
[1]
Rationale for prescription omega-3-acid ethyl ester therapy for hypertriglyceridemia: A primer for clinicians [J].
Bays, Harold .
DRUGS OF TODAY, 2008, 44 (03) :205-246
[2]
Bays Harold E, 2008, Expert Rev Cardiovasc Ther, V6, P391, DOI 10.1586/14779072.6.3.391
[3]
Effect of dietary fish oil on body fat mass and basal fat oxidation in healthy adults [J].
Couet, C ;
Delarue, J ;
Ritz, P ;
Antoine, JM ;
Lamisse, F .
INTERNATIONAL JOURNAL OF OBESITY, 1997, 21 (08) :637-643
[4]
Efficacy and tolerability of adding prescription omega-3 fatty acids 4 g/d to simvastatin 40 mg/d in hypertriglyceridemic patients: An 8-week, randomized, double-blind, placebo-controlled study [J].
Davidson, Michael H. ;
Stein, Evan A. ;
Bays, Harold E. ;
Maki, Kevin C. ;
Doyle, Ralph T. ;
Shalwitz, Robert A. ;
Ballantyne, Christie M. ;
Ginsberg, Henry N. .
CLINICAL THERAPEUTICS, 2007, 29 (07) :1354-1367
[5]
*GLAXOSMITHKLINE, 2008, LOV PACK INS
[6]
Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III) Final Report [J].
Grundy, SM ;
Becker, D ;
Clark, LT ;
Cooper, RS ;
Denke, MA ;
Howard, WJ ;
Hunninghake, DB ;
Illingworth, R ;
Luepker, RV ;
McBride, P ;
McKenney, JM ;
Pasternak, RC ;
Stone, NJ ;
Van Horn, L ;
Brewer, HB ;
Cleeman, JI ;
Ernst, ND ;
Gordon, D ;
Levy, D ;
Rifkind, B ;
Rossouw, JE ;
Savage, P ;
Haffner, SM ;
Orloff, DG ;
Proschan, MA ;
Schwartz, JS ;
Sempos, CT ;
Shero, ST ;
Murray, EZ ;
Keller, SA ;
Jehle, AJ .
CIRCULATION, 2002, 106 (25) :3143-3421
[7]
Harris W S, 1997, J Cardiovasc Risk, V4, P385, DOI 10.1097/00043798-199710000-00011
[8]
Hartweg J, 2008, COCHRANE DB SYST REV, DOI 10.1002/14651858.CD003205.pub2
[9]
The influence of n-3 polyunsaturated fatty acids and very low calorie diet during a short-term weight reducing regimen on weight loss and serum fatty acid composition in severely obese women [J].
Kunesová, M ;
Braunerová, R ;
Hlavaty, P ;
Tvrzická, E ;
Stanková, B ;
Skrha, J ;
Hilgertová, J ;
Hill, M ;
Kopecky, J ;
Wagenknecht, M ;
Hainer, V ;
Matoulek, M ;
Parízková, J ;
Zák, A ;
Svacina, S .
PHYSIOLOGICAL RESEARCH, 2006, 55 (01) :63-72
[10]
Omega-3 Polyunsaturated Fatty Acids and Cardiovascular Diseases [J].
Lavie, Carl J. ;
Milani, Richard V. ;
Mehra, Mandeep R. ;
Ventura, Hector O. .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2009, 54 (07) :585-594