Omega-3 supplementation and non-alcoholic fatty liver disease: A systematic review and meta-analysis

被引:420
作者
Parker, Helen M. [2 ]
Johnson, Nathan A. [2 ,4 ]
Burdon, Catriona A. [2 ]
Cohn, Jeffrey S. [3 ]
O'Connor, Helen T. [2 ,4 ]
George, Jacob [1 ,5 ]
机构
[1] Univ Sydney, Westmead Hosp, Dept Med, Westmead, NSW 2145, Australia
[2] Univ Sydney, Discipline Exercise & Sport Sci, Westmead, NSW 2145, Australia
[3] Heart Res Inst, Nutr & Metab Grp, Sydney, NSW, Australia
[4] Univ Sydney, Boden Inst Obes Nutr & Exercise, Westmead, NSW 2145, Australia
[5] Univ Sydney, Storr Liver Unit, Westmead Millennium Inst, Westmead, NSW 2145, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
Fatty liver; Fish oil; Polyunsaturated fatty acid; Obesity; Diet; INSULIN-RESISTANCE; HEPATIC STEATOSIS; WEIGHT-LOSS; HYPERTENSION PREVALENCE; CARDIOVASCULAR-DISEASE; METABOLIC SYNDROME; NATURAL-HISTORY; DIETARY HABITS; UNITED-STATES; FISH-OIL;
D O I
10.1016/j.jhep.2011.08.018
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Non-alcoholic fatty liver disease (NAFLD) is a frequent accompaniment of obesity and insulin resistance. With the prevalence approaching 85% in obese populations, new therapeutic approaches to manage NAFLD are warranted. A systematic search of the literature was conducted for studies pertaining to the effect of omega-3 polyunsaturated fatty acid (PUFA) supplementation on NAFLD in humans. Primary outcome measures were liver fat and liver function tests: alanine aminotransferase (ALT) and aspartate aminotransferase [1]. Data were pooled and meta-analyses conducted using a random effects model. Nine eligible studies, involving 355 individuals given either omega-3 PUFA or control treatment were included. Beneficial changes in liver fat favoured PUFA treatment (effect size = -0.97, 95% CI: -0.58 to -1.35, p <0.001). A benefit of PUFA vs. control was also observed for AST (effect size = -0.97, 95% CI: -0.13 to -1.82, p = 0.02). There was a trend towards favouring PUFA treatment on ALT but this was not significant (effect size = -0.56, 95% CI: -1.16 to 0.03, p = 0.06). Sub-analyses of only randomised control trials (RCTs) showed a significant benefit for PUFA vs. control on liver fat (effect size = -0.96, 95% CI: -0.43 to -1.48, p <0.001), but not for ALT (p = 0.74) or AST (p = 0.28). There was significant heterogeneity between studies. The pooled data suggest that omega-3 PUFA supplementation may decrease liver fat, however, the optimal dose is currently not known. Well designed RCTs which quantify the magnitude of effect of omega-3 PUFA supplementation on liver fat are needed. (c) 2011 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:944 / 951
页数:8
相关论文
共 69 条
[41]   Why and How Meet n-3 PUFA Dietary Recommendations? [J].
Molendi-Coste, Olivier ;
Legry, Vanessa ;
Leclercq, Isabelle A. .
GASTROENTEROLOGY RESEARCH AND PRACTICE, 2011, 2011
[42]   DOES FISH-OIL LOWER BLOOD-PRESSURE - A METAANALYSIS OF CONTROLLED TRIALS [J].
MORRIS, MC ;
SACKS, F ;
ROSNER, B .
CIRCULATION, 1993, 88 (02) :523-533
[43]   Dietary habits and their relations to insulin resistance and postprandial lipemia in nonalcoholic steatohepatitis [J].
Musso, G ;
Gambino, R ;
De Michieli, F ;
Cassader, M ;
Rizzetto, M ;
Durazzo, M ;
Fagà, E ;
Silli, B ;
Pagano, G .
HEPATOLOGY, 2003, 37 (04) :909-916
[44]   A Meta-Analysis of Randomized Trials for the Treatment of Nonalcoholic Fatty Liver Disease [J].
Musso, Giovanni ;
Gambino, Roberto ;
Cassader, Maurizio ;
Pagano, Gianfranco .
HEPATOLOGY, 2010, 52 (01) :79-104
[45]  
Nelson JE, 2009, GASTROENTEROLOGY, V136, pA847
[46]   Trends in hypertension prevalence, awareness, treatment, and control in older US Adults: Data from the National Health and Nutrition Examination Survey 1988 to 2004 [J].
Ostchega, Yechiam ;
Dillon, Charles F. ;
Hughes, Jeffery P. ;
Carroll, Margaret ;
Yoon, Sarah .
JOURNAL OF THE AMERICAN GERIATRICS SOCIETY, 2007, 55 (07) :1056-1065
[47]   Drug therapy - Adherence to medication [J].
Osterberg, L ;
Blaschke, T .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (05) :487-497
[48]   Nonalcoholic steatohepatitis, insulin resistance, and metabolic syndrome: Further evidence for an etiologic association [J].
Pagano, G ;
Pacini, G ;
Musso, G ;
Gambino, R ;
Mecca, F ;
Depetris, N ;
Cassader, M ;
David, E ;
Cavallo-Perin, P ;
Rizzetto, M .
HEPATOLOGY, 2002, 35 (02) :367-372
[49]   Enhancement in liver SREBP-1c/PPAR-α ratio and steatosis in obese patients: Correlations with insulin resistance and n-3 long-chain polyunsaturated fatty acid depletion [J].
Pettinelli, Paulina ;
del Pozo, Talia ;
Araya, Julia ;
Rodrigo, Ramon ;
Veronica Araya, A. ;
Smok, Gladys ;
Csendes, Attila ;
Gutierrez, Luis ;
Rojas, Jorge ;
Korn, Owen ;
Maluenda, Fernando ;
Diaz, Juan C. ;
Rencoret, Guillermo ;
Braghetto, Italo ;
Castillo, Jaime ;
Poniachik, Jaime ;
Videla, Luis A. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2009, 1792 (11) :1080-1086
[50]   Randomized Controlled Trial Testing the Effects of Weight Loss on Nonalcoholic Steatohepatitis [J].
Promrat, Kittichai ;
Kleiner, David E. ;
Niemeier, Heather M. ;
Jackvony, Elizabeth ;
Kearns, Marie ;
Wands, Jack R. ;
Fava, Joseph L. ;
Wing, Rena R. .
HEPATOLOGY, 2010, 51 (01) :121-129