4.5 Article

Additive benefits of long-chain n-3 polyunsaturated fatty acids and weight-loss in the management of cardiovascular disease risk in overweight hyperinsulinaemic women

Journal

INTERNATIONAL JOURNAL OF OBESITY
Volume 30, Issue 10, Pages 1535-1544

Publisher

SPRINGERNATURE
DOI: 10.1038/sj.ijo.0803309

Keywords

adiponectin; weight-loss; insulin sensitivity; fish oil; n-3 PUFA

Funding

  1. MRC [MC_U105960384, MC_U120063239] Funding Source: UKRI
  2. Medical Research Council [MC_U120063239, MC_U105960384] Funding Source: researchfish
  3. Medical Research Council [MC_U105960384, MC_U120063239] Funding Source: Medline

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Background: Obesity, inflammation, insulin resistance and cardiovascular disease (CVD) risk are inter-related. Both weight-loss and long-chain n-3 polyunsaturated fatty acids (LC n-3 PUFA) are independently known to reduce metabolic risk, but the combined effects are unclear. Objective: This study examines whether addition of LC n-3 PUFA to a low fat/high carbohydrate weight-loss programme results in greater improvements in inflammation, insulin sensitivity and CVD risk, than weight-loss alone. Design: One hundred and sixteen overweight insulin-resistant women entered a 24-week randomised intervention study. Thirty-nine women were randomised to a weight-loss programme, with LC n-3 PUFA (WLFO), 38 to a weight-loss programme with placebo oil (WLPO), and 39 to receive placebo oil, with no weight-loss programme (control). Results: Ninety-three women completed the study (35 WLFO, 32 WLPO and 26 control), with significant weight-loss in WLFO (10.871.0%) and WLPO (12.471.0%) compared to the control group (P < 0.0001). The WLFO, but not WLPO or control group, showed significant increases in adipose tissue LC n-3 PUFA (0.34 +/- 70.20 vs 0.17 +/- 0.10 and 0.16 +/- 0.10 %DHA, P < 0.0001). Weight-loss showed significant improvements in insulin sensitivity (P < 0.001), lipid profile (triglycerides P < 0.05) and inflammation (sialic acid P < 0.05). Time*group effects showed significant decreases in triglycerides (P < 0.05) and increases in adiponectin (P < 0.01) with LC n-3 PUFA, in the WLFO vs WLPO groups. Conclusions: Weight-loss improved risk factors associated with CVD, with some additional benefits of LC n-3 PUFA on triglycerides and adiponectin. Given the current low dietary intake of LC n-3 PUFA, greater attention should be given to increase these fatty acids in the treatment of obesity.

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