TY - JOUR
T1 - Effects of weight loss and seafood consumption on inflammation parameters in young, overweight and obese European men and women during 8 weeks of energy restriction
AU - Ramel, A.
AU - Martinez, J. A.
AU - Kiely, M.
AU - Bandarra, N. M.
AU - Thorsdottir, I.
PY - 2010/9
Y1 - 2010/9
N2 - Background/Objectives: In vitro studies have shown that long-chain n-3 polyunsaturated fatty acids (LC n-3 PUFAs) can affect inflammation; however, results from intervention studies in overweight or obese individuals are contradicting. The aim of this study was to investigate the effects of weight loss and seafood consumption on inflammation parameters during energy restriction. Subjects/Methods: In this 8-week intervention trial, 324 subjects (aged 20-40 years, body mass index 27.5-32.5 kg/m 2 from Iceland, Spain and Ireland) were randomized to one of four energy-restricted diets (30% relative to estimated requirements): salmon (3 × 150 g/week, 2.1 g LC n-3 PUFA per day); cod (3 × 150 g/week, 0.3 g LC n-3 PUFA per day); fish oil capsules (1.3 g LC n-3 PUFA per day); and control (sunflower oil capsules, no seafood). Body weight, high-sensitivity C-reactive protein (CRP), interleukin-6 (IL-6), glutathione reductase and prostaglandin F2 alpha (PGEF2α) were measured at baseline and end point. Results: Subjects experienced weight loss (5.23.2 kg, P<0.001). Taken together for all subjects, there were significant decreases in all inflammation parameters. On a group level, salmon consumption was most effective, three of the four inflammation parameters decreased in the salmon group (high-sensitivity CRP32.0%; IL-618.4%; PGEF2α18.5%; all P<0.05). Cod consumption decreased high-sensitivity CRP and IL-6 (21.5 and 10.8%, respectively, both P<0.05). Changes in the other two groups were not significant, which can be partly explained by the large s.d. Conclusions: The mean concentrations of inflammation parameters decreased during a period of weight loss and dietary intervention. In our study, salmon consumption was most effective, three of the four measured inflammation parameters decreased significantly in the salmon group.
AB - Background/Objectives: In vitro studies have shown that long-chain n-3 polyunsaturated fatty acids (LC n-3 PUFAs) can affect inflammation; however, results from intervention studies in overweight or obese individuals are contradicting. The aim of this study was to investigate the effects of weight loss and seafood consumption on inflammation parameters during energy restriction. Subjects/Methods: In this 8-week intervention trial, 324 subjects (aged 20-40 years, body mass index 27.5-32.5 kg/m 2 from Iceland, Spain and Ireland) were randomized to one of four energy-restricted diets (30% relative to estimated requirements): salmon (3 × 150 g/week, 2.1 g LC n-3 PUFA per day); cod (3 × 150 g/week, 0.3 g LC n-3 PUFA per day); fish oil capsules (1.3 g LC n-3 PUFA per day); and control (sunflower oil capsules, no seafood). Body weight, high-sensitivity C-reactive protein (CRP), interleukin-6 (IL-6), glutathione reductase and prostaglandin F2 alpha (PGEF2α) were measured at baseline and end point. Results: Subjects experienced weight loss (5.23.2 kg, P<0.001). Taken together for all subjects, there were significant decreases in all inflammation parameters. On a group level, salmon consumption was most effective, three of the four inflammation parameters decreased in the salmon group (high-sensitivity CRP32.0%; IL-618.4%; PGEF2α18.5%; all P<0.05). Cod consumption decreased high-sensitivity CRP and IL-6 (21.5 and 10.8%, respectively, both P<0.05). Changes in the other two groups were not significant, which can be partly explained by the large s.d. Conclusions: The mean concentrations of inflammation parameters decreased during a period of weight loss and dietary intervention. In our study, salmon consumption was most effective, three of the four measured inflammation parameters decreased significantly in the salmon group.
KW - fish
KW - inflammation
KW - LC n-3 PUFA
KW - seafood
KW - weight loss
KW - young adults
UR - https://www.scopus.com/pages/publications/77956345305
U2 - 10.1038/ejcn.2010.99
DO - 10.1038/ejcn.2010.99
M3 - Article
C2 - 20551965
AN - SCOPUS:77956345305
SN - 0954-3007
VL - 64
SP - 987
EP - 993
JO - European Journal of Clinical Nutrition
JF - European Journal of Clinical Nutrition
IS - 9
ER -