Dietary factors and low-grade inflammation in relation to overweight and obesity

被引:794
作者
Calder, Philip C. [1 ,2 ]
Ahluwalia, Namanjeet [3 ]
Brouns, Fred [4 ,21 ]
Buetler, Timo [5 ,22 ]
Clement, Karine [6 ]
Cunningham, Karen [7 ]
Esposito, Katherine [8 ]
Jonsson, Lena S. [1 ]
Kolb, Hubert [9 ]
Lansink, Mirian [10 ]
Marcos, Ascension [11 ]
Margioris, Andrew [12 ]
Matusheski, Nathan [13 ]
Nordmann, Herve [14 ]
O'Brien, John [5 ]
Pugliese, Giuseppe [15 ]
Rizkalla, Salwa [6 ]
Schalkwijk, Casper [16 ]
Tuomilehto, Jaakko [17 ]
Waernberg, Julia [11 ,18 ]
Watzl, Bernhard [19 ]
Winklhofer-Roob, Brigitte M. [20 ]
机构
[1] ILSI Europe Aisbl, Ave E Mounier 83,Box 6, B-1200 Brussels, Belgium
[2] Univ Southampton, Sch Med, Southampton SO16 6YD, Hants, England
[3] Univ Paris, INSERM, U557, F-93017 Bobigny, France
[4] Cargill R&D Ctr Europe, B-1800 Vilvoorde, Belgium
[5] Nestle Res Ctr, CH-1000 Lausanne, Switzerland
[6] Hop La Pitie Salpetriere, Human Nutr Res Ctr, INSERM, U872,Dept Nutr, F-75013 Paris, France
[7] Coca Cola Europe, London W6 9HQ, England
[8] Univ Naples Federico II, Div Metab Dis, I-80138 Naples, Italy
[9] Univ Dusseldorf, Fac Med, Res Grp Immunobiol, D-40225 Dusseldorf, Germany
[10] Danone Res, Ctr Specialised Nutr, NL-6700 CA Wageningen, Netherlands
[11] Spanish Natl Res Council, CSIC, Dept Metab & Nutr, Madrid 28040, Spain
[12] Univ Crete, Sch Med, Iraklion 71409, Greece
[13] Kraft Gen Foods Inc, Nutr Res, Glenview, IL 60025 USA
[14] Ajinomoto Europe, F-75817 Paris, France
[15] Univ Roma La Sapienza, Dept Clin & Mol Med, I-00161 Rome, Italy
[16] Univ Maastricht, NL-6202 AZ Maastricht, Netherlands
[17] Univ Helsinki, FIN-00014 Helsinki, Finland
[18] Univ Navarra, Dept Prevent Med & Publ Hlth, E-31080 Pamplona, Spain
[19] Max Rubner Inst, Fed Res Ctr Nutr & Food, D-76131 Karlsruhe, Germany
[20] Karl Franzens Univ Graz, Human Nutr & Metab Res & Training Ctr, Inst Mol Biosci, A-8010 Graz, Austria
[21] Maastricht Univ Med Ctr, Dept Nutr, NL-6200 MD Maastricht, Netherlands
[22] Univ Zurich, Inst Pharmacol & Toxicol, XeRR, CH-8057 Zurich, Switzerland
关键词
Inflammation; Cytokines; Adipose; Obesity; Diet; C-REACTIVE PROTEIN; GLYCATION END-PRODUCTS; POLYUNSATURATED FATTY-ACIDS; NF-KAPPA-B; CARDIOVASCULAR RISK-FACTORS; NECROSIS-FACTOR-ALPHA; CONJUGATED LINOLEIC-ACID; LONG-CHAIN N-3; MODERATE ALCOHOL-CONSUMPTION; BLOOD MONONUCLEAR-CELLS;
D O I
10.1017/S0007114511005460
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 [营养与食品卫生学];
摘要
Low-grade inflammation is a characteristic of the obese state, and adipose tissue releases many inflammatory mediators. The source of these mediators within adipose tissue is not clear, but infiltrating macrophages seem to be especially important, although adipocytes themselves play a role. Obese people have higher circulating concentrations of many inflammatory markers than lean people do, and these are believed to play a role in causing insulin resistance and other metabolic disturbances. Blood concentrations of inflammatory markers are lowered following weight loss. In the hours following the consumption of a meal, there is an elevation in the concentrations of inflammatory mediators in the bloodstream, which is exaggerated in obese subjects and in type 2 diabetics. Both high-glucose and high-fat meals may induce postprandial inflammation, and this is exaggerated by a high meal content of advanced glycation end products (AGE) and partly ablated by inclusion of certain antioxidants or antioxidant-containing foods within the meal. Healthy eating patterns are associated with lower circulating concentrations of inflammatory markers. Among the components of a healthy diet, whole grains, vegetables and fruits, and fish are all associated with lower inflammation. AGE are associated with enhanced oxidative stress and inflammation. SFA and trans-MUFA are pro-inflammatory, while PUFA, especially long-chain n-3 PUFA, are anti-inflammatory. Hyperglycaemia induces both postprandial and chronic low-grade inflammation. Vitamin C, vitamin E and carotenoids decrease the circulating concentrations of inflammatory markers. Potential mechanisms are described and research gaps, which limit our understanding of the interaction between diet and postprandial and chronic low-grade inflammation, are identified.
引用
收藏
页码:S1 / S78
页数:78
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