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Effect of diet-induced weight loss on inflammatory cytokines in obese women

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Abstract

Background: Obesity is associated with low-grade systemic inflammation which has been linked to the increased risk of cardiovascular disease and Type 2 diabetes in obese patients. Aim: To evaluate changes in pro/anti-inflammatory adipocytokines and metabolic profile after moderate diet-induced weight loss. Subjects and methods: Twenty-nine pre-menopausal obese women (body mass index ≥30 kg/m2) aged 21 to 54 years without diabetes, hypertension, or hyperlipidemia, were enrolled in this study. We measured anthropometric parameters, lipid and glucose profiles, interleukin (IL)-6, IL-10, and IL-18 in obese women, who then entered a medically supervised program aimed at reducing body weight by 10% or more. Obese women restricted their caloric intake (by 500–1000 kcal/day) and consumed 50 g/day of a fiber supplement (Slim Last Powder) for 12 weeks. Results: By completing the dietary intervention program, weight (Δ=−10.0%, p<0.0001), body mass index, waist circumference, triceps skinfold thickness, total cholesterol, triglyceride, and fasting plasma glucose significantly decreased, while HDL-cholesterol significantly increased. While plasma levels of IL-6 and IL-18 decreased by 27% after 12 weeks, no significant change was observed in circulating levels of IL-10. Conclusion: Our study suggests that an improved body composition induced by restriction of energy intake is associated with favorable serum concentrations of IL-6 and IL-18 in obese women. However, the anti-inflammatory IL-10 is not affected by a moderate weight decrease.

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References

  1. Fantuzzi G. Adipose tissue, adipokines, and inflammation. J Allergy Clin Immunol 2005, 115: 911–9; quiz 920.

    Article  PubMed  Google Scholar 

  2. Popkin BM, Gordon-Larsen P. The nutrition transition: worldwide obesity dynamics and their determinants. Int J Obes Relat Metab Disord 2004, 28(Suppl 3): S2–9.

    Article  PubMed  Google Scholar 

  3. Yudkin JS. Adipose tissue, insulin action and vascular disease: inflammatory signals. Int J Obes Relat Metab Disord 2003, 27(Suppl 3): S25–8.

    Article  PubMed  Google Scholar 

  4. Solá E, Jover A, López-Ruiz A, et al. Parameters of inflammation in morbid obesity: lack of effect of moderate weight loss. Obes Surg 2009, 19: 571–6.

    Article  PubMed  Google Scholar 

  5. Tajik N, Golpaie A, Keshavarz SA, et al. Decreased plasma levels of ceruloplasmin after diet-induced weight loss in obese women. J Endocrinol Invest 2012; 35: 566–9.

    PubMed  Google Scholar 

  6. Golpaie A, Tajik N, Masoudkabir F, et al. Short-term effect of weight loss through restrictive bariatric surgery on serum levels of vaspin in morbidly obese subjects. Eur Cytokine Netw 2011, 22: 181–6.

    PubMed  Google Scholar 

  7. Matthews DR, Hosker JP, Rudenski AS, Naylor BA, Treacher DF, Turner RC. Homeostasis model assessment: insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia 1985, 28: 412–9.

    Article  PubMed  Google Scholar 

  8. Esposito K, Pontillo A, Di Palo C, et al. Effect of weight loss and lifestyle changes on vascular inflammatory markers in obese women: a randomized trial. JAMA 2003, 289: 1799–804.

    Article  PubMed  Google Scholar 

  9. Bastard JP, Lagathu C, Caron M, Capeau J. Point-counterpoint: Interleukin-6 does/does not have a beneficial role in insulin sensitivity and glucose homeostasis. J Appl Physiol 2007, 102: 821–2; author reply 825.

    PubMed  Google Scholar 

  10. Mohamed-Ali V, Goodrick S, Rawesh A, et al. Subcutaneous adipose tissue releases interleukin-6, but not tumor necrosis factor-alpha, in vivo. J Clin Endocrinol Metab 1997, 82: 4196–200.

    PubMed  Google Scholar 

  11. Yudkin JS. Abnormalities of coagulation and fibrinolysis in insulin resistance. Evidence for a common antecedent? Diabetes Care 1999, 22(Suppl 3): C25–30.

    PubMed  Google Scholar 

  12. Fernández-Real JM, Broch M, Vendrell J, Richart C, Ricart W. Interleukin-6 gene polymorphism and lipid abnormalities in healthy subjects. J Clin Endocrinol Metab 2000, 85: 1334–9.

    Article  PubMed  Google Scholar 

  13. Ridker PM, Rifai N, Stampfer MJ, Hennekens CH. Plasma concentration of interleukin-6 and the risk of future myocardial infarction among apparently healthy men. Circulation 2000, 101: 1767–72.

    Article  PubMed  Google Scholar 

  14. Gallistl S, Sudi KM, Aigner R, Borkenstein M. Changes in serum interleukin-6 concentrations in obese children and adolescents during a weight reduction program. Int J Obes Relat Metab Disord 2001, 25: 1640–3.

    Article  PubMed  Google Scholar 

  15. Arvidsson E, Viguerie N, Andersson I, Verdich C, Langin D, Arner P. Effects of different hypocaloric diets on protein secretion from adipose tissue of obese women. Diabetes 2004, 53: 1966–71.

    Article  PubMed  Google Scholar 

  16. Bruun JM, Verdich C, Toubro S, Astrup A, Richelsen B. Association between measures of insulin sensitivity and circulating levels of interleukin-8, interleukin-6 and tumor necrosis factor-alpha. Effect of weight loss in obese men. Eur J Endocrinol 2003, 148: 535–42.

    Article  PubMed  Google Scholar 

  17. Vendrell J, Broch M, Vilarrasa N, et al. Resistin, adiponectin, ghrelin, leptin, and proinflammatory cytokines: relationships in obesity. Obes Res 2004, 12: 962–71.

    Article  PubMed  Google Scholar 

  18. Manco M, Fernandez-Real JM, Equitani F, et al. Effect of massive weight loss on inflammatory adipocytokines and the innate immune system in morbidly obese women. J Clin Endocrinol Metab 2007, 92: 483–90.

    Article  PubMed  Google Scholar 

  19. Kopp HP, Krzyzanowska K, Mohlig M, Spranger J, Pfeiffer AF, Schernthaner G. Effects of marked weight loss on plasma levels of adiponectin, markers of chronic subclinical inflammation and insulin resistance in morbidly obese women. Int J Obes (Lond) 2005, 29: 766–71.

    Article  Google Scholar 

  20. Barzilay JI, Forsberg C, Heckbert SR, Cushman M, Newman AB. The association of markers of inflammation with weight change in older adults: the Cardiovascular Health Study. Int J Obes (Lond) 2006, 30: 1362–7.

    Article  Google Scholar 

  21. Dvoráková-Lorenzová A, Suchánek P, Havel PJ, et al. The decrease in C-reactive protein concentration after diet and physical activity induced weight reduction is associated with changes in plasma lipids, but not interleukin-6 or adiponectin. Metabolism 2006, 55: 359–65.

    Article  PubMed  Google Scholar 

  22. Rankin JW, Turpyn AD. Low carbohydrate, high fat diet increases C-reactive protein during weight loss. J Am Coll Nutr 2007, 26: 163–9.

    Article  PubMed  Google Scholar 

  23. Esposito K, Pontillo A, Ciotola M, et al. Weight loss reduces inter-leukin-18 levels in obese women. J Clin Endocrinol Metab 2002, 87: 3864–6.

    Article  PubMed  Google Scholar 

  24. Thorand B, Kolb H, Baumert J, et al. Elevated levels of interleukin-18 predict the development of type 2 diabetes: results from the MONICA/KORA Augsburg Study, 1984–2002. Diabetes 2005, 54: 2932–8.

    Article  PubMed  Google Scholar 

  25. Hulthe J, Mcpheat W, Samnegard A, Tornvall P, Hamsten A, Eriksson P. Plasma interleukin (IL)-18 concentrations is elevated in patients with previous myocardial infarction and related to severity of coronary atherosclerosis independently of C-reactive protein and IL-6. Atherosclerosis 2006, 188: 450–4.

    Article  PubMed  Google Scholar 

  26. Blankenberg S, Tiret L, Bickel C, et al. Interleukin-18 is a strong predictor of cardiovascular death in stable and unstable angina. Circulation 2002, 106: 24–30.

    Article  PubMed  Google Scholar 

  27. Mallat Z, Heymes C, Ohan J, Faggin E, Leseche G, Tedgui A. Expression of interleukin-10 in advanced human atherosclerotic plaques: relation to inducible nitric oxide synthase expression and cell death. Arterioscler Thromb Vasc Biol 1999, 19: 611–6.

    Article  PubMed  Google Scholar 

  28. Gunnett CA, Heistad DD, Faraci FM. Interleukin-10 protects nitric oxide-dependent relaxation during diabetes: role of superoxide. Diabetes 2002, 51: 1931–7.

    Article  PubMed  Google Scholar 

  29. Manigrasso MR, Ferroni P, Santilli F, et al. Association between circulating adiponectin and interleukin-10 levels in android obesity: effects of weight loss. J Clin Endocrinol Metab 2005, 90: 5876–9.

    Article  PubMed  Google Scholar 

  30. Esposito K, Pontillo A, Giugliano F, et al. Association of low interleukin-10 levels with the metabolic syndrome in obese women. J Clin Endocrinol Metab 2003, 88: 1055–8.

    Article  PubMed  Google Scholar 

  31. Seidell JC, Björntorp P, Sjöström L, Kvist H, Sannerstedt R. Visceral fat accumulation in men is positively associated with insulin, glucose, and C-peptide levels, but negatively with testosterone levels. Metabolism 1990, 39: 897–901.

    Article  PubMed  Google Scholar 

  32. Manolio TA, Savage PJ, Burke GL, et al. Correlates of fasting insulin levels in young adults: the CARDIA study. J Clin Epidemiol 1991, 44: 571–8.

    Article  PubMed  Google Scholar 

  33. Zavaroni I, Bonora E, Pagliara M, et al. Risk factors for coronary artery disease in healthy persons with hyperinsulinemia and normal glucose tolerance. N Engl J Med 1989, 320: 702–6.

    Article  PubMed  Google Scholar 

  34. Yamada N, Yoshinaga H, Sakurai N, et al. Increased risk factors for coronary artery disease in Japanese subjects with hyperinsulinemia or glucose intolerance. Diabetes Care 1994, 17: 107–14.

    Article  PubMed  Google Scholar 

  35. Psyrogiannis AJ, Alexopoulos DK, Kyriazopoulou VE, Vagenakis AG. Insulin resistance, hyperinsulinemia, and hypertriglyceridemia in patients with coronary artery disease independent of obesity. Angiology 1998, 49: 607–12.

    Article  PubMed  Google Scholar 

  36. Ma Y, Hebert JR, Li W, et al. Association between dietary fiber and markers of systemic inflammation in the Women’s Health Initiative Observational Study. Nutrition 2008, 24: 941–9.

    Article  PubMed Central  PubMed  Google Scholar 

  37. Wannamethee SG, Whincup PH, Thomas MC, Sattar N. Associations between dietary fiber and inflammation, hepatic function, and risk of type 2 diabetes in older men: potential mechanisms for the benefits of fiber on diabetes risk. Diabetes Care 2009, 32: 1823–5.

    Article  PubMed Central  PubMed  Google Scholar 

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Correspondence to M. Djalali PhD, DsC.

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Tajik, N., Keshavarz, S.A., Masoudkabir, F. et al. Effect of diet-induced weight loss on inflammatory cytokines in obese women. J Endocrinol Invest 36, 211–215 (2013). https://doi.org/10.3275/8465

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