References
- Finkelstein EA, Trogdon JG, Cohen JW, Dietz W. Annual medical spending attributable to obesity: payer- and service-specific estimates. Health Aff (Millwood) 2009;28:w822-31. https://doi.org/10.1377/hlthaff.28.5.w822
- World Health Organization. Obesity [Internet]. Geneva: WHO; 2008 [cited 2009 Oct 22]. Available from: http://www.who.int/ topics/obesity/en/.
- Statistics Korea. Estimated future population 2010-2060. Daejeon: Statistics Korea; 2011 [cited 2011 Dec 7]. Available from: http://kosis.kr/statisticsList/ statisticsList_01List.jsp?vwcd=MT_ZTITLE& parentId=D.
- Korea Centers for Disease Control and Prevention. The Korean National Health and Nutrition Examination Survey (KNHANES), 2011. Available at http:// knhanes.cdc.go.kr/knhanes/.
- Trayhurn P, Wood IS. Adipokines: inflammation and the pleiotropic role of white adipose tissue. Br J Nutr 2004;92:347-55. https://doi.org/10.1079/BJN20041213
- Galic S, Oakhill JS, Steinberg GR. Adipose tissue as an endocrine organ. Mol Cell Endocrinol 2010;316:129-39. https://doi.org/10.1016/j.mce.2009.08.018
- Hajer GR, van Haeften TW, Visseren FL. Adipose tissue dysfunction in obesity, diabetes, and vascular diseases. Eur Heart J 2008;29:2959-71. https://doi.org/10.1093/eurheartj/ehn387
- Galland L. Diet and inflammation. Nutr Clin Pract 2010;25:634-40. https://doi.org/10.1177/0884533610385703
- Bullo M, Casas-Agustench P, Amigo-Correig P, Aranceta J, Salas-Salvado J. Inflammation, obesity and comorbidities: the role of diet. Public Health Nutr 2007;10:1164-72.
- Calder PC, Ahluwalia N, Brouns F, Buetler T, Clement K, Cunningham K, et al. Dietary factors and low-grade inflammation in relation to overweight and obesity. Br J Nutr 2011;106(Suppl 3):S5-78. https://doi.org/10.1017/S0007114511005460
- Calabro P, Yeh ET. Obesity, inflammation, and vascular disease: the role of the adipose tissue as an endocrine organ. Subcell Biochem 2007;42:63-91. https://doi.org/10.1007/1-4020-5688-5_3
- Tilg H, Moschen AR. Adipocytokines: mediators linking adipose tissue, inflammation and immunity. Nat Rev Immunol 2006;6:772-83. https://doi.org/10.1038/nri1937
- Ceddia RB, Koistinen HA, Zierath JR, Sweeney G. Analysis of paradoxical observations on the association between leptin and insulin resistance. FASEB J 2002;16:1163-76. https://doi.org/10.1096/fj.02-0158rev
- Ekmekci H, Ekmekci OB. The role of adiponectin in atherosclerosis and thrombosis. Clin Appl Thromb Hemost 2006;12:163-8. https://doi.org/10.1177/107602960601200203
- Fukuhara A, Matsuda M, Nishizawa M, Segawa K, Tanaka M, Kishimoto K, et al. Visfatin: a protein secreted by visceral fat that mimics the effects of insulin. Science 2005;307:426-30. https://doi.org/10.1126/science.1097243
- Steppan CM, Bailey ST, Bhat S, Brown EJ, Banerjee RR, Wright CM, et al. The hormone resistin links obesity to diabetes. Nature 2001;409:307-12. https://doi.org/10.1038/35053000
- Purohit A, Ghilchik MW, Duncan L, Wang DY, Singh A, Walker MM, et al. Aromatase activity and interleukin- 6 production by normal and malignant breast tissues. J Clin Endocrinol Metab 1995;80:3052-8.
- Koh KK, Han SH, Quon MJ. Inflammatory markers and the metabolic syndrome: insights from therapeutic interventions. J Am Coll Cardiol 2005;46:1978-85. https://doi.org/10.1016/j.jacc.2005.06.082
- Mandrup-Poulsen T. The role of interleukin-1 in the pathogenesis of IDDM. Diabetologia 1996;39:1005-29. https://doi.org/10.1007/BF00400649
- Horn F, Henze C, Heidrich K. Interleukin-6 signal transduction and lymphocyte function. Immunobiology 2000;202:151-67. https://doi.org/10.1016/S0171-2985(00)80061-3
- Brown MA, Hural J. Functions of IL-4 and control of its expression. Crit Rev Immunol 1997;17:1-32. https://doi.org/10.1615/CritRevImmunol.v17.i1.10
- Marchant A, Devière J, Byl B, De Groote D, Vincent JL, Goldman M. Interleukin-10 production during septicaemia. Lancet 1994;343:707-8. https://doi.org/10.1016/S0140-6736(94)91584-9
- Schroder K, Hertzog PJ, Ravasi T, Hume DA. Interferon-gamma: an overview of signals, mechanisms and functions. J Leukoc Biol 2004;75:163-89. https://doi.org/10.1189/jlb.0603252
- Gregor MF, Hotamisligil GS. Inflammatory mechanisms in obesity. Annu Rev Immunol 2011;29:415-45. https://doi.org/10.1146/annurev-immunol-031210-101322
- Hotamisligil GS. Inflammation and metabolic disorders. Nature 2006;444:860-7. https://doi.org/10.1038/nature05485
- Ron D, Walter P. Signal integration in the endoplasmic reticulum unfolded protein response. Nat Rev Mol Cell Biol 2007;8:519-29. https://doi.org/10.1038/nrm2199
- Urano F, Wang X, Bertolotti A, Zhang Y, Chung P, Harding HP, et al. Coupling of stress in the ER to activation of JNK protein kinases by transmembrane protein kinase IRE1. Science 2000;287:664-6. https://doi.org/10.1126/science.287.5453.664
- Deng J, Lu PD, Zhang Y, Scheuner D, Kaufman RJ, Sonenberg N, et al. Translational repression mediates activation of nuclear factor kappa B by phosphorylated translation initiation factor 2. Mol Cell Biol 2004;24: 10161-8. https://doi.org/10.1128/MCB.24.23.10161-10168.2004
- Gregor MF, Hotamisligil GS. Thematic review series: adipocyte biology. Adipocyte stress: the endoplasmic reticulum and metabolic disease. J Lipid Res 2007;48: 1905-14. https://doi.org/10.1194/jlr.R700007-JLR200
- Surmi BK, Hasty AH. Macrophage infiltration into adipose tissue: initiation, propagation and remodeling. Future Lipidol 2008;3:545-56. https://doi.org/10.2217/17460875.3.5.545
- Hosogai N, Fukuhara A, Oshima K, Miyata Y, Tanaka S, Segawa K, et al. Adipose tissue hypoxia in obesity and its impact on adipocytokine dysregulation. Diabetes 2007;56:901-11. https://doi.org/10.2337/db06-0911
- Ye J, Gao Z, Yin J, He Q. Hypoxia is a potential risk factor for chronic inflammation and adiponectin reduction in adipose tissue of ob/ob and dietary obese mice. Am J Physiol Endocrinol Metab 2007;293:E1118-28. https://doi.org/10.1152/ajpendo.00435.2007
- Shi H, Kokoeva MV, Inouye K, Tzameli I, Yin H, Flier JS. TLR4 links innate immunity and fatty acid-induced insulin resistance. J Clin Invest 2006;116:3015-25. https://doi.org/10.1172/JCI28898
- Jenkins DJ, Wolever TM, Taylor RH, Barker H, Fielden H, Baldwin JM, et al. Glycemic index of foods: a physiological basis for carbohydrate exchange. Am J Clin Nutr 1981;34:362-6. https://doi.org/10.1093/ajcn/34.3.362
- Salmeron J, Manson JE, Stampfer MJ, Colditz GA, Wing AL, Willett WC. Dietary fiber, glycemic load, and risk of non-insulin-dependent diabetes mellitus in women. JAMA 1997;277:472-7. https://doi.org/10.1001/jama.1997.03540300040031
- Levitan EB, Cook NR, Stampfer MJ, Ridker PM, Rexrode KM, Buring JE, et al. Dietary glycemic index, dietary glycemic load, blood lipids, and C-reactive protein. Metabolism 2008;57:437-43. https://doi.org/10.1016/j.metabol.2007.11.002
- Du H, van der A DL, van Bakel MM, van der Kallen CJ, Blaak EE, van Greevenbroek MM, et al. Glycemic index and glycemic load in relation to food and nutrient intake and metabolic risk factors in a Dutch population. Am J Clin Nutr 2008;87:655-61. https://doi.org/10.1093/ajcn/87.3.655
- Qi L, Meigs JB, Liu S, Manson JE, Mantzoros C, Hu FB. Dietary fibers and glycemic load, obesity, and plasma adiponectin levels in women with type 2 diabetes. Diabetes Care 2006;29:1501-5. https://doi.org/10.2337/dc06-0221
- Pischon T, Girman CJ, Rifai N, Hotamisligil GS, Rimm EB. Association between dietary factors and plasma adiponectin concentrations in men. Am J Clin Nutr 2005;81:780-6. https://doi.org/10.1093/ajcn/81.4.780
- Pittas AG, Roberts SB, Das SK, Gilhooly CH, Saltzman E, Golden J, et al. The effects of the dietary glycemic load on type 2 diabetes risk factors during weight loss. Obesity (Silver Spring) 2006;14:2200-9. https://doi.org/10.1038/oby.2006.258
- Shikany JM, Phadke RP, Redden DT, Gower BA. Effects of low- and high-glycemic index/glycemic load diets on coronary heart disease risk factors in overweight/ obese men. Metabolism 2009;58:1793-801. https://doi.org/10.1016/j.metabol.2009.06.006
- Vrolix R, Mensink RP. Effects of glycemic load on metabolic risk markers in subjects at increased risk of developing metabolic syndrome. Am J Clin Nutr 2010;92: 366-74. https://doi.org/10.3945/ajcn.2009.28339
- Joffe YT, Collins M, Goedecke JH. The relationship between dietary fatty acids and inflammatory genes on the obese phenotype and serum lipids. Nutrients 2013;5:1672-705. https://doi.org/10.3390/nu5051672
- Lopez-Garcia E, Schulze MB, Manson JE, Meigs JB, Albert CM, Rifai N, et al. Consumption of (n-3) fatty acids is related to plasma biomarkers of inflammation and endothelial activation in women. J Nutr 2004;134:1806-11. https://doi.org/10.1093/jn/134.7.1806
- Zampelas A, Panagiotakos DB, Pitsavos C, Das UN, Chrysohoou C, Skoumas Y, et al. Fish consumption among healthy adults is associated with decreased levels of inflammatory markers related to cardiovascular disease: the ATTICA study. J Am Coll Cardiol 2005;46:120-4. https://doi.org/10.1016/j.jacc.2005.03.048
- Ciubotaru I, Lee YS, Wander RC. Dietary fish oil decreases C-reactive protein, interleukin-6, and triacylglycerol to HDL-cholesterol ratio in postmenopausal women on HRT. J Nutr Biochem 2003;14: 513-21. https://doi.org/10.1016/S0955-2863(03)00101-3
- Lopez-Garcia E, Schulze MB, Meigs JB, Manson JE, Rifai N, Stampfer MJ, et al. Consumption of trans fatty acids is related to plasma biomarkers of inflammation and endothelial dysfunction. J Nutr 2005;135:562-6. https://doi.org/10.1093/jn/135.3.562
- Baer DJ, Judd JT, Clevidence BA, Tracy RP. Dietary fatty acids affect plasma markers of inflammation in healthy men fed controlled diets: a randomized crossover study. Am J Clin Nutr 2004;79:969-73. https://doi.org/10.1093/ajcn/79.6.969
- Lichtenstein AH, Erkkilä AT, Lamarche B, Schwab US, Jalbert SM, Ausman LM. Influence of hydrogenated fat and butter on CVD risk factors: remnant-like particles, glucose and insulin, blood pressure and C-reactive protein. Atherosclerosis 2003;171:97-107. https://doi.org/10.1016/j.atherosclerosis.2003.07.005
- Bhupathiraju SN, Tucker KL. Greater variety in fruit and vegetable intake is associated with lower inflammation in Puerto Rican adults. Am J Clin Nutr 2011;93:37-46. https://doi.org/10.3945/ajcn.2010.29913
- Salas-Salvado J, Garcia-Arellano A, Estruch R, Marquez-Sandoval F, Corella D, Fiol M, et al. Components of the Mediterranean-type food pattern and serum inflammatory markers among patients at high risk for cardiovascular disease. Eur J Clin Nutr 2008;62: 651-9. https://doi.org/10.1038/sj.ejcn.1602762
- Freese R, Vaarala O, Turpeinen AM, Mutanen M. No difference in platelet activation or inflammation markers after diets rich or poor in vegetables, berries and apple in healthy subjects. Eur J Nutr 2004;43:175-82. https://doi.org/10.1007/s00394-004-0456-4
- Morand C, Dubray C, Milenkovic D, Lioger D, Martin JF, Scalbert A, et al. Hesperidin contributes to the vascular protective effects of orange juice: a randomized crossover study in healthy volunteers. Am J Clin Nutr 2011;93:73-80. https://doi.org/10.3945/ajcn.110.004945
- Brady WE, Mares-Perlman JA, Bowen P, Stacewicz- Sapuntzakis M. Human serum carotenoid concentrations are related to physiologic and lifestyle factors. J Nutr 1996;126:129-37. https://doi.org/10.1093/jn/126.1.129
- Wang L, Gaziano JM, Norkus EP, Buring JE, Sesso HD. Associations of plasma carotenoids with risk factors and biomarkers related to cardiovascular disease in middle-aged and older women. Am J Clin Nutr 2008;88:747-54. https://doi.org/10.1093/ajcn/88.3.747
- Aasheim ET, Hofso D, Hjelmesaeth J, Birkeland KI, Bøhmer T. Vitamin status in morbidly obese patients: a cross-sectional study. Am J Clin Nutr 2008;87:362-9. https://doi.org/10.1093/ajcn/87.2.362
- Block G, Jensen C, Dietrich M, Norkus EP, Hudes M, Packer L. Plasma C-reactive protein concentrations in active and passive smokers: influence of antioxidant supplementation. J Am Coll Nutr 2004;23:141-7. https://doi.org/10.1080/07315724.2004.10719354
- Fumeron C, Nguyen-Khoa T, Saltiel C, Kebede M, Buisson C, Drueke TB, et al. Effects of oral vitamin C supplementation on oxidative stress and inflammation status in haemodialysis patients. Nephrol Dial Transplant 2005;20:1874-9. https://doi.org/10.1093/ndt/gfh928
- Chacko SA, Song Y, Nathan L, Tinker L, de Boer IH, Tylavsky F, et al. Relations of dietary magnesium intake to biomarkers of inflammation and endothelial dysfunction in an ethnically diverse cohort of postmenopausal women. Diabetes Care 2010;33:304-10. https://doi.org/10.2337/dc09-1402
- Guerrero-Romero F, Rodríguez-Morán M. Relationship between serum magnesium levels and C-reactive protein concentration, in non-diabetic, non-hypertensive obese subjects. Int J Obes Relat Metab Disord 2002;26:469-74. https://doi.org/10.1038/sj.ijo.0801954
- Landberg R, Sun Q, Rimm EB, Cassidy A, Scalbert A, Mantzoros CS, et al. Selected dietary flavonoids are associated with markers of inflammation and endothelial dysfunction in U.S. women. J Nutr 2011;141:618-25. https://doi.org/10.3945/jn.110.133843
- Chun OK, Chung SJ, Claycombe KJ, Song WO. Serum C-reactive protein concentrations are inversely associated with dietary flavonoid intake in U.S. adults. J Nutr 2008;138:753-60. https://doi.org/10.1093/jn/138.4.753
- Karlsen A, Retterstøl L, Laake P, Paur I, Bøhn SK, Sandvik L, et al. Anthocyanins inhibit nuclear factor- kappaB activation in monocytes and reduce plasma concentrations of pro-inflammatory mediators in healthy adults. J Nutr 2007;137:1951-4. https://doi.org/10.1093/jn/137.8.1951
- Karlsen A, Paur I, Bøhn SK, Sakhi AK, Borge GI, Serafini M, et al. Bilberry juice modulates plasma concentration of NF-kappaB related inflammatory markers in subjects at increased risk of CVD. Eur J Nutr 2010;49:345-55. https://doi.org/10.1007/s00394-010-0092-0
- Suomela JP, Ahotupa M, Yang B, Vasankari T, Kallio H. Absorption of flavonols derived from sea buckthorn (Hippophaë rhamnoides L.) and their effect on emerging risk factors for cardiovascular disease in humans. J Agric Food Chem 2006;54:7364-9. https://doi.org/10.1021/jf061889r
- D'Anna R, Baviera G, Corrado F, Cancellieri F, Crisafulli A, Squadrito F. The effect of the phytoestrogen genistein and hormone replacement therapy on homocysteine and C-reactive protein level in postmenopausal women. Acta Obstet Gynecol Scand 2005;84:474-7. https://doi.org/10.1080/j.0001-6349.2005.00661.x
- Yildiz MF, Kumru S, Godekmerdan A, Kutlu S. Effects of raloxifene, hormone therapy, and soy isoflavone on serum high-sensitive C-reactive protein in postmenopausal women. Int J Gynaecol Obstet 2005;90: 128-33. https://doi.org/10.1016/j.ijgo.2005.05.005
- Clerici C, Setchell KD, Battezzati PM, Pirro M, Giuliano V, Asciutti S, et al. Pasta naturally enriched with isoflavone aglycons from soy germ reduces serum lipids and improves markers of cardiovascular risk. J Nutr 2007;137:2270-8. https://doi.org/10.1093/jn/137.10.2270
- Aubertin-Leheudre M, Lord C, Khalil A, Dionne IJ. Effect of 6 months of exercise and isoflavone supplementation on clinical cardiovascular risk factors in obese postmenopausal women: a randomized, double- blind study. Menopause 2007;14:624-9. https://doi.org/10.1097/gme.0b013e31802e426b
- Salminen S, Bouley C, Boutron-Ruault MC, Cummings JH, Franck A, Gibson GR, et al. Functional food science and gastrointestinal physiology and function. Br J Nutr 1998;80(Suppl 1):S147-71. https://doi.org/10.1079/BJN19980108
- Nova E, Wärnberg J, Gómez-Martínez S, Díaz LE, Romeo J, Marcos A. Immunomodulatory effects of probiotics in different stages of life. Br J Nutr 2007; 98(Suppl 1):S90-5.
- Olivares M, Díaz-Ropero MP, Gómez N, Lara-Villoslada F, Sierra S, Maldonado JA, et al. The consumption of two new probiotic strains, Lactobacillus gasseri CECT 5714 and Lactobacillus coryniformis CECT 5711, boosts the immune system of healthy humans. Int Microbiol 2006;9:47-52.
- Olivares M, Paz Díaz-Ropero M, Gómez N, Sierra S, Lara-Villoslada F, Martín R, et al. Dietary deprivation of fermented foods causes a fall in innate immune response. Lactic acid bacteria can counteract the immunological effect of this deprivation. J Dairy Res 2006;73:492-8. https://doi.org/10.1017/S0022029906002068
- Kekkonen RA, Lummela N, Karjalainen H, Latvala S, Tynkkynen S, Jarvenpaa S, et al. Probiotic intervention has strain-specific anti-inflammatory effects in healthy adults. World J Gastroenterol 2008;14: 2029-36. https://doi.org/10.3748/wjg.14.2029
- Pineiro M, Asp NG, Reid G, Macfarlane S, Morelli L, Brunser O, et al. FAO technical meeting on prebiotics. J Clin Gastroenterol 2008;42(Suppl 3 Pt 2):S156-9. https://doi.org/10.1097/MCG.0b013e31817f184e
- Guigoz Y, Rochat F, Perruisseau-Carrier G, Rochat I, Schiffrin EJ. Effects of oligosaccharide on the faecal flora and non-specific immune system in elderly people. Nutr Res 2002;22:13-25. https://doi.org/10.1016/S0271-5317(01)00354-2
- Schiffrin EJ, Thomas DR, Kumar VB, Brown C, Hager C, Van't Hof MA, et al. Systemic inflammatory markers in older persons: the effect of oral nutritional supplementation with prebiotics. J Nutr Health Aging 2007;11:475-9.
Cited by
- Repeated measures of body mass index and C-reactive protein in relation to all-cause mortality and cardiovascular disease: results from the consortium on health and ageing network of cohorts in Europe vol.29, pp.12, 2013, https://doi.org/10.1007/s10654-014-9954-8
- Involvement of Proteasome and Macrophages M2 in the Protection Afforded by Telmisartan against the Acute Myocardial Infarction in Zucker Diabetic Fatty Rats with Metabolic Syndrome vol.2014, pp.None, 2014, https://doi.org/10.1155/2014/972761
- Immunomodulatory Effects of Kimchi in Chinese Healthy College Students: A Randomized Controlled Trial vol.3, pp.2, 2013, https://doi.org/10.7762/cnr.2014.3.2.98
- Body Mass Index and Comorbidities in Adult Severe Asthmatics vol.2014, pp.None, 2013, https://doi.org/10.1155/2014/607192
- A Rosemary Extract Rich in Carnosic Acid Selectively Modulates Caecum Microbiota and Inhibits β-Glucosidase Activity, Altering Fiber and Short Chain Fatty Acids Fecal Excretion in Lean and Obese vol.9, pp.4, 2013, https://doi.org/10.1371/journal.pone.0094687
- Diisopropylamine Dichloroacetate, a Novel Pyruvate Dehydrogenase Kinase 4 Inhibitor, as a Potential Therapeutic Agent for Metabolic Disorders and Multiorgan Failure in Severe Influenza vol.9, pp.5, 2013, https://doi.org/10.1371/journal.pone.0098032
- Diet components can suppress inflammation and reduce cancer risk vol.8, pp.3, 2014, https://doi.org/10.4162/nrp.2014.8.3.233
- The effect of obesity and tobacco smoke exposure on inflammatory mediators and matrix metalloproteinases in rat model vol.24, pp.9, 2013, https://doi.org/10.3109/15376516.2014.956911
- Classification of pro-inflammatory status for interleukin-6 affects relative muscle strength in obese elderly women vol.27, pp.6, 2013, https://doi.org/10.1007/s40520-015-0349-9
- A Hyperlipidic Diet Combined with Short-Term Ovariectomy Increases Adiposity and Hyperleptinemia and Decreases Cytokine Content in Mesenteric Adipose Tissue vol.2015, pp.None, 2013, https://doi.org/10.1155/2015/923248
- Influenza virus pathogenicity regulated by host cellular proteases, cytokines and metabolites, and its therapeutic options vol.91, pp.8, 2013, https://doi.org/10.2183/pjab.91.351
- Obesity and asthma: current knowledge and future needs vol.21, pp.1, 2013, https://doi.org/10.1097/mcp.0000000000000119
- Dietary proteins improve endothelial function under fasting conditions but not in the postprandial state, with no effects on markers of low-grade inflammation vol.114, pp.11, 2013, https://doi.org/10.1017/s0007114515003530
- Effect of Diet and Exercise on the Peripheral Immune System in Young Balb/c Mice vol.2015, pp.None, 2013, https://doi.org/10.1155/2015/458470
- Epigallocatechin Gallate (EGCG) Suppresses Lipopolysaccharide-Induced Toll-like Receptor 4 (TLR4) Activity via 67 kDa Laminin Receptor (67LR) in 3T3-L1 Adipocytes vol.63, pp.10, 2013, https://doi.org/10.1021/jf505531w
- Obesity-related immune responses and their impact on surgical outcomes vol.39, pp.6, 2013, https://doi.org/10.1038/ijo.2015.21
- Anti-inflammatory effect of anthocyanins via modulation of nuclear factor- B and mitogen-activated protein kinase signaling cascades vol.73, pp.6, 2015, https://doi.org/10.1093/nutrit/nuu066
- Sleep Deficiency is a Modifiable Risk Factor for Obesity and Cognitive Impairment and Associated with Elevated Visfatin vol.3, pp.2, 2013, https://doi.org/10.3889/oamjms.2015.063
- The dietary inflammatory index is associated with colorectal cancer in the National Institutes of Health-American Association of Retired Persons Diet and Health Study vol.113, pp.11, 2013, https://doi.org/10.1017/s000711451500104x
- Insulin-independent reversal of type 1 diabetes in nonobese diabetic mice with brown adipose tissue transplant vol.308, pp.12, 2013, https://doi.org/10.1152/ajpendo.00570.2014
- Dietary factors and biomarkers of systemic inflammation in older people: the Lothian Birth Cohort 1936 vol.114, pp.7, 2013, https://doi.org/10.1017/s000711451500210x
- Correlation between Dietary Intake and Inflammatory Biomarkers in a Tunisian Obese Group vol.3, pp.11, 2013, https://doi.org/10.4236/jbm.2015.311014
- Impact of Nutrition on Cerebral Circulation and Cognition in the Metabolic Syndrome vol.7, pp.11, 2015, https://doi.org/10.3390/nu7115477
- Associations of total and abdominal adiposity with risk marker patterns in children at high-risk for cardiovascular disease vol.2, pp.1, 2013, https://doi.org/10.1186/s40608-015-0043-7
- Epicardial Fat: Physiological, Pathological, and Therapeutic Implications vol.2016, pp.None, 2013, https://doi.org/10.1155/2016/1291537
- Severe but Not Moderate Vitamin B12 Deficiency Impairs Lipid Profile, Induces Adiposity, and Leads to Adverse Gestational Outcome in Female C57BL/6 Mice vol.3, pp.None, 2013, https://doi.org/10.3389/fnut.2016.00001
- Association between dietary inflammatory potential and breast cancer incidence and death: results from the Women's Health Initiative vol.114, pp.11, 2013, https://doi.org/10.1038/bjc.2016.98
- Development and Validation of an Empirical Dietary Inflammatory Index vol.146, pp.8, 2013, https://doi.org/10.3945/jn.115.228718
- Chronic transgenerational vitamin B12 deficiency of severe and moderate magnitudes modulates adiposity-probable underlying mechanisms : Chronic transgenerational vitamin B12 deficiency vol.43, pp.3, 2013, https://doi.org/10.1002/biof.1350
- Association between diet-related inflammation, all-cause, all-cancer, and cardiovascular disease mortality, with special focus on prediabetics: findings from NHANES III vol.56, pp.3, 2017, https://doi.org/10.1007/s00394-016-1158-4
- High Sensitivity C-reactive Protein may be used as a Marker for Cognitive Impairment in Obese Egyptian Middle Age Females vol.9, pp.1, 2013, https://doi.org/10.3923/ajcn.2017.17.23
- Polymorphism of -308 G/A TNF- gene correlated with the concentration of TNF- and lipid profile in obese subject of Javanese population vol.16, pp.37, 2017, https://doi.org/10.5897/ajb2017.16150
- Dietary Pea Fiber Supplementation Improves Glycemia and Induces Changes in the Composition of Gut Microbiota, Serum Short Chain Fatty Acid Profile and Expression of Mucins in Glucose Intolerant Rats vol.9, pp.11, 2013, https://doi.org/10.3390/nu9111236
- A high-fat diet impairs reproduction by decreasing the IL1β level in mice treated at immature stage vol.7, pp.None, 2013, https://doi.org/10.1038/s41598-017-00505-0
- Down-regulation of miRNAs in the brain and development of diet-induced obesity vol.64, pp.None, 2013, https://doi.org/10.1016/j.ijdevneu.2017.06.005
- Military Sexual Trauma and Obesity Among Women Veterans vol.27, pp.3, 2013, https://doi.org/10.1089/jwh.2016.6105
- Structure–Activity Relationship and Molecular Docking of Natural Product Library Reveal Chrysin as a Novel Dipeptidyl Peptidase-4 (DPP-4) Inhibitor: An Integrated In Silico and In Vitro Study vol.23, pp.6, 2013, https://doi.org/10.3390/molecules23061368
- Effects of postweaning calorie restriction on accelerated growth and adiponectin in nutritionally programmed microswine offspring vol.315, pp.2, 2018, https://doi.org/10.1152/ajpregu.00162.2017
- Functional and systemic effects of whole body electrical stimulation post bariatric surgery: study protocol for a randomized controlled trial vol.19, pp.1, 2013, https://doi.org/10.1186/s13063-018-2844-8
- Potential therapeutic antibodies targeting specific adiponectin isoforms in rheumatoid arthritis vol.20, pp.None, 2013, https://doi.org/10.1186/s13075-018-1736-3
- Carnosic Acid Modulates Increased Hepatic Lipogenesis and Adipocytes Differentiation in Ovariectomized Mice Fed Normal or High-Fat Diets vol.10, pp.12, 2013, https://doi.org/10.3390/nu10121984
- Nutrition and Cardiovascular Health vol.19, pp.12, 2013, https://doi.org/10.3390/ijms19123988
- Challenging Case in Clinical Practice: Use of the Elimination Diet as a Broad-Spectrum Approach for the First-Line Treatment of a Multi-Symptomatic Client vol.25, pp.2, 2013, https://doi.org/10.1089/act.2019.29207.kch
- The effects of meal-timing on self-rated hunger and dietary inflammatory potential among a sample of college students vol.67, pp.4, 2013, https://doi.org/10.1080/07448481.2018.1481074
- Anti-inflammatory Action of Curcumin and Its Use in the Treatment of Lifestyle-related Diseases vol.14, pp.2, 2019, https://doi.org/10.15420/ecr.2019.17.2
- Nutrient intake is a predictor of lung function in obese asthmatic adolescents undergoing interdisciplinary therapy vol.122, pp.9, 2013, https://doi.org/10.1017/s0007114519001739
- Omega-3 polyunsaturated fatty acids have beneficial effects on visceral fat in diet-induced obesity model vol.97, pp.6, 2013, https://doi.org/10.1139/bcb-2018-0361
- Dexmedetomidine-Associated Hyperpyrexia in Three Critically Ill Patients With Coronavirus Disease 2019 vol.2, pp.9, 2013, https://doi.org/10.1097/cce.0000000000000213
- The immune remodel: Weight loss-mediated inflammatory changes to obesity vol.245, pp.2, 2013, https://doi.org/10.1177/1535370219900185
- The Dietary Inflammatory Index and Chronic Lymphocytic Leukaemia in the MCC Spain Study vol.12, pp.1, 2013, https://doi.org/10.3390/nu12010048
- Effects of a Low-Dose Spirulina/Turmeric Supplement on Cardiometabolic and Antioxidant Serum Markers of Patients With Abdominal Obesity vol.7, pp.None, 2013, https://doi.org/10.3389/fnut.2020.00065
- Special Attention to Diet and Physical Activity in Children and Adolescents With Obesity During the Coronavirus Disease-2019 Pandemic vol.8, pp.None, 2013, https://doi.org/10.3389/fped.2020.00407
- Endothelial Dysfunction in Obesity-Induced Inflammation: Molecular Mechanisms and Clinical Implications vol.10, pp.2, 2013, https://doi.org/10.3390/biom10020291
- Intergenerational associations of dietary inflammatory index with birth outcomes and weight status at age 5 and 9: Results from the Lifeways cross‐generation cohort study vol.15, pp.3, 2013, https://doi.org/10.1111/ijpo.12588
- Research update on the association between SFRP5, an anti‐inflammatory adipokine, with obesity, type 2 diabetes mellitus and coronary heart disease vol.24, pp.5, 2013, https://doi.org/10.1111/jcmm.15023
- Characterization of burning mouth syndrome profiles based on response to a local anaesthetic lozenge vol.26, pp.3, 2013, https://doi.org/10.1111/odi.13267
- The effect of α-terpineol enantiomers on biomarkers of rats fed a high-fat diet vol.6, pp.4, 2020, https://doi.org/10.1016/j.heliyon.2020.e03752
- Beneficial effects of lingonberry ( Vaccinium vitis-idaea L.) supplementation on metabolic and inflammatory adverse effects induced by high-fat diet in a mouse model of obesity vol.15, pp.5, 2013, https://doi.org/10.1371/journal.pone.0232605
- Maternal Obesity and the Uterine Immune Cell Landscape: The Shaping Role of Inflammation vol.21, pp.11, 2020, https://doi.org/10.3390/ijms21113776
- Virgin Coconut Oil Associated with High-Fat Diet Induces Metabolic Dysfunctions, Adipose Inflammation, and Hepatic Lipid Accumulation vol.23, pp.7, 2020, https://doi.org/10.1089/jmf.2019.0172
- Factors Associated with Increased Morbidity and Mortality of Obese and Overweight COVID-19 Patients vol.9, pp.9, 2013, https://doi.org/10.3390/biology9090280
- Beneficial Effects of Newly Isolated Akkermansia muciniphila Strains from the Human Gut on Obesity and Metabolic Dysregulation vol.8, pp.9, 2013, https://doi.org/10.3390/microorganisms8091413
- Serum MicroRNA on inflammation: a literature review of mouse model studies vol.25, pp.7, 2013, https://doi.org/10.1080/1354750x.2020.1810320
- Diabetes-Specific Nutrition Formulas in the Management of Patients with Diabetes and Cardiometabolic Risk vol.12, pp.12, 2013, https://doi.org/10.3390/nu12123616
- Detecting Cognitive Impairment in Idiopathic Intracranial Hypertension Using Ocular Motor and Neuropsychological Testing vol.12, pp.None, 2013, https://doi.org/10.3389/fneur.2021.772513
- Changes of Urinary Cytokines in Non-Diabetic Obese Patients After Laparoscopic Sleeve Gastrectomy vol.14, pp.None, 2013, https://doi.org/10.2147/ijgm.s302418
- Alterations in Lysosome Homeostasis in Lipid-Related Disorders: Impact on Metabolic Tissues and Immune Cells vol.9, pp.None, 2013, https://doi.org/10.3389/fcell.2021.790568
- Does C-C Motif Chemokine Ligand 2 (CCL2) Link Obesity to a Pro-Inflammatory State? vol.22, pp.3, 2013, https://doi.org/10.3390/ijms22031500
- Obesity, Early Life Gut Microbiota, and Antibiotics vol.9, pp.2, 2013, https://doi.org/10.3390/microorganisms9020413
- Retraction notice for: “Characteristics and risk factors for COVID-19 diagnosis and adverse outcomes in Mexico: an analysis of 89,756 laboratory-confirmed COVID-19 cases.” Theodoros V. G vol.57, pp.3, 2013, https://doi.org/10.1183/13993003.02144-2020
- Protective effect of Curcuma amada acetone extract against high-fat and high-sugar diet-induced obesity and memory impairment vol.24, pp.3, 2021, https://doi.org/10.1080/1028415x.2019.1616436
- Impact of Obesity-Induced Inflammation on Cardiovascular Diseases (CVD) vol.22, pp.9, 2013, https://doi.org/10.3390/ijms22094798
- The triumvirate: why hypertension, obesity, and diabetes are risk factors for adverse effects in patients with COVID-19 vol.58, pp.7, 2013, https://doi.org/10.1007/s00592-020-01636-z
- Obesity Has a Systemic Effect on Immune Cells in Naïve and Cancer-Bearing Mice vol.22, pp.16, 2013, https://doi.org/10.3390/ijms22168803
- Aberrant Neurogliovascular Unit Dynamics in Cerebral Small Vessel Disease: A Rheological Clue to Vascular Parkinsonism vol.13, pp.8, 2021, https://doi.org/10.3390/pharmaceutics13081207
- Maternal Dietary Quality and Dietary Inflammation Associations with Offspring Growth, Placental Development, and DNA Methylation vol.13, pp.9, 2013, https://doi.org/10.3390/nu13093130
- DASH Diet as a Proposal for Improvement in Cellular Immunity and Its Association with Metabolic Parameters in Persons with Overweight and Obesity vol.13, pp.10, 2013, https://doi.org/10.3390/nu13103540
- A tale of two proteins: PACT and PKR and their roles in inflammation vol.288, pp.22, 2013, https://doi.org/10.1111/febs.15691
- Antioxidant and Anti-Inflammatory Activity of Cynanchum acutum L. Isolated Flavonoids Using Experimentally Induced Type 2 Diabetes Mellitus: Biological and In Silico Investigation for NF-κB Path vol.10, pp.11, 2013, https://doi.org/10.3390/antiox10111713
- Effects of Lingonberry (Vaccinium vitis-idaea L.) Supplementation on Hepatic Gene Expression in High-Fat Diet Fed Mice vol.13, pp.11, 2021, https://doi.org/10.3390/nu13113693
- Inflammation, epigenetics, and metabolism converge to cell senescence and ageing: the regulation and intervention vol.6, pp.1, 2013, https://doi.org/10.1038/s41392-021-00646-9
- Plasma lipocalin-2/NGAL is stable over 12 weeks and is not modulated by exercise or dieting vol.11, pp.1, 2013, https://doi.org/10.1038/s41598-021-83472-x
- Comparative epidemiology of gestational diabetes in ethnic Chinese from Shanghai birth cohort and growing up in Singapore towards healthy outcomes cohort vol.21, pp.1, 2013, https://doi.org/10.1186/s12884-021-04036-5
- COVID-19 Pandemic as Risk Factors for Excessive Weight Gain in Pediatrics: The Role of Changes in Nutrition Behavior. A Narrative Review vol.13, pp.12, 2013, https://doi.org/10.3390/nu13124255
- Different associations of specific non-alcoholic beverages with elevated high-sensitivity C-reactive protein in Korean adults: results from the Korea National Health and Nutrition Examination Survey ( vol.70, pp.1, 2013, https://doi.org/10.3164/jcbn.21-20
- The dietary inflammatory index, obesity, type 2 diabetes, and cardiovascular risk factors and diseases vol.23, pp.1, 2022, https://doi.org/10.1111/obr.13349