The role of bioactives in energy metabolism and metabolic syndrome

Some food bioactives potentially exert anti-obesity effects. Anthocyanins (ACN), catechins, β-glucan (BG) and n-3 long chain PUFA (LCPUFA) are among the most promising candidates and have been considered as a strategy for the development of functional foods counteracting body weight gain. At present, clinical trials, reviews and meta-analyses addressing anti-obesity effects of various bioactives or bioactive-rich foods show contradictory results. Abdominal obesity is an important criterion for metabolic syndrome (MetS) diagnosis along with glucose intolerance, dyslipidaemia and hypertension. Food bioactives are supposed to exert beneficial effects on these parameters, therefore representing alternative therapy approaches for the treatment of MetS. This review summarises outcomes on MetS biomarkers in recent clinical trials supplementing ACN, catechins, BG and n-3 LCPUFA, focusing mainly on anti-obesity effects. Overall, it is clear that the level of evidence for the effectiveness varies not only among the different bioactives but also among the different putative health benefits suggested for the same bioactive. Limited evidence may be due to the low number of controlled intervention trials or to inconsistencies in trial design, i.e. duration, dose and/or the method of bioactive supplementation (extracts, supplements, rich or enriched food). At present, the question ‘Are bioactives effective in weight management and prevention of metabolic syndrome?’ remains inconclusive. Thus, a common effort to harmonise the study design of intervention trials focusing on the most promising bioactive molecules is urgently needed to strengthen the evidence of their potential in the treatment of obesity, MetS and related diseases.

[1]  K. Djafarian,et al.  Effect of anthocyanin supplementation on cardio-metabolic biomarkers: A systematic review and meta-analysis of randomized controlled trials. , 2019, Clinical nutrition.

[2]  Pengfei Guo,et al.  A meta-analysis of randomized controlled trials , 2019, Medicine.

[3]  D. Baer,et al.  Blackberry Feeding Increases Fat Oxidation and Improves Insulin Sensitivity in Overweight and Obese Males , 2018, Nutrients.

[4]  D. Luna-Vital,et al.  Anthocyanins from purple corn activate free fatty acid-receptor 1 and glucokinase enhancing in vitro insulin secretion and hepatic glucose uptake , 2018, PloS one.

[5]  L. Gong,et al.  Blackberry and Blueberry Anthocyanin Supplementation Counteract High-Fat-Diet-Induced Obesity by Alleviating Oxidative Stress and Inflammation and Accelerating Energy Expenditure , 2018, Oxidative medicine and cellular longevity.

[6]  H. Takase,et al.  Efficacy of tea catechin-rich beverages to reduce abdominal adiposity and metabolic syndrome risks in obese and overweight subjects: a pooled analysis of 6 human trials. , 2018, Nutrition research.

[7]  C. Nyachoti,et al.  Barley β-glucan increases fecal bile acid excretion and short chain fatty acid levels in mildly hypercholesterolemic individuals. , 2018, Food & function.

[8]  J. Bernatonienė,et al.  The Role of Catechins in Cellular Responses to Oxidative Stress , 2018, Molecules.

[9]  P. Wilde,et al.  Processing of oat: the impact on oat's cholesterol lowering effect , 2018, Food & function.

[10]  Zezhong Tian,et al.  Role of Purified Anthocyanins in Improving Cardiometabolic Risk Factors in Chinese Men and Women with Prediabetes or Early Untreated Diabetes—A Randomized Controlled Trial , 2017, Nutrients.

[11]  S. Nabavi,et al.  Dietary Anthocyanins and Insulin Resistance: When Food Becomes a Medicine , 2017, Nutrients.

[12]  W. Ling,et al.  Effects of Anthocyanins on Cardiometabolic Health: A Systematic Review and Meta-Analysis of Randomized Controlled Trials. , 2017, Advances in nutrition.

[13]  Hock Eng Khoo,et al.  Anthocyanidins and anthocyanins: colored pigments as food, pharmaceutical ingredients, and the potential health benefits , 2017, Food & nutrition research.

[14]  G. Reglero,et al.  Winemaking by-products as anti-inflammatory food ingredients , 2017 .

[15]  Ian R. Lanza,et al.  Very-long-chain ω-3 fatty acid supplements and adipose tissue functions: a randomized controlled trial. , 2017, The American journal of clinical nutrition.

[16]  P. Tessari,et al.  A Multifunctional Bread Rich in Beta Glucans and Low in Starch Improves Metabolic Control in Type 2 Diabetes: A Controlled Trial , 2017, Nutrients.

[17]  N. Damasceno,et al.  The benefits of ω-3 supplementation depend on adiponectin basal level and adiponectin increase after the supplementation: A randomized clinical trial. , 2017, Nutrition.

[18]  W. Hall,et al.  Drinks containing anthocyanin-rich blackcurrant extract decrease postprandial blood glucose, insulin and incretin concentrations☆☆☆★ , 2016, The Journal of nutritional biochemistry.

[19]  P. Kris-Etherton,et al.  Effects of canola and high‐oleic‐acid canola oils on abdominal fat mass in individuals with central obesity , 2016, Obesity.

[20]  N. Rigby,et al.  Increasing dietary oat fibre decreases the permeability of intestinal mucus , 2016, Journal of functional foods.

[21]  I. Björck,et al.  A multifunctional diet improves cardiometabolic-related biomarkers independently of weight changes: an 8-week randomized controlled intervention in healthy overweight and obese subjects , 2016, European Journal of Nutrition.

[22]  C. Del Bo’,et al.  Berry Fruit Consumption and Metabolic Syndrome , 2016, Antioxidants.

[23]  M. Pervin,et al.  Beneficial Effects of Tea and the Green Tea Catechin Epigallocatechin-3-gallate on Obesity , 2016, Molecules.

[24]  M. Gidley,et al.  Reduction in circulating bile acid and restricted diffusion across the intestinal epithelium are associated with a decrease in blood cholesterol in the presence of oat β‐glucan , 2016, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[25]  M. Amiot,et al.  Effects of dietary polyphenols on metabolic syndrome features in humans: a systematic review , 2016, Obesity reviews : an official journal of the International Association for the Study of Obesity.

[26]  J. Horowitz,et al.  Dietary supplementation with omega‐3 fatty acids and oleate enhances exercise training effects in patients with metabolic syndrome , 2016, Obesity.

[27]  W. Hall,et al.  Conference on ‘ The future of animal products in the human diet : health and environmental concerns ’ Postgraduate Winner Berries and anthocyanins : promising functional food ingredients with postprandial glycaemia-lowering effects , 2016 .

[28]  E. D. de Mejia,et al.  Phenolic Compounds from Fermented Berry Beverages Modulated Gene and Protein Expression To Increase Insulin Secretion from Pancreatic β-Cells in Vitro. , 2016, Journal of agricultural and food chemistry.

[29]  Li-Xia He,et al.  The difference between oats and beta-glucan extract intake in the management of HbA1c, fasting glucose and insulin sensitivity: a meta-analysis of randomized controlled trials. , 2016, Food & function.

[30]  Xiaoyun Xie,et al.  Effects of 4 month exercise on left ventricular remodeling and autonomic nervous system in hypertensive patients. , 2016, Panminerva Medica (Testo stampato).

[31]  T. Wallace,et al.  Systematic Review of Anthocyanins and Markers of Cardiovascular Disease , 2016, Nutrients.

[32]  C. Drevon,et al.  Insulin resistance determines a differential response to changes in dietary fat modification on metabolic syndrome risk factors: the LIPGENE study. , 2015, The American journal of clinical nutrition.

[33]  P. Jones,et al.  Effect of consuming novel foods consisting high oleic canola oil, barley β-glucan, and DHA on cardiovascular disease risk in humans: the CONFIDENCE (Canola Oil and Fibre with DHA Enhanced) study – protocol for a randomized controlled trial , 2015, Trials.

[34]  S. Asgary,et al.  Evaluation of the Effects of Cornus mas L. Fruit Extract on Glycemic Control and Insulin Level in Type 2 Diabetic Adult Patients: A Randomized Double-Blind Placebo-Controlled Clinical Trial , 2015, Evidence-based complementary and alternative medicine : eCAM.

[35]  A. Bosy-Westphal,et al.  Assessment of fat and lean mass by quantitative magnetic resonance: a future technology of body composition research? , 2015, Current opinion in clinical nutrition and metabolic care.

[36]  H. Isoda,et al.  Cyanidin-3-glucoside derived from black soybeans ameliorate type 2 diabetes through the induction of differentiation of preadipocytes into smaller and insulin-sensitive adipocytes. , 2015, The Journal of nutritional biochemistry.

[37]  S. Faure,et al.  Epigallocatechin Gallate: A Review of Its Beneficial Properties to Prevent Metabolic Syndrome , 2015, Nutrients.

[38]  D. Venturini,et al.  Effects of Extra‐Virgin Olive Oil and Fish Oil on Lipid Profile and Oxidative Stress in Patients with Metabolic Syndrome , 2015, Nutrition.

[39]  E. Nahas,et al.  Effects of omega-3 on metabolic markers in postmenopausal women with metabolic syndrome , 2015, Climacteric : the journal of the International Menopause Society.

[40]  D. Greenwood,et al.  Effects of dietary fibre type on blood pressure: a systematic review and meta-analysis of randomized controlled trials of healthy individuals , 2015, Journal of hypertension.

[41]  T. Dinan,et al.  A natural solution for obesity: Bioactives for the prevention and treatment of weight gain. A review , 2015, Nutritional neuroscience.

[42]  Peixin Yang,et al.  Vascular and Metabolic Actions of the Green Tea Polyphenol Epigallocatechin Gallate , 2014, Current medicinal chemistry.

[43]  P. Ivester,et al.  The impact of polyunsaturated fatty acid-based dietary supplements on disease biomarkers in a metabolic syndrome/diabetes population , 2014, Lipids in Health and Disease.

[44]  P. Ivester,et al.  The impact of polyunsaturated fatty acid-based dietary supplements on disease biomarkers in a metabolic syndrome/diabetes population , 2014, Lipids in Health and Disease.

[45]  K. Koh,et al.  Omega-3 fatty acid therapy dose-dependently and significantly decreased triglycerides and improved flow-mediated dilation, however, did not significantly improve insulin sensitivity in patients with hypertriglyceridemia. , 2014, International journal of cardiology.

[46]  A. Whitehead,et al.  Cholesterol-lowering effects of oat β-glucan: a meta-analysis of randomized controlled trials1234 , 2014, The American journal of clinical nutrition.

[47]  P. Ellis,et al.  Oat β-glucan: physico-chemical characteristics in relation to its blood-glucose and cholesterol-lowering properties , 2014, British Journal of Nutrition.

[48]  M. Orešič,et al.  Isoenergetic diets differing in their n-3 fatty acid and polyphenol content reflect different plasma and HDL-fraction lipidomic profiles in subjects at high cardiovascular risk. , 2014, Molecular nutrition & food research.

[49]  G. Srzednicki,et al.  Composition and inhibitory activities towards digestive enzymes of polyphenolic-rich fractions of Davidson's plum and quandong , 2014 .

[50]  M. Xia,et al.  Anthocyanin supplementation improves HDL-associated paraoxonase 1 activity and enhances cholesterol efflux capacity in subjects with hypercholesterolemia. , 2014, The Journal of clinical endocrinology and metabolism.

[51]  T. Spector,et al.  Intakes of anthocyanins and flavones are associated with biomarkers of insulin resistance and inflammation in women. , 2014, The Journal of nutrition.

[52]  J. Margareto,et al.  Effects of dietary supplementation with epigallocatechin-3-gallate on weight loss, energy homeostasis, cardiometabolic risk factors and liver function in obese women: randomised, double-blind, placebo-controlled clinical trial , 2013, British Journal of Nutrition.

[53]  M. Ladomery,et al.  The relationship between the structure and biological actions of green tea catechins. , 2013, Food chemistry.

[54]  R. Amani,et al.  Effects of Freeze-Dried Strawberry Supplementation on Metabolic Biomarkers of Atherosclerosis in Subjects with Type 2 Diabetes: A Randomized Double-Blind Controlled Trial , 2013, Annals of Nutrition and Metabolism.

[55]  S. Engelsen,et al.  Extracted oat and barley β-glucans do not affect cholesterol metabolism in young healthy adults. , 2013, The Journal of nutrition.

[56]  I. Björck,et al.  Combining functional features of whole-grain barley and legumes for dietary reduction of cardiometabolic risk: a randomised cross-over intervention in mature women , 2013, British Journal of Nutrition.

[57]  M. Moreno-Aliaga,et al.  Role of omega-3 fatty acids in obesity, metabolic syndrome, and cardiovascular diseases: a review of the evidence , 2013, Journal of Physiology and Biochemistry.

[58]  A. Clarke,et al.  Green and black tea for the primary prevention of cardiovascular disease. , 2013, The Cochrane database of systematic reviews.

[59]  N. Osakabe Flavan 3-ols improve metabolic syndrome risk factors: evidence and mechanisms , 2013, Journal of clinical biochemistry and nutrition.

[60]  S. Tosh Review of human studies investigating the post-prandial blood-glucose lowering ability of oat and barley food products , 2013, European Journal of Clinical Nutrition.

[61]  S. Kjeldsen,et al.  Effects of anthocyanins on cardiovascular risk factors and inflammation in pre-hypertensive men: a double-blind randomized placebo-controlled crossover study , 2013, Journal of Human Hypertension.

[62]  E. López-Huertas The effect of EPA and DHA on metabolic syndrome patients: a systematic review of randomised controlled trials , 2012, British Journal of Nutrition.

[63]  E. Martínez-Victoria,et al.  Omega 3 polyunsaturated fatty acids and body weight , 2012, British Journal of Nutrition.

[64]  E. Rimm,et al.  Effects of chocolate, cocoa, and flavan-3-ols on cardiovascular health: a systematic review and meta-analysis of randomized trials. , 2012, The American journal of clinical nutrition.

[65]  E. Cummins,et al.  Meta-analysis of the effect of β-glucan intake on blood cholesterol and glucose levels. , 2011, Nutrition.

[66]  G. Silecchia,et al.  Cyanidin-3-O-β-Glucoside and Protocatechuic Acid Exert Insulin-Like Effects by Upregulating PPARγ Activity in Human Omental Adipocytes , 2011, Diabetes.

[67]  L. Tapsell,et al.  Effect of 6 weeks' consumption of β-glucan-rich oat products on cholesterol levels in mildly hypercholesterolaemic overweight adults , 2011, British Journal of Nutrition.

[68]  J. Gaziano,et al.  Effects of cocoa products/dark chocolate on serum lipids: a meta-analysis , 2011, European Journal of Clinical Nutrition.

[69]  N. Kalupahana,et al.  (n-3) Fatty acids alleviate adipose tissue inflammation and insulin resistance: mechanistic insights. , 2011, Advances in nutrition.

[70]  T. Tsai,et al.  Does supplementation with green tea extract improve insulin resistance in obese type 2 diabetics? A randomized, double-blind, and placebo-controlled clinical trial. , 2011, Alternative medicine review : a journal of clinical therapeutic.

[71]  J. Viikari,et al.  Different berries and berry fractions have various but slightly positive effects on the associated variables of metabolic diseases on overweight and obese women , 2011, European Journal of Clinical Nutrition.

[72]  T. Wolever,et al.  Physicochemical properties of oat β-glucan influence its ability to reduce serum LDL cholesterol in humans: a randomized clinical trial. , 2010, The American journal of clinical nutrition.

[73]  D. Cherkin,et al.  Unanticipated benefits of CAM therapies for back pain: an exploration of patient experiences. , 2010, Journal of alternative and complementary medicine.

[74]  L. Tapsell,et al.  Oat β-glucan supplementation does not enhance the effectiveness of an energy-restricted diet in overweight women , 2009, British Journal of Nutrition.

[75]  C. Lavie,et al.  Omega-3 polyunsaturated fatty acids and cardiovascular diseases. , 2009, Journal of the American College of Cardiology.

[76]  Donald A Williamson,et al.  Comparison of weight-loss diets with different compositions of fat, protein, and carbohydrates. , 2009, The New England journal of medicine.

[77]  Yun Hu,et al.  Tea Consumption and Risk of Type 2 Diabetes: A Meta-Analysis of Cohort Studies , 2009, Journal of General Internal Medicine.

[78]  J. Martínez,et al.  A diet rich in long chain omega-3 fatty acids modulates satiety in overweight and obese volunteers during weight loss , 2008, Appetite.

[79]  K. M. Behall,et al.  Whole-grain diets reduce blood pressure in mildly hypercholesterolemic men and women. , 2006, Journal of the American Dietetic Association.

[80]  F. Danesi,et al.  Polyunsaturated fatty acids: From diet to binding to ppars and other nuclear receptors , 2006, Genes & Nutrition.

[81]  S. Grundy,et al.  The metabolic syndrome. , 2008, Endocrine reviews.

[82]  H. Iso,et al.  Randomized controlled trial for an effect of green tea consumption on insulin resistance and inflammation markers. , 2005, Journal of nutritional science and vitaminology.

[83]  G. Norman,et al.  Randomized controlled trials. , 2004, AJR. American journal of roentgenology.

[84]  K. Shimada,et al.  Oolong tea increases plasma adiponectin levels and low-density lipoprotein particle size in patients with coronary artery disease. , 2004, Diabetes research and clinical practice.

[85]  R. Mensink,et al.  Cholesterol-lowering effect of β-glucan from oat bran in mildly hypercholesterolemic subjects may decrease when β-glucan is incorporated into bread and cookies , 2003 .

[86]  B. Clevidence,et al.  Antihyperglycemic effect of oolong tea in type 2 diabetes. , 2003, Diabetes care.

[87]  P. Wilson,et al.  Whole-grain intake is favorably associated with metabolic risk factors for type 2 diabetes and cardiovascular disease in the Framingham Offspring Study. , 2002, The American journal of clinical nutrition.

[88]  S. Roberts,et al.  High-protein weight-loss diets: are they safe and do they work? A review of the experimental and epidemiologic data. , 2002, Nutrition reviews.

[89]  B. Charbonnel [Treatment of type 2 diabetes]. , 2000, Diabetes & metabolism.

[90]  P. Åman,et al.  Molecular Weight, Structure, and Shape of Oat (1→3),(1→4)-β-d-Glucan Fractions Obtained by Enzymatic Degradation with Lichenase , 2000 .

[91]  Christine M. Williams,et al.  Modest doses of beta-glucan do not reduce concentrations of potentially atherogenic lipoproteins. , 2000, The American journal of clinical nutrition.

[92]  R. Vandongen,et al.  A randomized controlled trial of the effect of dietary fibre on blood pressure. , 1987, Clinical science.

[93]  M. Lila,et al.  Berries containing anthocyanins with enhanced methylation profiles are more effective at ameliorating high fat diet-induced metabolic damage. , 2018, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

[94]  D. Różańska,et al.  The significance of anthocyanins in the prevention and treatment of type 2 diabetes. , 2018, Advances in clinical and experimental medicine : official organ Wroclaw Medical University.

[95]  Frank Schoenlau,et al.  Delphinol® standardized maqui berry extract significantly lowers blood glucose and improves blood lipid profile in prediabetic individuals in three-month clinical trial. , 2016, Panminerva medica.

[96]  Guillermo I Carrillo,et al.  A Controlled Clinical Trial , 2015 .

[97]  J. Cryan,et al.  A natural solution for Obesity , 2014 .

[98]  I. Mackay,et al.  A double-blind controlled trial , 2011 .

[99]  G. Schuler,et al.  Effect of cocoa products on blood pressure: systematic review and meta-analysis. , 2010, American journal of hypertension.

[100]  J. Sikora,et al.  Aronia melanocarpa extract reduces blood pressure, serum endothelin, lipid, and oxidative stress marker levels in patients with metabolic syndrome. , 2010, Medical science monitor : international medical journal of experimental and clinical research.

[101]  W. Howard Whole-grain intake is inversely associated with the metabolic syndrome and mortality in older adults , 2007 .

[102]  B. Blaine a review and meta-analysis , 2006 .

[103]  P. Jacques,et al.  Whole-grain intake is inversely associated with the metabolic syndrome and mortality in older adults. , 2006, The American journal of clinical nutrition.

[104]  R. Mensink,et al.  Changes in serum lipids and postprandial glucose and insulin concentrations after consumption of beverages with β-glucans from oats or barley: a randomised dose-controlled trial , 2005, European Journal of Clinical Nutrition.

[105]  R. Mensink,et al.  Cholesterol-lowering effect of beta-glucan from oat bran in mildly hypercholesterolemic subjects may decrease when beta-glucan is incorporated into bread and cookies. , 2003, The American journal of clinical nutrition.

[106]  R. Andersson,et al.  Molecular weight, structure, and shape of oat (1-->3),(1-->4)-beta-D-glucan fractions obtained by enzymatic degradation with lichenase. , 2000, Biomacromolecules.

[107]  G. Burch [Cardiovascular diseases]. , 1956, Revista medica cubana.