Display options
Share it on

Food Nutr Res. 2016 Jan 29;60:29268. doi: 10.3402/fnr.v60.29268. eCollection 2016.

Effect of long chain omega-3 polyunsaturated fatty acids on inflammation and metabolic markers in hypertensive and/or diabetic obese adults: a randomized controlled trial.

Food & nutrition research

Mohammed S Ellulu, Huzwah Khaza'ai, Ismail Patimah, Asmah Rahmat, Yehia Abed

Affiliations

  1. Department of Nutrition and Dietetics, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Selangor, Malaysia.
  2. Department of Biomedical Science, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Selangor, Malaysia; [email protected].
  3. Department of Biomedical Science, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Selangor, Malaysia.
  4. Faculty of Public Health, Al Quds University of Gaza, Gaza City, Palestine.

PMID: 26829184 PMCID: PMC4734034 DOI: 10.3402/fnr.v60.29268

Abstract

BACKGROUND: Obesity is a degree of excess weight that predisposes people to metabolic syndromes via an inflammatory mechanism. Hypertensive and diabetic people have higher risks of developing systemic inflammation. Long chain omega-3 polyunsaturated fatty acids (LC ω-3 PUFAs) can reduce the cardiovascular events and help against inflammation.

OBJECTIVE: To identify the effects of LC ω-3 PUFAs on reducing the levels of inflammatory markers on hypertensive and/or diabetic obese adults.

MATERIALS AND METHODS: Sixty-four patients, who were hypertensive and/or diabetic obese with high levels of inflammatory markers, from primary healthcare centers of Gaza City, Palestine, enrolled in two groups of an open-label, parallel, randomized, controlled trial for 8 weeks. Thirty-three patients were in the control group, and 31 patients were in the experimental group. The experimental group was treated with a daily dose of 300 mg eicosapentaenoic acid and 200 mg of docosahexaenoic acid.

RESULTS: Treatment with LC ω-3 PUFAs significantly reduced the level of high sensitivity C reactive protein (hs-CRP) [14.78±10.7 to 8.49±6.69 mg/L, p<0.001], fasting blood glucose (FBG) [178.13±58.54 to 157.32±59.77 mg/dL, p=0.024], and triglyceride (TG) [209.23±108.3 to 167.0±79.9 mg/dL, p<0.05] after 8 weeks of treatment, whereas no significant changes appeared in interleukin 6 (IL-6) and total cholesterol (TC). In the control group, significant reduction was detected for FBG [187.15±64.8 to 161.91±37.9 mg/dL, p<0.05] and TG [202.91±107.0 to 183.45±95.82 mg/dL, p<0.05], and no changes for hs-CRP, IL-6, or TC. By comparing the experimental group with the changes of control group at the endpoint, LC ω-3 PUFAs did not reach the clinical significance in treating effectiveness for any of the clinical variables.

CONCLUSION: LC ω-3 PUFAs have recommended effects on health; the obtained results can improve the role of LC ω-3 PUFAs as a protective factor on inflammation and metabolic dysregulation. The time allowed or the dose used could be insufficient to achieve full treatment affectivity.

Keywords: DHA; EPA; diabetes; hypertension; inflammation; obesity; omega-3 fatty acids

References

  1. Biochem Biophys Res Commun. 2009 Feb 6;379(2):476-9 - PubMed
  2. Science. 1993 Jan 1;259(5091):87-91 - PubMed
  3. Atherosclerosis. 2012 Apr;221(2):514-20 - PubMed
  4. BMC Obes. 2014 Apr 22;1:7 - PubMed
  5. Mar Drugs. 2013 Sep 20;11(9):3569-81 - PubMed
  6. J Clin Psychiatry. 2007 Jul;68(7):1056-61 - PubMed
  7. Eur J Clin Nutr. 2009 Sep;63(9):1154-6 - PubMed
  8. East Mediterr Health J. 2013 Apr;19(4):307-13 - PubMed
  9. J Obes. 2012;2012:213547 - PubMed
  10. J Cardiovasc Pharmacol. 2011 Apr;57(4):489-94 - PubMed
  11. Nature. 2008 Jul 24;454(7203):428-35 - PubMed
  12. Biochem Biophys Res Commun. 2002 Feb 1;290(4):1295-9 - PubMed
  13. East Mediterr Health J. 2004 Nov;10 (6):789-93 - PubMed
  14. J Nutr Metab. 2012;2012:476380 - PubMed
  15. Drug Des Devel Ther. 2015 Jul 01;9:3405-12 - PubMed
  16. World Health Organ Tech Rep Ser. 2000;894:i-xii, 1-253 - PubMed
  17. Br J Nutr. 2007 Oct;98 Suppl 1:S29-35 - PubMed
  18. Clin Nutr. 2015 Jun;34(3):388-93 - PubMed
  19. Prostaglandins Leukot Essent Fatty Acids. 2009 Feb-Mar;80(2-3):85-91 - PubMed
  20. Klin Med (Mosk). 2009;87(4):37-41 - PubMed
  21. Br J Nutr. 2012 Jun;107 Suppl 2:S228-39 - PubMed
  22. Atherosclerosis. 2014 Jan;232(1):10-6 - PubMed
  23. Br J Nutr. 2012 Jun;107 Suppl 2:S201-13 - PubMed
  24. Am J Clin Nutr. 2012 Nov;96(5):1137-49 - PubMed
  25. Br J Nutr. 2012 Jun;107 Suppl 2:S159-70 - PubMed
  26. Diabetes Metab Syndr Obes. 2010 May 26;3:173-86 - PubMed
  27. J Biol Chem. 2002 Aug 23;277(34):31270-8 - PubMed
  28. Nutr Metab Cardiovasc Dis. 2007 Oct;17(8):590-7 - PubMed
  29. Biotechnol Adv. 2011 Sep-Oct;29(5):508-18 - PubMed
  30. Am J Clin Nutr. 2011 Feb;93(2):243-52 - PubMed
  31. J Int Med Res. 2009 Nov-Dec;37(6):1831-41 - PubMed
  32. J Nutr Biochem. 2010 Sep;21(9):781-92 - PubMed
  33. Prostaglandins Leukot Essent Fatty Acids. 2014 Oct;91(4):161-8 - PubMed
  34. BMJ. 2012 Oct 30;345:e6698 - PubMed
  35. Nat Rev Immunol. 2008 May;8(5):349-61 - PubMed
  36. CMAJ. 2008 Jan 15;178(2):150 - PubMed
  37. Am J Cardiol. 2015 Jan 15;115(2):196-201 - PubMed
  38. Mol Cell Biochem. 2014 Nov;396(1-2):9-22 - PubMed

Publication Types