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