Long Chain n-3 Fatty Acids Improve Depression Syndrome in Type 2 Diabetes Mellitus

Maryam Mazaherioun, Ahmad Saedisomeolia, Mohammad Hassan Javanbakht, Fariba Koohdani, Mahnaz Zarei, Samaneh Ansari, Fatemeh Khoshkhoo Bazargani, Mahmoud Djalali, Maryam Mazaherioun, Ahmad Saedisomeolia, Mohammad Hassan Javanbakht, Fariba Koohdani, Mahnaz Zarei, Samaneh Ansari, Fatemeh Khoshkhoo Bazargani, Mahmoud Djalali

Abstract

Background: Type 2 diabetes mellitus (T2DM) is commonly associated with depressive symptoms, which affect prognosis and quality of life. We investigated the antidepressant effects of n-3 fatty acids (n-3FAs) monotherapy (without conventional antidepressants) for T2DM patients with mild to moderate depressive symptoms.

Methods: A 10-wk, placebo-controlled, double-blind, parallel-group (1:1 ratio) randomized trial of n-3FAs (2700 mg/day EPA: DHA ratio=2) versus placebo in 88 Iranian diabetic patients with mild to moderate depression based on Beck Depression Inventory II (BDI-II-PERSIAN) was conducted. This study started from July 2014 to January 2015 in Tehran University of Medical Sciences, Tehran, Iran. The primary event was defined as worsened, non-changed, or inconsiderably improved depression (<5 unit decrease in BDI-II-PERSIAN depression scores after treatment) (ClinicalTrials.gov Identifier: NCT02261545).

Results: Randomly, 44 T2DM patients were treated with n-3FAs supplements and 44 cases received placebo (three patients discontinued). n-3FAs could significantly protect patients against the aforesaid event and exhibit satisfactory prevention (number needed to treat with 95% confidence interval: 2.52, 1.71-4.74). No serious adverse reactions were reported.

Conclusion: n-3FAs supplementation had significant antidepressant effects in T2DM patients with mild to moderate depressive symptoms, not confounded by metabolic factors and disease duration.

Keywords: Depression; Randomized controlled trial; Type 2 diabetes mellitus; n-3 fatty acids.

Conflict of interest statement

Conflicts of Interest The authors declared no conflict of interest.

Figures

Fig. 1:
Fig. 1:
Changes in BDI-II scores of patients with type II diabetes mellitus before and after intervention

References

    1. Inzucchi SE, Bergenstal RM, Buse JB, et al. (2012). Management of Hyperglycemia in Type 2 Diabetes: A Patient-Centered Approach: Position Statement of the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD). Diabetes Care, 35:1364–1379.
    1. Saydah SH, Fradkin J, Cowie CC. (2004). POor control of risk factors for vascular disease among adults with previously diagnosed diabetes. JAMA, 291:335–342.
    1. Papelbaum M, Moreira RO, Coutinho W, et al. (2011). Depression, glycemic control and type 2 diabetes. Diabetol Metab Syndr, 3:26.
    1. O’Connor PJ, Crain AL, Rush WA, et al. (2009). Does diabetes double the risk of depression? Ann Fam Med, 7:328–35.
    1. Group DCCTR (1993). The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent diabetes mellitus. N Engl J Med, 329:977–986.
    1. de Groot M, Anderson R, Freedland KE, et al. (2001). Association of depression and diabetes complications: a meta-analysis. Psychosom Med, 63:619–30.
    1. Lustman PJ, Anderson RJ, Freedland KE, et al. (2000). Depression and poor glycemic control: a meta-analytic review of the literature. Diabetes Care, 23:934–942.
    1. Black SA, Markides KS, Ray LA. (2003). Depression Predicts Increased Incidence of Adverse Health Outcomes in Older Mexican Americans With Type 2 Diabetes. Diabetes Care, 26:2822–8.
    1. Katon WJ, Rutter C, Simon G, et al. (2005). The Association of Comorbid Depression With Mortality in Patients With Type 2 Diabetes. Diabetes Care, 28:2668–2672.
    1. Lucas M, Asselin G, Mérette C, Poulin M-J, Dodin S. (2009). Ethyl-eicosapentaenoic acid for the treatment of psychological distress and depressive symptoms in middle-aged women: a double-blind, placebo-controlled, randomized clinical trial. Am J Clin Nutr, 89:641–651.
    1. Rubin RR, Ma Y, Marrero DG, et al. (2008). Elevated Depression Symptoms, Antidepressant Medicine Use, and Risk of Developing Diabetes During the Diabetes Prevention Program. Diabetes Care, 31:420–6.
    1. Flachs P, Rossmeisl M, Kopecky J. (2014). The effect of n-3 fatty acids on glucose homeostasis and insulin sensitivity. Physiol Res, 63 Suppl 1:S93–118.
    1. Grosso G, Pajak A, Marventano S, et al. (2014). Role of omega-3 fatty acids in the treatment of depressive disorders: a comprehensive meta-analysis of randomized clinical trials. PLoS One, 9(5): e96905.
    1. Flachs P, Rossmeisl M, Bryhn M, Kopecky J. (2009). Cellular and molecular effects of n-3 polyunsaturated fatty acids on adipose tissue biology and metabolism. Clin Sci (Lond), 116:1–16.
    1. Hansen HS, Diep TA. (2009). N-acylethanolamines, anandamide and food intake. Biochem Pharmacol, 78:553–560.
    1. Ghassemzadeh H, Mojtabai R, Karamghadiri N, Ebrahimkhani N. (2005). Psychometric properties of a Persian-language version of the Beck Depression Inventory--Second edition: BDI-II-PERSIAN. Depress Anxiety, 21:185–92.
    1. Mazaherioun M, Djalali M, Koohdani F, et al. (2017). Beneficial Effects of n-3 Fatty Acids on Cardiometabolic and Inflammatory Markers in Type 2 Diabetes Mellitus: A Randomized Placebo-Controlled Double-blind Clinical Trial. Med Princ Pract, 26:535–541.
    1. Mazaherioun M, Saedisomeolia A, Javanbakht MH, et al. (2017). Beneficial effects of n-3 polyunsaturated fatty acids on adiponectin levels and AdipoR gene expression in patients with type 2 diabetes mellitus: a randomized, placebo-controlled, double-blind clinical trial. Arch Med Sci, 13:716–724.
    1. Vasheghani-Farahani A, Tahmasbi M, Asheri H, et al. (2011). The Persian, last 7-day, long form of the International Physical Activity Questionnaire: translation and validation study. Asian J Sports Med, 2:106–16.
    1. Antypa N, Van der Does A, Smelt A, Rogers R. (2009). Omega-3 fatty acids (fish-oil) and depression-related cognition in healthy volunteers. J Psychopharmacol, 23:831–840.
    1. DeFina LF, Marcoux LG, Devers SM, et al. (2011). Effects of omega-3 supplementation in combination with diet and exercise on weight loss and body composition. Am J Clin Nutr, 93:455–62.
    1. Fontani G, Corradeschi F, Felici A, et al. (2005). Blood profiles, body fat and mood state in healthy subjects on different diets supplemented with Omega-3 polyunsaturated fatty acids. Eur J Clin Invest, 35:499–507.
    1. Kiecolt-Glaser JK, Belury MA, Andridge R, et al. (2011). Omega-3 supplementation lowers inflammation and anxiety in medical students: a randomized controlled trial. Brain Behav Immun, 25:1725–1734.
    1. Kiecolt-Glaser JK, Belury MA, Andridge R, et al. (2012). Omega-3 supplementation lowers inflammation in healthy middle-aged and older adults: a randomized controlled trial. Brain Behav Immun, 26:988–995.
    1. van de Rest O, Geleijnse JM, Kok FJ, et al. (2008). Effect of fish-oil supplementation on mental well-being in older subjects: a randomized, double-blind, placebo-controlled trial. Am J Clin Nutr, 88:706–713.
    1. Ginty AT, Conklin SM. (2015). Short-term supplementation of acute long-chain omega-3 polyunsaturated fatty acids may alter depression status and decrease symptomology among young adults with depression: A preliminary randomized and placebo controlled trial. Psychiatry Res, 229:485–489.
    1. Bot M, Pouwer F, Assies J, et al. (2010). Eicosapentaenoic acid as an add-on to antidepressant medication for co-morbid major depression in patients with diabetes mellitus: a randomized, double-blind placebo-controlled study. J Affect Disord, 126:282–286.
    1. Mocking RJ, Assies J, Bot M, et al. (2012). Biological effects of add-on eicosapentaenoic acid supplementation in diabetes mellitus and co-morbid depression: a randomized controlled trial. PLoS One, 7:e49431.
    1. McNamara RK, Carlson SE. (2006). Role of omega-3 fatty acids in brain development and function: potential implications for the pathogenesis and prevention of psychopathology. Prostaglandins Leukot Essent Fatty Acids, 75:329–349.
    1. Kodas E, Galineau L, Bodard S, et al. (2004). Serotoninergic neurotransmission is affected by n-3 polyunsaturated fatty acids in the rat. J Neurochem, 89:695–702.
    1. Hibbeln JR, Linnoila M, Umhau JC, et al. (1998). Essential fatty acids predict metabolites of serotonin and dopamine in cerebrospinal fluid among healthy control subjects, and early-and late-onset alcoholics. Biol Psychiatry, 44:235–242.
    1. Farooqui AA, Horrocks LA, Farooqui T. (2007). Modulation of inflammation in brain: a matter of fat. J Neurochem, 101:577–599.
    1. Gross R, Olfson M, Gameroff MJ, et al. (2005). Depression and glycemic control in Hispanic primary care patients with diabetes. J Gen Intern Med, 20:460–466.

Source: PubMed

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