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Completed

NCT Number: NCT03258840

EPA Supplementation on Vascular Inflammation, and Gene Expression of PON2 in Patients With Type II Diabetes Mellitus

The aim of this study is to determining of the effects of Eicosapentaenoic acid (EPA) supplementation on serum activities of Paraoxonase-1 and Homocystein thiolactonase, and serum levels of some indicators of vascular inflammation, and the gene expression of PON2 in the peripheral blood mononuclear cell (PBMC) in the patients with type II diabetes mellitus.

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Key information

Age range

35 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Tehran University of Medical Sciences (TUMS), School of Nutritional Sciences and Dietetics, Department of Cellular and Molecular Nutrition

Tehran, 1471613151, Iran

About this study

The aim of this study is to determining of the effects of Eicosapentaenoic acid (EPA) supplementation on serum activities of Paraoxonase-1 and Homocystein thiolactonase and several indicators of vascular inflammation and the gene expression of PON2 in the peripheral blood mononuclear cell (PBMC) in the patients with type II diabetes mellitus. In this randomized, double-blind clinical trial, placebo-controlled, single-center, 36 men and women aged 35-50 years with type 2 diabetes are enrolled in the study from the Iranian Diabetes Association. After signing informed consent, all individuals complete a general information form. a 24-hour food recall for 3 days will be taken from the participants at the beginning and the end of the study,. Selected samples are randomly classified into 2 blocks of groups receiving supplement and placebo. Two groups will be classified (blocked) based on sex. The supplement group, will receive 2 g/day EPA for 8 weeks and the placebo group will also receive placebo (containing 2 g of edible paraffin) (similar in terms of color, shape and size). Patients are recommended to sustain their diets and medication dose (s) during the study and also advised to maintain a constant level of physical activity. Blood samples will be collected after 8-12 hours fasting and anthropocentric variables, biochemical parameters, target gene expression and physical activity before and after the trial will be measured.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Willingness to collaborate in the study
  • aged 35-50 years
  • having a history of at least 1 year of type 2 diabetes mellitus before the participation in the study based on FBS ≥126 mg/dl or 2hPG ≥200 mg/dl (2-hour plasma glucose),
  • 25≤BMI<30 kg/m2

Exclusion criteria

  • pregnant and breastfeeding women
  • using insulin, alcohol consumption, smoking and other drugs
  • taking drugs (lipid-lowering, β-blockers, diuretics, estrogens, progesterones, vitamin supplements and ω-3 fatty acid supplements
  • followers of the special diet
  • history of diabetic retinopathy or diabetic nephropathy
  • type 1 diabetes mellitus and other disorders
  • any need to take insulin, change in the dose (s) and type of medication or physical activity

Treatment and study plan

EPA Supplement

Dietary Supplement

EPA supplement, 4 × 500 mg softgel daily (2 g per day), 2 times a day, for 8 weeks.

Other names: Eicosapentaenoic acid

EPA Placebo

Dietary Supplement

EPA- placebo softgel (Containing 2 g edible paraffin oil), 4 × 500 mg softgel daily, 2 times a day, for 8 weeks.

Primary outcomes

  1. HbA1c

    Time frame: Change from Baseline at 8 weeks after the intervention

    Hemoglobin A1c (HbA1c) measurement by related kits according their protocols

Secondary outcomes

  1. PON2 gene expression

    Time frame: Baseline, 8 weeks after the intervention

    measurement of paraoxonase-2(PON-2) gene expression using quantitative Real-time PCR

  2. Systolic blood pressure

    Time frame: Change frome baseline at 8 weeks

    Systolic blood pressure changes measurement by manometer

  3. Diastolic blood pressure

    Time frame: Change frome baseline at 8 weeks

    Diastolic blood pressure changes measurement by manometer

  4. serum paraoxonase-1(PON-1) activity

    Time frame: Baseline, 8 weeks after the intervention

    serum paraoxonase-1(PON-1) activity by kit according related protocol

  5. PON1/HDL-c Ratio

    Time frame: Baseline, 8 weeks after the intervention

    calculating the ratio after measurement of PON1 and HDL-c by related kits according their protocols

  6. serum paraoxonase lactonase (PON-HCTLase) activity

    Time frame: Baseline, 8 weeks after the intervention

    measurement of paraoxonase lactonase (PON-HCTLase) activity by related kit according its protocol

  7. HDL-c

    Time frame: Baseline, 8 weeks after the intervention

    high density lipoprotein- cholesterol (HDL-c) measurement by related kits according their protocols

  8. FBS

    Time frame: Baseline, 8 weeks after the intervention

    Fasting blood sugar (FBS) measurement by related kits according their protocols

  9. HDL2-c

    Time frame: Baseline, 8 weeks after the intervention

    high density lipoprotein 2- cholesterol (HDL2-c) measurement by related kits according their protocols

  10. HDL3-c

    Time frame: Baseline, 8 weeks after the intervention

    high density lipoprotein 3- cholesterol (HDL3-c) measurement by related kits according their protocols

  11. Serum apo B

    Time frame: Baseline, 8 weeks after the intervention

    Serum apo-protein B measurement by related kits according their protocols

  12. Serum apo A-I

    Time frame: Baseline, 8 weeks after the intervention

    Serum apo-protein A-I measurement by related kits according their protocols

  13. apo B/apo A-I Ratio

    Time frame: Baseline, 8 weeks after the intervention

    calculating the ratio after measurement of apo B and apo A-1 by related kits according their protocols

  14. Serum methionine

    Time frame: Baseline, 8 weeks after the intervention

    measurement of serum levels of methionine by related kit according its protocol

  15. Serum malondialdehyde (MDA)

    Time frame: Baseline, 8 weeks after the intervention

    measurement of serum levels of malondialdehyde (MDA)by related kit according its protocol

  16. Serum homocysteine (Hcy)

    Time frame: Baseline, 8 weeks after the intervention

    measurement of serum levels of homocysteine (Hcy) by related kit according its protocol

  17. Serum sE-Selectin

    Time frame: Baseline, 8 weeks after the intervention

    measurement of serum levels of soluble E-Selectin by related kit according its protocol

  18. sVCAM-1

    Time frame: Baseline, 8 weeks after the intervention

    measurement of serum levels of soluble Vascular cell adhesion molecule-1 (VCAM-1) by related kit according its protocol

  19. Serum cysteine

    Time frame: Baseline, 8 weeks after the intervention

    measurement of serum levels of cysteine by related kit according its protocol

  20. Serum Lpa

    Time frame: Baseline, 8 weeks after the intervention

    measurement of serum levels of lipoprotein-a (Lpa)by related kit according its protocol

Sponsors and collaborators

Lead sponsor

Tehran University of Medical Sciences

Other

Registry information

Official study title

The Effect of EPA on the Serum Activities of Paraoxonase 1, Homocystein, Thiolactonase and Some Indicators of Vascular Inflammation and PON2 Gene Expression in PBMC Ofthe Patients With Type II Diabetes

Important dates

Study start
2013
Primary completion
2013
Study completion
2014
First posted
Aug 23, 2017
Registry last updated
Aug 23, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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