Tehran University of Medical Sciences (TUMS), School of Nutritional Sciences and Dietetics, Department of Cellular and Molecular Nutrition
Tehran, 1471613151, Iran
NCT Number: NCT03258840
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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Notify Me35 year–50 year
All sexes
Interventional
Not applicable
Tehran, 1471613151, Iran
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
EPA supplement, 4 × 500 mg softgel daily (2 g per day), 2 times a day, for 8 weeks.
Other names: Eicosapentaenoic acid
EPA- placebo softgel (Containing 2 g edible paraffin oil), 4 × 500 mg softgel daily, 2 times a day, for 8 weeks.
Time frame: Change from Baseline at 8 weeks after the intervention
Hemoglobin A1c (HbA1c) measurement by related kits according their protocols
Time frame: Baseline, 8 weeks after the intervention
measurement of paraoxonase-2(PON-2) gene expression using quantitative Real-time PCR
Time frame: Change frome baseline at 8 weeks
Systolic blood pressure changes measurement by manometer
Time frame: Change frome baseline at 8 weeks
Diastolic blood pressure changes measurement by manometer
Time frame: Baseline, 8 weeks after the intervention
serum paraoxonase-1(PON-1) activity by kit according related protocol
Time frame: Baseline, 8 weeks after the intervention
calculating the ratio after measurement of PON1 and HDL-c by related kits according their protocols
Time frame: Baseline, 8 weeks after the intervention
measurement of paraoxonase lactonase (PON-HCTLase) activity by related kit according its protocol
Time frame: Baseline, 8 weeks after the intervention
high density lipoprotein- cholesterol (HDL-c) measurement by related kits according their protocols
Time frame: Baseline, 8 weeks after the intervention
Fasting blood sugar (FBS) measurement by related kits according their protocols
Time frame: Baseline, 8 weeks after the intervention
high density lipoprotein 2- cholesterol (HDL2-c) measurement by related kits according their protocols
Time frame: Baseline, 8 weeks after the intervention
high density lipoprotein 3- cholesterol (HDL3-c) measurement by related kits according their protocols
Time frame: Baseline, 8 weeks after the intervention
Serum apo-protein B measurement by related kits according their protocols
Time frame: Baseline, 8 weeks after the intervention
Serum apo-protein A-I measurement by related kits according their protocols
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
Time frame: Baseline, 8 weeks after the intervention
measurement of serum levels of methionine by related kit according its protocol
Time frame: Baseline, 8 weeks after the intervention
measurement of serum levels of malondialdehyde (MDA)by related kit according its protocol
Time frame: Baseline, 8 weeks after the intervention
measurement of serum levels of homocysteine (Hcy) by related kit according its protocol
Time frame: Baseline, 8 weeks after the intervention
measurement of serum levels of soluble E-Selectin by related kit according its protocol
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
Time frame: Baseline, 8 weeks after the intervention
measurement of serum levels of cysteine by related kit according its protocol
Time frame: Baseline, 8 weeks after the intervention
measurement of serum levels of lipoprotein-a (Lpa)by related kit according its protocol
Tehran University of Medical Sciences
Other
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
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