Hyperlipidemia. Hyperlipidemia, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Willingness to cooperate Age 20-55 Years suffering from hyperlipidemia based on laboratory documentation (total cholesterol more than 240, LDL-c more than 160 and triglyceride more than 200 BMI:25-34.9
Exclusion criteria
Exclusion criteria: Unwillingness to cooperate Pregnancy, breastfeeding and menopause History of other cardiovascular diseases, diabetes, liver and kidney failure, thyroid and parathyroid diseases, chronic diseases of the digestive system and cancer Use of cigarettes, tobacco and alcohol Regular consumption of probiotic foods (kefir, probiotic yogurt) (daily consumption of kefir buttermilk or probiotic yogurt in a person's usual diet) Using food supplements that may affect metabolic parameters (prebiotics and omega 3) Intolerance or allergy to milk and dairy products Receive antibiotic treatment one month before the study Under any diet, especially the blood fat-lowering diet Taking drugs that reduce cholesterol or triglycerides
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The percentage of people with hyperlipidemia( total cholesterol above 240, LDL-cholesterol above 160, triglyceride above 200 mg/dL) and The percentage of overweight people with a BMI between 25 and 34.9. Timepoint: Measurement of anthropometric indices and blood lipids at the beginning of the study (before the start of the intervention) and 60 days after the start of kefir buttermilk consumption. Method of measurement: Use Seka digital scale to measure weight, tape measure to measure height, laboratory kits of Byrex Fars company to measure blood fat indicators. | — |
Secondary
| Measure | Time frame |
|---|---|
| Total cholesterol-LDL-TG laboratory value. Timepoint: The beginning of the study and 60 days after the start of the study. Method of measurement: medical laboratory. | — |
Countries
Iran (Islamic Republic of)
Contacts
Esfahan University of Medical Sciences