The Clinical Study on Isoflavone Genistein in Restructuring the Gut Microbiota of Hyperlipidemia Patients

NCT ID: NCT06895954

Last Updated: 2025-03-26

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 36 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-10-13
• Study Completion Date: 2025-02-20

Brief Summary

: In preliminary animal experiments, we found that the soybean isoflavone compound Genistein could reduce serum TMAO levels in high-fat diet (HFD) mice, and this effect was dependent on the gut microbiota. Furthermore, we discovered that Genistein's regulatory effect on the gut microbiota in high-fat diet mice relies on the host colonic PKI-Nos2 pathway. Genistein is an isoflavone compound extracted from soybeans and is the most effective functional ingredient in soybean isoflavone products. It has multiple physiological functions, and several randomized controlled trials (RCTs) have shown that the intake of Genistein can effectively alleviate hyperlipidemia, obesity, metabolic syndrome, and cardiovascular diseases, suggesting its safety and efficacy as a clinical health supplement. Therefore, we aim to conduct clinical trials to further demonstrate that Genistein also influences the gut microbiota in hyperlipidemia patients, thereby reducing serum TMAO levels.

Conditions

Hyperlipidemia

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Genistein

Dietary Supplement: Genistein Hyperlipidemia patients take a 125mg Genistein capsule daily, once a day.

Group Type: EXPERIMENTAL

Genistein

Intervention Type: DIETARY_SUPPLEMENT

Hyperlipidemia patients take a 125mg Genistein capsule daily, once a day.

Control

The control group does not take the Genistein medication.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Genistein

Hyperlipidemia patients take a 125mg Genistein capsule daily, once a day.

Intervention Type: DIETARY_SUPPLEMENT

Eligibility Criteria

Inclusion Criteria

• Aged between 30-65 years old, regardless of gender
• Abnormal donation and loan: including elevated total cholesterol and triglycerides, high triglycerides, and high triglycerides
• Volunteer to participate in clinical trials, understand and sign the informed consent form

• Patients with gastrointestinal or chronic infectious diseases (i.e., diarrhea, Crohn's disease, ulcerative colitis, irritable bowel syndrome, diverticular disease, gastric or duodenal ulcer, hepatitis, HIV, cancer, etc.), or with a history of such diseases
• Chronic or acute kidney disease, eGFR < 50 in two or more laboratory tests in the past 6 months; diagnosis of cirrhosis or liver failure; hyperkalemia (defined as potassium > 5.4 in two or more laboratory tests in the past 6 months)
• Severe immunodeficiency (HIV positive, transplant patients, taking anti-rejection drugs, taking steroids for > 30 days, or receiving chemotherapy or radiotherapy in the past year)
• Alarm features such as weight loss, rectal bleeding, recent changes in bowel habits (< 3 months), or abdominal pain
• Patients with malignant diseases or any concomitant end-stage organ diseases
• Patients who have taken any antibiotics or dietary supplements (prebiotics, probiotics, fiber, resveratrol, fish oil, seed oil, ginkgo leaf, ginseng, fruit powder extract and DHA) within one month
• Patients who have taken any Chinese patent medicine or Chinese herbal decoction within one month
• Avoid eating seafood or fish 24 hours before each visit
• Vegetarian/vegan diet or food allergies or other food problems that will prevent the intake of research products
• Pregnant or preparing for pregnancy and breastfeeding women
• Allergic constitution, or known allergy to isoflavone genistein
• Participating in other drug clinical studies within 1 month
• According to the investigator's judgment, the patient cannot complete this study or cannot comply with the requirements of this study (due to management reasons or other reasons)

• Minimum Eligible Age: 30 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Shenzhen Hospital of Southern Medical University

OTHER

Sponsor Role: lead

Responsible Party

Hongwei Zhou

Shenzhen Hospital of Southern Medical University

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Shenzhen Hospital of Southern Medical University

Guangzhou, Guangdong, China

Countries

China

Other Identifiers

NYSZYYEC2024K072R001

Identifier Type: -

Identifier Source: org_study_id