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Study on the role of gut microbiota and metabolites in metabolic associated fatty liver disease

Study on the role of gut microbiota and metabolites in metabolic associated fatty liver disease

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300068404
Enrollment
Unknown
Registered
2023-02-17
Start date
2023-02-20
Completion date
Unknown
Last updated
2023-05-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

fatty liver disease

Interventions

Health group:No
Overweight/obese group of MAFLD patients :No
A lean/normal-weight group of MAFLD patients with metabolic dysfunction:No
MAFLD patients with type 2 diabetes:No

Sponsors

Liyuan Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Voluntary signing of informed consent; 2. Age 18-70 years old, gender unlimited; 3. The subject is willing to collect and send samples in strict accordance with the sampling procedures; 4. Vital signs, physical examination, blood routine, blood biochemistry and urine routine were all within the normal range or abnormal but considered meaningless by researchers; body mass index (BMI) was 19.0-23.0kg/m^2 (including the boundary value, calculated by formula = weight/height^2); waist circumference = 23kg/m^2; (2) History of type 2 diabetes mellitus or fasting blood glucose >=7.0mmol/L; (3) Metabolic dysfunction, with at least the following two risk factors for metabolic abnormalities: 1) Waist circumference: Asian men and women >=90 and 80cm, respectively; 2) Blood pressure: >=130/85mmHg or receiving blood pressure lowering drugs; 3) Blood triglycerides: >=150mg/dL (>=1.70mmol/L) or receive treatment with lipid-lowering drugs; 4) Plasma HDL cholesterol: =2.5; 7) Blood hypersensitive C-reactive protein: >2mg/L;

Exclusion criteria

Exclusion criteria: 1. Accompanied by chronic diseases that may interfere with the study data, including but not limited to chronic infections, any intestinal diseases or symptoms (including but not limited to constipation, diarrhea and other symptoms, colitis, Crohn's disease, intestinal obstruction, intestinal tumors, etc.); 2. Severe acute illness occurred within 1 month prior to screening that may interfere with the study data; 3. Cirrhosis of the liver; 4. Subjects deemed unsuitable for the study by the researcher, such as poor spirits and poor compliance.

Design outcomes

Primary

MeasureTime frame
gut microbiota;Microbial metabolites;

Countries

China

Contacts

Public ContactXiong Zhifan

Liyuan Hospital, Tongji Medical College, Huazhong University of Science and Technology

xiongzhifan@126.com+86 135 1728 1937

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026