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The role of fat-liver crosstalk in the non-alcoholic fat liver disease development, Nrf2 regulation in liver, and hepatic mitochondria ß-oxidation

The role of fat-liver crosstalk in the non-alcoholic fat liver disease development, Nrf2 regulation in liver, and hepatic mitochondria ß-oxidation

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000036270
Enrollment
Unknown
Registered
2020-08-22
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-09-07

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

Conditions

Nonalcoholic fatty liver disease

Interventions

normal group:none

Sponsors

Department of Thyroid Biliary Deweighting and Metabolic Surgery, the Fourth Clinical College Affiliated to China Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: NAFLD group: 1. Meet the clinical, pathological or imaging diagnostic criteria for nonalcoholic fatty liver disease. 2. Meet the indications for metabolic surgery, and sign the informed consent. 3. Understand and agree to conduct intraoperative liver biopsy in the surgery, and agree to keep the biological sample in the biobank for the remaining liver tissue, fat tissue and blood after normal pathological diagnosis and treatment. 4. 18 to 60 years old (including values at both ends) at the time of signing the informed consent. 5. Able to understand and sign the informed consent. If illiterate, press the handprint. Normal group: 1. Consistent with the indications for the cholecystectomy. 2. After cholecystectomy, there was residual liver tissue on the specimen surface. 3. At the time of signing the informed consent, the person shall be at least 18 to 60 years old (including values at both ends). 4. Able to understand and sign the informed consent. If illiterate, press the handprint.

Exclusion criteria

Exclusion criteria: NAFLD group: 1. There are other liver diseases that can cause the fatty liver, including Autoimmune liver disease, drug liver injury (DILI), viral hepatitis, metabolic liver disease, Wilson's disease, alpha-1 antitrypsin deficiency and other diseases. 2. Patients with liver malignant tumor, biliary tract infection and other diseases, and use of drugs that may cause abnormal ALT, AST, GGT, etc. related to serum liver function previously or currently. 3. Patients with serious organic diseases, such as heart disease, and malignant tumors. 4. Patients with a history of long-term heavy drinking, male: alcohol intake was >30g/day (female: alcohol intake was > 20g/day). 5. The researchers considered the patients unsuitable for the study. Normal group: 1. Exclude various liver diseases that can cause the fatty liver, including non-alcoholic fatty liver, alcoholic fatty liver, Autoimmune liver disease, DILI, viral hepatitis, metabolic liver disease, Wilson's disease, alpha-1 antitrypsin deficiency and other diseases. 2.Patients with liver malignant tumor, biliary tract infection and other diseases, and use of drugs that may cause abnormal ALT, AST, GGT, etc. related to serum liver function previously or currently. 3. Patients with serious organic diseases, such as heart disease, and malignant tumors. 4. Patients with a history of long-term heavy drinking, male: alcohol intake was > 30g/day (female: alcohol intake was > 20g/day). 5. The researchers considered the patients unsuitable for the study.

Design outcomes

Primary

MeasureTime frame
adiponectin;Nrf2;hepatic mitochondrial ß-oxidation;

Countries

China

Contacts

Public ContactYong Wang

The Fourth Affiliated Hospital of China Medical University

wangyong@cmu.edu.cn+86 18940259733

Outcome results

None listed

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