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Study on early biomarkers of nonalcoholic fatty liver disease patients with different BMI based on serum exosomal circRNA and metabolomics

Study on early biomarkers of nonalcoholic fatty liver disease patients with different BMI based on serum exosomal circRNA and metabolomics

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200055441
Enrollment
Unknown
Registered
2022-01-09
Start date
2019-01-01
Completion date
Unknown
Last updated
2023-01-30

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

Conditions

nonalcoholic fatty liver disease (NAFLD)

Interventions

obese patients with nonalcoholic fatty liver disease:Nil
obese patients with normal liver:Nil
non-obese patients with nonalcoholic fatty liver disease:Nil
non-obese patients with normal liver:Nil

Sponsors

Shanghai Putuo District Center Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 16-75 years, gender is not limited; 2. Weekly alcohol intake: no more than 210g for men and no more than 70g for women; 3. There are imaging changes of fatty liver in B-ultrasound or CT examination; 4. Exclude viral hepatitis, drug-induced liver disease, autoimmune liver disease and other autoimmune diseases, thyroid disease and other conditions that lead to fatty liver; 5. No history of major gastrointestinal surgery, such as subtotal gastrectomy and gastrointestinal anastomosis, radical colonectomy, small bowel resection, etc., except appendectomy, peptic ulcer perforation repair, etc.; 6. No serious heart, lung, brain, kidney disease and malignant tumor; 7. Women who are pregnant or who are willing to become pregnant in the near future are excluded.

Exclusion criteria

Exclusion criteria: 1. Combined with extrahepatic fibrotic diseases, including systemic lupus erythematosus, rheumatic diseases, renal failure, chronic obstructive pulmonary disease, tumor diseases, diabetes, hypertension, coronary heart disease, etc.; 2. Patients with alcoholic liver disease, cholestatic liver disease, hereditary metabolic liver disease and advanced liver cirrhosis with liver tumor were excluded; 3. Those who are currently or have received anti-hepatic fibrosis therapy or anti-viral therapy in the past, and those who have used enzyme-lowering drugs; 4. With jaundice, ALT and/or AST exceeds the upper limit of normal by 2 times or more; 5. Patients with incomplete clinical data related to this study.

Design outcomes

Primary

MeasureTime frame
blood routine;hepatic function;renal function;blood lipid level;blood glucose;glycosylated hemoglobin;tumor marker;thyroid function;microelement;coagulation function;immunologic function;interleukin;indicators of hepatic fibrosis;

Countries

China

Contacts

Public ContactCao Qin

Shanghai Putuo District Center Hospital

caoqin434@sina.com+86 13681858591

Outcome results

None listed

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