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Construction and Clinical Translation of a Steatotic Liver Disease Cohort in Cardiovascular Populations

Construction and Clinical Translation of a Steatotic Liver Disease Cohort in Cardiovascular Populations

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500114912
Enrollment
Unknown
Registered
2025-12-18
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Metabolic dysfunction–Associated Steatotic Liver Disease

Interventions

Adult patients undergoing assessment for cardiovascular metabolic diseases:None

Sponsors

The First Affiliated Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Age >=18 years and <80 years. 2.Suspected coronary artery disease, with completed coronary angiography or CTA examination. 3.Completed non-invasive FibroScan assessment, with available liver stiffness measurement (LSM) and controlled attenuation parameter (CAP) values for baseline and follow-up analysis.

Exclusion criteria

Exclusion criteria: 1.Patients with other definite liver diseases at baseline or during follow-up, including those positive for hepatitis B surface antigen, untreated active hepatitis C virus infection, drug-induced liver injury, autoimmune liver disease, and hereditary liver diseases. 2.Patients with active viral infections, such as HIV infection or other active infections that may affect liver function and metabolism, to avoid confounding effects on the analysis. 3.Patients with a history of malignancy at baseline or within the past five years, to prevent interference from tumors and related treatments on liver and cardiovascular status. 4.Pregnant or breastfeeding women, to avoid physiological influences on liver fat metabolism and fluid status. 5.Patients with incomplete key assessments or missing critical follow-up data, such as missing FibroScan, imaging, or laboratory measurements, to ensure the integrity of primary outcome measures.

Design outcomes

Primary

MeasureTime frame
Follow-up content: Dynamic monitoring of FibroScan results (liver stiffness and CAP value), liver-related events (LRE), major adverse cardiovascular events (MACE), control of blood pressure, blood glucose, and lipids, medication adjustments, and occurrences of liver and kidney function abnormalities and adverse events.;Baseline characteristics, including: 1. Demographic features (age, sex, BMI, lifestyle factors, and family history); 2. Cardiovascular and metabolic risk factors (blood pressure, blood glucose, lipids, HDL-C, and history of prior cardiovascular events); 3. Liver-related parameters (ALT, AST, FibroScan LSM and CAP values, imaging-based assessment of hepatic fat); 4. Laboratory parameters (complete blood count, liver and kidney function, inflammatory and metabolic biomarkers); 5. Medicat;

Secondary

MeasureTime frame
Demographic information: age, sex, height, weight, body mass index (BMI), lifestyle, and family history.;

Countries

China

Contacts

Public ContactZheng Minghua

The First Affiliated Hospital of Wenzhou Medical University

zhengmh@wmu.edu.cn+86 139 6778 1644

Outcome results

None listed

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