Risk Factors and Prediction Model for Liver-Related Adverse Outcomes in Elderly Patients With Steatotic Liver Disease
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 10,000
- 试验地点
- 1
- 主要终点
- Incidence of Significant Fibrosis
研究概览
简要总结
This is a single-center, retrospective cohort study based on data from the Nanjing Elderly Steatotic Liver Disease Cohort. The study aims to investigate risk factors for liver-related adverse outcomes (including significant fibrosis, advanced fibrosis, cirrhosis, hepatocellular carcinoma, and liver-related death) and extrahepatic outcomes (new-onset type 2 diabetes, chronic kidney disease, and cardiovascular disease) in elderly patients (aged ≥60 years) with steatotic liver disease. A total of approximately 10,000 participants will be included. Baseline and annual follow-up data on demographics, lifestyle, anthropometric measurements, laboratory tests, abdominal ultrasound, and medication use will be collected. Risk prediction models will be developed using machine learning algorithms. The study is observational and does not involve any intervention.
详细描述
Background: Steatotic liver disease (SLD) is highly prevalent among the elderly and can progress to cirrhosis and hepatocellular carcinoma. However, large-scale longitudinal studies focusing on risk prediction in Chinese elderly populations are limited.
Objectives: Primary objective is to identify risk factors and develop a prediction model for significant fibrosis. Secondary objectives include models for advanced fibrosis, cirrhosis, hepatocellular carcinoma, liver-related death, and extrahepatic outcomes (type 2 diabetes, chronic kidney disease, cardiovascular disease), as well as comparison of outcomes across SLD subtypes (MASLD, MetALD, ALD).
Methods: This is a single-center, retrospective cohort study using data from the Nanjing Elderly Steatotic Liver Disease Cohort (initiated in 2018). Approximately 10,000 participants aged ≥60 years with imaging or biopsy-proven hepatic steatosis will be included. Baseline and annual follow-up data include demographics, lifestyle factors (smoking, alcohol, diet, physical activity), anthropometric measurements, laboratory tests (glucose, lipids, liver and kidney function), abdominal ultrasound, and medication use. The primary outcome is significant fibrosis (FIB-4 ≥2.67); secondary outcomes include advanced fibrosis, cirrhosis, hepatocellular carcinoma, liver-related death, and extrahepatic outcomes. Cox regression will be used for univariate and multivariate analyses. Machine learning algorithms (random forest, XGBoost, Cox-boost) will be applied to develop prediction models, with performance evaluated by time-dependent ROC curves, calibration curves, and decision curve analysis. A competing risk model will account for death as a competing event. The study has been approved by the Ethics Committee of the Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Retrospective
入排标准
- 年龄范围
- 60 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age ≥60 years
- •Presence of hepatic steatosis confirmed by baseline imaging (e.g., ultrasound, transient elastography) or liver biopsy
排除标准
- •Missing data for key variables
- •Pre-existing hepatocellular carcinoma or history of liver transplantation at baseline
研究组 & 干预措施
Elderly SLD Cohort
Elderly patients (aged ≥60 years) with steatotic liver disease (SLD) confirmed by imaging or biopsy, enrolled from the Nanjing Elderly Steatotic Liver Disease Cohort.
结局指标
主要结局
Incidence of Significant Fibrosis
时间窗: From baseline (first eligible visit) up to study completion (March 2026), assessed annually
Significant fibrosis defined as FIB-4 ≥ 2.67. Occurrence during follow-up will be assessed.
次要结局
- Incidence of Advanced Fibrosis(From baseline up to March 2026, assessed annually)
- Incidence of Cirrhosis(From baseline up to March 2026, assessed annually)
- Incidence of Hepatocellular Carcinoma (HCC)(From baseline up to March 2026, assessed annually)
- Liver-Related Mortality(From baseline up to March 2026, assessed annually)
- New-Onset Type 2 Diabetes Mellitus(From baseline up to March 2026, assessed annually)
- New-Onset Chronic Kidney Disease (CKD)(From baseline up to March 2026, assessed annually)
- Incidence of Cardiovascular and Cerebrovascular Events(From baseline up to March 2026, assessed annually)
