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临床试验/NCT06888310
NCT06888310进行中(未招募)不适用

Optimizing Noninvasive assessMent Of DysmEtabolic Compensated Advanced Liver Disease by Integration of Artificial Intelligence Model and omicS Data

Fondazione Policlinico Universitario Agostino Gemelli IRCCS3 个研究点 分布在 1 个国家目标入组 408 人开始时间: 2024年12月6日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
408
试验地点
3
主要终点
number of patients identified with single diagnostic method

研究概览

简要总结

Non-alcoholic fatty liver disease (NAFLD) is responsible for a significant proportion of liver-related deaths and healthcare costs in the United States, accounting for approximately 36% of liver-related deaths and over one billion dollars in annual healthcare expenses. [PMID: 34863359] A recent analysis of healthcare costs in Italy showed that out of the 9,729 NAFLD/NASH patients who were hospitalized and analyzed, the vast majority (97%) did not have advanced liver disease, while 1.3% had compensated advanced liver disease (cACLD), 3.1% had decompensated cirrhosis, 0.8% had hepatocellular carcinoma, and 0.1% underwent liver transplantation.

The burden of comorbidities was high across all patient cohorts, and patients with cACLD required a greater number of inpatient services, outpatient visits, and the pharmacy fills compared to those without advanced liver disease. As disease severity increased, mean total annual costs also increased primarily due to higher inpatient services costs. In Italy, as in other EU countries, most of the healthcare costs for patients were attributed to NAFLD/NASH-related liver complications. Thus, the optimization of the non-invasive diagnosis of cACLD represents an urgent need in dysmetabolic liver disease. These advancements will play a crucial role in early detection, risk stratification, and effective management of highly prevalent liver diseases such as NAFLD/NASH and their progression.

详细描述

The study aims to significantly enhance diagnostic innovation and contribute to the existing literature on the stratification of cACLD caused by metabolic-dysfunction liver disease, a major factor leading to cirrhosis, liver cancer, and liver transplant in individuals with non-communicable diseases. By integrating radiomics, digital pathology, non-invasive scores, and omics the results are expected to provide novel evidence for diagnostic advancements.

The incorporation of AI is anticipated to lead to more efficient diagnostic management, effectively addressing the impact of cACLD on healthcare systems. The outcomes of this research will yield a substantial database and intellectual content, both of which will be made available to the scientific community and multiple stakeholders, including patient associations, policymakers, healthcare providers, and industry players.

The primary goal is to foster innovation in diagnostics and mitigate the impact of cACLD on national health systems. By accurately predicting individuals at higher risk of liver or extra-hepatic complications, this study aims to revolutionize diagnostic methods, ultimately leading to improved patient outcomes and resource optimization in healthcare settings.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • age>=18; sex (M,F);
  • dysmetabolic liver disease according new nomenclature definition;
  • suspicion of cACLD by LSM>=10 with VCTE;
  • routine esogastroduodenoscopy report within 12 months of VCTE for identification of high-risk varices (HRV).

排除标准

  • portal vein thrombosis,
  • infiltrative liver neoplasms, and conditions are known for their potential influence on the LSM results (congestive liver disease, extrahepatic biliary obstruction, ALT > 5x upper normal limit).

研究组 & 干预措施

patients with MASLD and LSM>=10kPa

Experimental

To set an interventional prospective, cohort study where individuals will have a liver health check to identify cACLD.

We will exclude subjects with decompensation (ascites, encephalopathy, gastrointestinal bleeding, or in case of the presence of transjugular intrahepatic portosystemic shunt). We aim to recruit a prospective cohort and randomize after the end of the study to derivation (2/3) and validation cohort (1/3). The cohort will be stratified according to the presence of Type 2 diabetes (T2D) and obesity (BMI>= 30Kg/m2).

干预措施: extra blood sampling (Procedure)

结局指标

主要结局

number of patients identified with single diagnostic method

时间窗: 24 months

evaluate the efficacy of risk-stratification pathways for cACLD detection and outcome prediction in adults (age\>18 years) with dysmetabolic liver disease in a tertiary care setting.

次要结局

  • number of patients identified with innovative diagnostic method omic-based(24 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

MIELE LUCA

Head of UOS Pre Liver Trasplant

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

研究点 (3)

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