Type 2 DIAbeTes With NAFLD: innOvative Biomarkers of Disease progressioN and clInical outComes

Hospices Civils de Lyon4 个研究点分布在 1 个国家目标入组 500 人2024年9月25日

适应症Metabolic Dysfunction-Associated Liver Disease

干预措施Non-invasive test for the screening of MASLD-related advanced fibrosis in patients with T2D.

概览

阶段: 不适用
干预措施: Non-invasive test for the screening of MASLD-related advanced fibrosis in patients with T2D.
疾病 / 适应症: Metabolic Dysfunction-Associated Liver Disease
发起方: Hospices Civils de Lyon
入组人数: 500
试验地点: 4
主要终点: Progression of MASLD for T2D and MASLD patients without AF at baseline (cohort A) or progression to confirmed diagnosis of cirrhosis for T2D and MASLD patients with presence of AF at baseline and without cirrhosis (cohort B).
状态: 招募中
最后更新: 3个月前

概览研究者入排标准研究组 & 干预措施结局指标研究点相似试验

概览

简要总结

详细描述

Type 2 diabetes (T2DM) patients are at high-risk for advanced fibrosis (AF) due to non-alcoholic fatty liver disease (NAFLD), recently renamed Metabolic dysfunction-Associated Liver Disease (MASLD). Thus, patients with T2DM are recognized as a priority target for the screening of MASLD-related advanced fibrosis and a systematic screening for AF is currently recommended in T2DM patients using FIB-4 and liver stiffness measurement (LSM). Hence, these Non-Invasive Tests (NITs) are expected to be integrated in the management of T2DM in a near future. Indeed diabetologists are becoming more aware of the need for liver assessment in patients with T2DM recently reinforced by recent clear recommendations supporting the use of non-invasive test (NITs) such as LSM for the detection of liver fibrosis. Several studies indicate that MASLD increases the risk of T2DM complications. However, there are very limited data and no prospective longitudinal data assessing the progression of MASLD and relevant clinical outcomes in T2DM patients included in liver screening using these NITs. This provides a unique opportunity to better stratify T2DM and to understand the heterogeneity among patients with T2DM by defining patient's profiles linked the progression of MASLD and relevant clinical outcomes. Therefore, the main objective of the project is to investigate the ability of baseline non-invasive biomarkers to discriminate patients with a progression of MASLD from patients without progression of MASLD among patients with T2DM and to investigate the association between clinical outcomes related to the natural evolution of MASLD and T2DM and baseline biomarkers.

注册库

clinicaltrials.gov

开始日期

2024年9月25日

结束日期

2027年5月25日

最后更新

3个月前

研究类型

Interventional

研究设计

Parallel

性别

All

研究者

发起方

Hospices Civils de Lyon

责任方

Sponsor

入排标准

入选标准

•Patients with T2D and meeting the other inclusion criteria of the NAFLD-Care study:
•Patient aged between 40 and 80 years old,
•Patient with hepatic steatosis determined by conventional abdominal ultrasound as defined by the EASL/EASO/EASD European guidelines.
•Patient who agrees to be included in the study and who signs the informed consent form,
•Patient affiliated to a healthcare insurance plan.

排除标准

•\- Participants with a diagnosis of cirrhosis defined by a liver biopsy with histological stage of fibrosis F4 or a proven diagnosis of cirrhosis by magnetic resonance imaging.
•The main non-inclusion criteria for the NAFLD-CARE study are:
•Evidence of other causes of chronic liver disease :
•Hepatitis B as defined as presence of hepatitis B surface antigen (HBsAg).
•Previous or current infection with Hepatitis C as defined by presence of hepatitis C virus Ab in serum (anti-HCV Ab).
•Autoimmune hepatitis as defined by anti-nuclear antibody (ANA) of 1:160 or greater and liver histology consistent with autoimmune hepatitis or previous response to immunosuppressive therapy.
•Autoimmune cholestatic liver disorders as defined by elevation of alkaline phosphatase and anti-mitochondrial antibody of greater than 1:80 or liver histology consistent with primary biliary cirrhosis or elevation of alkaline phosphatase and liver histology consistent with sclerosing cholangitis.
•Wilson disease as defined by ceruloplasmin below the limits of normal and liver histology consistent with Wilson disease.
•Alpha-1-antitrypsin deficiency as defined by alpha-1-antitrypsin level less than normal and liver histology consistent with alpha-1-antitrypsin deficiency.
•Hemochromatosis as defined by presence of 3+ or 4+ stainable iron on liver biopsy and homozygosity for C282Y or compound heterozygosity for C282Y/H63D.

研究组 & 干预措施

Patients with T2D and MASLD without advanced fibrosis (AF) (COHORT A)

Patients with T2D and MASLD without advanced fibrosis (AF) at baseline in the NAFLD-Care study.

干预措施: Non-invasive test for the screening of MASLD-related advanced fibrosis in patients with T2D.

Patients with T2D and MASLD, without diagnosis of cirrhosis (COHORT B)

Patients with T2D and MASLD with presence of advanced fibrosis (AF) and without cirrhosis at baseline in the NAFLD-Care study

干预措施: Non-invasive test for the screening of MASLD-related advanced fibrosis in patients with T2D.

结局指标

主要结局

Progression of MASLD for T2D and MASLD patients without AF at baseline (cohort A) or progression to confirmed diagnosis of cirrhosis for T2D and MASLD patients with presence of AF at baseline and without cirrhosis (cohort B).

时间窗: One time visit planned according to standard care at 4 years+/- 6 months after inclusion in the NAFLD-CARE study

COHORT A = Composite outcome defined by either histological stage of fibrosis ≥ F3 if a liver biopsy is performed in clinical care or concordant patented Fibrotest≥ F3 and LSM≥ 8 kPa according to EASL guidelines or overt imaging evidence of cirrhosis via ultrasound, computed tomography (CT), or MRI COHORT B = Histological stage of fibrosis 4 or imaging evidence of cirrhosis via ultrasound, computed tomography (CT), or MRI

次要结局

Assessment of clinical events associated with the natural history of MASLD and T2D for both cohorts(One time visit planned according to standard care at 4 years+/- 6 months after inclusion in the NAFLD-CARE study)