Prevalence, Incidence and Characteristics of NAFLD/NASH in Type 1 Diabetes Mellitus
Last updated on July 2021Recruitment
- Recruitment Status
- Recruiting
- Estimated Enrollment
- Same as current
Summary
- Conditions
- Cardiovascular Diseases
- NAFLD
- Type 1 Diabetes
- Design
- Observational Model: Case-ControlTime Perspective: Prospective
Participation Requirements
- Age
- Between 18 years and 125 years
- Gender
- Both males and females
Description
This study aims to characterize and follow a thoroughly characterized cohort of adult type 1 diabetes patients free from secondary liver disease due to excessive alcohol usage, viral hepatitis, alfa-1 antitrypsin deficiency, Wilson's disease or steatogenic or hepatotoxic drug use. The investigators ...
This study aims to characterize and follow a thoroughly characterized cohort of adult type 1 diabetes patients free from secondary liver disease due to excessive alcohol usage, viral hepatitis, alfa-1 antitrypsin deficiency, Wilson's disease or steatogenic or hepatotoxic drug use. The investigators will screen for NAFLD and fibrosis using multiple non-invasive techniques including ultrasound controlled attenuation parameter fatty liver index human steatosis index transient elastography FIB-4 NAFLD fibrosis score NASH algorithm based on multiple parameters Subjects will be screened for microvascular and microvascular complications with: ECG microfilament examination 24hour urine collection for microalbuminuria serum kidney test (creatinine, eGFR) fundoscopy peripheral arterial pulsation palpation The investigators will subsequently thoroughly characterize various metabolic and anthropometric parameters and document any microvascular or macrovascular complications. The patients will be annually rescreened for both NAFLD-related as cardiovascular variables. Therefore this study will assess the correlation between NAFLD, cardiovascular risk, and type 1 diabetes in a prospective manner.
Tracking Information
- NCT #
- NCT04664036
- Collaborators
- Not Provided
- Investigators
- Principal Investigator: Christophe De Block, M.D., PhD Universiteit Antwerpen Principal Investigator: Sven Francque, M.D., PhD Universiteit Antwerpen