RecruitingNCT03178630

MRI Biomarkers in as Predictor of Clinical Endpoints in Pediatric Autoimmune Liver Disease

Longitudinal Study for the Assessment of MRI Based Biomarkers as a Predictors of Clinical Endpoints in Pediatric Onset Autoimmune Liver Disease


Sponsor

Children's Hospital Medical Center, Cincinnati

Enrollment

150 participants

Start Date

Feb 20, 2017

Study Type

OBSERVATIONAL

Conditions

Summary

Autoimmune liver diseases (AILD), which include Primary Sclerosing Cholangitis (PSC) and Autoimmune Hepatitis (AIH) are a common etiological factor for chronic liver disease among adolescents. This is a longitudinal study to identify surrogate endpoints with an accurate predictive value for the progression of hepatobiliary damage in subjects with pediatric onset AILD. This study will involve collection of MRI-based data at the time of enrollment and at year 1 and 2 of follow up, and collection of clinical data for 10 years following enrollment. There is a strong possibility that MRI quantitative techniques may be more sensitive to disease progression than standard clinical and laboratory tests. To investigate predictivity of MRI based biomarkers, summary measures of MRCP/MREL from baseline, Year 1 and Year 2, e.g. change rate, maximum, and average will be calculated as predictors for Year 10 clinical outcomes. The same predictors will also be used to model native liver survival in a proportional hazard regression. Findings from this study may be used to assess disease progression and to predict complications and survival of liver disease patients.


Eligibility

Min Age: 6 YearsMax Age: 23 Years

Inclusion Criteria2

  • Age 6-23 years old.
  • Established clinical diagnosis of AIH or PSC.

Exclusion Criteria8

  • History of liver transplantation.
  • Chronic Hepatitis B or untreated hepatitis C virus infection.
  • Pregnancy.
  • Absolute contraindication for MRI (e.g. pacemaker, metallic implants, claustrophobia).
  • Diagnosis of cystic fibrosis or biliary atresia
  • Diagnosis of cardiac hepatopathy.
  • Diagnosis of Wilson's disease, Alpha-1 Antitrypsin deficiency, or Glycogen storage disease.
  • Skin conditions which could be aggravated by MREL (i.e. Epidermolysis bullosa).

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Locations(1)

Cincinnati Children's Hospital and Medical Center

Cincinnati, Ohio, United States

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NCT03178630


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