MRI Based Biomarkers in Pediatric Autoimmune Liver Disease

Sponsor
Children's Hospital Medical Center, Cincinnati (Other)
Overall Status
Recruiting
CT.gov ID
NCT03175471
Collaborator
(none)
115
1
120.4
1

Study Details

Study Description

Brief Summary

Autoimmune liver diseases (AILD), which include Primary Sclerosing Cholangitis (PSC) and Autoimmune Hepatitis (AIH) are a common etiological factors for chronic liver disease among adolescents. In all these conditions, autoimmune lymphocyte responses are thought to orchestrate inflammatory injury against hepatocytes (primarily in AIH) or cholangiocytes (in PSC). In this proposal we aim to evaluate the Magnetic Resonance Imaging (MRI) modalities; MR cholangiopancreatography (MRCP) and MR elastography (MREL), as non-invasive biomarkers to assess two primary pathophysiological processes of AILD: bile duct damage and liver fibrosis. In this cross-sectional study MRI based findings of bile duct injury and liver fibrosis will be correlated with both liver histology and circulating biomarkers of these disease processes.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    115 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Cross-sectional Study for Assessment of MRI Based Biomarkers of Bile Duct Injury and Hepatic Fibrosis in Pediatric Onset Autoimmune Liver Disease
    Actual Study Start Date :
    Jan 17, 2017
    Anticipated Primary Completion Date :
    Jan 30, 2023
    Anticipated Study Completion Date :
    Jan 30, 2027

    Arms and Interventions

    Arm Intervention/Treatment
    Patients with autoimmune liver disease

    Patients (6-23 y.o.) with established clinical diagnosis of AIH or suspected diagnosis of AIH based on elevated serum AST or ALT, elevated IgG level >1.1 ULN, elevated titer of autoantibodies, including ANA, SMA, LKM, LC-1 or SLA, which is consistent with the simplified criteria for the diagnosis of AIH in children will be enrolled. Patients (6-23 y.o.) with established clinical diagnosis of PSC or Suspected diagnosis of PSC supported by abnormal cholangiogram (ERCP or MRCP) or elevated GGT>1.5 ULN and dilated bile ducts by liver ultrasound will be enrolled.

    Outcome Measures

    Primary Outcome Measures

    1. MRI based outcomes [36 months]

      MRCP based assessment of intrahepatic and extrahepatic duct irregularities by Majoie classification (on 4 and 5 point scale of 0-3 and 0-4 respectively; 0: No visible abnormalities, 1: minimal dilatation/irregularities, 2: saccular dilatations/segmental stricture, 3: severe pruning, 4: Extremely irregular margin). MREL based quantification of mean shear stiffness (kPa) of liver.

    2. Liver histopathology based assessment of bile duct injury by ISHAK Score [36 months]

      Assessment of bile duct injury by ISHAK Score (Confluent necrosis: on the 7 point scale of 0-6; Focal necrosis on the 4 point scale of 0-4 and portal inflammation on the 4 point scale of 0-4).

    3. Liver histopathology based assessment of bile duct injury by Ludwig score [36 months]

      Assessment of bile duct injury by Ludwig score (on five point scale of 0-4; 0: No ductal injury, 1: portal inflammation, 2: periportal inflammation, 3: Portal bridging, 4: Nodular cirrhosis).

    4. Liver histopathology based assessment of liver fibrosis by Nakanuma score [36 months]

      Assessment of liver fibrosis by Nakanuma score for on the 4 point scale of 0-3 (0; No portal fibrosis, 1; Portal fibrosis; 2; Bridging fibrosis, 3; Liver cirrhosis) .

    5. Liver histopathology based assessment of liver fibrosis by Ishak score [36 months]

      Assessment of liver fibrosis by Ishak score on the 7 point scale of 0-6 (0; Absent, 1; confluent necrosis, 2; necrosis in some areas, 3; necrosis in most areas, 4; necrosis with occasional portal-central bridging necrosis, 5; necrosis with multiple portal-central bridging necrosis, 6; Panacinar or multiacinar necrosis).

    6. Liver histopathology based assessment of cholangitis and hepatic activity [36 months]

      Cholangitis and hepatic activity by Nakanuma score for on the 4 point scale of 0-3 (0; No bile duct loss, 1; Bile duct loss in <1/3 of portal tracts; 2; Bile duct loss in 1/3-2/3 of portal tracts, 3; Bile duct loss in >2/3 of portal tracts).

    7. Serum based outcome [36 months]

      Quantification of serum alkaline phosphatase (ALP in U/L) and Gamma-glutamyl transpeptidase (GGT in U/L).

    8. Enhanced Liver Fibrosis (ELF) score [36 months]

      Assesment of Enhanced Liver Fibrosis (ELF) score on continuous scale of 1-10; <7.7 none -mild. ≥7.7 -<9.8 moderate, >9.8 sever).

    Secondary Outcome Measures

    1. MR T1rho, T1, T2 Imaging [36 Months]

      Mean of MR T1rho, T1, T2 signal in msec to measure the inflammation.

    2. Liver Morphometry [36 Months]

      Collagen deposition in percent area fibrosis by image analysis

    3. Liver histopathology based outcomes [36 Months]

      Liver histopathology based grade of inflammation by Scheuer score on 5 point scale of 0-4; (0: No ductal injury, 1: portal inflammation, 2: periportal inflammation, 3: Portal to portal bridging, 4: Nodular cirrhosis).

    4. Serum based outcomes [36 Months]

      Quantification of serum fractionated ALP (U/L)

    5. Serum MMP7 [36 Months]

      Quantification of serum MMP7 (pg/mL)

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    6 Years to 23 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Age 6-23 years old.

    2. Established or suspected clinical diagnosis of AIH or PSC.

    Exclusion Criteria:
    1. History of liver transplantation.

    2. Chronic Hepatitis B or untreated hepatitis C virus infection.

    3. Pregnancy.

    4. Absolute contraindication for MRI (e.g. pacemaker, metallic implants, claustrophobia).

    5. Diagnosis of cystic fibrosis or biliary atresia

    6. Diagnosis of cardiac hepatopathy.

    7. Diagnosis of Wilson's disease, Alpha-1 Antitrypsin deficiency, or Glycogen storage disease.

    8. Skin conditions which could be aggravated by MREL (i.e. Epidermolysis bullosa).

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Cincinnati Childrens Hospital Medical Center Cincinnati Ohio United States 45229

    Sponsors and Collaborators

    • Children's Hospital Medical Center, Cincinnati

    Investigators

    • Principal Investigator: Alexander Miethke, MD, Cincinnati Childrens Hospital Medical Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Children's Hospital Medical Center, Cincinnati
    ClinicalTrials.gov Identifier:
    NCT03175471
    Other Study ID Numbers:
    • CIN001-MRI biomarkers in AILD
    First Posted:
    Jun 5, 2017
    Last Update Posted:
    Jun 22, 2021
    Last Verified:
    Jun 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 22, 2021