Quantitative Magnetic Resonance Imaging to Aid Clinical Decision Making in Autoimmune Hepatitis.

This will be a single centre quantitative study recruiting 60 participants from those patients attending the hepatology outpatient clinic at Kings College Hospital NHS (National Health Service) Trust. It will set out to determine the impact of quantitative Magnetic Resonance Imaging (MRI) (using LiverMultiScan (LMS)) on intended patient management for Autoimmune Hepatitis (AIH) patients in comparison with the current usual standard of care. Participants will be made aware of the study by a member of clinical care team.

All participants will attend their planned outpatient hepatology appointment. The consultant will document the intended treatment plan for each participant in line with their usual care pathway. Following this, participants will be required to attend one dedicated study visit with no continued follow-up. This will involve an Magnetic Resonance Image (MRI) scan. This visit will be scheduled for the same day as their outpatient appointment, or within a 7-day window around their appointment with the consultant.

The results of this scan will be analysed, and a report securely sent to the consultant who will review participants original documented care plan alongside the LMS report. The consultant will be asked to describe any changes he would have made based on the new information that is provided by the scan. Consideration will also be taken for quantifying the potential cost-effectiveness of adding LMS to the standard care pathway.

The study Magnetic Resonance Imaging (MRI) will be conducted within a London based MRI imaging centre where LMS is installed and compatible with the allocated scanner (1.5Tesla/3Tesla).

Sample size: The primary endpoint of the study is to determine the proportion of patients for whom a change in intended treatment would occur following clinical review of LMS data.

Based on the following assumptions, the investigators will aim to recruit 60 patients from the autoimmune clinic at Kings College Hospital, London, and expect to observe at least a 24% change in intended clinical management.

• In clinic, returning patients have their liver function tests reviewed to assess response to therapy, new patients are referred for both labs and biopsy for initial diagnosis.
• In an observational study of N=60 AIH participants, 19% were experiencing a biochemical flare at baseline (raised Alanine aminotrasferase (ALT) with an associated rise in Immunoglobulin G (IgG)). After removing these patients, in the remaining 50 stable/biochemical responders, 35 were considered low risk (normal liver function tests (LFTs) and requiring <10mg prednisolone to maintain remission). In total 16 (32%) went on to flare in the following 12 months, 8 of those were 'low risk'.
• The average Corrected T1 (cT1) for patients who had a flare was 35 ms higher at baseline than the non-flaring patients and cT1 had an Area Under the Receiver Operating Characteristic Curve (AUROC) of 0.72 for discriminating these patients (cT1 cut-off ≥ 810ms, 81% sensitivity, 59% specificity and positive and negative predictive values of 48% and 87%, respectively).
• The proportion of patients who may have benefiting from a change in management using LMS was 36%: 15 originally classified "low risk" who had cT1 ≥ 810 and 3 "high risk" with a cT1 < 810 ms [(18/50)*100].
• With an estimated proportion of change using LMS of 36%, the lower-bound 95% confidence interval is 24% which reflects a 5% chance the investigators would see a change smaller than 24% in this sample, if the true population change was 36%.

For the secondary endpoint exploring correlations between multi-parametric MRI metrics with other measurements of AIH, of the 60 patients the investigators expect biopsy-paired data from ~30 patients - 10 new patients and 20 returning patients based on the following assumptions:

• Biopsy is performed at the clinic for diagnosis of incidence patients, for clinical indications in returning patients (abnormal transaminase or IgG levels, suspected azathioprine hepatotoxicity is suspected), or every 2 years since diagnosis to confirm histological remission (to prevent relapse of AIH and confirm no progression to liver fibrosis). Stable patients' laboratory results are reviewed every 6 months.
• Given the reported rate of 30 returning and 2 incidence patients to the autoimmune clinic at Kings College hospital a month the investigators would expect ~6% to be treatment naive at baseline.

Recruitment: Participants will be identified by a secondary care clinic where those patients with autoimmune hepatitis (AIH) or those awaiting confirmation of AIH diagnosis will be identified by a member of their care team and sent an invitation letter and Participant Information Sheet (PIS) 2-3 weeks before their appointment date. All potential participants will receive the PIS for a minimum of 24 hours and will have an opportunity to discuss the study with an investigator prior to the informed consent process during the first study visit.

Prior to the date of patient clinic visit, the patient will be given a telephone call by a member of their care team. Once a potential participant, identified by these means, and expresses an interest in the study, they will have the opportunity to discuss their eligibility and the details of the study, discuss the logistics around the MRI scan, and If happy to participate, the participant will be introduced to a member of the research team during their clinic visit.

Inclusion criteria

• Adult patients aged 18 years or over
• Patient due to attend the hepatology clinic for AIH diagnostics/review
• Participant is willing and able to give informed consent

Exclusion criteria

• The participant may not enter the study if they have any contraindication to magnetic resonance imaging (inc pregnancy, extensive tattoos, pacemaker, shrapnel injury, severe claustrophobia).
• Any other cause, including a significant disease or disorder which, in the opinion of the investigator, may either put the participant at risk because of participation in the study, or may influence the result of the study, or the participant's ability to participate in the study