Adverse Outcomes and Mortality in Liver Transplant
Primary Purpose
End Stage Liver DIsease, Sarcopenia, Sarcopenic Obesity
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
MAsS
Sponsored by
About this trial
This is an interventional diagnostic trial for End Stage Liver DIsease
Eligibility Criteria
Inclusion Criteria:
- All patients with end-stage liver disease undergoing evaluation for liver transplantation
- Patient clinically indicated for MRI during transplant candidacy evaluation
- Adult
Exclusion Criteria:
1. Contra indication to MRI
Sites / Locations
- Mayo Clinic ArizonaRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Define MAsS cut-point at transplant evaluation to identify those with high risk for adverse outcomes
Arm Description
Outcomes
Primary Outcome Measures
Muscle assessment score (MAsS)
The MAsS is a composite score of muscle fat index (% of muscle fat normalized to sex, weight in kg and height in meters) and muscle volume index (muscle volume in liters normalized to patient sex, height in meters and weight in kg)
Adverse outcomes
Number of pre- and post-transplant inpatient days
Adverse outcomes
Number of pre- and post-transplant ICU days
Adverse outcomes
Number of days alive outside of the hospital in the first year after liver transplant
Adverse outcomes
Mortality within the first year after liver transplant
MAsS changes while waiting for liver transplant
In patients who remain on the waitlist, serial MAsS measurements (see Outcome 1) will be taken and changes over time will be assessed
Secondary Outcome Measures
Full Information
NCT ID
NCT05477277
First Posted
July 12, 2022
Last Updated
October 19, 2023
Sponsor
Mayo Clinic
Collaborators
Amra Medical AB
1. Study Identification
Unique Protocol Identification Number
NCT05477277
Brief Title
Adverse Outcomes and Mortality in Liver Transplant
Official Title
Adverse Outcomes and Mortality in Liver Transplant
Study Type
Interventional
2. Study Status
Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
November 2, 2022 (Actual)
Primary Completion Date
July 2024 (Anticipated)
Study Completion Date
July 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mayo Clinic
Collaborators
Amra Medical AB
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
Prospective natural history pilot study to explore the link between muscle composition using an MRI-based Muscle Assessment Score (MAsS) and adverse outcomes in liver transplant candidates.
Detailed Description
Sarcopenia, characterized by the progressive loss of muscle volume and function, is a common and major complication in end-stage liver disease which significantly contributes to adverse outcomes and mortality as well as hampers successful outcomes for treatments such as liver transplant (LT). High resolution image-based techniques have been instrumental in furthering our understanding of body composition in sarcopenia specifically and human health in general. While several methods exist to evaluate body composition, imaging techniques, such as computed tomography (CT) and magnetic resonance imaging (MRI) enable capitalization of images taken as part of standard practice as well as append already clinical examinations with brief sequences tailored for mapping muscle and body composition. Opportunistic application of this imaging-based body composition assessment to patients in a liver transplant context has revealed a high prevalence of sarcopenia (low muscle volume relative to age and sex) and pathological muscle fat infiltration (myosteatosis). Furthermore, a recent long-term (6-years post-LT) MRI-based retrospective study showed associations of myosteatosis to increased graft loss and mortality after transplant.
The combination of MRI-based thigh muscle volume and fat infiltration has been suggested as a more complete description of muscle composition with a stronger link to hospitalization, poor functional activities of daily life, and metabolic co-morbidities in general population and subjects presenting with non-alcoholic fatty liver disease. A recently submit paper explored the predictive power of this combination based on 40 000 participants in the UK biobank and found that the presence of adverse muscle composition, that is the combination of lower-than-expected muscle volume and high muscle fat infiltration, showed to be a strong and independent predictor of all-cause mortality comparable to that of previous cancer diagnosis and smoking. The same MRI-sequence and body composition assessment has successfully been implemented in small pilot studies before and after LT, both within weeks and years after LT, and presented at recent scientific conferences.
There is a lack of knowledge in how to fully identity patients indicted for liver transplant that are of very high risk for adverse outcomes and mortality in standardized fashion. The aim is to use an MRI-based Muscle Assessment Score (MAsS), which includes both muscle volume and fat infiltration, at the transplant candidacy evaluation and other follow-up MRI examinations as clinically indicated, as an objective, standardized, and quantitative measure of muscle health and explore the link between muscle composition and adverse outcomes and mortality. In addition, there are growing numbers of high-risk donor livers, such as presenting with steatosis or exposed to prolonged ischemia time. A co-primary aim is to gather information on the association between transplant recipient muscle composition and donor liver characteristics to one-year post-LT adverse outcomes and mortality.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
End Stage Liver DIsease, Sarcopenia, Sarcopenic Obesity, Cirrhosis
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Define MAsS cut-point at transplant evaluation to identify those with high risk for adverse outcomes
Arm Type
Experimental
Intervention Type
Diagnostic Test
Intervention Name(s)
MAsS
Intervention Description
Add MAsS to standard of care MRI scan
Primary Outcome Measure Information:
Title
Muscle assessment score (MAsS)
Description
The MAsS is a composite score of muscle fat index (% of muscle fat normalized to sex, weight in kg and height in meters) and muscle volume index (muscle volume in liters normalized to patient sex, height in meters and weight in kg)
Time Frame
1 year
Title
Adverse outcomes
Description
Number of pre- and post-transplant inpatient days
Time Frame
1 year
Title
Adverse outcomes
Description
Number of pre- and post-transplant ICU days
Time Frame
1 year
Title
Adverse outcomes
Description
Number of days alive outside of the hospital in the first year after liver transplant
Time Frame
1 year
Title
Adverse outcomes
Description
Mortality within the first year after liver transplant
Time Frame
1 year
Title
MAsS changes while waiting for liver transplant
Description
In patients who remain on the waitlist, serial MAsS measurements (see Outcome 1) will be taken and changes over time will be assessed
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
All patients with end-stage liver disease undergoing evaluation for liver transplantation
Patient clinically indicated for MRI during transplant candidacy evaluation
Adult
Exclusion Criteria:
1. Contra indication to MRI
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Latasha Bunkley
Phone
480.342.5756
Email
bunkley.latasha@mayo.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elizabet Carey, MD
Organizational Affiliation
Mayo Cinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mayo Clinic Arizona
City
Phoenix
State/Province
Arizona
ZIP/Postal Code
85259
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Elizabeth Carey, MD
Phone
480-342-1094
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
26768490
Citation
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Citation
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Citation
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Citation
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Citation
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Adverse Outcomes and Mortality in Liver Transplant
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