Is Adrenal Insufficiency Under-diagnosed in Hospitalized Cirrhosis Patients?
Primary Purpose
Adrenal Insufficiency, Cirrhosis, Spur Cell Anemia
Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Cosyntropin
Sponsored by
About this trial
This is an interventional diagnostic trial for Adrenal Insufficiency
Eligibility Criteria
Inclusion Criteria:
- Age >=18 years
- Diagnosis of cirrhosis
- Admission to hospital
Exclusion Criteria:
- Age < 18 years
- Prior enrollment in study (i.e. readmission)
- Prisoner
- Pregnancy
- Prednisone or Hydrocortisone use in last 24 hours
Sites / Locations
- University of Virginia Health System
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Hospitalized cirrhosis patients
Arm Description
Administration of cortisol stimulation test to assess for presence or absence of adrenal insufficiency
Outcomes
Primary Outcome Measures
Number of Participants With Cholesterol Esterification Deficiency
A percent quantification of serum cholesterol esterification will be measured via blood draw. Low values represent deficiency in esterification, which is a surrogate measure of lecthicin-cholesterol acetyltransferase (LCAT) enzymatic deficiency.
Number of Participants With Spur Cell Anemia
A peripheral blood smear will be obtained and assessed for presence of acanthocytes (spur cells). Spur cell anemia is defined as a serum hemoglobin < 10g/dL and the presence of >= 5% spur cells on blood smear.
Participant Transplant-Free Survival
Transplant and Death are considered equivalent outcomes
Secondary Outcome Measures
Number of Participants With Relative Adrenal Insufficiency (RAI)
A baseline total cortisol level will be obtained and then patients will receive a standard-dose synthetic ACTH (250mcg of Cosyntropin) stimulation test to assess for the presence of adrenal insufficiency. RAI is defined as a change in the total cortisol level in response to the stimulation test of <9mcg/dL when measured 60 minutes after the Cosyntropin is administered.
Number of Participants With Low Free Cortisol
Patients will have their free cortisol levels measured to assess for deficiency.
Number of Participants Who Received Liver Transplantation at 90 Days
Patients who received a liver transplant within 90 days of enrollment
Number of Participants Who Received Liver Transplantation at 6 Months
Patients who received a liver transplant within 6 months of enrollment
Number of Participants Who Died Within Index Hospitalization
Patients who died within the same hospitalization as enrollment
Number of Participants Who Died at 30 Days
Patients who died within 30 days of enrollment
Number of Participants Who Died at 90 Days
Patients who died within 90 days of enrollment
Number of Participants Who Died at 6 Months
Patients who died within 6 months of enrollment
Full Information
NCT ID
NCT03368066
First Posted
November 20, 2017
Last Updated
December 8, 2021
Sponsor
University of Virginia
1. Study Identification
Unique Protocol Identification Number
NCT03368066
Brief Title
Is Adrenal Insufficiency Under-diagnosed in Hospitalized Cirrhosis Patients?
Official Title
Is Adrenal Insufficiency Under-diagnosed in Hospitalized Cirrhosis Patients?
Study Type
Interventional
2. Study Status
Record Verification Date
December 2021
Overall Recruitment Status
Completed
Study Start Date
January 29, 2018 (Actual)
Primary Completion Date
March 12, 2019 (Actual)
Study Completion Date
March 12, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Virginia
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
The hepatoadrenal syndrome has been well described in the literature and is known to be associated with poorer outcomes in both stable and critically ill cirrhotic patients. In chronic liver disease, adrenal (and more specifically cortisol) insufficiency is thought to be a byproduct of altered lipid metabolism that results in decreased HDL production and thus decreased delivery of cholesterol to the adrenal for subsequent corticosteroid production. Studies to date have implicated lecithin-cholesterol acetyltransferase (LCAT) as the key enzyme which is deficient in some cirrhotic patients, leading to an impaired ability to esterify cholesterol and thus a loss of normal cellular functioning and membrane stability. The investigators seek to quantify this LCAT deficiency in a cohort of cirrhotic patients and demonstrate its association with various abnormal physiologies associated with chronic liver disease, including spur cell anemia, low HDL levels, and adrenal insufficiency.
Hospitalized cirrhotic patients at UVA that meet study eligibility criteria will be approached by a member of the study team to obtain consent for participation. If a patient agrees to become a study subject, they will have an approximate total of 35ml of blood drawn the following morning. Lab tests to be performed include: peripheral blood smear, lipid panel, free cortisol, cortisol binding globulin, serum cholesterol esters (surrogate for LCAT enzyme activity), and a standard-dose cortisol stimulation test. The latter involves blood drawn with the initial collection, administration of an intravenous 250mcg dose of synthetic ACTH, and then repeat small-volume blood draws at 30 minutes and 60 minutes later.
Subjects will be classified as adrenally sufficient or insufficient on the basis of as standard-dose cortisol stimulation test. Variables of interest for comparison between the groups include MELD score, Child-Turcotte-Pugh (CTP) classification, high-density lipoprotein (HDL) levels, presence of spur cell anemia, serum cholesterol ester percentage (surrogate for LCAT enzymatic activity), cortisol binding globulin levels, and free cortisol levels. Student's t-test and Chi Square tests will be utilized to determine significance; a p <0.05 value will be used as our threshold for significance. If multiple factors are found to be significantly different in a univariate fashion between classification groups, a multivariate logistic regression analysis will be performed for adjusted analysis. The investigators will also seek to define any correlations between variables. Furthermore, the investigators will assess correlation between MELD score and serum cholesterol ester percentage, spur cell anemia, HDL levels, cortisol binding globulin levels, and free cortisol levels; similar correlate analysis will be done using CTP classification instead of MELD score.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adrenal Insufficiency, Cirrhosis, Spur Cell Anemia, Lecithin Acyltransferase Deficiency
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
100 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Hospitalized cirrhosis patients
Arm Type
Experimental
Arm Description
Administration of cortisol stimulation test to assess for presence or absence of adrenal insufficiency
Intervention Type
Drug
Intervention Name(s)
Cosyntropin
Intervention Description
Administer 250mcg cosyntropin to hospitalized cirrhosis patients to assess for the presence of adrenal insufficiency
Primary Outcome Measure Information:
Title
Number of Participants With Cholesterol Esterification Deficiency
Description
A percent quantification of serum cholesterol esterification will be measured via blood draw. Low values represent deficiency in esterification, which is a surrogate measure of lecthicin-cholesterol acetyltransferase (LCAT) enzymatic deficiency.
Time Frame
24 hours
Title
Number of Participants With Spur Cell Anemia
Description
A peripheral blood smear will be obtained and assessed for presence of acanthocytes (spur cells). Spur cell anemia is defined as a serum hemoglobin < 10g/dL and the presence of >= 5% spur cells on blood smear.
Time Frame
24 hours
Title
Participant Transplant-Free Survival
Description
Transplant and Death are considered equivalent outcomes
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Number of Participants With Relative Adrenal Insufficiency (RAI)
Description
A baseline total cortisol level will be obtained and then patients will receive a standard-dose synthetic ACTH (250mcg of Cosyntropin) stimulation test to assess for the presence of adrenal insufficiency. RAI is defined as a change in the total cortisol level in response to the stimulation test of <9mcg/dL when measured 60 minutes after the Cosyntropin is administered.
Time Frame
24 hours
Title
Number of Participants With Low Free Cortisol
Description
Patients will have their free cortisol levels measured to assess for deficiency.
Time Frame
24 hours
Title
Number of Participants Who Received Liver Transplantation at 90 Days
Description
Patients who received a liver transplant within 90 days of enrollment
Time Frame
90 days
Title
Number of Participants Who Received Liver Transplantation at 6 Months
Description
Patients who received a liver transplant within 6 months of enrollment
Time Frame
6 months
Title
Number of Participants Who Died Within Index Hospitalization
Description
Patients who died within the same hospitalization as enrollment
Time Frame
Within Hospitalization
Title
Number of Participants Who Died at 30 Days
Description
Patients who died within 30 days of enrollment
Time Frame
30 days
Title
Number of Participants Who Died at 90 Days
Description
Patients who died within 90 days of enrollment
Time Frame
90 days
Title
Number of Participants Who Died at 6 Months
Description
Patients who died within 6 months of enrollment
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
110 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age >=18 years
Diagnosis of cirrhosis
Admission to hospital
Exclusion Criteria:
Age < 18 years
Prior enrollment in study (i.e. readmission)
Prisoner
Pregnancy
Prednisone or Hydrocortisone use in last 24 hours
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zachary Henry, MD
Organizational Affiliation
University of Virginia School of Medicine, Department of Medicine, Division of Gastroenterology & Hepatology
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Virginia Health System
City
Charlottesville
State/Province
Virginia
ZIP/Postal Code
22903
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
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Is Adrenal Insufficiency Under-diagnosed in Hospitalized Cirrhosis Patients?
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