Number of Participants With Cholesterol Esterification Deficiency
| Group | Value (Participants) |
|---|---|
| Normal Adrenal Response | 10 |
| Relative Adrenal Insufficiency | 11 |
Trial · Interventional
CompletedPhase 3Results postedRegistry dataUnited States
1 trial · 1 completed · 1 with posted results
Is Adrenal Insufficiency Under-diagnosed in Hospitalized Cirrhosis Patients?
NCT0336806629 Jan 2018 to 12 Mar 2019
Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.
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.
Experimental
Hospitalized cirrhosis patients
Administration of cortisol stimulation test to assess for presence or absence of adrenal insufficiency
Outcomes the sponsor listed as primary.
Number of Participants With Cholesterol Esterification Deficiency
Time frame · 24 hours
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
Time frame · 24 hours
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
Time frame · 6 months
Transplant and Death are considered equivalent outcomes
Number of Participants With Relative Adrenal Insufficiency (RAI)
Time frame · 24 hours
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
Time frame · 24 hours
Patients will have their free cortisol levels measured to assess for deficiency.
Number of Participants Who Received Liver Transplantation at 90 Days
Time frame · 90 days
Patients who received a liver transplant within 90 days of enrollment
Number of Participants Who Received Liver Transplantation at 6 Months
Time frame · 6 months
Patients who received a liver transplant within 6 months of enrollment
Number of Participants Who Died Within Index Hospitalization
Time frame · Within Hospitalization
Patients who died within the same hospitalization as enrollment
Number of Participants Who Died at 30 Days
Time frame · 30 days
Patients who died within 30 days of enrollment
Number of Participants Who Died at 90 Days
Time frame · 90 days
Patients who died within 90 days of enrollment
Number of Participants Who Died at 6 Months
Time frame · 6 months
Patients who died within 6 months of enrollment
Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.
| Group | Value (Participants) |
|---|---|
| Normal Adrenal Response | 10 |
| Relative Adrenal Insufficiency | 11 |
| Group | Value (Participants) |
|---|---|
| Normal Adrenal Response | 6 |
| Relative Adrenal Insufficiency | 8 |
| Group | Value (Participants) |
|---|---|
| Normal Adrenal Response | 41 |
| Relative Adrenal Insufficiency | 16 |
| Group | Value (Participants) |
|---|---|
| Hospitalized Cirrhosis Patients | 37 |
| Group | Value (Participants) |
|---|---|
| Normal Adrenal Response | 6 |
| Relative Adrenal Insufficiency | 1 |
| Group | Value (Participants) |
|---|---|
| Normal Adrenal Response | 6 |
| Relative Adrenal Insufficiency | 5 |
| Group | Value (Participants) |
|---|---|
| Normal Adrenal Response | 8 |
| Relative Adrenal Insufficiency | 6 |
| Group | Value (Participants) |
|---|---|
| Normal Adrenal Response | 1 |
| Relative Adrenal Insufficiency | 1 |
| Group | Deaths | Serious events | Other events |
|---|---|---|---|
| Hospitalized Cirrhosis PatientsAdministration of cortisol stimulation test to assess for presence or absence of adrenal insufficiency Cosyntropin: Administer 250mcg cosyntropin to hospitalized cirrhosis patients to assess for the presence of adrenal insufficiency | 25 / 100 | 25 / 100 | 1 / 100 |
Each cell reads participants affected / participants at risk, as the registry posted them.
Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works
Studies that cite this trial.
2 studies on this page
PubMed tag: none · 2011
Fede et al. 2011Journal of hepatologycited by 61
PMID 21056503DOI 10.1016/j.jhep.2010.06.034PUB-21056503
PubMed tag: none · 2010
Tan et al. 2010Journal of hepatologycited by 66
PMID 20739086DOI 10.1016/j.jhep.2010.05.020PUB-20739086
Who could join, as posted.
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