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Effects and Interactions of Liquorice and Grapefruit on Glucocorticoid Replacement Therapy in Addison's Disease

Primary Purpose

Addison Disease

Status
Completed
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Liquorice
Grapefruit Juice
Sponsored by
Haukeland University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Addison Disease focused on measuring Addison Disease, Pharmacokinetics, Hormone Replacement Therapy, cortisone acetate, Quality of Life

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Verified diagnosis of adrenal insufficiency (Addison's disease)
  • Stable cortisone acetate replacement therapy
  • Written informed consent

Exclusion Criteria:

  • Malignant disease
  • Pharmacological treatment with other glucocorticoids
  • Pregnancy
  • Current minor disease (ie the flu)
  • Major disease or accident requiring hospitalization the last three months
  • Use of grapefruit juice or liquorice the last two weeks before study start
  • Blood pressure above 150mmHg systolic or 90 mmHg diastolic.

Sites / Locations

  • Haukeland University Hospital, Helse-Bergen HF

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

No Intervention

Arm Label

Liquorice

Grapefruit juice

Baseline

Arm Description

Liquorice eq to 150 mg glycyrrhizinic acid. Results are compared to a baseline assessment without liquorice/grapefruit juice ingestion.

200 ml pink grapefruit juice three times a day. Results are compared to a baseline assessment without liquorice/grapefruit juice ingestion.

Baseline assessment without intake of liquorice or grapefruit juice

Outcomes

Primary Outcome Measures

AUC Serum Cortisol - Levels of cortisol in serum during the first 2.6 hours after oral administration of cortisone acetate.
The area under the curve (AUC) of cortisol is calculated based on serum time-series sampling (every 20 minutes for 2.6 h after oral administration of cortisone acetate). The AUCs obtained during liquorice and grapefruit juice intakes are compared to the baseline assessment (without these nutritional compounds). All other pharmacokinetic properties (primary and secondary outcome measures) are compared analogously.

Secondary Outcome Measures

Serum Cortisol levels at the end of time-series sampling (t=160min)
At the end of time series sampling (160 minutes after orally administered cortisone acetate) on all three assessments
Serum Cortisone levels at the end of time-series sampling (t=160min)
At the end of time series sampling (160 minutes after orally administered cortisone acetate) on all three assessments
Saliva Cortisol levels at the end of time-series sampling (t=160min)
At the end of time series sampling (160 minutes after orally administered cortisone acetate) on all three assessments
Saliva Cortisone levels at the end of time-series sampling (t=160min)
At the end of time series sampling (160 minutes after orally administered cortisone acetate) on all three assessments
Time of maximum concentration of serum Cortisol
Based on time-series sampling at each of the three assessments
Time of maximum concentration of serum Cortisone
Based on time-series sampling at each of the three assessments
Time of maximum concentration of Saliva Cortisol
Based on time-series sampling at each of the three assessments
Time of maximum concentration of Saliva Cortisone
Based on time-series sampling at each of the three assessments
Half life of serum cortisol
Based on time-series sampling at each of the three assessments
Half life of serum cortisone
Based on time-series sampling at each of the three assessments
Urinary aTHF/THF-ratio
Measured in 24h urine obtained at the three assessments. aTHF = allo-tetrahydrocortisol, THF = tetrahydrocortisol
AUC Serum Cortisone
Similar to primary outcome Serum AUC Cortisol
Urine total metabolites (Urinary cortisol+cortisone+6OHF+aTHF+THF+THE)
24-hour urine collected on each of the three assessments aTHF = allo-tetrahydrocortisol, THF = tetrahydrocortisol, THE = tetrahydrocortisone, 6OHF = 6beta-hydroxycortisol
Urinary ratio (aTHF+THF)/THE
Assessed in 24h urine obtained at the three assessments (baseline, after liquorice and after grapefruit juice). It is an index of 5-reductase activity. 24-hour urine collected on each of the three assessments aTHF = allo-tetrahydrocortisol, THF = tetrahydrocortisol, THE = tetrahydrocortisone
Urinary Ratio Cortisol/6beta-OH-Cortisol
Assess the enzymatic activity of CYP3A4 by the index urinary cortisol/6beta-oh cortisol ratio obtained at the three assessments (baseline, after liquorice and after grapefruit juice. 6OHF = 6beta-hydroxycortisol
Urine total metabolites (Urinary cortisol+cortisone+6OHF+aTHF+THF+THE)
24-hour urine collected on each of the three assessments 24-hour urine collected on each of the three assessments aTHF = allo-tetrahydrocortisol, THF = tetrahydrocortisol, THE = tetrahydrocortisone, 6OHF = 6beta-hydroxycortisol
AUC Saliva cortisone
Similar to primary outcome Saliva AUC Cortisol, but for cortisone.
AUC Serum Cortisone
Similar to primary outcome Serum AUC Cortisol, but for cortisone.
AUC Saliva Cortisol
Similar to AUC Serum Cortisol, but measurements are on saliva.

Full Information

First Posted
December 22, 2010
Last Updated
January 13, 2011
Sponsor
Haukeland University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01271296
Brief Title
Effects and Interactions of Liquorice and Grapefruit on Glucocorticoid Replacement Therapy in Addison's Disease
Official Title
Use of Liquorice and Grapefruit in Patients With Addison's Disease
Study Type
Interventional

2. Study Status

Record Verification Date
December 2010
Overall Recruitment Status
Completed
Study Start Date
April 2008 (undefined)
Primary Completion Date
January 2009 (Actual)
Study Completion Date
January 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Haukeland University Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Addison's disease is a rare disease, wherein the adrenals can not produce sufficient steroid hormones (cortisol and aldosterone). Patients with Addison's disease report impaired subjective health status, and they have increased all-cause mortality. Conventional therapy is by oral replacement of glucocorticoid and mineralocorticoid hormones, but this strategy imperfectly mimic the diurnal cortisol variations, and render the patients both over- and under-treated. Anecdotally, some patients with adrenal insufficiency may benefit from the use of various nutritional compounds. We hypothesised that liquorice and grapefruit altered the metabolism and absorption of cortisone acetate.
Detailed Description
In the present study, cortisone acetate absorption and metabolism are assessed in subjects with Addison's disease on three occasions. On the first occasion, the subjects are on their regular diet, but avoid ingestion of grapefruit and liquorice. At the end of the baseline assessment the order of the nutritional compounds (liquorice-grapefruit juice or grapefruit juice-liquorice) to be investigated in the next two assessments are randomised. On the two next occasions, the absorption and metabolism of cortisone acetate is studied when study subjects consume liquorice and grapefruit juice. Between the use of grapefruit and liquorice there is a wash out period of at least 3 weeks. For studies on liquorice effects, the subjects ingest 24-gram liquorice per day (equivalent of 150-mg glycyrrhizinic acid per day). For studies on grapefruit juice effects, subjects drink 200-ml grapefruit juice three times a day for three days. They maintain their regular medication and usual diet. Time-series of cortisol and cortisone are obtained in serum and saliva samples on the third day of liquorice/grapefruit juice use. 24-hour urine is also collected. Measurements of cortisol and metabolites in serum and saliva are used to calculate pharmacokinetical parameters. The measurements from samples obtained when using the investigated nutritional compounds are compared to the baseline assessment in each subject. Metabolites in 24-hour urine are compared similarly to investigate changes in urinary excretion, and to estimate the activity of enzymes involved in the metabolism of cortisol (5alfa-reductase, 5beta-reductase, cytochrome P450 3A4 system, 11-beta hydroxysteroid dehydrogenase).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Addison Disease
Keywords
Addison Disease, Pharmacokinetics, Hormone Replacement Therapy, cortisone acetate, Quality of Life

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
17 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Liquorice
Arm Type
Active Comparator
Arm Description
Liquorice eq to 150 mg glycyrrhizinic acid. Results are compared to a baseline assessment without liquorice/grapefruit juice ingestion.
Arm Title
Grapefruit juice
Arm Type
Active Comparator
Arm Description
200 ml pink grapefruit juice three times a day. Results are compared to a baseline assessment without liquorice/grapefruit juice ingestion.
Arm Title
Baseline
Arm Type
No Intervention
Arm Description
Baseline assessment without intake of liquorice or grapefruit juice
Intervention Type
Dietary Supplement
Intervention Name(s)
Liquorice
Intervention Description
24 gram liquorice eq. to 150 mg glycyrrhizinic acid, taken orally, for three days.
Intervention Type
Dietary Supplement
Intervention Name(s)
Grapefruit Juice
Intervention Description
200 ml pink grapefruit juice three times a day, taken orally, for three days.
Primary Outcome Measure Information:
Title
AUC Serum Cortisol - Levels of cortisol in serum during the first 2.6 hours after oral administration of cortisone acetate.
Description
The area under the curve (AUC) of cortisol is calculated based on serum time-series sampling (every 20 minutes for 2.6 h after oral administration of cortisone acetate). The AUCs obtained during liquorice and grapefruit juice intakes are compared to the baseline assessment (without these nutritional compounds). All other pharmacokinetic properties (primary and secondary outcome measures) are compared analogously.
Time Frame
Outcome measures are assessed when all subjects have completed the study, approximately 1.5-2.0 years after study start.
Secondary Outcome Measure Information:
Title
Serum Cortisol levels at the end of time-series sampling (t=160min)
Description
At the end of time series sampling (160 minutes after orally administered cortisone acetate) on all three assessments
Time Frame
Outcome measures are assessed when all subjects have completed the study, approximately 1.5-2.0 years after study start.
Title
Serum Cortisone levels at the end of time-series sampling (t=160min)
Description
At the end of time series sampling (160 minutes after orally administered cortisone acetate) on all three assessments
Time Frame
Outcome measures are assessed when all subjects have completed the study, approximately 1.5-2.0 years after study start.
Title
Saliva Cortisol levels at the end of time-series sampling (t=160min)
Description
At the end of time series sampling (160 minutes after orally administered cortisone acetate) on all three assessments
Time Frame
Outcome measures are assessed when all subjects have completed the study, approximately 1.5-2.0 years after study start.
Title
Saliva Cortisone levels at the end of time-series sampling (t=160min)
Description
At the end of time series sampling (160 minutes after orally administered cortisone acetate) on all three assessments
Time Frame
Outcome measures are assessed when all subjects have completed the study, approximately 1.5-2.0 years after study start.
Title
Time of maximum concentration of serum Cortisol
Description
Based on time-series sampling at each of the three assessments
Time Frame
Outcome measures are assessed when all subjects have completed the study, approximately 1.5-2.0 years after study start.
Title
Time of maximum concentration of serum Cortisone
Description
Based on time-series sampling at each of the three assessments
Time Frame
Outcome measures are assessed when all subjects have completed the study, approximately 1.5-2.0 years after study start.
Title
Time of maximum concentration of Saliva Cortisol
Description
Based on time-series sampling at each of the three assessments
Time Frame
Outcome measures are assessed when all subjects have completed the study, approximately 1.5-2.0 years after study start.
Title
Time of maximum concentration of Saliva Cortisone
Description
Based on time-series sampling at each of the three assessments
Time Frame
Outcome measures are assessed when all subjects have completed the study, approximately 1.5-2.0 years after study start.
Title
Half life of serum cortisol
Description
Based on time-series sampling at each of the three assessments
Time Frame
Outcome measures are assessed when all subjects have completed the study, approximately 1.5-2.0 years after study start.
Title
Half life of serum cortisone
Description
Based on time-series sampling at each of the three assessments
Time Frame
Outcome measures are assessed when all subjects have completed the study, approximately 1.5-2.0 years after study start.
Title
Urinary aTHF/THF-ratio
Description
Measured in 24h urine obtained at the three assessments. aTHF = allo-tetrahydrocortisol, THF = tetrahydrocortisol
Time Frame
Outcome measures are assessed when all subjects have completed the study, approximately 1.5-2.0 years after study start.
Title
AUC Serum Cortisone
Description
Similar to primary outcome Serum AUC Cortisol
Time Frame
Outcome measures are assessed when all subjects have completed the study, approximately 1.5-2.0 years after study start.
Title
Urine total metabolites (Urinary cortisol+cortisone+6OHF+aTHF+THF+THE)
Description
24-hour urine collected on each of the three assessments aTHF = allo-tetrahydrocortisol, THF = tetrahydrocortisol, THE = tetrahydrocortisone, 6OHF = 6beta-hydroxycortisol
Time Frame
Outcome measures are assessed when all subjects have completed the study, approximately 1.5-2.0 years after study start.
Title
Urinary ratio (aTHF+THF)/THE
Description
Assessed in 24h urine obtained at the three assessments (baseline, after liquorice and after grapefruit juice). It is an index of 5-reductase activity. 24-hour urine collected on each of the three assessments aTHF = allo-tetrahydrocortisol, THF = tetrahydrocortisol, THE = tetrahydrocortisone
Time Frame
Outcome measures are assessed when all subjects have completed the study, approximately 1.5-2.0 years after study start.
Title
Urinary Ratio Cortisol/6beta-OH-Cortisol
Description
Assess the enzymatic activity of CYP3A4 by the index urinary cortisol/6beta-oh cortisol ratio obtained at the three assessments (baseline, after liquorice and after grapefruit juice. 6OHF = 6beta-hydroxycortisol
Time Frame
Outcome measures are assessed when all subjects have completed the study, approximately 1.5-2.0 years after study start.
Title
Urine total metabolites (Urinary cortisol+cortisone+6OHF+aTHF+THF+THE)
Description
24-hour urine collected on each of the three assessments 24-hour urine collected on each of the three assessments aTHF = allo-tetrahydrocortisol, THF = tetrahydrocortisol, THE = tetrahydrocortisone, 6OHF = 6beta-hydroxycortisol
Time Frame
Outcome measures are assessed when all subjects have completed the study, approximately 1.5-2.0 years after study start.
Title
AUC Saliva cortisone
Description
Similar to primary outcome Saliva AUC Cortisol, but for cortisone.
Time Frame
Outcome measures are assessed when all subjects have completed the study, approximately 1.5-2.0 years after study start.
Title
AUC Serum Cortisone
Description
Similar to primary outcome Serum AUC Cortisol, but for cortisone.
Time Frame
Outcome measures are assessed when all subjects have completed the study, approximately 1.5-2.0 years after study start.
Title
AUC Saliva Cortisol
Description
Similar to AUC Serum Cortisol, but measurements are on saliva.
Time Frame
Outcome measures are assessed when all subjects have completed the study, approximately 1.5-2.0 years after study start.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Verified diagnosis of adrenal insufficiency (Addison's disease) Stable cortisone acetate replacement therapy Written informed consent Exclusion Criteria: Malignant disease Pharmacological treatment with other glucocorticoids Pregnancy Current minor disease (ie the flu) Major disease or accident requiring hospitalization the last three months Use of grapefruit juice or liquorice the last two weeks before study start Blood pressure above 150mmHg systolic or 90 mmHg diastolic.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paal Methlie, MD
Organizational Affiliation
University of Bergen. Helse-Bergen HF
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Kristian Løvås, MD, PhD
Organizational Affiliation
University of Bergen. Helse-Bergen HF.
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Eystein S Husebye, Prof, MD
Organizational Affiliation
University of Bergen. Helse-Bergen HF.
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ernst A Lien, Prof. MD.
Organizational Affiliation
University of Bergen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Haukeland University Hospital, Helse-Bergen HF
City
Bergen
ZIP/Postal Code
5020
Country
Norway

12. IPD Sharing Statement

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Effects and Interactions of Liquorice and Grapefruit on Glucocorticoid Replacement Therapy in Addison's Disease

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