The Influence of Different Hydrocortisone Replacement Doses on the Partitioning and Flexibility of Ectopic Lipids in Patients With Corticotropic Hypopituitarism
Study Details
Study Description
Brief Summary
This study aims at assessing the effect of today's standard of hydrocortisone dosage versus previous hydrocortisone dosage on flexibility and partitioning of ectopic lipid depots (IMCL and IHCL) after a standardised fat load followed by a short-term aerobic exercise in patients with corticotropic pituitary insufficiency.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
Background
The investigators and others have shown that long-term hydrocortisone replacement therapy at higher doses of hydrocortisone replacement therapy at higher doses of hydrocortisone replacement (as previously recommended) is associated with higher mortality. The pathophysiology for the association of hydrocortisone-replacement dose and mortality remains unclear. A possible underlying mechanism is nonalcoholic fatty liver disease which is more prevalent in patients with hypopituitarism. Patients with non-alcoholic fatty liver disease are at a higher risk for overall-mortality.
It remains to be established whether the insulin resistance, associated with increased intrahepatocellular lipids and increased intramusculoskeletal lipids, is implicated in the pathophysiology of these epidemiological findings.
Interestingly, it has been shown that a reduction of hydrocortisone replacement dose from 20-30mg/d to 10-15mg/d resulted in a loss of body fat and a significant decrease of plasma total cholesterol and triglyceride concentration. The effect of IMCL and IHCL is so far unknown.
Patients with hypopituitarism with hydrocortisone replacement therapy provide a unique disease model to study the short-term effects of previously recommended dose (higher dose) of hydrocortisone versus lower dose of HC replacement therapy on ectopic lipids (IMCL; IHCL) lipids, as well as on subcutaneous and visceral fat mass and on parameters of insulin resistance. Combining MRI and MR-spectroscopy techniques, different fat mass (subcutaneous and visceral) and ectopic lipids can be repeatedly and non-invasively assessed.
Objective
To investigate the impact of today's standard of hydrocortisone dosage (lower) versus previous (higher) hydrocortisone dosage on flexibility and partitioning of ectopic lipid depots after a standardised fat load followed by a short-term aerobic exercise in patients with corticotropic pituitary insufficiency.
Methods
Ectopic lipids are measured by MR-spectroscopy, separate assessment of visceral and subcutaneous fat mass will be performed by MR-imaging, standardized exercise capacity test using spiroergometry. Short-time exercise consists of 2h aerobic cycling at 50% VO2max. Laboratory analysis include lipid profile, free fatty acids, HOMA-Index, hormones.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Other: Higher hydrocortisone dose Established hydrocortisone replacement therapy plus 10mg of hydrocortisone |
Drug: Hydrocortisone
Established Hydrocortisone replacement therapy plus Hydrocortisone (10mg/day)
|
| Other: Lower hydrocortisone dose Established hydrocortisone replacement therapy plus placebo |
Drug: Placebo
Established Hydrocortisone replacement therapy plus Placebo (0mg Hydrocortisone)
|
Outcome Measures
Primary Outcome Measures
- Change from baseline in flexibility of Intramyocellular Lipids (IMCL) Measured in mmol/L [3 months]
Measured in mmol/L
- Change from baseline in flexibility of Intrahepatocellular Lipids (IHCL) Measured in mmol/L [3 months]
Measured in mmol/L
Secondary Outcome Measures
- Free Fatty Acids (FFA) availability during exercise before and after additional hydrocortisone/placebo Measured in mmol/L [At baseline, 3 months]
Measured in mmol/L
- Flexibility of ectopic fat stores, defined as difference between intramyocellular/intrahepatocellular lipid concentration before and after exercise, and their possible relation to insulin sensitivity before and after additional hydrocortisone/placebo [At baseline, 3 months]
- Free Fatty Acids (FFA) availability during exercise and the possible relation to insulin sensitivity before and after additional hydrocortisone/placebo Measured in mmol/L [At baseline, 3 months]
Measured in mmol/L
- Effect of exercise on insulin at baseline [At baseline]
- Effect of exercise on insulin at 3 months [3 months]
- Effect of exercise on catecholamines at baseline [At baseline]
- Effect of exercise on catecholamines at 3 months [3 months]
- Effect of exercise on growth hormone at baseline [At baseline]
- Effect of exercise on growth hormone at 3 months [3 months]
- Effect of exercise on cortisol at baseline [At baseline]
- Effect of exercise on cortisol at 3 months [3 months]
- Effect of exercise on lactate at baseline [At baseline]
- Effect of exercise on lactate at 3 months [3 months]
- Effect of exercise on glucose at baseline [At baseline]
- Effect of exercise on glucose at 3 months [3 months]
- Effect of exercise on inflammatory markers at baseline [At baseline]
- Effect of exercise on inflammatory markers at 3 months [3 months]
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Written informed consent
-
Male and female patients
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Corticotropic pituitary insufficiency
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Capable to exercise during 120 minutes on a bicycle
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Normal ECG during ergometry
Exclusion Criteria
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Concomitant medication with NSAID, anticoagulants, digoxin, salbutamol, anticonvulsants, cholinesterase inhibitor, pancuronium
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Abnormal liver, renal or thyroid function, heart failure
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Hemophilia
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Diabetes mellitus
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Severe dyslipidemia
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Active neoplasia
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Women who are pregnant or breast feeding
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Intention to become pregnant during the course of the study
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Lack of safe contraception
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Known or suspected non-compliance
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Drug or alcohol abuse
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Inability to follow the procedures of the study
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Participation in another study with investigational drug within the 30 days preceding and during the study
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Previous enrolment into current study
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Enrolment of the investigator, his/her family members, employees and other dependent persons
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Inability to exercise
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Contraindications to exposure to a 3 T magnetic field
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Major depression, psychosis, claustrophobia
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Division of Endocrinology, Diabetes and Clinical Nutrition, University Hospital Berne | Berne | Switzerland | 3010 |
Sponsors and Collaborators
- University Hospital Inselspital, Berne
Investigators
- Principal Investigator: Emanuel Christ, MD, PhD, Division of Endocrinology, Diabetes and Clinical Nutrition, University Hospital Bern
- Principal Investigator: Chris Boesch, MD, PhD, AMSM; Division of Radiology, University Hopsital of Bern, Inselspital
Study Documents (Full-Text)
None provided.More Information
Publications
- Boesch C, Slotboom J, Hoppeler H, Kreis R. In vivo determination of intra-myocellular lipids in human muscle by means of localized 1H-MR-spectroscopy. Magn Reson Med. 1997 Apr;37(4):484-93.
- Danilowicz K, Bruno OD, Manavela M, Gomez RM, Barkan A. Correction of cortisol overreplacement ameliorates morbidities in patients with hypopituitarism: a pilot study. Pituitary. 2008;11(3):279-85. doi: 10.1007/s11102-008-0126-2.
- 211/14
- 2014 DR 4137