This study is designed to collect data on individuals with adrenal insufficiency who are changing treatments from hydrocortisone to prednisolone, or vice versa. It will compare anthropometric, biochemical and subjective health outcomes between both treatments.
In the UK, oral immediate release hydrocortisone divided in three doses daily has been the traditional treatment. The most common regimen in clinical practice uses doses of 10 mg on waking, 5 mg at lunch time and 5 mg in the afternoon. Once daily prednisolone is another regimen in clinical use and now prescribed at less than 5mg daily. It has a longer duration of action and a smoother pharmacokinetic profile compared to hydrocortisone. Moreover, prednisolone is much more cost-effective than hydrocortisone with 5mg tablets. Prednisolone is less commonly used due to perceived concerns regarding loss of bone mineral density leading to osteoporosis, increased insulin resistance leading to steroid induced diabetes, and rises in blood pressure and weight leading to increased cardiovascular risk. This belief is perhaps driven by the fact that most clinicians encounter prednisolone in the context of the treatment of asthma, rheumatoid arthritis etc. where far higher doses are employed. Where effects on bone health have been noted, they have been in association with higher doses of prednisolone (7.5mg) than those employed today (2-5mg). Although conventionally prednisolone 5 mg is assumed to be bioequivalent to HC 20 mg (ratio 1:4), newer studies suggest that the ratio may be nearer 1:6-8 i.e. lower doses can be used.
Study Type
OBSERVATIONAL
Enrollment
100
There is no specific intervention other than an individual changing their treatment as part of their usual care
Imperial College Healthcare NHS Trust
London, United Kingdom
RECRUITINGP1NP
measurement of bone turnover markers: P1NP,
Time frame: Minimum 4 months of stable treatment
NTX
measurement of bone turnover markers: NTX
Time frame: Minimum 4 months of stable treatment
Heart rate
recording observations- heart rate
Time frame: Minimum 4 months of stable treatment
Blood pressure
recording observations- blood pressure
Time frame: Minimum 4 months of stable treatment
Waist-hip circumference
recording observations- waist-hip circumference ratios
Time frame: Minimum 4 months of stable treatment
Lipid profile (Total cholesterol, HDL, LDL and triglycerides)
measuring biochemical indicators of cardiovascular risk: total cholesterol, HDL, LDL and triglycerides
Time frame: Minimum 4 months of stable treatment
High sensitivity CRP
measuring biochemical indicators of cardiovascular risk: high sensitivity CRP
Time frame: Minimum 4 months of stable treatment
Glucose
assessed by measuring glucose
Time frame: Minimum 4 months of stable treatment
HbA1c
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assessed by measuring HBA1c
Time frame: Minimum 4 months of stable treatment
Frequency and severity of steroid replacement related symptoms
assessed by reporting of symptoms of steroid deficiency, their frequency and severity stratified by the patient's current replacement regimen. Symptoms include nausea, lethargy, muscle pain, headaches etc.)
Time frame: Minimum 4 months of stable treatment
Efficacy of replacement and wellbeing
assessed using subjective health questionnaire
Time frame: Minimum 4 months of stable treatment