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Introduction Adrenal insufficiency (AI) is characterised by inadequate adrenal corticosteroid hormone production and is classified as primary, secondary or tertiary ( 1 ). Primary adrenal insufficiency (PAI) is caused by pathological processes
Department of Endocrinology, Sahlgrenska University Hospital, Gothenburg, Sweden
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Department of Endocrinology, Sahlgrenska University Hospital, Gothenburg, Sweden
Wallenberg Center for Molecular and Translational Medicine, University of Gothenburg, Gothenburg, Sweden
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Introduction Oral glucocorticoid (GC) treatment can lead to adrenal insufficiency by suppressing the hypothalamic–pituitary–adrenal axis. This can result in life-threatening adrenal crisis if the patient does not receive an increased GC dose
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Introduction Primary adrenal insufficiency (PAI) is a rare disease, most commonly of auto-immune origin. There is a global variation in prevalence from 80 to 145 per million in Europe, with the highest case numbers reported in Scandinavian
Department of Endocrinology, Imperial College Healthcare NHS Trust, London, UK
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Department of Endocrinology, Imperial College Healthcare NHS Trust, London, UK
Department of Clinical Biochemistry, North West London Pathology, London, UK
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Department of Endocrinology, Imperial College Healthcare NHS Trust, London, UK
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Department of Endocrinology, Imperial College Healthcare NHS Trust, London, UK
Department of Clinical Biochemistry, North West London Pathology, London, UK
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Introduction Patients with adrenal insufficiency (AI) have premature morbidity and mortality ( 1 ). Mildly elevated levels of glucocorticoids or non-circadian timing of therapy may contribute towards cardiovascular disease and increased
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Introduction Adrenal insufficiency (AI) is characterized by high morbidity and mortality, likely due to inappropriate glucocorticoid (GC) treatment and no physiological daily exposure. Indeed, conventional GC treatment, with hydrocortisone (HC
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principal cause of euvolemic hyponatremia (EuVHNa). Although SIAD has a specific diagnostic criteria, it remains a diagnosis of exclusion and needs the absence of secondary adrenal insufficiency (AI) and hypothyroidism as an essential criterion for the
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Department of Endocrinology, Diabetes and Metabolism, Karolinska University Hospital, Stockholm, Sweden
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Department of Medicine, Haukeland University Hospital, Bergen, Norway
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The number of individuals in Europe with primary and secondary adrenal insufficiency (AI) is estimated to be 20–50 per 100,000 ( 1 ). AI is characterised by a deficit in synthesis and release of cortisol, with symptoms including tiredness
Diabetes and Endocrine Clinic, Mediclinic Airport Road Hospital, Abu Dhabi, United Arab Emirates
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attracted the most attention with the largest volume of literature ( 5 ). Nevertheless, significant deficiencies remain in guidance toward the management of other endocrinological disorders during Ramadan ( 6 ). Adrenal insufficiency (AI) represents a
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cortisone, resulting in higher systemic availability of the active 11β-hydroxy form, prednisolone ( 12 ). Prednisolone is used in some patients with adrenal insufficiency (AI) as hormone replacement therapy. Advocates of prednisolone highlight that it
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GR functionality. In patients with bronchial asthma, the Bcl I polymorphism seems to at least partially explain the development of a severe form of asthma associated with resistance to glucocorticoids ( 10 ). Patients with adrenal insufficiency