The Glucocorticoid Axis Flashcards

To understand the glucocorticoid axis

1
Q

Describe the adrenal glands?

A
  1. Outer cortex producing cortisol, aldosterone and androgens
  2. Inner medulla secreting catecholines
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2
Q

Describe the adrenal glands?

A
  1. Outer cortex producing cortisol, aldosterone and androgens
  2. Inner medulla secreting catecholines
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3
Q

How is cortisol released?

A
  1. Corticotrophin releasing hormone (CRH) from the hypothalamus stimulates ACTH from the anterior pituitary.
  2. This stimulates cortisol production from the adrenal glands.
  3. Cortisol feeds back to the hypothalamus and pituitary to suppress further CRH/ACTH release
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4
Q

Describe Addison’s disease: primary hypoadrenalism?

A
  1. 90% of cases arise from adrenal cortex destruction by organ specific auto antibodies
  2. Associated with other autoimmune conditions:
    - autoimmune thyroid disease
    - ovarian failure
    - pernicious anaemia
    - type 1 diabetes mellitus
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5
Q

What are the clinical features of Addison’s?

A
  1. Lethargy, depression, anorexia
  2. Postural hypotension caused by salt and water loss is an early sign
  3. Hyperpigmentation due to stimulation if melanocytes by xs ACTH
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6
Q

What are the appropriate investigations for Addison’s disease

A
  1. Single cortisol measurement - random daytime cortisol below 100nmol/l suggestive above 550 makes diagnosis unlikely
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7
Q

What are the appropriate investigations for Addison’s disease?

A
  1. The short ACTH test over 30 mins tests if ACTH raises cortisol levels
  2. Measure plasma ACTH levels: a high level with low or low/normal levels confirms primary hypoadrenalism
  3. Long ACTH test detects secondary hypoadrenalism and steroid suppression
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8
Q

What is the management for Addison’s disease?

A
  1. Hydrocortisone: 20mg morning, 10mg evening

2. Fludrcortisone: 50-300mcgs

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9
Q

Describe secondary hypoadrenalism?

A
  1. May arise from hypothalamic-pituitary disease or from long term steroid therapy
  2. Clinical features same as Addison’s but no pigmentation as ACTH levels are low
  3. A long ACTH will differentiate between primary and secondary hypoadrenalism
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10
Q

Describe Cushing’s syndrome?

A
  1. Persistently and innappropriately elevated glucocorticoid levels.
  2. Most cases result from administration for other conditions
  3. Spontaneous Cushing’s can result from xs ACTH secretion
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11
Q

Describe the clinical features of Cushing’s?

A
  1. Obese, fat distribution is central, affecting the trunk, abdomen and neck
  2. Moon face, skin bruising, striations, pigmentation
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