growth hormone Flashcards

1
Q

What is the pattern of release of GH?

A

Pulsatile release, increased release at night.

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2
Q

In which stage of life are GH levels the greatest?

A

puberty

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3
Q

What are the functions of GH?

A

Promotes growth of bone and muscle, and increases blood glucose levels

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4
Q

How does GH stimulate bone and muscle growth?

A

GH stimulates the release of IGF-1 (insulin-like growth factor), which stimulates mitosis in bone and muscle

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5
Q

What are the metabolic effects of GH?

A

Restricts cellular uptake of glucose to raise blood glucose. Stimulates lipolysis in adipose tissue to supply fatty acids for energy. Increases gluconeogenesis in the liver. Stimulates protein synthesis in muscle

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6
Q

What are the negative feedback loops for GH?

A

GH and IGF-1 provide negative feedback to the hypothalamus

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7
Q

What hormone inhibits release of GH?

A

Growth Hormone Inhibiting Hormone (GHIH), AKA somatostatin

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8
Q

What condition is caused by excess secretion of GH in childhood?

A

Gigantism

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9
Q

What are the causes of gigantism?

A

pituitary adenoma, genetic mutations

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10
Q

What are the symptoms of gigantism?

A

Abnormally rapid childhood growth of height/size. Enlarged hands, feet, facial features. Joint pain

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11
Q

What investigations may diagnose gigantism?

A

Bloods may show elevated GH or IGF-1,
Oral glucose tolerance test may fail to supress GH levels indicating adenoma.
MRI/CT may show adenoma

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12
Q

What are the non-pharmalogical treatments for gigantism?

A

surgical/radiation tumor removal

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13
Q

What are the pharmalogical treatments for gigantism?

A

Somatostatin analogue (potent inhibitor of growth hormone release)

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14
Q

What condition is caused by excess GH in adults?

A

Acromegaly

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15
Q

What are the causes of acromegaly?

A

Pituitary adenoma, ectopic GH or GHRH producing tumor

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16
Q

What are the symptoms of acromegaly?

A

enlarged hands, feet, jaw, nose, brow. Thickened skin, deepened voice, increased tooth spacing, glucose intolerance

17
Q

What investigations are used to diagnose acromegaly?

A

Bloods may show elevated GH/IGF-1, oral glucose tolerance test not supressed suggests adenoma, MRI/CT may show adenoma

18
Q

What are the non-pharmalogical treatments for acromegaly?

A

Surgery/radiation removal of adenoma

19
Q

What are the pharmacological treatments for acromegaly?

A

somatostatin analogues

20
Q

What condition is caused by a lack of growth hormone?

A

Pituitary dwarfism/growth hormone deficiency

21
Q

What are the causes of GH deficiency?

A

Congenital pituitary abnormalities, pituitary damage from trauma/tumours/radiation/infection

22
Q

What are the symptoms of GH deficiency?

A

slow growth rate, short stature, reduced muscle mass, delayed puberty, high lipids

23
Q

What are the investigations used to diagnose GH deficiency?

A

GH stimulation test will show no response to insulin, Bloods will show low GH/IGF-1, xrays will show delayed bone age

24
Q

What is the pharmacological intervention for GH deficiency?

A

Somatotrophin (growth hormone analogue) injections

25
Q

What is a glucose supression test?

A

Glucose is given to a patient and GH levels are tested to see if they are inhibited normally. If suppression does not occur then there is likely a GH secreting tumor