Disorders of GH (Paulson, Exam 3) Flashcards
What is the most common cause of GH deficiency in adults?
Pituitary tumor
If you are concerned about a GH deficiency, what is the 1st lab test you should order?
IGF-1
You are concerned your pt might have GH deficiency, so you decide to order an IGF-1 test and it comes back as low. Is this sufficient for your diagnosis of GH deficiency?
Nope. If IGF-1 comes back low, you need to confirm with 2 provocative stimulation tests that there’s an inadequate rise of GH. Examples of stimuli include insulin, deep sleep, glucagon, L-DOPA, vigorous exercise, and arginine.
You could also get an MRI of the hypothalamic-pituitary region.
How do you treat children with GH deficiency?
- GH SQ daily
- Start ASAP for best results
- Adjust based upon IGF-1 levels and growth response
- S/E: HA most common
- If tumor: cut that sh*t out!
What are the risks involved with untreated GH deficiency?
- Increased mortality
- Decreased lean body mass
- Decreased bone density
- Increased fractures
- Increased HTN
- Increased HLD
What’s the difference between gigantism and acromegaly?
- Gigantism: occurs in children before closure of epiphyses, so there is excess growth of long bones
- Acromegaly: occurs in adults after closure of epiphyses, so there isn’t long bone involvement → hands, feet, jaw, internal organs affected
*Both are cause by excessive GH
What is the most common cause of GH excess?
Pituitary adenoma
People with acromegaly are at increased risk of…..
HTN, DM, cardiomegaly, and CHF
Mixed cell tumors in the pituitary can often secrete __________ in addition to excess GH.
Mixed cell tumors in the pituitary can often secrete prolactin in addition to excess GH.
Brosef Brad comes into your office and you immediately notice his jaw is huge! He tells you his wedding ring no longer fits and he had to buy 3 new pairs of golf shoes over the past couple years because his feet started growing. Being the genius PA that you are, you immediately think, ah yes, acromegaly! How do you go about confirming BB’s suspected diagnosis?
- 1st: check IGF-1
- Next (fasting for 8 hrs):
- Serum IGF-1, prolactin, glucose, LFTs, BUN/Cr, TSH
- 1 hour glucose tolerance test (gold standard)
- Shows failure of GH to suppress
- Finally: pituitary MRI to identify lesion
The results came back on Brosef Brad and you were right, he has acromegaly! How are you going to treat him?
- Transsphenoidal resection if possible
-
Somatostatin analogs: octreotide or lanreotide
- can shrink the pituitary adenoma
- used if surgery is unsuccessful
-
Dopamine agonists: cabergoline or bromocriptine (you tx broseph brad with bromocriptine because he’s a bro, duh)
- May inhibit GH secretion
-
Pegvisomant:
- GH receptor antagonist
- Blocks production of IGF-1
Brosef Brad asks you what the prognosis is for his new diagnosis of acromegaly. What do you tell the poor guy?
- Lifespan decreased 10-15 yrs
- Mortality rate 2-3x higher than general population
- most due to CV disease
- also increased cancer
- BB needs to go see endocrinology