Endocrinology Flashcards
Tests for DM-I
C-peptide: endogenous insulin production (will be very low in type 1)
GAD antibodies: attack islet cells (will be elevated in type 1)
What lab test is important before starting metformin
Creatinine clearance
can cause lactic acidosis if CrCl<30
be cautious in patients with Cr>1.4
MOA of sulfonylureas
think milk insulin from pancreas
works better for newly dx DM-II in younger pts
glipizide
glyburide
Metformin MOA
dec glucose production by liver
sensitizes insulin to use glucose
Thiazolidinediones MOA
helps muscle utilize glucose
Avandia (rosiglitazone)
Actos (pioglitazone)
SGLT-2 MOA
pee out glucose (NOT kidney protective) Steglatro (ertugliflozin) Invokana (canagliflozin) Jardiance (empagliflozin) Farxiga (dapagliflozin)
GLP-1 MOA
activated glucagon-like-peptide-1 (GLP-1) receptor: -increasing insulin secretion -decreasing glucagon secretion -delays gastric emptying decrease appetite cardio and nephro protective Bydureon (exenatide) Byetta (exenatide) Lyxumia (lixisenatide) Trulicity (dulaglutide) Victoza (liraglutide) Ozempic (semaglutide) Rybelsus (semaglutide)
Xigduo generic
dapagliflozin/metformin
SGLT2
Soliqua generic
lixisenatide/insulin glargine
GLP-1
Xultophy generic
liraglutide and insulin degludec
GLP-1
Diabetes Mellitus
Path:
Pt:
Dx:
Path: Abnormal carbohydrate metabolism
Pt:polydipsia, polyphagia, polyuria, weight loss, blurry vision
Dx:
- Symptoms + random plasma glucose >/= 200
- Fasting plasma glucose >/= 126 on 2 separate occasions
- Plasma glucose >200 2 hours after a 75g glucose load during oral glucose tolerance test
- HgA1c >/= 6.5% (adults only)
Which class of antidiabetic drug should be avoided in patients with a family or personal history of medullary thyroid carcinoma?
GLP-1 (-tide)
type 2 non-insulin dependent diabetes mellitus presents to the clinic with recurrent vaginal yeast infections. Which of the following medications is most likely contributing to her chief complaint?
SGLT-2 (-gliflozin)
Cushing Disease Path: Pt: Dx: Tx:
Path: ACTH-secreting pituitary tumor
Pt: amenorrhea, central obesity, depressive symptoms, and easy bruising
bitemporal hemianopsia (pituitary adenoma)
PE: purple striae, moon face (facial adiposity), buffalo hump (increased adipose tissue in the neck and upper back), and hypertension
Dx: 24 hr urine cortisol and testing ACTH levels
Tx: transsphenoidal removal
Adrenal insufficiency Path: Pt: Dx: Tx:
Path:
Primary (Addison’s disease)- destruction of adrenal gland-> lack of cortisol, aldosterone, and sex hormones
Secondary- deficient ACTH from pituitary-> lack of cortisol (aldosterone & RASS intact)
-Glucocorticoid cessation- esp w/ prolonged use and abrupt cessation
-Hypopituitarism (rare)
Pt:
Low cortisol:
weakness, myalgias, fatigue, weight/appetite loss, N/V/D, abdominal pain, headaches, sweats, irregular periods
Mild hyponatremia, salt craving, hypotension, hypoglycemia
Primary only (dec aldo and sex hormones, inc ACTH)
-Hyperpigmentation-> inc ATCH stimulation of melanocytes
-Dec aldo: orthostatic hypotension, hyponatremia, hyperkalemia, non-anion gap acidosis, hypoglycemia, dec BUN
-Dec sex hormones: dec libido, amenorrhea, loss of axillary and public hair
Dx:
-Cosyntropin (ACTH) stimulation test- screening for adrenal insufficiency, little/no inc cortisol-> adrenal insufficiency
-CRH stimulation test- differentiates etiologies
Primary/Addisons (Adrenal)- inc ACTH levels and dec cortisol
Secondary (pituitary)- dec ACTH and dec cortisol (pituitary can’t produce enough ACTH)
Tx:
Hormone replacement
Addisons-> glucocorticoids + mineralocorticoids
Synthetic glucocorticoids: hydrocortisone (1st line), prednisone, dexamethasone
Synthetic mineralocorticoid: fludrocortisone (aldosterone)
Secondary-> only glucocorticoids