Disorders of the endocrine pancreas: Howell Flashcards
Type 1 DM incidence
-familial predisposition (HLA-D)
-sometimes after infection: cox sackie, mumps, rubella
type 1 DM onset
usually in the first 2 decades of life
-first peak: 5-7 years old
2nd peak: puberty `
type 1 dm etiology
autoimmune destruction of beta cells
-antibodies against those cells found in 80% of pts
twin to twin concordance in type 1 DM
Less than 50% of the time the second time has the condition
sx of type 1 DM
-Polydipsia, polyuria, dehydration, polyphagia, wt loss, fatigue, abdominal pain, nausea, glycosuria possible , metabolic acidosis
dx of type 1 DM
-measure fasting blood glucose:
greater than 126 mg.dl after fasting on 2 occasions
-glucose is usually 300
- Glycosylated hb (HBA1C):
- Good: less than 6%, bad 9-12%
incidence of type II DM
adult onset, usually
-10X more common than type 1
twin to twin concordance in type 2 dm
greater than 90%, meaning that this is much more familial than type 1
sx of type 2 DM
-Mostly Asx
-women may develop recurrent vaginal candidiasis
average time to dx type 2 DM
usually 5-7 year lapse occurs before dx is confirmed
clinical presentation of hyperosmolar hyperglycemic non-ketonic syndrome
osmotic duresis leads to dehydration
what leads to hyperosmolar hyperglycemic non-ketonic syndrome
type 2 DM
DIagnostic for hyperosmolar hyperglycemic nonketotic syndrome
-glucose over 1,000 mg/dl
lack of significant ketosism
Mortality rate of hyperosmolar hyperglycemic non-ketonic syndrome
50% mortality rate
Causes of DKA
-Complication of type 1 dm
- absolute insulin deficiency
-precipitated by stress, trauma, insulin withholding