Osteo/ Vitamin D Flashcards
Process of de novo vitamin D synthesis
cholesterol becomes reduced, converted in the skin by UV light producing previtamin D3, previtamin is processed by the liver to 25- hydroxyvitamin D3, further hydroxylation takes place in kidney to form 1-25 dihydroxy-vitamin D (calcitrol)- which is the active form of vitamin D.
Role of Vitamin D
positive regulator of calcium homeostasis from phosphate metabolism is affected by vitamin D in a manner parallel to calcium
How does Vitamin D maintain normal concentrations of calcium and phosphate?
- facilitate absorption by the small intestine
- interact w/ PTH to enhance their mobilization from bone
- decrease excretion by kidneys
MOA of calcitrol
same as steroid and thyroid hormones
Binds to cytosolic receptors within target cells, and the receptor-hormone complex interacts w/ DNA to modify gene transcription
What happens in vitamin D deficiency?
inadequate absorption of calcium and phosphate
decrease in plasma calcium stimulates PTH secretion, which acts to restore plasma concentration
Phosphate decreases due to effect of PTH
Ergocalciferol
pure vitamin D2
given PO, IM, IV
Dihydrotachysterol
reduction product of vitamin D2
Given PO
Calcitriol
given PO & IV, important in renal failure
Hypervitaminosis
Toxicity results from excessive intake of Vitamin C or over treatment of hypoparathyroidism
Greatest risk is severe hypercalcemia
Primary Osteoporosis
2 different condition:
- type 1- loss of trabecular bone due to estrogen lack at menopause
- type 2- loss of cortical and trabecular bone in men and women due to long term modeling inefficiency, dietary inadequacy, and activation of parathyroid axis w/ age
Calcium Carbonate
inexpensive, more elemental calcium than other salt forms
can be constipating in doses upward of 2000 mg/day
Vitamin D and analogs
directly suppress parathyroid function and reduce bone turnover - possible toxicity
Estrogen
used for post menopausal women
conjugated equine estrogens with or without progestins
Raloxifene
acts as estrogen agonist in liver and bone, inactive on the uterus, anti estrogen on breast tissue
Calcitonin
inhibitor of osteoclastic bone resorption