Calcium metabolism Flashcards
Parathyroid glands
3rd and 4th branchial arch derivatives
Chief cells – principal cells
Produce PTH
Oxyphil cells – packed w/ mt
Appear at puberty and increase w/ age
Innervated by nerves off cervical sympathetic ganglia
-control blood flow
Vit D
Increase dietary Ca2+ and PO43- absorption
Regulates bone turnover
Calcitonin
Produced by parafollicular (c) cells of thyroid
Neural crest cells
Decreased bone resorption of Ca2+
PTH
Increase serum Ca2+ levels
Increase bone turnover – rev up osteoclasts – resorb bone
Osteoblasts have the PTH receptor -> RANKL which activates osteoclasts
Increased resorption of Ca2+ at DCT
Increased 1 alpha hydroxylase in kidney to activate Vit D3 -> calcitriol -> Ca2+ absorption in gut
Hypercalciemia – 90%
Primary hyperparathyroidism:
Solitary parathyroid adenoma 90-95%
Parathyroid hyperplasia 5%
Malignancy: Squamous cell cancers esp lung via PTHrP Renal cell carcinoma Breast metastasis Multiple myeloma –local osteolytic factors
Hypercalcemia – 10%
Excess Vit D ingestion
Excess calcium ingestion – milk-alkali sn – antacids
Granulomatous disease – excess vit D d/t sarcoid or TB
Increased bone turnover – hyperthyroidism, vit A intoxication, immobilization
Thizide diuretics -> decreased renal excretion of calcium
PTH regulation
Ca2+ suppresses chief cell secretion of PTH
Low Ca2+ stimulates secretion
Mg2+ inhibits PTH secretion
-slightl low Mg2+ cuases PTH secretion
prolonged, severely low Mg2+ causes decreased PTH secretion
low Mg2+: diruetics, etOH, diarrhea, aminoglycosides
S/S of primary hyperthyroidism
Stones: Renal stones MC Nephrocalcinosis Polyuria/polydipsia Uremia
Bones:
Osteoporosis
Osteitis fibrosa cystica
OA
Abdominal groans: Constipation N/V Peptic ulcers (elevated calcium increases gastrin) Pancreatitis
Psychiatric overtones: Lethargy and fatigue Depression Psychosis Confusion, stupor, coma
Other: Proximal m. weakness Keratitis and conjunctivitis HTN Itching
Classic signs of hypocalcemia
Chvostek and Trousseau
Hypoparathyroidism
Parathyroidectomy from damage during thyroidectomy
Autoimmune destruction of parathyroids
Pseudohypoparathyroidsim – kidney tubules unresponsive to PTH
-GNAS1 mutation
DiGeorge Sn at birth
Vit D deficiency
Nutritional deficiency and paucity of sunlight
Chronic renal failure
Acute pancreatitis in hypocalcemia
Ca2+ precipitate into abdomen combine w/ fatty acids -> soaps
Type 1A – Albright hereditary osteodystrophy
AD
GNAS mutation – codes PTH g protein receptor at kidney
Short stature
Obesity
Underdevelopment of 4th and 5th digits
Severe: osteitis fibrosa cystica
Osteitis fibrosa cystica
Subperiosteal bone absorption of middle phalanges radial aspect
Tapering of distal clavicles
Salt and pepper appearance of skull
Bone cysts
Brown tumors of long bone
Secondary hyperparathyroidism
Chronic hypocalcemia
- chronic renal dz
- renal osteodystrophy
labs: elevated BUN/Cr, high phosphate
severe Vit D deficiency – rickets low Ca2+ high or low phosphate labs: high PTH, low Ca2+, low or nl phosphate low vit D