Calcium metabolism Flashcards

1
Q

Parathyroid glands

A

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

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2
Q

Vit D

A

Increase dietary Ca2+ and PO43- absorption

Regulates bone turnover

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3
Q

Calcitonin

A

Produced by parafollicular (c) cells of thyroid
Neural crest cells

Decreased bone resorption of Ca2+

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4
Q

PTH

A

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

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5
Q

Hypercalciemia – 90%

A

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
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6
Q

Hypercalcemia – 10%

A

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

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7
Q

PTH regulation

A

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

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8
Q

S/S of primary hyperthyroidism

A
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
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9
Q

Classic signs of hypocalcemia

A

Chvostek and Trousseau

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10
Q

Hypoparathyroidism

A

Parathyroidectomy from damage during thyroidectomy
Autoimmune destruction of parathyroids
Pseudohypoparathyroidsim – kidney tubules unresponsive to PTH
-GNAS1 mutation

DiGeorge Sn at birth

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11
Q

Vit D deficiency

A

Nutritional deficiency and paucity of sunlight

Chronic renal failure

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12
Q

Acute pancreatitis in hypocalcemia

A

Ca2+ precipitate into abdomen combine w/ fatty acids -> soaps

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13
Q

Type 1A – Albright hereditary osteodystrophy

A

AD
GNAS mutation – codes PTH g protein receptor at kidney

Short stature
Obesity
Underdevelopment of 4th and 5th digits

Severe: osteitis fibrosa cystica

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14
Q

Osteitis fibrosa cystica

A

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

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15
Q

Secondary hyperparathyroidism

A

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
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16
Q

Tertiary hyperparathyroidism

A

Long standing secondary hyperparathyroidism – chronic renal dz
Parathyroid hyperplasia
Autonomously functioning parathyroid

High calcium but keep making PTH anyway

17
Q

Calcium and phosphate levels in primary, secondary and tertiary hyperparathyroidism

A

Primary: high calcium, low phosphate
Secondary: low calcium, high phosphate
Tertiary: high calcium