Parathyroid Flashcards

1
Q

Where is calcium stored?

A

Mitochondria and ER

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2
Q

What is “pump-leak” transport?

A

Ca2+ leaks into cytosolic compartment and is pumped into storage sites in organelles

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3
Q

How is calcium stored in serum?

A
  • Ionized (50%)
  • Protein-bound (40%) - 9/10 of this is bound to albumin, rest to globulins
  • Complexed to serum constituents (10%) - like citrate and phosphate
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4
Q

Why are patients with acute respiratory alkalosis prone to seizures?

A

Low ionized calcium in ECF (increased binding to proteins) and therefore increased permeability to sodium ions

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5
Q

Normal calcium range in plasma:

A

8.5-10 mg/dL

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6
Q

Where does Vitamin D3 synthesis occur?

A

Keratinocytes in skin (stimulated by PTH)

The active metabolite is 1,25-dihydroxy-D

Skin/diet –> liver –> kidney –> bone/intestine

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7
Q

What is the point of regulation in Vitamin D synthesis?

A

1alpha-hydroxylase (mitochondrial P450 enzyme in kidney)

PTH stimulates this

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8
Q

Order of best calcium absorption (and phosphate)?

A

Duodenum > jejunum > ileum

Dependent on vitamin D

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9
Q

What type of activation regulates PTH?

A

G-protein (phospholipase C and IP3); decrease in cAMP

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10
Q

Overall action of PTH:

A

Increase plasma Ca2+, decrease plasma phosphate

  • bone resorption
  • kidney reabsorption (distal tubule)
  • inhibit phosphate reabsorption
  • stimulate 1,25-(OH)2-D synthesis (Vitamin D activity)
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11
Q

Normal plasma phosphate?

A

3-4.5 mg/dL

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12
Q

Parathyroid chief cells have a…

A

Calcium sensing receptor (CaSR)

Regulate ionized calcium via PTH secretion (low levels will stimulate PTH)

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13
Q

What produces calcitonin?

A

Parafollicular cells of thyroid (NEURAL CREST DERIVED - rest of thyroid is endoderm)

  • Inhibit osteoclast resorption and promote renal excretion of calcium
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14
Q

Calcitonin acts via ______

A

Increased cAMP concentrations in bone and kidney (inhibit osteoclast; also inhibit urinary excretion of calcium/phosphate)

  • Probably not necessary for survival, but can be used to treat hypercalcemia
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15
Q

List some bone formation stimulants:

A
  • GH
  • Insulin-like GF
  • Insulin
  • Estrogen
  • Androgens
  • Vitamin D
  • Calcitonin

** Inhibitor is cortisol

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16
Q

Bone reabsorption stimulators:

A
  • PTH
  • Cortisol
  • Thyroid hormone
  • Prostaglandins
  • IL-1, IL-6, TNF-alpha and beta
17
Q

Bone reabsorption inhibitors:

A
  • Estrogen, androgen
  • Calcitonin
  • gamma-interferon
  • NO
  • Transforming GF beta
18
Q

What is a cause of Pseudohypoparathyroidism?

A

End organ PTH resistance (PTH high, but no response, so calcium is low)

  • Classic sign is “knuckle knuckle dimple dimple” on metacarpals
  • Short, obese, variable mental retardation, Elfin faces, enamel hypoplasia
19
Q

What is an important cause of hypercalcemia of malignancy?

A

Parathyroid hormone related protein (PTHrP)

  • Can activate PTH receptor
  • May be important in lactation
  • Associated with a few cancers (can be secreted by them)
20
Q

What does vitamin D deficiency lead to in children?

A

Rickets (prior to closure of growth plates)

Sufficient osteoid, poor mineralization
- Osteomalacia occurs at any age

21
Q

Consequences of primary hyperparathyroidism? Treatment?

Caused by adenoma, hyperplasia, carcinoma

A
  • Nephrolithiasis / nephrocalcinosis
  • CNS disturbances (depression, seizures)
  • Constipation, peptic ulcer disease, acute pancreatitis
  • Osteitis fibrosa cystica

Surgical excision or Cinacalcet (Sensipar)

22
Q

Primary hyperparathyroidism labs…

PTH, calcium, phosphate, urinary cyclic AMP, alkaline phosphatase

A
Increased PTH
Increased calcium
Decreased phosphate
Increased urinary cyclic AMP
Increased alkaline phosphatase
23
Q

What is secondary hyperparathyroidism?

A

Excess PTH in response to problem outside of glands - chronic renal failure or after gastric bypass surgery

24
Q

Describe the process of secondary hyperparathyroidism in RENAL INSUFFICIENCY

A
  • Decreased kidney phosphate excretion
  • Increased phosphate binds calcium
  • PTH released (free calcium lower)
  • More bone resorption
25
Q

Labs for secondary hyperparathyroidism…

A

Inc PTH
Dec serum calcium
Inc phosphate
Inc alkaline phosphatase

26
Q

DiGeorge syndrome has hypoparathyroidism with hypocalcemia

A

Don’t forget, now!

27
Q

Trosseau’s sign? (in hypoparathyroidism)

A

indication of latent tetany in which carpal spasm occurs when the upper arm is compressed

28
Q

Chvostek’s sign? (in hypoparathyroidism)

A

twitching of the facial muscles in response to tapping over the area of the facial nerve

29
Q

Hypoparathyroidism treatment?

A

Calcitriol and calcium supplements / NatPara

30
Q

Causes of Rickets / Osteomalacia:

A
  • Nutritional deficiency (Vitamin D, calcium chelators, antacids)
  • GI absorption defects
  • Renal tubular defects / osteodystrophy
31
Q

What is Paget’s Disease?

A

Disease of bone remodeling; accelerated resorption and formation

  • Increased vascularity and fibrosis
  • Cause unknown (virus?)
32
Q

What is osteogenesis imperfecta?

A

Brittle Bone Disease; heritable disorder of connective tissue

  • Bone fragility, tendency to fracture
  • BLUE SCLERA (rare)