Calcium Metabolism 1 Flashcards

1
Q

Function of Calcium?

A

Calcium causes depolarisation and is therefore essential for

  • > Nervous activity
  • > Muscle Control
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2
Q

Describe the flow of Calcium through the body?

A

Calcium enters through the gut.

Calcium is excreted in the urine.

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3
Q

Describe how Calcium is stored in the body?

A

99% of Calcium is stored in the skeleton (Calcium Reservoir) - along with Phosphate and Magnesium.

The remaining 1% is exists in the Serum in 3 Forms - Total Serum Calcium is 2.2-2.6mmol/L

i) Free ‘ionised’, 50% BIOLOGICALLY ACTIVE
ii) Protein bound, 40% - Albumin
iii) Complexes, 10% i.e. Citrate*/Phosphate

*Blood transfusions with Citrate present can chelate the bloods calcium and cause a Hypocalcaemia

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4
Q

What is Corrected Calcium?

A

Corrected Calcium = Measured total Ca + (0.02*40-Albumin)

-> Normal Albumin is 40g/L, and each g/L carries 0.02mmol/L

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5
Q

What level of serum calcium will be there in a patient with chronic liver disease and why?

A
  • > Many patients have Hypoalbuminaemia as a result of Chronic Liver Disease etc.
  • > Their total serum calcium will therefore be lower, but the amount of Biologically Active, Free Ionised Calcium will be normal
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6
Q

What is the most reliable way to measure Serum Free Calcium?

A

Arterial Blood Gas

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7
Q

How does pH affect Calcium?

A
  • > H+ and Ca+ both compete for Albumin
  • > In Alkalosis, H+ leaves the Albumin and more Ca+ is taken up therefore reducing the amount of Serum Free Biologically Active Ca+ (Hypocalcaemic)
  • > In Acidosis, H+ is taken up the Albumin, displacing Ca+ therefore the patient will show symptoms of Hypercalcaemia
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8
Q

What are the 2 key hormones in calcium homeostasis?`

A

Vitamin D and PTH

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9
Q

What is Vitamin D2 – Ergocalciferol?

A

The plant version of Vitamin D3

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10
Q

How can 1-alpha hydroxylase be aberrantly produced?

A

Physiologically – Kidney (under PTH)

Pathologically – Lung (Sarcoidosis

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11
Q

What does Osteoblast activity cause?

A

Raised ALP

  • Post Fracture
  • Certain Bone Diseases
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12
Q

What is Osteoporosis?

A

Thinning of bones due to loss of bone density (normal mineralisation and structure)
-> Loss of bone mass
Physiological part of ageing i.e. loss of bone mass, but in Osteoporosis it occurs quicker

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13
Q

Risk factors for osteoporosis?

A
  • > Failure to attain peak bone mass in childhood
  • > Early menopause (Earlier increased deceleration in bone mass)
  • > Age
  • > Lifestyle; Alcohol, Smoking, Poor Diet
  • > Endocrine Causes – Thyrotoxicosis, Hyperprolactinaemia, Cushings
  • > Iatrogenic - Steroids
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14
Q

What is usually the first presenting complaint of someone with osteoporosis?

A

-> Fracture is usually first symptom (Neck of femur, vertebral, Wrist i.e. Colle’s)

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15
Q

Investigations for osteoporosis?

A
  • > Biochemistry, Ca and Phosphate normal
  • > DEXA Scan
DEXA - Dual Energy X Ray Absorptiometry 
T - Score >-1 Normal
T - Score [-1 to -2.5] Ostepaenia
T - Score < -2.5 Osteoporosis
NB Raised Bone Density - Osteosclerosis

T Score – S.D. from mean of young healthy population (useful for #risk)
Z Score – S.D from mean of age-matched control (useful to identify accelerated bone loss)

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16
Q

Management of osteoporosis

A

Conservative

  • > Weight bearing exercises
  • > Stop Smoking
  • > Reduce alcohol

Medical

  • > Vit D + Calcium
  • > Bisphosphonates i.e. Alendronate -> Inhibits Osteoclast mediated bone-resorption
  • > Teriparatide (PTH derivative)
  • > Strontium Ranelate -> Stimulates Osteoblasts and Inhibits Osteoclasts
  • > Raloxifene // HRT -> Oestrogen like effects
17
Q

What is osteomalacia?

A

Metabolic bone disorder caused by Vitamin D Deficiency

-> Abnormal decalcified bone [Demineralised]

18
Q

Risk factors and epidemiology of osteomalacia

A

Epidemiology
Over 50% of adults have a Vitamin D Deficiency
-> 16% are severely deficient during winter and spring

Risk Factors

  • > Lack of sunlight
  • > Dark Skin
  • > Dietary / Gut Malabsorption
  • > Renal Failure
  • > Older AntiConvulsants i.e. Phenytoin induce Vitamin D breakdown
  • > Chappati’s, Phytic Acid chelates Vitamin D
19
Q

What are the features of osteomalacia?

A
  • > Bone and muscle pain
  • > Increased Fracture Risk
  • > LOW Ca, High PTH, LOW Phosphate, Raised ALP (Osteoblast function)
  • > Looser Zones, Pseudofractures i.e. fracture secondary to insufficiency of bone
20
Q

What is osteomalacia known as in childhood? and what are some features/

A

In Childhood - Osteomalacia is known as Rickets

  • > bowed legs
  • > costochondral swellings
  • > widened epiphyses at the wrists
  • > myopathy
21
Q

What is Paget’s disease?

A

Focal disorder of bone remodelling

-> Unknown aetiology i.e. may be due to a virus

22
Q

What are the main presenting symptoms of paget’s disease?

A

-> Pain, warmth, deformity
-> Nerve compression, malignancy, and cardiac failure
Typically Affects;
-> Pelvis, Femur, Skull, Tibia

23
Q

What are the investigations for paget’s?

A
  • > Bloods; Raised ALP

- > Radioactive bisphosphonate injection – Technetium Bisphosphonate Scan.

24
Q

What is the treatment for paget’s?

A

-> Treated with Bisphosphonates i.e. Alendronate

25
Q

What is Parathyroid Bone Disease?

A

o.e. Osteitis Fibrosa

Increased PTH, causing Bone Resorption; Loss of Cortical Bone

26
Q

What is Renal Osteodystrophy?

A

Aluminium Toxicity from Dialysis inhibits 1alpha Hydroxylase

-> Low Calcium, Secondary increased PTH.

27
Q

What is the normal total serum calcium?

A

2.2 - 2.6 mmol/L

28
Q

Why does Paget’s disease sometimes present as malignancy?

A

Fewer than 5% of patients with Paget’s disease will undergo malignant transformation to a sarcoma. The risk of a patient developing a sarcoma is greater the more extensive the Paget’s disease and the longer the patient has been affected.

29
Q

Why does Paget’s disease sometimes present with cardiac failure?

A

Paget’s disease causes increased blood flow to the bones, and sometimes it is difficult for the heart to keep up with the demand for increased blood flow. This can lead to heart failure.