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Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh
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Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Jan 15, 2016

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Page 1: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Bone Metabolism

CM RobinsonSenior Lecturer

Royal Infirmary of Edinburgh

Page 2: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Outline

• Normal bone structure

• Normal calcium/phosphate metabolism

• Presentation and investigation of bone metabolism disorders

• Common disorders of bone metabolism

Page 3: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Normal Bone Structure• What are the normal types of bone

in the mature skeleton?• Lamellar

– Cortical– Cancellous

• Woven– Immature– Healing– Pathological

Page 4: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

• What is the composition of bone?• The matrix

– 40% organic • Type 1 collagen (tensile strength)• Proteoglycans (compressive strength)• Osteocalcin/Osteonectin• Growth factors/Cytokines/Osteoid

– 60% inorganic• Calcium hydroxyapatite

• The cells – osteo-clast/blast/cyte/progenitor

Page 5: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Bone structure

• Structure of lamellar bone?

• Structure of woven bone?

Page 6: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Bone turnover

• How does normal bone grow……..– In length?– In width?

• How does normal bone remodel?

• How does bone heal?

Page 7: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Bone turnover

• What happens to bone……….– in youth?– aged 20-40’s?– aged 40+?– aged over 70?

Page 8: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Calcium metabolism

• What is the recommended daily intake?

• 1000mg• What is the plasma concentration?• 2.2-2.6mmol/L• How is calcium excreted?• Kidneys - 2.5-10mmol/24 hrs• How are calcium levels regulated?• PTH and vitamin D (+others)

Page 9: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Phosphate metabolism

• Normal plasma concentration?• 0.9-1.3 mmol/L• Absorption and excretion?• Gut and kidneys• Regulation• Not as closely regulated as calcium

but PTH most important

Page 10: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

PTH• Physiological role• Production related to plasma

calcium levels• Control of calcium levels

– target organs• bone - increased Ca/PO4 release• kidneys

– increased reabsorption of Ca– increased excretion of PO4

• gut - indirect increase in calcium reabs by stimulting activation of vitamin D metabolism

Page 11: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Calcitonin

• Physiological role

• Levels increased when serum Ca >2.25mmol/L

• Target organs– Bone - suppresses resorption– Kidney - increases excretion

Page 12: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Vitamin D (cholecalciferol)

• Sources of vit D• Diet• u.v. light on precursors in skin• Normal daily requirement• 400IU/day• Target organs

– bone - increased Ca release– gut - increased Ca absorption

Page 13: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

• Normal metabolism

Vit D

25-HCC (Liver)

Ca/PTH 1,25-DHCC 24,25-DHCC (Kidney) (Kidney)

Page 14: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Factors affecting bone turnover

• Other hormones• Oestrogen

– gut - increased absorption– bone - decreased re-absorption

• Glucocorticoids– gut - decrease absorption– bone - increased re-absorption/decreased

formation• Thyroxine

– stimulates formation/resorption– net resorption

Page 15: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Factors affecting bone turnover

• Local factors• I-LGF 1 (somatomedin C)

– increased osteoblast prolifn• TGF

– increased osteoblast activity• IL-1/OAF

– increased osteoclast activity (myeloma)• PG’s

– increased bone turnover (#’s/inflammn) • BMP

– bone formation

Page 16: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Factors affecting bone turnover

• Other factors• Local stresses• Electrical stimuln• Environmental

– temp– oxygen levels– acid/base balance

Page 17: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Bone metabolic disorders• Presentation?• Skeletal abnormality

– osteopenia - osteomalacia/osteoporosis– osteitis fibrosa cystica - replacement of bone

with fibrous tissue usually due to PTH excess• Hypercalcaemia• Underlying hormonal disorder• When to investigate?

– Under 50– repeated fractures or deformity– systemic features or signs of hormonal

disorder

Page 18: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Bone metabolic disorders• Assessment• History

– duration of sx– drug rx– causal associations

• Examn• X-rays - plain and specialist (cort

index/Singh index/DEXA)• Biochemical tests• Bone biopsy

Page 19: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Biochemical tests• Which investigations?• Ca/PO4 - plasma/excretion• Alkaline phosphatase/osteocalcin

(o’blast activity)• PTH• vit D uptake • hydroxyproline excretion

Page 20: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Osteoporosis

• Definition?• Decrease in bone mass per unit

volume

• Fragility (perfn of trabecular plates)

• Primary (post-menopausal/senile) Secondary

Page 21: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Primary osteoporosis

• Post-menopausal• Aetiology?• Menopausal loss 3% vs 0.3% previously• Loss of oestrogen - incr osteoclastic activity• Risk factors?• Race• Heredity• Build• Early menopause/hysterectomy• Smoking/alcohol/drug abuse• ?Calcium intake

Page 22: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Primary osteoporosis

• Post-menopausal

• Clinical features?

• Prevention and treatment?• General health measures/diet• HRT• Bisphosphonates• Calcium• Vitamin D

Page 23: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Primary osteoporosis• Senile• Aetiology?• 7-8th decade steady loss of 0.5%• physiological manifestation of aging• Risk factors?• Prolonged uncorrected post-menopausal loss• chronic illness• urinary insuff• muscle atrophy• diet def/lack of exposure to sun/mild

osteomalacia

Page 24: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Primary osteoporosis• Senile• Clinical features?• as for post-menopausal• Treatment?• general health measures• treat fractures• as for post-menopausal (HRT not

acceptable)

Page 25: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Secondary Osteoporosis• Aetiology?• Nutrition - scurvy, malnutr,malabs• Endocrine - Hyper PTH, Cush, Gonad, Thyroid• Drug induced - steroid, alcohol, smoking, phenytoin• Malignancy - ca’tosis, myeloma (o’clasts), leukaemia• Chronic disease - RA, AS, TB, CRF• Idiopathic - juvenile, post-climacteric• Genetic -OI• Clin features?• Investigation?• Treatment?

Page 26: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Osteomalacia• Definition?• Rickets - growth plates affected, children• Osteomalacia - incomplete mineralisation

of osteoid, adults• Types - vit D def, vit-D resist (fam

hypophos)

• Aetiology?• Decr intake/production(sun/diet/malabs)• Decreased processing (liver/kidney)• Increased excretion (kidney)

Page 27: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Osteomalacia

• Clinical features?• In child• In adult

• Investign• Ca/PO4 decr, alk ph incr, Ca excr

decr• Ca x PO4 <2.4• Bone biopsy

Page 28: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Osteomalacia

• Types• Vitamin D deficient• Hypophosphataemic

– growth decr +++ and severe deformity with wide epiphyses

– x-linked dominant– decreased tubular reabs of PO4– Ca normal but low PO4– Rx PO4 and vit D

Page 29: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Osteomalacia vs osteoporosis

Osteomal Osteopor Ageing fem, #, decreased bone densIll Not illGeneral ache Asympt till #Weak muscles normalLoosers nilAlk ph incr normalPO4 decr normalCa x PO4 <2.4 Ca x PO4 >2.4

Page 30: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Hyperparathyroidism

• Excessive PTH• Due to prim (adenoma), sec

(hypocalc), tert (second hyperact -> autonomous overact)

• Osteitis due to fibr repl of bone• Clin feat - hypercalc• Invest - Calc incr, PO4 decr, incr PTH• Rx surg

Page 31: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Renal osteodystrophy

• Combination of• osteomalacia• secondary PTH incr• osteoporosis/sclerosis• CF - renal disorder, depends on

predom pathology• Rx - vit D or 1,25-DHCC• renal disorder correction

Page 32: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Pagets

• Bone enlargement and thickening• Incr o-clast/blast activity -> increased tunrover• Aet - unknown but racial diff ?viral• CF - M=F, >50, ache but not severe unless

fracture or tumour• Inv - x-ray app characteristic, alk ph is

increased and increased hydroxyproline in urine

• Rx - bisphos, calcitonin

Page 33: Bone Metabolism CM Robinson Senior Lecturer Royal Infirmary of Edinburgh.

Endocrine disorders

• Cushings

• Hypopituitarism - GH def - prop dwarf or

Frohlich adiposogenital syndrome

• Hyperpituitarism - gigantism or acromegaly

• Hypothyroidism - cretinism or myxoedema

• Hyperthyroidism - o’porosis

• Pregnancy - backache, CTS, rheumatoid

improves SLE gets worse