Lecture 17 Metabolic Bone Disease Flashcards

1
Q

What is the function of osteoclasts

A

Bone resorption

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2
Q

What is the function of osteblasts

A

Bone formation

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3
Q

What is Paget’s Disease

A

Increased bone resorption followed by increased bone formation

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4
Q

What are the symptoms of Paget’s disease

A
  • Presents >40 years
  • Bone pain
  • Occasionally bone deformity, excessive heat over the Pagetic bone
  • Neurological complications such as nerve deafness
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5
Q

What are the presentation of Paget’s disease

A
  • Isolated elevation of serum alkaline phosphatase
  • Bone pain and local heat
  • Bone deformity or fracture
  • Hearing loss
  • Rarely the development of osteosarcoma in affected bone
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6
Q

What is the treatment of Paget’s Disease

A
  • No evidence to treat asymptomatic Paget’s unless in skull or in area requiring surgical intervention.
  • Do not treat based on a raised alkaline phosphatase alone
  • Intravenous Bisphosphonate therapy-One off zoledronic acid infusion
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7
Q

What are the causes of Ricketts and Osteomalacia?

A

Severe nutritional Vitamin D deficiency or calcium deficiency
Osteomalacia in the adult when the epiphyseal lines are closed

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8
Q

What is Osteomalacia

A

Softening of bones caused by impaired bone metabolism primarily due to inadequate levels of available phosphate, calcium and vitamin D

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9
Q

What are the symptoms of Osteomalacia

A

Bone pain, muscle weakness, increased falls risk

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10
Q

What is osteogenesis imperfects?

A

Genetic disorder of connectivity tissue characterised by fragile bones from mild trauma

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11
Q

Name the 4 most common Type 1 collagen of Osteogenesis Imperfects

A

Type 1: milder form
Type 2: lethal by age 1
Type 3: progressive reforming with severe bone dysplasia and poor growth
Type 4: similar to type 1 but more severe

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12
Q

Name other clinical features of defects in Osteogenesis Imperfects

A
Growth deficiency
Defective tooth formation
Hearing loss
Blue sclera
Scoliosis/Barrel Chest
Ligamentous laxity
Easy bruising
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13
Q

What is the management of Osteogenesis Imperfects

A
  • Surgical - to treat fractures
  • Medical - to prevent fracture Intravenous Bisphosphonates
  • Social-educational and social adaptions
  • Genetic - genetic counselling for parents and next generation
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14
Q

What is Osteoporosis

A

Metabolic bone disease characterised by low bone mass and micro architectural deterioration of bone tissue, leading to enhanced bone fragility and a consequent increase in fracture risk

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15
Q

Name the endocrine causes of osteoporosis

A
  • Thyrotoxicosis
  • Hyper and Hypoparathyroidim
  • Cushings
  • Hyperprolactinaemia
  • Hypopituitarism
  • Low sex hormone levels
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16
Q

Name the rheumatic cause of osteoporosis

A

RA, ankylosing spondylitis, polymyalgia rheumatica

17
Q

Name the gastroenterological causes of osteoporosis

A
  • Inflammatory diseases: UC and crohns
  • Liver diseases: PBC, CAH, Alcoholic cirrhosis, Viral cirrhosis (Hep C)
  • Malabsorption: Cystic Fibrosis, chronic pancreatitis, coeliac disease, whipples disease, short gut syndromes and ischaemic bowel
18
Q

Name some medications which cause osteoporosis

A
  • Steroids
  • PPI
  • Enzyme inducting antiepileptic medications
  • Aromatase inhibitors
  • GnRH inhibitors
  • Warfarin
19
Q

Name medications that help prevent osteoporotic fractures

A

HRT, SERM (Selective oEstrogen Receptor Modulator-Raloxifene), Bisphosphates, Denosumab

20
Q

What are the side effects of Denosumab

A
  • Allergy/rash
  • Symptomatic hypocalcaemia if given when vitamin D deplete
  • ?ONJ- Osteonecrosis of the jaw (ONJ) is a severe bone disease (osteonecrosis) that affects the jaws (the maxilla and the mandible)
  • ? Atypical femoral shaft fractures