5 - Ageing and Metabolic Bone Conditions Flashcards

1
Q

What percent of bone mass is usually lost in a year from the age of 40+?

A

0.7% a year

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2
Q

After menopause, what is the percentage of bone mass loss in women?

A

2-9% a year

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3
Q

What is a T score

A

number of standard deviations from the mean young (30 yr) same gender and ethnicity

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4
Q

What is the Z score

A

number of standard deviations from mean aged, same gender and ethnicity

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5
Q

What is osteopenia

A

A precursor to osteoporosis

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6
Q

Where do you usually measure for osteoporosis

A

Neck of femur

Vertebral bodies

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7
Q

What does the DEXA scan measure

A

Bone density

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8
Q

Osteopenia T score

A

-1 to -2.4

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9
Q

Osteoporosis T score

A

below -2.5

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10
Q

What does DEXA stand for

A

Dual Energy X-ray Absorptiometry

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11
Q

Prevalence of osteoporosis

A

2% at 50 years

Greater than 25% at 80 years

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12
Q

What bones are more susceptible to osteoporotic bone loss

A

Neck of femur
Vertebral bodies
High proportion of trabecular bone

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13
Q

What treatments are given for osteoporosis?

A
Calcium supplements
Vitamin D supplements
HRT
Selective oestrogen receptor modulator
Biphosphonates 
Denosumab
Teriparatide
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14
Q

What is the minimum time HRT is given for

A

5 years

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15
Q

Example of a Selective Oestrogen Receptor Modulator

A

Raloxifene

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16
Q

What is the MoA of biphosphonates

A
Inhibitors of bone reabsorption
Inhibit osteoclast activity
Promote osteoclast apoptosis
Increase OPG production
Decrease RANKL expression
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17
Q

Complications of biphosphonates

A

Giant osteoclasts
Osteoncrosis of the jaw
Atypical fractures

18
Q

What is teriparatide

A

A recombinant PTH

Will activate osteoblasts without activating osteoclasts

19
Q

What is Denosumab + how often does it need to be given

A

Monoclonal antibody which binds to RANKL and prevents it’s signalling
therefore inhibits the formation of osteoclasts

Needs to be given every 6 months via subcutaneous injection

20
Q

What is osteomalacia

A

Insufficient calcium and phosphate to mineralise bone osteoid
The bones are softer and more liable to bend or fracture

21
Q

Cause of osteomalacia

A

Lack of vitamin D

22
Q

What is rickets and why is it more deforming

A

Childhood osteomalacia

More deforming as in children the epiphyseal growth plate is open

23
Q

What would lab results show in osteomalacia

A

Low serum calcium and phosphorus

High alkaline phosphatase

24
Q

Why is alkaline phosphatase high in osteomalacia

A

Due to high osteoblast activity

25
What would an X-ray look like in someone with osteomalacia
Pseudofractures = unmineralised sections of bone | Areas of unmineralised bone
26
What is the normal level of unmineralised osteoid?
<20%
27
What colour is unmineralised and mineralised osteoid on biopsy
Orange - unmineralised (up to 100% in osteomalacia) | Green - mineralised
28
How do you treat osteomalacia
Vitamin D supplements Increase calcium in diet Sun or UV exposure
29
Calcium containing foods
Milk Bread Beans Green leafy vegetables
30
What is Pagets disease also called
Osteitis Deformans
31
Percentage population with pagets
3% >50 y/o
32
What are the 3 stages of Pagets disease
1) Increased rate of bone resorption (large no of giant osteoclasts) 2) Compensatory phase (Increased bone formation as woven bone, accelerated deposition in a disorganised manner) 3) Burn out phase (Sclerotic) - Bone hypercellularity may deminish leaving dense pagetic bone Hypervascular bone marrow Irregular thickened trabeculae Bone marrow replaced by fibrovascular CT
33
Which bones are most commonly affected in osteomalacia?
``` Pelvis Femur Vertebrae Skull Tibia ```
34
What is osteosarcoma?
A rare complication of pagets disease where a cancer forms
35
Where are osteosarcomas usually
Long bone | Near the knee
36
How do you treat osteosarcoma
Remove part of the bone | Limb amputation
37
How do you treat osteomalacia
Biphosphates Calcium and vitamin D supplements Pain management Surgery
38
How long does an osteomalacia patient have to take biphosphates
Oral - 2-6 months | IV single infusion to 3 infusions
39
What is sclerostosis also known as
Aka van buchem syndrome
40
Genetics of sclerostosis
Autosomal recessive
41
Features of sclerostosis
Endosteal hyperostosis Resistance to fracture Excessive height
42
Pathophysiology of sclerostosis
Absence or reduced production of sclerostin | therefore osteoblasts are not inhibited