1+ Ankylosing Spondylitis Flashcards

1
Q

What is ankylosing spondylitis?

A

A chronic inflammatory disease of the spine and sacroiliac joints that leads to partial or complete fusion and rigidity of the spine

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2
Q

What is the epidemiology of AS?

A

M>F
15-40 yo
Onset is BEFORE 40, often begins in 30s

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3
Q

What is the aetiology of SpA?

A

Likely genetic
- HLA-B27
- Lots of other genes seem to contribute (HLA-B60)

But environmental interplay

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4
Q

What is the pathophysiology of AS?

A
  1. Fluctuating inflammation
  2. Erosive damage + repair
  3. New bone formation/osteoproliferation –> syndesmophytes so spine progressively stiffens
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5
Q

What are the characteristics of the back pain in AS?

A
  • Insidious onset before 40
  • Duration of back pain longer than 3 months
  • Morning stiffness
  • Decreased pain with exercise
  • Good response to NSAIDs
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6
Q

What are the extra-skeletal featutes of AS?

A
  • Anterior uveitis
  • CVS involvement
  • Pul involvement e.g. fibrosis
  • Cauda equina syndrome
  • Enteric mucosal lesions
  • Amyloidosis
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7
Q

What are the skeletal features of AS?

A

Skeletal:
- Axial arthritis= sacroiliitis and spondylitis
- Arthritis of the girdle joints
- Peripheral arthritis UNCOMMON
- Other: enthesitis, OP, vertebral fractures

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8
Q

What are the features of AS on examination?

A
  • Decreased spinal ROM in all directions
  • Loss of lumbar lordosis (increased kyphosis)
  • Neck hyperextension (occiput to wall test and tragus to wall)
  • Modified Schober’s test (<5cm)
  • Lateral spinal flexion reduced
  • Tenderness over sacroiliac joint
  • Reduced chest expansion
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9
Q

How can you monitor AS?

A
  • Number of joints
  • Stiffness duration
  • CRP and ESR
  • Fatigue with BASDAI
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10
Q

What Ix do you do for AS?

A

Biochemical:
- Increased CRP and ESR
- RF, ANA, Anti-ccp negative
- HLA-B27 positive

Imaging:
- Not always required by X-RAY
- Sacroiliitis: sclerosis, erosions, joint space widening, ankylosis
- Spine: loss of lordosis, straightening of the spine, syndesmophytes (bamboo spine)

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11
Q

What is the pharmacological management of AS?

A
  1. NSAIDs
  2. Biologic DMARDs: TNFalpha inhibitors (infliximab, entanercept, adalimumab)
  3. Other biologics: secukinumab (IL-17 inhibitor)

Traditional DMARDs and steroids are really only for peripheral arthritis and DONT help axial SpA

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12
Q

What is the role of HLA-B27/theories of aetiology in ankylosing spondylitis?

A

Canonical:

  1. AI arthritogenic peptide
  2. HLA-B27 is poor at clearing infections so you have chronic immune stimulation

Non-Canonical:
3. HLA-B27 forms homodimers, there is heavy chain misfolding in the ER –> proinflammatory unfolded protein response –> IL-23 release which activates T cells at enthesis (ankylosing) + activates Th17 to release IL-17 which makes the T cell produce pro-inflammatory cytokines –> inflammation

  1. HLA-B27 is an autoantigen
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13
Q

What are the two types of ‘predominantly axial’ SpA?

A
  1. Non-radiographic axial SpA
    - IBP
    - Sacroilitis on MRI
  2. Ankylosing Spondylitis
    - IBP
    - Sacroiliitis on X-Ray
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14
Q

How does the inflammation of RA and AS differ?

A

RA = persistent –> just get erosions

AS= fluctuating –> inflammation –> repair –> syndesmophytes

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15
Q

Summary of Ankylosing Spondylitis

A

Male
<40
Insidious onset
Sacroiliitis and spondylitis = 100%
Peripheral joints only 25%
HLA-B27 = 97%
Eye: anterior uveitis
Cardiac
Pulmonary

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