Crystal Induced Arthritis Flashcards

1
Q

Crystal Induced Arthritis - General

A

Endogenous Crystals

  • Monosodium Urate (GOUT)
  • Calcium Pyrophosphate (PSEUDOGOUT)
  • Calcium Phosphate

Exogenous Crystals

  • Corticosteroid Ester
  • Talcum

Crystals cause disease by TRIGGERING CASCADE that results in CYTOKINE-mediated CARTILAGE DESTRUCTION

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2
Q

Primary Gout - Classification

A
90% of cases
OVERPRODUCTION of URIC ACID
- Diet 
- Enzyme Defects
REDUCED EXCRETION
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3
Q

Secondary Gout - Classification

A
10% of cases
OVERPRODUCTION w/ INCREASED EXCRETION
- Increased Nucleic Acid Turnover(Leuke)
- Inborn Metabolism error (HGPRT def)
DECREASED EXCRETION w/ NORMAL PRODUCTION
- Chronic Renal Disease
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4
Q

Formation of Uric Acid ( 2 ways)

A

De Novo Pathway - Purines are synthesized from nonpurine precursors

Salvage Pathway - free purine bases derived from breakdown of nucleic acids are recaptured

  • HGPRT is the gatekeeper enzyme
  • Deficiency of HGPRT causes more product to push towards Uric Acid and results in more Purines being synthesized via the De Novo Pathway
  • X-Linked Lesch Nyhan Syndrome –> defiecincy in HGPRT (causes retardation, self mutilation)
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5
Q

Process of Gout

A
  1. Monosodium Urate Crystals Precipitate in Joint
  2. The urates in the joint fluid become supersaturated and crystals/microtophi develop
  3. Crystals are “released” (possibly to a traumatic event) and initiate inflammatory response
    - chemotaxis and C3 and C5a generation
    - INCREASED Nuetrophils and Macrophages
  4. Crystals are phagocytized
    - Free radicals and LTB4 released causing tissue injury and inflammation
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6
Q

What factors help turn hyperuricemia (7mg/dL) into GOUT?

A

Age and Duration - usually older than 20-30
Genetic Predisposition - multifactorial
Heavy Alcohol Consumption
Obesity
Drugs - like thiazides (reduce excretion)
Lead toxicity

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7
Q

For arthritis via crystals (gout) to occur - precipitation of MSU crystals is central to the disease process. What allows for crystalization?

A
  1. Low temperatures - this is why extremities are more affected
  2. High intra-articular concentration
  3. Nucleating agents
    - insoluble collagen fibers
    - chondroitin sulfate
    - proteoglycans
    - cartilage fragments
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8
Q

Gout - Morphology

A

Acute Arthritis

  • Neutrophils with bifringent crystals permeate synovium and synovial fluid
  • CRYSTALS ACTIVATE NUETROPHILS
  • Synovial Fluid congested w/ various inflammatory cells
  • Attacks stop when crystals are gone
  • See PODAGRA here

Chronic Tophaceous Arthritis

  • Repetative build-up of crystals in synovium and periarticular tissue during acute attacks
  • TOPHI arise here (white/chalky and surrounded by fibrosis)
  • PATHONOMONIC for gout
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9
Q

Gout - Clinical

A

Acute Arthritis

  • Podagra (first metatarsophalangeal joint)
  • Sudden Joint Pain
  • Warmth, Tenderness

Chronic Tophaceous Gout
- takes 12 years to develop

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10
Q

Gout - Labs

A

Labs

  • HYPERURICEMIA
  • Athrocentesis
  • High WBC
  • NEGATIVE, LAY LOW, YELLOW, BIREFRINGENET NEEDLE-SHAPED INTRACELLULAR CRYSTALS
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11
Q

Gout - Common Complications

A

Cardiovascular

Renal - 20% of chronic gout pts die of renal failure

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