Download - Rheumatoid arthritis
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RHEUMATOID ARTHRITIS
ByDr.ESSAM T. ATWA
PROFESSOR OF RHEUMATOLOGY & REHABILITATION
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Rheumatoid arthritis (RA) is a systemic disease characterized predominantly by a chronic inflammatory polyarthritis, with frequent progression to joint destruction and disability.
The clinical picture seen in RA is the result of a complex cascade involving T cells, B cells, antigen-presenting cells, and a complex set of costimulation signals that lead to the production of proinflammatory cytokines, including tumor necrosis factor (TNF)-alpha, interleukins, and other mediators.
Definition
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The hallmarks of RA are inflammation and synovitis leading to joint damage, and an overexpression of inflammatory cytokines, such as TNF-alpha, IL-1, and IL-6.
Although disease activity is the major cause for active joint damage in RA leading to disability, measuring disease activity in patients with RA remains a challenging issue.
A number of composite disease scoring systems have been developed over the past decade, which consider physical and radiographic evaluations as well as overall physician and patient assessment.
In addition, acute-phase reactant inflammatory markers, such as CRP and ESR, can provide additional information of the disease state.
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RA Is Characterized by Synovitis and Joint Destruction
NORMAL RA
Synovial membrane
Cartilage
CapsuleSynovial
fluid
Inflamed synovial
membrane
Pannus
Major cell types•T lymphocytes•macrophages
Minor cell types•fibroblasts•plasma cells•endothelium•dendritic cells
Major cell type•neutrophils
Feldmann M, et al. Annu Rev Immunol. 1996;14:397-440.
Cartilage thinning
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Pannus formation
Expansion of the synovial membrane forms an invasive pannus1
Synovial cells and chondrocytes release destructive enzymes that degrade cartilage1
Pannus invades cartilage, leading to bone erosion and joint instability1
1Harris ED Jr. N Engl J Med. 1990;322:1277-1289 .
Surgically resected pannus from a patient with
advanced RA
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Antigen presentation
Foreign antigens bind to receptors on antigen-presenting cells1
Complementary receptors on T cells recognize the antigens, triggering an immune response1
1Harris ED Jr. N Engl J Med. 1990;322:1277-1289.
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The inflammatory cascade
Activation of T cells triggers a series of intercellular reactions1
Lymphocytes and macrophages release proinflammatory cytokines1,2
Cytokines induce synovial proliferation and release of destructive enzymes1,2
1Rosenberg AE. In: Cotran RS, Kumar V, Robbins SL, eds. Robbins Pathologic Basis of Disease. 5th ed. Philadelphia, Pa: W.B. Saunders Company; 1994:1213-1271 .
2Goronzy JJ, Weyand CM. In: Klippel JH, ed. Primer on the Rheumatic Diseases. 11th ed. Atlanta, Ga: Arthritis Foundation; 1997:155-161.
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Protein
Inflammation
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Cytokine in Inflammation
PROINFLAMMATORY
ANTI-INFLAMMATORY
TNF
IL-1
IL-6
IL-8
IFN-LT
IL-4
IL-10
TGF
sTNFR
sIL-1R
IL-1Ra
Adapted from Feldmann M et al. Cell 85:307-310, 1996 and Moreland LW et al. Arthritis Rheum 40:397-409, 1997.
disequilibrium
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TNF Is a Key Pathogen in Rheumatic Disease
TNF
Macrophages
Endothelium
Hepatocytes
Synoviocytes
Pro-inflammatory cytokines Chemokines
Adhesion molecules
Acute phase response
Metalloproteinase synthesis
Vascular endothelial growth factor (VEGF)
Articularcartilage
degradation
IncreasedCRP in serum
Increasedangiogenesis
Increased cellinfiltration
Increasedinflammation
Osteoclast Progenitors RANKL expression
Bone erosions
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TNF
osteoclasts synoviocytes chondrocytes
bone resorption
bone erosion
joint inflammation
cartilage degradation
joint space narrowing
pain/joint inflammation
Central Role of TNF in Rheumatoid Arthritis
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The diagnosis of RA is made using :
The patient's history and examination results
In conjunction with laboratory and radiographic data.
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CLINICAL
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◦ Symmetric joint pain◦ Swelling of small
peripheral joints◦ Morning joint stiffness of
variable duration◦ Other diffuse achingFatigue, malaise, and depressionmay precede other symptomsby weeks or months
Grassi W et al. Eur J Radiol. 1998;27(suppl 1):S18–S24.
RHEUMATOID ARTHRITISPresenting Signs and Symptoms
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INVESTIGATIONS
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RADIOLOGY
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1987 Revised American Rheumatism Association Criteria for the Classification of Rheumatoid Arthritis
Definition Criterion
Morning stiffness in and around the joints, lasting at least 1 h.
1. Morning stiffness
At least three joint areas simultaneously have had soft tissue swelling or fluid (not bony overgrowth alone) observed by a physician. The 14 possible areas are right or left PIP, MCP, wrist, elbow, knee, ankle, and MTP joints.
2. Arthritis in three or more joint areas
At least one area swollen (as defined above) in a wrist, MCP, or PIP joint.
3. Arthritis of hand joints
Simultaneous involvement of the same joint areas (as defined in Criterion 2) on both sides of the body (bilateral involvement of PIPs, MCPs, or MTPs is acceptable without absolute symmetry).
4. Symmetric arthritis
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Cont.Definition Criterion
Subcutaneous nodules over bony prominences or extensor surfaces or juxtaarticular regions observed by a physician.
5. Rheumatoid nodules
Demonstration of abnormal amounts of serum rheumatoid factor by any method for which the result has been positive in <5% of normal control subjects.
6. Serum rheumatoid factor
Radiographic changes typical of rheumatoid arthritis on the posteroanterior hand and wrist radiographs, which must include erosions or unequivocal decalcification localized in, or most marked adjacent to, the involved joints (osteoarthritis changes alone do not qualify).
7. Radiographic changes
MCP, metacarpophalangeal; MTP, metatarsophalangeal; PIP, proximal interphalangeal.
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For classification purposes, a patient shall be said to have rheumatoid arthritis if he or she has satisfied at least four of these seven criteria.
Criteria 1 through 4 must have been present for at least 6 weeks.
Patients with two clinical diagnoses are not excluded.
Designation as classic, definite, or probable rheumatoid arthritis is not to be made.
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The 2010 American College of Rheumatology/European League Against Rheumatism classificationcriteria for rheumatoid arthritis
Target population (Who should be tested?): Patients who
1) have at least 1 joint with definite clinical synovitis (swelling)
2) with the synovitis not better explained by another disease
Classification criteria for RA (score-based algorithm: add score of categories A–D; a score of 6/10 is needed for classification of a patient
as having definite RA)
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A-Joint Involvement Score
1- large joint. 0
2- 10 large joints 1
1-3 small joints (with or without involvement of large joints)
2
4-10 small joints (with or without involvement of large joints)
3
>10 joints (at least 1 small joint) 5
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B. Serology (at least 1 test result is needed for classification)
Score
Negative RF and negative ACPA
0
Low-positive RF or low-positive ACPA
2
High-positive RF or high-positive ACPA
3
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C. Acute-phase reactants (at least 1 test result is needed for classification)
Score
Normal CRP and normal ESR
0
Abnormal CRP or abnormal ESR
1
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D.Duration of symptoms
Score
< 6 weeks 0
> 6 weeks 1
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TREATMENT
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Characteristics of ideal RA therapy
°Provides both rapid and sustained efficacy
°Highly effective for symptom relief
°Leads to prevention of joint destruction
° Prevents functional disability
° Useful in combination treatment
° Well tolerated, with minimal monitoring required
° Allows for simple dosing and administration
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Modern history of RA treatment
1928
1948
1985
2000
Milestones Steps foreward
Parenteral Gold
Corticosteroids
Methotrexate
TNF blockers
Antimalarials
Modern NSAIDs
Azathioprine
D-Penicillamine
Sulfasalazine
Cyclosporin A
Leflunomide
COXIBS
DMARDCombination
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If DiseaseControlled
Wolfe F, et al. J Rheumatol. 2001;28:1704-11 .Fleischmann RM. Clin Ther. 1999;21:1429-42 .Matteson EL. Mayo Clin Proc. 2000;75:69-74.
The Evolving RA Treatment Paradigm
Initial Treatment Initial Treatment
Monotherapy or Combination
Current Approach Evolving Paradigm
Conventional DMARDs DMARDBiologic
agent
If Poor Response
Add additional DMARDs
Add biologic
agent
If Poor Response
Combinationtherapy
Discontinuation/reduction of
DMARDs
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THANK YOU