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1 IN THE NAME OF GOD
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Rheumatoid Arthritis A chronic multisystem disease Characteristic feature: Persistent inflammatory synovitis Peripheral joints Symmetric Cartilage damage and bone erosions Destruction 3
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Epidemiology Most common form of chronic inflammatory arthritis Prevalence :~1% (range 0.3–2.1%) women: 3 times more often than men Throughout world; all races 5
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Epidemiology Onset: 4 and 5 decades of life Incidence between 25 and 50 y 6
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Genetics First-degree relative 2-10 times Concordant in monozygotic twins 15–20% 7
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Genetics Major genetic risk factors class II HLA HLA-DR4 (DR1*0401) and related alleles 8
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Environmental factors Climate and urbanization Incidence and severity of RA Smoking : Relative Risk: 1.5-3.5 Severe RA with antibodies to CCP 9
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11 ANTIGEN Genetic Background MACROPHAGE
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12 DR MACROPHAGE IL -1 CD80/86
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13 ANTIGEN DR MACROPHAGET-CELL CD4+ IL -1 CD80/86 CD 28
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14 Genetic Background IL- 1 ANTIGEN MACROPHAGE T CELL IL 2 B Cell ANTIBODY
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15 AUTOIMMUNE REACTION Genetic Background IL- 1 ANTIGEN MACROPHAGE T CELL IL 2 B Cell IMMUNE COMPLEX ANTIBODY
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16 AUTOIMMUNE REACTION Genetic Background IL- 1 ANTIGEN MACROPHAGE T CELL IL 2 B Cell ANTIBODY IMMUNECOMPLEX COMPLEMENT TARGET INFLAMMATION
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17 HYPOTHALAMUS PITUITARY GLAND ADRENAL CORTISOL IL-1, IL-6, TNF DHEA BRAIN STEM ESTROGEN AUTONOM SYNOVITIS RA: Plasma cortisol Nature 2007 Cortisol Cortisone 11 β-HSD1 11 β-HSD2 Arth Rheum 2005 Abnormal receptor Abnormal postreceptor ADENOSIN
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Onset In 2/3 of patients begins with: - Fatigue, anorexia, generalized weakness This prodrome may persist for weeks or months 19
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Onset Specific symptoms appear gradually - Especially: hands, wrists, knees, feet - Symmetric 1/3 of patients Initially one or a few joints 20
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Articular Most common manifestation: - Pain An almost invariable feature: - Morning stiffness of >1-h Constitutional symptoms: - Weakness, easy fatigability, anorexia, and weight loss 22
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Articular Synovial inflammation causes: Swelling Tenderness Limitation of motion Warmth 23
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Articular Initially, impairment in physical function is caused by: - Pain and inflammation Later: - Fibrous or bony ankylosis 24
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Articular Symmetric Certain specific joints: - Wrist joints - MCP, PIP - Synovitis of the elbow Flexion contractures - Knee - Forefoot, ankles, and subtalar - Hip & shoulder DIP: rare Not affect lumbar and thoracic spine 25
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Articular Synovial joints of C1-C2: - On occasion - Atlantoaxial subluxation - Pain in the occiput - Rarely: compression of the cord 26
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Articular Characteristic joint changes: Hand: - "Z" deformity Radial deviation at wrist Ulnar deviation digits 27
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Articular Characteristic joint changes: Hand: - Swan-neck deformity PIP hyperextension DIP Flexion 28
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Articular Characteristic joint changes: Hand: - Boutonnière deformity PIP flexion DIP extension 29
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Articular Characteristic joint changes: Hand: - Thumb Hyperextension of the first IP Flexion of the first MCP 30
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Articular Characteristic joint changes: Foot: - Hallux valgus - Eversion at hindfoot - Plantar subluxation of the metatarsal heads - Widening of the forefoot - Lateral deviation and dorsal subluxation of the toes 31
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Extraarticular Manifestation RA is a systemic disease 40% of patients As a rule: occur in high titers of RF or antiCCP 33
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Rheumatoid nodule In 20–30% On areas subjected to mechanical pressure Elsewhere 34
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Rheumatoid nodule Common locations: Olecranon bursa, proximal ulna, Achilles tendon, occiput 35
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Vasculitis Severe RA and high titers of RF Can affect nearly any organ Polyneuropathy and mononeuritis multiplex Cutaneous ulceration and dermal necrosis Digital gangrene Visceral infarction 36
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Vasculitis Uncommon Renal vasculitis is rare 37
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Pleuropulmonary Pleuritis: - Most common pulmonary manifestation - Autopsy Common - Symptomatic Infrequent 38
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Pleuropulmonary ILD Pulmonary nodules 39
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Cardiovascular Pericarditis: - Asymptomatic - 50% in autopsy Congestive heart failure IHD 40
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Cardiovascular Most common cause of death Inflammatory markers 41
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Nervous system Central nervous system Spare Vasculitis Peripheral neuropathy Atlantoaxial subluxation Nerve entrapment 42
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Eye <1% Long-standing disease and nodules Episcleritis, scleritis 15–20% of patients Sjögren's syndrome 43
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Felty’s syndrome Consists of: - Splenomegaly - Neutropenia Leukopenia is selective neutropenia (PMN <1500 cells/L) Late stage of sever RA High titers of RF, nodules 44
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Osteoporosis Inflammation Glucocorticoid 45
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Laboratory RF autoantibodies reactive with Fc portion of IgG 2/3 of patients No specific 5% of healthy Rheumatic & infectiuse 47
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Laboratory Predictive value: low <1/3 of patients with a positive test for RF have RA Not useful as screening Prognostic 48
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Laboratory Anti-CCP: - Sensitivity: 70% - Specificity: 90% - Prognostic - 1.5% of population 49
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Laboratory Normochromic, normocytic anemia Anemia and thrombocytosis disease activity ESR & CRP Synovial fluid: WBC 50
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Radiography Early: soft tissue swelling Juxtaarticular osteopenia Loss of articular cartilage Bone erosions 51
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Radiography 52
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Patholog Pannus: - Invades bone-cartilage 53
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Clinical course Persistent but fluctuating disease activity Early aggressive treatment 54
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Diagnosis No pathognomonic finding in: Clinic Paraclinic Almost exclusively on: History Physical examination 55
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Diagnosis Typical picture: - Bilateral symmetric polyarthritis - Small and large joints - Upper and lower extremities - Sparing of the axial skeleton except cervical spine Constitutional features Morning stiffness Nodules RF & AntiCCP Radiography 56
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57 2010 ACR-EULAR criteria for classification of RA Joint involvement: Score - 1 large joint 0 - 2-10 large joint 1 - 1-3 small joint 2 - 4-10 small joint 3 - > 10 joint (at least small joint) 5
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58 2010 ACR-EULAR criteria for classification of RA Serology: Score - Negative RF or Anti-CCP 0 - Low positive (< 3 times) 2 - High (> 3 times) 3
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59 2010 ACR-EULAR criteria for classification of RA Acute Phase reactants: Score - ERS/CRP NL 0 - Abnormal 1 Duration - <6 weeks 0 - ≥6 weeks 1 Definite RA ≥6
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Treatment NSAIDs Glucocorticoid DMARDs Biologic 60
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61 YAZD-GHALAH THANKS FOR YOUR ATTENTION
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