Rheumatoid arthritis is a chronic systemic inflammatory disease of unknown cause triggered by an autoimmune reaction leading to synovial membrane hypertrophy and chronic joint inflammation often with extra-articular manifestations.
The trigger for the reaction could be external and is thought to occur in genetically susceptible individuals.
Wrist and joints are most commonly involved and the disease is often symmetrical i.e. the same joints typically involved on both sides of the body. The disease may also affect other parts of the body.
While the cause of rheumatoid arthritis is not clear, it is believed to involve a combination of genetic and environmental factors. It is a kind of auto-immune disease which implies that body’s tissues are attacked by its own cells.
The term rheumatoid arthritis is based on the Greek for watery and inflamed joints.
Prevalence of rheumatoid arthritis is about 1%. The incidence increases with increasing age and peaks around middle age.
First-degree relatives of individuals with RA are at 2 to 3-fold higher risk for the disease.
Women are affected by RA approximately 3 times more often than men are, but sex differences diminish in older age groups.
RA primarily affects joints, but it also affects other organs in 15–25% of affected people.
The pathogenesis of rheumatoid arthritis is not completely understood. An external trigger like cigarette smoking, infection, or trauma triggers an autoimmune reaction, leading to synovial hypertrophy and chronic joint inflammation and other extraarticular manifestations.
Rheumatoid arthritis is a kind of uncontrolled inflammation and inflammatory mediators like CD4 T cells, mononuclear phagocytes, fibroblasts, osteoclasts, neutrophils and B cells play major role in the pathophysiology. Various cytokines, chemokines, and other inflammatory mediators including the following –
- Tumor necrosis factor alpha
- Transforming growth factor beta
- Fibroblast growth factor
- Platelet-derived growth factor
Inflammation and proliferation of the synovium [pannus] leads to destruction of joint cartilage, bone, tendons, ligaments, and blood vessels and other tissues.
The various phases of progression of rheumatoid arthritis are
- Initiation phase – non-specific inflammation.
- Amplification phase – T cell activation
- Chronic inflammatory phase and tissue injury – cytokines IL–1, TNF-alpha and IL–6.
Joint Deformities and Other Changes in Rheumatoid Arthritis
- Boutonniere deformity
- Nonreducible flexion at the proximal interphalangeal joint along with hyperextension of the distal interphalangeal joint of the finger.
- Synovitis leads to stretching or rupturing of the proximal interphalangeal joint through the central extensor tendon, with concomitant volar displacement of the lateral bands.
- Lateral bands when beyond the transverse axis of the joint, become flexors of the joint
- Gradual shortening of tendons leads to hyperextension of the distal interphalangeal joint. A compensatory and reducible hyperextension may occur at the MCP joint.
- Swan-neck deformity of the finger
- Hyperextension at the PIP joint with flexion of the DIP join
- Disruption of the extensor tendon occurs at the distal interphalangeal joint causing secondary shortening of the central extensor tendon and hyperextension of the proximal interphalangeal joint.
- Another mechanism of this deformity is volar herniation of the proximal interphalangeal joint capsule and subsequent tightening of the lateral bands and central extensor tendon.
- Flexor tenosynovitis
- Trigger finger
- Thickening or nodule formation of the tendon
- Tendon rupture [especially the flexor pollicis longus]
- Arthritis mutilans
- Severe and extensive arthritis with dissolution of bone leading to shortening of phalanges and gross instability of joints.
- Subluxation and ulnar deviation of metacarpophalangeal joints
- Sretching and attenuation of the volar plate and collateral ligaments,
- Dislocation of the flexor tendon volarward and ulnarward.
- Z-thumb or Z-deformity
- Hyperextension of the interphalangeal joint,
- Fixed flexion and subluxation of the metacarpophalangeal joint
- Disruption of the radioulnar joint with dorsal subluxation of the ulna
- Rotation of the carpus on the distal radius
- Entrapment neuropathy
- Median nerve
- Ulnar nerve .
- Flexion deformity
- Olecranon bursitis
- Rotator cuff degeneration
- Due to synovitis
- Superolateral migration of the humerus with complete tears
- Acromioclavicular arthritis
- Flexion deformity
- Large effusions
- Quadriceps inhibition by spinal reflexes leading to atrophy
- Knee instability may develop after progressive loss of cartilage and weakening of ligaments
Ankles and Feet
- Posterior tibialis tendon involvement or rupture
- Subtalar subluxation
- Loss of arches leading to flattening of the feet.
- Hallux valgus or bunion
- Hammer toes
- Subluxation at the metatarsophlangeal joint
- Compensatory flexion of toes
- C1-C2 instability
- Neck pain and stiffness
- Radicular pain
- Transient ischemic attacks
- Vertebral artery impingement
- Myelopathy secondary to rupture of the transverse ligament
- Rheumatoid nodules
- Seen in 25% of patients
- Olecranon process
- Proximal ulna
- Back of the heel
- Ischial tuberosities
- Heel pads
Rheumatoid factor is almost invariably present in patients with rheumatoid nodules. If rehumatoid factor is absent, other diagnoses should be considered.
- Subcutaneous nodules
- Vasculitic lesions of the skin
- Palpable purpura
- Skin ulceration
- Palmar erythema
- Poderma gangrenosum may be noted.
- Myocardial infarction
- Myocardial dysfunction
- Pericardial effusions
- Pericarditis, Myocarditis, coronary vasculitis
- Valvular disease, and conduction defects
- Pleural effusions
- Interstitial fibrosis
- Bronchiolitis obliterans
- Vasculitis esp in skin
- Anemia of chronic disease
- Nerve entrapment
- Mononeuritis multiplex
- Cervical myelopathy
- Peripheral myopathy
- Keratoconjunctivitis sicca
- Nodular scleritis that may lead to scleromalacia
Etiology of Rheumatoid Arthritis
The cause of rheumatoid arthritis not known is unknown. Follolwing factors are thought to be involved.
Genetic factors account for 50% of the risk for developing rheumatoid arthritis.
Following genetic associations are known
- Human leukocyte antigen (HLA)-DR4
- PTPN22 and TRAF5 genes
Numerous infectious agents have been suggested as potential causes
- Mycoplasma organisms
- Epstein-Barr virus
- Rubella virus
- Porphyromonas gingivalis
- Sex hormones may play a role suggested by
- Female preponderance
- Amelioration of the disease during pregnancy
- Postpartum recurrence
- Reduced incidence in women using oral contraceptives
- Hyperprolactinemia may be a risk factor
- Synovial macrophages and fibroblasts may become autonomous
- B cells produce numerous autoantibodies
Tobacco use is the main environmental risk
Clinical Presentation of Rheumatoid Arthritis
Patient classically presents with persistent symmetric polyarthritis that includes hands and feet though any synovial joint may be involved.
Constitutional symptoms like fatigue, fever, malaise, morning stiffness, loss of appetite and loss of weight may be present.
The symptoms of rheumatoid arthritis wax and wane over time. Over the time progressive destruction of joints occur, eventually leading to deformities and decreased function.
Extra-articular involvement of organs such as the skin, heart, lungs, and eyes can also be significant.
Patients with RA may report difficulty performing activities of daily living like dressing, standing, walking, personal hygiene, or use of hands.
Most of the patients have insidious onset which may begin with systemic symptoms and signs.
The joints are examined for swelling, warmth, deformity, tenderness, limitation of motion. Patients are also examined for extra-articular manifestations and rheumatoid nodules
Joints involved in decreasing frequency are
- Proximal interphalangeal joint
- Meetatarsophalangeal joint
- Shoulder joint
- Cervical spine
- Temporomandibular joints
Direct palpation can elicit joint tenderness.
Thickening of the synovium is most evident in the small joints of the hands and feet, and is felt as doughy texture on palpation.
Baker cyst may be seen in knee.
Stages of Rheumatoid Arthritis
Stage I or Early Rheumatoid Arthritis
- No destructive changes on x-ray
- Osteoporosis may be seen
Stage II or Moderate Progression
- Periarticular osteoporosis with or without subchondral bone destruction
- Mild cartilage destruction
- Limited joint mobility
- No joint deformities
- Adjacent muscle atrophy
- Extra-articular lesions
Stage III or Severe Progression
- Radiographic evidence of cartilage and bone destruction
- Periarticular osteoporosis
- Joint deformities without fibrous or bony ankylosis
- Extensive muscle atrophy is extensive
- Extra-articular soft tissue lesions
Stage IV or Terminal Progression
- Stage III + Criteria of stage III
Patients with RA are categorized into 4 functional classes:
- Class I – Completely able to perform usual activities of daily living
- Class II – Able to perform usual self-care and vocational activities but limited in avocational activities
- Class III – Able to perform usual self-care activities but limited in vocational and avocational activities
- Class IV – Limited in ability to perform usual self-care, vocational, and avocational activities
- Lyme Disease
- Myelodysplastic Syndrome
- Paraneoplastic Syndromes
- Relapsing Polychondritis
- Polymyalgia Rheumatica
- Psoriatic Arthritis
- Sjogren Syndrome
- Systemic Lupus Erythematosus
There is no specific test for rheumatoid arthritis which is pathognomic. The diagnosis is established using a combination of clinical, laboratory, and imaging features.
Following tests are helpful in rheumatoid arthritis
Markers of inflammation
- CRP [Over a period correlates with radiographic progression]
- Shows chronic anemia
- Leukopenia [Consequence of therapy or a component of Felty syndrome]
- Detects IgM antibody against the Fc fragment of IgG
- Fluctuate somewhat with disease activity, though titers remain.
- Also present in connective tissue disorders and 1-5% healthy people
- Predictive of radiographic progression
- Anti-CCP antibodies
- Assays for Anti-cyclic citrullinated peptide
- More specific
- Detectable early in the disease course
- Anti nuclear antibodies
Joints and spine should be assessed with standard views. Varying degree of joint destruction and seformities may be noted.
Magnetic Resonance Imaging
MRI provides a better assessment and is able to detect lesions earlier than x-rays. But the practical use is limited to cervical spine because of the smaller joints and high cost.
- To confirm or rule out differentials
- Specially indicated in single joint involvement
- Synovial fluid analysis
- Gram staining
- Cell count
- In rheumatoid arthritis, the picture is that of inflammation
- Leucocyte count >2000/µL
- Lower glucose levels than serum
Treatment of Rheumatoid Arthritis
The main treatment goals are to control disease activity and slow the rate of joint damage, in addition improving the symptoms.
Successful treatment of rheumatoid arthritis includes drugs, exercise, massage, physical therapy and surgery. Counseling and stress reduction also form part of the treatment wherever required.
Various medications used in treatment of rheumatoid arthritis are
- Nonbiologic and biologic disease-modifying antirheumatic drugs
An early treatment with DMARDs is the standard of care as it stops the disease and can induce remissions.
American college of rheumatology recommends vaccination for pneumococcal, hepatitis and influenza before patient are put on nonbiologic or biologic disease modifying antirheumatic [DMARDS] .
Vaccination against human papiloma and herpes zoster virus are also recommended in recent guidelines.
Disease-modifying Antirheumatic Drugs
DMARDs can retard or prevent disease progression and, thus, joint destruction and subsequent loss of function. These agents can eliminate the need for other anti-inflammatory or analgesic medications.
After DMARDs are started anti-inflammatory or analgesic medications may be required initially as bridging therapy to reduce pain and swelling.
Early treatment of rheumatoif arthriris has potential to retard progression and may also induce remissions.
- Gold salts
Methotrexaate and sulphsalazine are the most active compounds and provide the best risk-benefit ratios. Methtrexate either alone or in combination with other agents, has become the standard of care for moderate to severe RA.
Gold salts and penicillamine are rarely used now due to availability of better drug have largely been supplanted by more effective agents.
Tumor Necrosis Factor inhibitors
These drugs bind TNF [tumor necrosis factor] and prevent its interaction with its receptors. The drugs include etanercept, infliximab, adalimumab, certolizumab, and golimumab.
The indications for their use arises when at least one nonbiologic DMARD, usually MTX, has been administered without sufficient success.
These drugs are contraindicated in infections, demyelinating disorders, class III or IV heart failure, and presence or recent history of malignancy.
Patients should be tested for latent tuberculosis before treatment is commenced as the infection could become active when on treatment.
Patients taking anti-TNF agents must avoid live-virus vaccines. Giving live vaccines to patients receiving immunosuppressive drugs leads to a higher risk for serious infection.
A patient with hepatitis B surface infection/history should receive antiviral prophylaxis.
Adverse Effects are
- Generation of antibodies against these compounds
- Emergence of antinuclear
- Drug-induced lupuslike syndromes
- Demyelination disorders
- Bone marrow suppression occur
These agents are indicated in moderately to severely active rheumatoid arthritis when response to TNF inhibitors is inadequate
- Most often used in combination with methotrexate.
- Decrease in CD20+ B cells seen as adverse effect
- Inhibits T-cell activation
- Binds to CD80 and CD86
- Blocks their interaction with CD28 [required for T-cell activation]
- Monthly intravenous infusion or weekly subcutaneous injection
- Indicated in treatment failure with anti-TNF therapy
- IL-6 receptor inhibitor
- IV infusion or subcutaneous injection.
- Used alone or in combination with methotrexate or other DMARDs.
- Oral Janus Kinase Inhibitor [A group of intracellular tyrosine kinases that modulate signals to maintain the inflammatory conditionin rheumatoid arthritis]
- Monotherapy or in combination with methotrxate
- Should not be used along with biologic DMARDs or potent immunosuppressive agents like azathioprine or cyclosporine.
- Recombinant glycosylated IL-1 receptor antagonist
- Has shown improvement in patients in clinical trials.
Patients may require 2-3 months to achieve a full response to DMARDs
Combination therapy of DMARDs
Most successful combinations are
- Methotrxate + sulphasalazine+Hydroxychloroquine
- Methotrxate plus leflunomide
- Methotrxate plus biologic DMARDs.
Corticosteroids are potent anti-inflammatory drugs that are commonly used in patients with RA to bridge the time until treatment with DMARDs is effective.
As rheumatoid arthritis is an auto-immune disease, suppressing the immune system helps reduce the damage to good tissue. Cyclosporine, Azathioprine and cyclophosphamide are commonly used agents.
Nonsteroidal anti-inflammatory drugs
NSAIDs interfere with prostaglandin synthesis through inhibition of the enzyme cyclooxygenase (COX), thus reducing swelling and pain.
These drugs however, do not retard joint destruction and thus are not sufficient to treat rheumatoid arthritis when used alone
- Goals of rehabilitation for RA patients include relief of pain, improving range of motion, enhancement of strength and endurance and prevention or correction of deformities
Following measures are included in rehabilitation
- Heat and cold therapies
- Orthotics and splints
- Therapeutic exercise
- Aerobic conditioning
- Isometric exercises restore
- Resistance exercises
- Occupational therapy
Surgical intervention in patients with RA can achieve pain relief, deformity correction, and functional improvement. Following surgical procedures are available to obtain these goals –
- Tendon realignment
- Reconstructive surgery or arthroplasty
Prognosis of Rheumatoid Arthritis
Course of rheumatoid arthritis is generally one of exacerbations and remissions.
Early treatment is associated with better outcomes.
Some patients experience a relatively self-limited disease, whereas others have a chronic progressive illness.
Complications associated with rheumatoid arthritis are
- Gastrointestinal problems
- Lung disease
- Heart disease
- Sjogren syndrome – Keratoconjunctivitis sicca
- Felty syndrome
- Recurrent bacterial infections
- Lmphoma and other malignancies
Following correlate with an unfavorable prognosis
- HLA-DRB1*04/04 genotype
- High serum titer of autoantibodies (RF, anti-CCP)
- Extra-articular manifestations
- Large number of involved joints
- Age < 30 years
- Female sex
- Systemic disease
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