Psoriatic arthritis

Psoriatic arthritis
Classification and external resources

Severe psoriatic arthritis of both feet and ankles. Note the changes to the nails.
ICD-10 L40.5, M07
ICD-9 696.0
MedlinePlus 000413
eMedicine radio/578
MeSH D015535

Psoriatic arthritis (also arthritis psoriatica, arthropathic psoriasis or psoriatic arthropathy) is a type of inflammatory arthritis[1][2] that, according to the National Psoriasis Foundation, will develop in up to 30 percent of people who have the chronic skin condition psoriasis.[3] Psoriatic arthritis is said to be a seronegative spondyloarthropathy and therefore occurs more commonly in patients with tissue type HLA-B27.

Contents

Signs and symptoms

Common symptoms of psoriatic arthritis include:

Psoriatic arthritis may remain mild, or may progress to more destructive joint disease. Periods of active disease, or flares, will typically alternate with periods of remission.

Because prolonged inflammation can lead to joint damage, early diagnosis and treatment to slow or prevent joint damage is recommended[4]

Causes

The exact causes are not yet known, but a number of genetic associations have been identified in a genome-wide association study of psoriasis and psoriatic arthritis including HLA-B27.[5][6]

Diagnosis

There is no definitive test to diagnose psoriatic arthritis. Symptoms of psoriatic arthritis may closely resemble other diseases, including rheumatoid arthritis. A rheumatologist (a doctor specializing in diseases affecting the joints) may use physical examinations, health history, blood tests and x-rays to accurately diagnose psoriatic arthritis.

Factors that contribute to a diagnosis of psoriatic arthritis include:

Other symptoms that are more typical of psoriatic arthritis than other forms of arthritis include inflammation in the Achilles tendon (at the back of the heel) or the Plantar fascia (bottom of the feet), and dactylitis (sausage-like swelling of the fingers or toes).[7]

Classification

There are five main types of psoriatic arthritis:

Treatments

The underlying process in psoriatic arthritis is inflammation, therefore treatments are directed at reducing and controlling inflammation. Milder cases of psoriatic arthitis may be treated with NSAIDS alone; however there is a trend toward earlier use of Disease-modifying antirheumatic drugs or biological response modifiers to prevent irreversible joint destruction.

Nonsteroidal anti-inflammatory drugs

Typically the medications first prescribed for psoriatic arthritis are NSAIDs such as ibuprofen and naproxen followed by more potent NSAIDs like diclofenac, indomethacin, and etodolac. NSAIDs can irritate the stomach and intestine, and long-term use can lead to gastrointestinal bleeding.[8][9] Other potential adverse effects include damage to the kidneys and cardiovascular system.

Disease-modifying antirheumatic drugs

Rather than just reducing pain and inflammation, this class of drugs helps limit the amount of joint damage that occurs in psoriatic arthritis. Most DMARDs act slowly, and may take weeks or even months to take full effect. Drugs such as methotrexate or leflunomide are commonly prescribed; other DMARDS used to treat psoriatic arthritis include ciclosporin, azathioprine and sulfasalazine. These immunosuppressant drugs can also reduce psoriasis skin symptoms, but can lead to liver and kidney problems and an increased risk of serious infection.

Biological response modifiers

Recently, a new class of therapeutics called biological response modifiers or biologics has been developed using recombinant DNA technology. Biologic medications are derived from living cells cultured in a laboratory. Different from the traditional DMARDS that impact the entire immune system, biologics target specific parts of the immune system. They are given by injection or intravenous (IV) infusion.

Biologics prescribed for psoriatic arthritis are TNF-α inhibitors, including infliximab, etanercept, golimumab, certolizumab pegol and adalimumab.

Biologics may increase the risk of both minor and serious infections. More rarely, they may be associated with nervous system disorders, blood disorders or certain types of cancer.

Other treatments

Doctors may use joint injections with corticosteroids in cases where one joint is severely impacted. In psoriatic arthritis patients with severe joint damage orthopedic surgery may be implemented to correct joint destruction, usually with use of a joint replacement. Surgery is effective for pain alleviation, correcting joint disfigurement, and reinforcing joint usefulness and strength.

Self care

People with psoriatic arthritis and other forms of arthritis may find day to day tasks difficult. Adjustments include using gadgets such as jar openers to twist the lids from jars, lifting heavy pans or other objects with both hands, etc.

Maintaining a healthy weight places less strain on the joints, leading to reduced pain and increased energy and mobility.

Regular exercise is recommended for people with arthritis to help maintain flexibility and strength. Biking, swimming and walking are commonly recommended.

Hot and cold packs can relieve inflamed joints. Cold has a numbing effect and can dull the sensation of pain. Heat can help relax tense muscles and relieve pain.

Epidemiology

Seventy percent of people who develop psoriatic arthritis first show signs of psoriasis on the skin, 15 percent develop skin psoriasis and arthritis at the same time, and 15 percent develop skin psoriasis following the onset of psoriatic arthritis.[10]

Psoriatic arthritis can develop in people who have any level severity of psoriatic skin disease from mild to very severe.[11]

Psoriatic arthritis tends to appear about 10 years after the first signs of psoriasis. For the majority of people this is between the ages of 30 and 55, but the disease can also affect children. The onset of psoriatic arthritis symptoms before symptoms of skin psoriasis is more common in children than adults.[12]

More than 80% of patients with psoriatic arthritis will have psoriatic nail lesions characterized by nail pitting, separation of the nail from the underlying nail bed, ridging and cracking, or more extremely, loss of the nail itself (onycholysis).[13]

Men and women are equally affected by this condition. Like psoriasis, psoriatic arthritis is more common among Caucasians than African or Asian Americans.[14]

Additional images

References

  1. ^ Freedberg, Irwin M.; Fitzpatrick, Thomas B. (2003). Fitzpatrick's dermatology in general medicine (6th ed.). New York: McGraw-Hill. pp. 427–436. ISBN 0-07-138076-0. 
  2. ^ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology (10th ed.). Saunders. p. 194. ISBN 0-7216-2921-0. 
  3. ^ About psoriatic arthritis. National Psoriasis Foundation. http://www.psoriasis.org/about/psa/. Retrieved 2008-08-31 
  4. ^ Farragher TM, Lunt M, Plant D, Bunn DK, Barton A, Symmons DP (May 2010). "Benefit of early treatment in inflammatory polyarthritis patients with anti-cyclic citrullinated peptide antibodies versus those without antibodies.". Ann. Rheum. Dis. 62 (5): 664–75. doi:10.1002/acr.20207. PMC 2962800. PMID 20461787. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2962800. 
  5. ^ Liu Y, Helms C, Liao W, et al. (March 2008). Leal, Suzanne M.. ed. "A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci". PLoS Genet. 4 (3): e1000041. doi:10.1371/journal.pgen.1000041. PMC 2274885. PMID 18369459. http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1000041. 
  6. ^ Rahman P, Elder JT (March 2005). "Genetic epidemiology of psoriasis and psoriatic arthritis". Ann. Rheum. Dis. 64 (Suppl 2): ii37–9; discussion ii40–1. doi:10.1136/ard.2004.030775. PMC 1766868. PMID 15708933. http://ard.bmj.com/cgi/pmidlookup?view=long&pmid=15708933. 
  7. ^ Psoriatic Arthritis. The Johns Hopkins University School of Medicine and the Johns Hopkins Arthritis Center. http://www.hopkins-arthritis.org/arthritis-info/psoriatic-arthritis/diagnosis.html. Retrieved 2011-05-04 
  8. ^ Warner TD, Giuliano F, Vojnovic I, Bukasa A, Mitchell JA, Vane JR (1999). "Nonsteroid drug selectivities for cyclo-oxygenase-1 rather than cyclo-oxygenase-2 are associated with human gastrointestinal toxicity: a full in vitro analysis". Proc Natl Acad Sci U S A 96 (13): 7563–8. doi:10.1073/pnas.96.13.7563. PMC 22126. PMID 10377455. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=22126. 
  9. ^ Scholer DW, Ku EC, Boettcher I, Schweizer A (April 1986). "Pharmacology of diclofenac sodium". Am. J. Med. 80 (4B): 34–8. doi:10.1016/0002-9343(86)90077-X. PMID 3085490. 
  10. ^ Psoriatic Arthritis. The Johns Hopkins University School of Medicine and the Johns Hopkins Arthritis Center. http://www.hopkins-arthritis.org/arthritis-info/psoriatic-arthritis/#epidemiology. Retrieved 2011-05-04 
  11. ^ Who's At Risk. National Psoriasis Foundation and Arthritis Foundation. http://www.bejointsmart.org/psoriatic-arthritis-whos-at-risk. Retrieved 2011-05-04 
  12. ^ Psoriatic Arthritis. WebMD LLC. http://emedicine.medscape.com/article/331037-overview. Retrieved 2011-05-04 
  13. ^ Psoriatic Arthritis. WebMD LLC. http://emedicine.medscape.com/article/331037-overview. Retrieved 2011-05-04 
  14. ^ Epidemiology of Psoriatic Arthritis. WebMD LLC. http://emedicine.medscape.com/article/331037-overview#aw2aab6b6. Retrieved 2011-05-04 

External links