January 07, 2008

Blood test can predict severe ankylosing spondylitis

Measuring blood levels of a protein called matrix metalloproteinase 3 (MMP3) may help predict which people with ankylosing spondylitis will develop severe joint damage, particularly among people with pre-existing damage visible on X-ray, according to new findings presented at the American College of Rheumatology Annual Scientific Meeting in Washington, DC.

Ankylosing spondylitis (AS) is an inflammatory form of the disease which causes a breakdown of bone and cartilage, primarily in the spine and large joints. It can lead to inflammation of the eyes, lungs and heart valves. AS typically develops in men between the ages of 20 and 40. Until now there has been no way to predict which patients will go on to develop more severe forms of the disease.

Researchers analyzed blood samples for numerous protein biomarkers that indicate cartilage breakdown and are associated with deformities in other related diseases in 100 people with AS. Of all the proteins assessed, MMP3 proved to be most strongly associated with progressive joint and bone damage at two years, particularly in those patients with pre-existing damage visible on X-rays. In fact, MMP3 levels correctly identified two-thirds of patients who progressed.
"Being able to predict disease activity and damage in AS in patients can lead to more aggressive treatment when the disease is active and (hence) more aggressive." says lead researcher Walter P. Maksymowych, MD, Professor of Medicine, university of Alberta, Edmonton, Alberta, Canada.

Reference:
"Blood test can predict severe ankylosing spondylitis." Health News 13.2 (Feb 2007): 4(1).

Ankylosing spondylitis patients miss effective Tx due to lack of referrals; primary care docs 'a major barrier'

Primary care physicians have proved to be one of the biggest obstacles to getting the new highly effective therapies for ankylosing spondylitis to affected patients, Dr. Christopher T. Ritchlin said at a symposium sponsored by the American College of Rheumatology. Tumor necrosis factor (TNF) inhibitors constitute a major therapeutic advance in ankylosing spondylitis. But rheumatologists have had a tough time getting out word of this new therapeutic option to the huge number of disaffected patients who were lost to follow up during the era of less-satisfactory treatment.

"We've had all these patients who've come to us, usually young very active males or females who had early ankylosing spondylitis (AS) and may have had minor radiographic changes, [to whom] we gave NSAIDs and exercises to do. We'd say, 'OK, come back in 6 months.' And we've just never seen them again," explained Dr. Ritchlin, director of the clinical immunology research center at the University of Rochester (N.Y.). With varying degrees of success, these patients have adapted to the limitations imposed by their disease. Upon learning about the new treatment options, some patients simply aren't interested; many others with more severe disease who have come in to the office have been helped enormously by anti-TNF therapy, he said.

Meanwhile, large numbers of patients with early AS continue to be misdiagnosed or diagnosed late and undertreated by primary care physicians, according to the rheumatologist. Dr. Ritchlin has mounted an aggressive local effort aimed at educating patients and clinicians about the new therapy for AS. The Arthritis Foundation has been a big help in making contact with new and former patients. Efforts to reach out to primary care physicians and get them to consider AS in the differential diagnosis of chronic back pain in young patients have been less successful.

"The primary care physicians have been a major barrier for us. They really haven't looked for or found ankylosing spondylitis. The referrals we get are mostly from a big orthopedics group that does a lot of joint injections. We need to become more active in helping primary care physicians diagnose the disorder], especially in women, where it's a much harder diagnosis to make," Dr. Ritchlin continued.

In women with AS, axial spinal involvement is often milder than in men. Affected women have more cervical spine and peripheral disease. Their higher self-rated pain scores and impairment of daily activities indicate a generally less favorable long-term course. Until anti-TNF therapy came along, standard treatment involved a gradual escalation from NSAIDs and physical therapy to off-label use of methotrexate and other disease-modifying antirheumatic drugs. But at best the older DMARDs controlled signs and symptoms without altering progression of ankylosis, a key factor in the disease's substantial disability.
TNF inhibitors offer much faster onset of action and substantially greater improvements in symptoms, quality of life, and function.

Clinical measures such as chest expansion and occiput-to-wall distance have shown significant gains. Toxicity is substantially less than with older DMARDs, too, at least out to about 1 year (the length of studies to date). Whether TNF inhibitors are truly disease modifying hasn't been settled, although MRI studies are encouraging, Dr. Ritchlin said. Etanercept is the only TNF inhibitor with FDA approval for AS. Infliximab is approved in Europe, and a phase III U.S. randomized trial is close to completion.

Reference:
Jancin, B. "Ankylosing spondylitis patients miss effective Tx due to lack of referrals; primary care docs 'a major barrier'." Family Practice News 34.8 (April 15, 2004): 44(1).

Juvenile-onset spondylitis does damage to hips

Patients with juvenile-onset ankylosing spondylitis have functional outcomes similar to adult-onset disease, but more often have less severe lumbar degeneration and more hip involvement requiring total hip arthroplasty, Ms. Lianne S. Gensler said in a poster session at the annual meeting of the American College of Rheumatology.

Ms. Gensler and her associates compared the disease characteristics of a cohort of 53 patients with juvenile-onset ankylosing spondylitis (JoAS) and 349 patients with adult-onset AS (AoAS) in a multicenter, cross-sectional study.

Compared with AoAS patients, JoAS patients were significantly younger (average 50 vs. 56 years), had significantly longer duration of AS (37 vs. 31 years), and included significantly more women (40% vs. 23%), said Ms. Gensler of the University of California, San Francisco.
Although each group had similar functional outcomes, JoAS patients were 45% less likely to have severe lumbar disease than were AoAS patients. The comparison was adjusted for disease duration, gender, white race, having ever been a smoker, family history of AS, and occupational activity. But JoAS patients were more than twice as likely as AoAS patients to need total hip arthroplasty.

Reference:
Evans, J. "Juvenile-onset spondylitis does damage to hips." Family Practice News 37.8 (April 15, 2007): 38(1).

Disease with a funny name

AS is not a new disease. The spines of 4,000-year-old mummies excavated from Egyptian tombs show conclusive evidence of the affliction. Yet today, because of the lack of proper diagnosis, no one knows exactly how many people are affected. At present, 500,000 people are reported to have AS in this country and studies strongly indicate it may be much more.
AS is extremely difficult to diagnose in its early stages. Studies show the average spondylitis victim endures many years of misdiagnosis before their condition is correctly identified, even though it is the third most common form of chronic arthritis in the United States. AS is not restricted to humans either. Primate studies indicate gorillas also suffer from a form of AS.

Reference:
Winston, C. "The mysterious back disease." AFAA's American Fitness 7.n2 (March-April 1989): 6

January 02, 2008

Ottawa Half Training Starts Today

I am excited to start training today for the ING Ottawa Half Marathon. My running partners and I have extended base training to allow our bodies to adjust to winter running. Today, we're running a mere 3K after work. Easy enough.

Racing Accomplishments

  • 2002 Nov--Run For Life 10K
  • 2002 Oct--Canadian International Marathon 5K
  • 2002 Sept--Community Power Challenge 5K
  • 2003 Oct--Canadian International Marathon 21.1K
  • 2003 Sept--Longboat Toronto Island 10K
  • 2004 May--Ottawa National Capital Race 21.1K
  • 2004 Oct--Toronto International Marathon 21.1K
  • 2004 Sept--Scotiabank Waterfront Marathon 21.1K
  • 2006 April--London Spring Run Off 10K
  • 2006 Aug--Midsummer's Night Run 15K
  • 2006 Dec--Honolulu Marathon 42.2K
  • 2006 July--5 Peaks Durham Regional Forest 5K
  • 2006 June--Race the Lake 10K
  • 2006 Oct--Vulture Bait Ultra Trail 10K
  • 2006 Sept--Scotiabank Waterfront Marathon 21.1K
  • 2007 March--Around the Bay 30K
  • 2007 April--Harry's Spring Run Off 8K
  • 2007 May--SportingLife 10K
  • 2007 Oct--Toronto International Marathon 21.1K
  • 2008 May--Ottawa National Capital Race 21.1K
  • 2008 Aug--Iroquois Trail Test 32K
  • 2008 Sept--Scotiabank Waterfront Marathon 21.1K
  • 2008 Oct--Run for the Toad 50K
  • 2008 Oct--Toronto Zoo Run 10K