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Mortality Higher in Some
with Rheumatoid Arthritis

NEW YORK (Reuters Health) - Rheumatoid arthritis may raise the risk of death in older women, study findings suggest.

In the report, elderly women with rheumatoid arthritis who tested positive for rheumatoid factor, a type of antibody found in the blood of most patients with the disease, were 90% more likely to die during the 10-year study period than healthy women. But women with rheumatoid arthritis who were not positive for rheumatoid factor had no greater death risk than healthy women, the researchers report in the October issue of the Annals of the Rheumatic Diseases.

Rheumatoid arthritis is a chronic inflammatory condition in which the body's own immune system attacks the tissue lining the joints. It can also damage other parts of the body, such as the heart, lungs and kidneys.

The findings point to a growing health problem among women as the population ages, conclude Dr. Ted R. Mikuls from the University of Alabama at Birmingham and colleagues.

"Our findings provide important insight into the impact of rheumatoid arthritis on a demographic group commonly affected by the disease," they write. "Future research must focus on identifying modifiable risk factors for mortality in this rheumatoid arthritis population."

At this point, they add, it is not clear how rheumatoid arthritis affects survival. They note that several aspects of the disease, such as the number of swollen joints and the degree of functional disability, have been individually linked to an increased mortality risk.

While there was some evidence that women with rheumatoid arthritis were more likely to die from infection or circulatory disease, rheumatoid arthritis patients did not appear to have an increased risk of dying from cancer.

The study began in 1986 and included more than 31,000 women aged 55 to 69 years without a history of rheumatic arthritis. Over the following decade, 158 women were diagnosed with the disorder.

SOURCE: Annals of Rheumatic Diseases 2002;61:994-999.

Reference Source 89

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