The researchers found people who had no osteoarthritis for two years and were afterward diagnosed with asthma or eczema, then followed them. For a control group, they followed patients who also had two years without osteoarthritis but had no subsequent diagnosis of asthma or eczema. The researchers then matched each diagnosed person to someone in the control group with similar demographics, outpatient visit frequency, presence of other diseases and several additional factors, to see who developed osteoarthritis. In the primary cohort, each group ended up having about 110,000 patients.

Paving the way for successful treatment

The authors found that if a patient had asthma or eczema, there was a 58% increased risk of developing osteoarthritis over about 10 years. If they had both asthma and eczema, the risk increased to 115%.

To see the effect of another lung disease, one that isn’t mediated by allergens, the researchers compared chronic obstructive pulmonary disease — in which airflow from the lungs is constricted — with asthma. They found that asthma patients had an 83% increased risk of developing osteoarthritis compared with COPD patients. They concluded that lung disease without an allergic response doesn’t predispose one to osteoarthritis, again suggesting that the activation of allergic pathways is the critical factor.

The claims data from the primary analysis did not include body mass index, a risk factor for osteoarthritis, so the researchers validated their results in an independent data set using the Stanford Research Repository. The results were similar, demonstrating that allergic diseases increase the risk of developing osteoarthritis, even after taking into account the key variable of body mass index.

According to Baker, existing medications for asthma attacks and for mast cell activation syndrome — a condition in which a patient experiences repeated episodes of anaphylaxis symptoms — could be candidates for treatment of osteoarthritis. These medications inhibit mast cells and allergic cytokines (byproducts of mast cells that cause inflammation).

“We now have a strong basis for studying this as an intervention, to see if targeting pathways like inhibiting mast cells or allergic cytokines can actually reduce the development and, or progression of osteoarthritis,” Baker said.

Researchers from Chinook Therapeutics in Seattle, the Boston University School of Medicine and the VA Palo Alto Health Care System contributed to the work.

The study was funded by the National Institutes of Health (grants R25 AI 147369 and P30 072571), the Department of Veterans Affairs, the Department of Defense, and the Stanford Center for Clinical and Translational Research and Education.