Study on the genetics of osteoarthritis

NewsGuard 100/100 Score

Interleukin Genetics, Inc. (NYSE Amex: ILI) and NYU Langone Medical Center announced findings from a study performed in collaboration with Duke University on the genetics of osteoarthritis have been published this week in the "Online First" version of the Annals of Rheumatic Diseases and is available at http://ard.bmj.com/cgi/rapidpdf/ard.2009.113043v1.pdf. Results from the study highlight importance of inter-individual variations in the IL-1 receptor antagonist (IL-1Ra) gene as a likely determinant for whether patients with knee osteoarthritis will go on to develop a severe form of the disease. Three commonly occurring variations in the gene for IL-1Ra were found to be strongly and significantly associated with severe knee osteoarthritis, as measured on radiographs.

"This publication helps validate a predominant theory over the last five years that IL-1 is an important driver of osteoarthritis," said Steven B. Abramson, MD, Director of the Division of Rheumatology at the Hospital for Joint Diseases at NYU Langone Medical Center. "This observation for the first time shows that variations of the IL-1 receptor antagonist gene, the natural blocker of IL-1's damaging actions, may determine who is more likely to progress with the disease and require surgery. This finding can help in the clinical management of patients, facilitate the clinical testing of drugs in various stages of development for slowing progression of osteoarthritis and could lead to new treatments for the disease where there currently are none."

Osteoarthritis (OA) is the most prevalent form of arthritis, affecting more than 20 million adults in the U.S., with that number expected to double over the next 50 years. OA is caused by the breakdown of the cartilage cushion in one or more joints of the body leading to pain, limitation in movement, and in many cases joint replacement. Therapy for OA patients involves mostly pain management, and no drugs are currently available to limit the progression of the disease.

"Many trials for osteoarthritis therapies have failed due to the inability to identify the group at highest risk for progression over short periods of time," said Virginia Byers Kraus, MD, PhD, collaborator at Duke University. "The identification of these variations in the IL-1 receptor antagonist gene may form one strategy of identifying such individuals that could help release this major roadblock to developing more effective drugs for osteoarthritis."

Interleukin Genetics identified and holds patents on genetic patterns that lead to over-production of interleukin-1, one of the key chemicals involved in cartilage and bone destruction, and on specific genetic patterns that are predictive of OA progression.

"We're excited at the potential for clinical use of our genetic biomarkers to aid drug companies in the development of a treatment to halt the progression of this crippling disease," said Ken Kornman, PhD, Chief Scientific Officer, Interleukin Genetics, Inc. "This publication is the positive culmination of Interleukin Genetics' research on genetic patterns related to interleukin-1 and dedication by our university partners to better understand and treat this disease."

SOURCE Interleukin Genetics, Inc.

Comments

The opinions expressed here are the views of the writer and do not necessarily reflect the views and opinions of News Medical.
Post a new comment
Post

While we only use edited and approved content for Azthena answers, it may on occasions provide incorrect responses. Please confirm any data provided with the related suppliers or authors. We do not provide medical advice, if you search for medical information you must always consult a medical professional before acting on any information provided.

Your questions, but not your email details will be shared with OpenAI and retained for 30 days in accordance with their privacy principles.

Please do not ask questions that use sensitive or confidential information.

Read the full Terms & Conditions.

You might also like...
Risk factors for serious inflammatory conditions in IBD patients identified