Treatment of rheumatoid arthritis (RA) has improved dramatically in the last 10 years. No single drug, however, is effective in every patient, and there is great variability in toxicity and price, ranging from ~$400/year for methotrexate (MTX) to up to $15,000/year for biologic agents. This proposal is based on the premise that the next major advance needed in the treatment of RA is not additional drugs, but rather a dramatic improvement in the efficiency and cost-effectiveness of the use of drugs for individual patients with RA. One of the major obstacles to identifying clinically useful markers of treatment response in RA is the lack of cohorts with prospectively collected treatment response data coupled with biological samples. To date, there has been no attempt to harmonize the efforts of the US academic RA research community to create a public resource. Our proposal will thus fill a critical need: establishing an infrastructure of academic investigators to lay the foundation for future collaborative large-scale registries;and to align and unite the efforts of many organizations with the common goal of improving care of RA patients. By unifying the efforts of academic researchers, we can create resources that would not otherwise be available, such as a bank of cryopreserved blood cells to allow sophisticated immunologic research to dissect molecular signals of successful treatment of RA.
Our specific aims are: 1) To create a collaborative network of leading academic investigators committed to collecting treatment response data and biologic samples in RA patients starting MTX or biologic agents;2) To implement a protocol to facilitate uniform data and specimen collection;3a) To perform a """"""""proof of concept"""""""" study to determine the feasibility of this infrastructure by enrolling a small number of RA patients at 10 sites;3b) To utilize financial and in-kind contributions from the Arthritis Foundation and corporate partners to perform pilot projects to facilitate future grant funding;4) To stimulate collaborative efforts of federal funding agencies, voluntary health agencies, professional organizations and industry partners to enable creation of a large, sustainable database and repository to better understand the molecular basis of treatment and rapidly accelerate translational research in RA.

Public Health Relevance

Rheumatoid arthritis (RA) is the most common type of inflammatory arthritis;while there are now many effective medications to treat it, these drugs vary greatly in cost (up to $15,000/year) and side effects and there is no way to predict which drug is best for an individual with this disease. This project will address one of the major roadblocks to personalized medicine in RA, which is the lack of coordinated effort of federal funding agencies (e.g. NIH), voluntary health agencies (e.g. Arthritis Foundation), professional organizations (e.g. American College of Rheumatology) and industry partners (e.g. pharmaceutical and biotechnology companies) to enable creation of a large, sustainable database of treatment response data and repository of accompanying samples of DNA and blood cells from RA patients starting treatment with different drugs. The ultimate goal of these studies is to better understand the molecular basis of treatment response and to rapidly accelerate research in RA to allow prediction of which drugs will work best in individual patients.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
High Impact Research and Research Infrastructure Programs (RC2)
Project #
5RC2AR058964-02
Application #
7943908
Study Section
Special Emphasis Panel (ZAR1-KM-J (M2))
Program Officer
Wang, Yan Z
Project Start
2009-09-30
Project End
2012-08-31
Budget Start
2010-09-01
Budget End
2012-08-31
Support Year
2
Fiscal Year
2010
Total Cost
$1,613,452
Indirect Cost
Name
University of Alabama Birmingham
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
063690705
City
Birmingham
State
AL
Country
United States
Zip Code
35294
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Lu, Bing; Rho, Young Hee; Cui, Jing et al. (2014) Associations of smoking and alcohol consumption with disease activity and functional status in rheumatoid arthritis. J Rheumatol 41:24-30
Halilova, Karina I; Brown, Elizabeth E; Morgan, Sarah L et al. (2012) Markers of treatment response to methotrexate in rheumatoid arthritis: where do we stand? Int J Rheumatol 2012:978396
Curtis, Jeffrey R; van der Helm-van Mil, Annette H; Knevel, Rachel et al. (2012) Validation of a novel multibiomarker test to assess rheumatoid arthritis disease activity. Arthritis Care Res (Hoboken) 64:1794-803