Six separate projects related to outcomes of patients with rheumatic diseases are included in this report. The first project, Genetic determinants of ankylosing spondylitis severity, is a prospective observational study of 600 subjects with ankylosing spondylitis (AS) that seeks to identify genetic determinants of ankylosing spondylitis severity. The severity of AS varies widely among patients, but the reasons for this variation are unknown. Because the susceptibility to AS is largely genetically determined, it is possible that the severity of AS may also be largely genetically determined. This project will test genotype-phenotype correlations in a large sample, stratified by duration of AS to capture inflammatory signs in early duration subjects and the degree of fusion and functional impairment in late duration subjects. Over 650 subjects have been enrolled, and genetic testing and data analysis has begun. Radiographic data and HLA data have been finalized on 666 patients. Recent findings have included the identification of immunogenetic markers associated with more severe spinal fusion, the finding that hip arthritis has larger impact on physical functioning than spinal damage, and characterization of the typical pattern of radiographic involvment of different joint areas. Collaborators include Drs. J. Reveille, M. Weisman, J. Davis, T. Learch, and J. Malley. In a related case-control study, we recently identified ARTS1 and IL23R as genes important in the susceptibility to AS, and are in the process of replicating these findings in another set of patients. ? ? The second project, Progression of spinal fusion in ankylosing spondylitis, is a feasibility study with a goal to develop and test a measure of spinal fusion in AS based on quantification of calcification of the lumbar intervertebral discs by computed tomography. Twenty-four subjects have been enrolled, and 22 have completed follow-up scans at 1 and 2 years. The collaborators on this project are Drs. J. Flynn, L. Yao, Y. Yao, S. Tan, and R. Summers.? ? The third project, Clinically important changes in rheumatoid arthritis, is a prospective observational study of clinically important changes in rheumatoid arthritis (RA) activity. Current criteria for improvement in RA have not emphasized the patients perspective. It is also not known if patients rate changes in their symptoms and signs of RA similarly as their physicians, or if different patients are concordant in their judgments of how much of an improvement in symptoms represents an important improvement. The goals of this project are to identify benchmarks of important improvement in pain, functioning, and global arthritis status in RA based on the self-assessment by patients of changes in their symptoms. A secondary goal is to examine the measurement properties of preference measures. To date, 173 patients have been assessed before and after escalation of their anti-rheumatic treatment. In an initial study, we found that a new method of measuring patient global asessment, using a rating scale with marker states, was no more valid than the traditionally used visual analog scale. ? ? The fourth project, Measurement of physical functioning, uses secondary analysis of clinical trial and observational data to understand what aspects of functioning are being measured in commonly used self-report instruments. One focus has been to deconstruct measures of functional limitation in rheumatoid arthritis into reversible components related to active synovitis and irreversible components related to joint damage. This work has recently been published, and testing this concept in osteoarthritis and ankylosing spondylitis is planned. The second focus is to study the relationship between measures of physical performance and measures of self-reported functional limitations. We have developed and tested a model of this relationship using data from NHANES III, annd found that performance measures are neither sensitive nor specific indicators of self-reported functional limitations. ? ? The fifth project, Malignancy in patients with rheumatoid arthritis, uses the Medicare-SEER database to compare the incidence and survival from cancer between patients with RA and those without RA. Rheumatoid arthritis may modify the risk of malignancy, increasing the risk of certain types of cancer (lymphoma, lung) and decreasing the risk of other types of cancer (colorectal). However, risks of malignancy are not well defined in patients with RA, nor is it known if the outcomes of cancer are similar between patients with RA and those without RA. The Medicare-SEER database is a large population-based linked database that combines clinical information from Medicare billing records with cancer data from SEER locations. SEER is the nation's primary cancer epidemiology program, operated by the National Cancer Institute. Patients with RA are identified from Medicare records, while cancer incidence is obtained from SEER. Data analysis is currently underway. ? ? The goals of the sixth project, Clinical epidemiology of systemic lupus erythematosus, are to better estimate the prevalence of systemic lupus erythematosus (SLE), to investigate health disparities among patients with SLE, and to identify clinical features and health care practices that are associated with mortality. Administrative data have been used to chart changes in the incidence of end-stage renal disease due to lupus nephritis over time, identify socioeconomic differences in the incidence of end-stage renal disease due to lupus nephritis, and racial differences in laboratory tests at the start of dialysis, which suggest disparities in care. We are beginning a study of quality of care indicators for hospitalized patients with systemic lupus erythematosus.

Project Start
Project End
Budget Start
Budget End
Support Year
4
Fiscal Year
2008
Total Cost
$667,988
Indirect Cost
Name
National Institute of Arthritis and Musculoskeletal and Skin Diseases
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Lati, Chili; Guthrie, Lori C; Ward, Michael M (2010) Comparison of the construct validity and sensitivity to change of the visual analog scale and a modified rating scale as measures of patient global assessment in rheumatoid arthritis. J Rheumatol 37:717-22
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Masters, Seth L; Simon, Anna; Aksentijevich, Ivona et al. (2009) Horror autoinflammaticus: the molecular pathophysiology of autoinflammatory disease (*). Annu Rev Immunol 27:621-68
Liang, Matthew H; Simard, Julia F; Costenbader, Karen et al. (2009) Methodologic issues in the validation of putative biomarkers and surrogate endpoints in treatment evaluation for systemic lupus erythematosus. Endocr Metab Immune Disord Drug Targets 9:108-12
Ward, Michael M (2008) Interpreting studies of cardiovascular mortality in rheumatoid arthritis: the importance of timing. Arthritis Rheum 59:1687-9
Aletaha, D; Strand, V; Smolen, J S et al. (2008) Treatment-related improvement in physical function varies with duration of rheumatoid arthritis: a pooled analysis of clinical trial results. Ann Rheum Dis 67:238-43
Gensler, L S; Ward, M M; Reveille, J D et al. (2008) Clinical, radiographic and functional differences between juvenile-onset and adult-onset ankylosing spondylitis: results from the PSOAS cohort. Ann Rheum Dis 67:233-7
Ward, Michael M (2007) Primer: measuring the effects of treatment in clinical trials. Nat Clin Pract Rheumatol 3:291-7
Ward, Michael M (2007) Laboratory abnormalities at the onset of treatment of end-stage renal disease: are there racial or socioeconomic disparities in care? Arch Intern Med 167:1083-91
Ward, Michael M (2007) Interpreting measurements of physical function in clinical trials. Ann Rheum Dis 66 Suppl 3:iii32-4

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