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Abstract Number: 712

Factors Associated with Anti-TNF Treatment in a Longitudinally Followed Ankylosing Spondylitis (AS) Cohort

Mary Gibson1, MinJae Lee2, Michael M. Ward3, Lianne S. Gensler4, Matthew A. Brown5, Shervin Assassi6, Colton Pence1, Laura A. Diekman7, Mohammad H. Rahbar8, Michael H. Weisman9 and John D. Reveille1, 1Rheumatology, University of Texas Health Science Center at Houston, Houston, TX, 2Biostatistics/Epidemiology/Research Design (BERD) Core | Center for Clinical and Translational Sciences, University of Texas Health Science Center at Houston, Houston, TX, 3NIH/NIAMS, Bethesda, MD, 4Medicine/Rheumatology, University of California, San Francisco, San Francisco, CA, 5The University of Queensland Diamantina Institute, Brisbane, Australia, 6Rheumatology, University of Texas Medical School at Houston, Houston, TX, 7Rheumatology, University of Texas Medical School, Houston, TX, 8The University of Texas Health Science Center at Houston, Houston, TX, 9Rheumatology, Cedars-Sinai Medical Center, Los Angeles, CA

Meeting: 2015 ACR/ARHP Annual Meeting

Date of first publication: September 29, 2015

Keywords: Ankylosing spondylitis (AS), anti-TNF therapy, longitudinal studies, multicenter study and outcomes

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Session Information

Date: Sunday, November 8, 2015

Title: Spondylarthropathies and Psoriatic Arthritis - Clinical Aspects and Treatment Poster I: Clinical Aspects and Assessments

Session Type: ACR Poster Session A

Session Time: 9:00AM-11:00AM

Background/Purpose: TNF-α inhibitor therapy is recommended by ASAS/EULAR guidelines for ankylosing spondylitis (AS) patients with moderate-to-high disease activity despite inadequate response to NSAIDs  in addition to education and exercise.  The purpose of this study is to evaluate factors associated with anti-TNF-α use over a 13 year period in a longitudinal cohort of AS patients enrolled between 2003 and 2013.

Methods: A prospective cohort study of 607 AS patients meeting modified New York criteria were followed for at least 2 years from 5 sites. Patients underwent a comprehensive standardize clinical evaluation and completed questionnaires assessing their disease activity and functional impairment by the BASDAI and BASFI respectively.  Demographic, social, and psychological variables were collected. Current medication lists as well as ESR and CRP levels were determined at each visit. Multivariable longitudinal analyses using mixed effect logistic regression models were conducted to assess the clinical, demographic, and lab features associated with anti TNF-α usage accounting for correlation of repeated measures over time.  

Results: The patients were 73% male and 82% of white race, with a mean age of 42.7 years (SD = 13.8), mean disease duration of 18 years (SD = 13.2) and average length of follow up of 4.96 years.  TNF-α inhibitor therapy was used in 45% of patients at baseline visit, with increased rate of usage over the 13 year study period (p=0.0001).  Multivariable longitudinal associations between independent variables and anti TNF-α usage for the 607 AS patients (Table 1) demonstrated significant associations with greater disease activity in the previous week (by patient global assessment) and higher baseline BASRI scores.  On the other hand, patients with disease duration of more than 20 years, those with elevated CRP, or those using NSAIDs or prednisone were less likely to be using anti-TNFα therapy.  Male gender, BASFI score, BASDAI score, Center for Epidemiologic Studies Depression (CES-D) scale score, greater pain severity (on a visual analog scale), acetaminophen and tramadol use were not  significantly associated with usage of TNF-α inhibitors.

Conclusion: This large, prospective, longitudinal cohort study shows multiple subjective and objective factors associated with anti TNF-α therapy. Patients with longstanding disease, laboratory evidence of inflammation and using anti-inflammatory medications were less likely to be using anti-TNF therapy. Those with more severe radiographic changes at baseline and higher patient global assessment of disease activity were more likely to be using TNF-α inhibitors.

Table 1 Multivariable Associations of Selected Variables on Longitudinal anti TNF-α use (N = 607)

Variable

Odds Ratio (95% CI)

p value 

Male

1.22 (0.65, 2.3)

0.54

Disease Duration at baseline ≥ 20yrs

0.44 (0.25, 0.8)

0.007

BASFI  ≥ 40

1.11 (0.69, 1.79)

0.67

BASDAI  ≥ 40

0.85 (0.55, 1.31)

0.46

CES-D >16

0.93 (0.61, 1.42)

0.75

Elevated CRP

0.3 (0.22, 0.42)

<0.0001

Pain severity score ≥ 50

0.68 (0.43, 1.05)

0.085

Patient Global Assessment ≥ 23

2.22 (1.26, 3.93)

0.006

BASRI baseline≥ 6

2.08 (1.12, 3.85)

0.02

NSAID use

0.32 (0.23, 0.44)

<0.0001

Prednisone use

0.53 (0.27, 1.03)

0.059

Tramadol use

1.5 (0.6, 3.74)

0.38

Acetaminophen use

1.17 (0.79, 1.75)

0.43

Diabetic medication use

0.68 (0.24, 1.94)

0.47

Osteoporosis medication use

1.34 (0.59, 3.03)

0.49


Disclosure: M. Gibson, None; M. Lee, None; M. M. Ward, None; L. S. Gensler, Amgen, 5,Janssen Pharmaceutica Product, L.P., 5,UCB, 5,Celgene, 9; M. A. Brown, Abbvie, Pfizer, UCB, Wyeth, Leo Pharma, NIAMS, NHMRC, Arthritis Australia, Qld Government, 2,Pfizer, Abbvie, UCB, 5,Pfizer, Abbvie, UCB, 8; S. Assassi, None; C. Pence, None; L. A. Diekman, None; M. H. Rahbar, None; M. H. Weisman, None; J. D. Reveille, None.

To cite this abstract in AMA style:

Gibson M, Lee M, Ward MM, Gensler LS, Brown MA, Assassi S, Pence C, Diekman LA, Rahbar MH, Weisman MH, Reveille JD. Factors Associated with Anti-TNF Treatment in a Longitudinally Followed Ankylosing Spondylitis (AS) Cohort [abstract]. Arthritis Rheumatol. 2015; 67 (suppl 10). https://acrabstracts.org/abstract/factors-associated-with-anti-tnf-treatment-in-a-longitudinally-followed-ankylosing-spondylitis-as-cohort/. Accessed .
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