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Abstract Number: 2005

Predictors Of Outcomes In Tophaceous Gout- Results From a Prospective Cohort At The Veterans Affairs

Puja Khanna1,2, Cleopatra Aquino-Beaton3, Jasvinder A. Singh4, Erin Duffy5, David Elashoff6 and Dinesh Khanna7, 1Division of Rheumatology, University of Michigan Medical Center, Ann Arbor, MI, 2Rheumatology, Ann Arbor VA, Ann Arbor, MI, 3Rheumatology, VA Greater Los Angeles Healthcare System, Los Angeles, CA, 4Department of Medicine, University of Alabama, Tuscaloosa, AL, 5Medicine, University of California Los Angeles, Los Angeles, CA, 6Medicine- Statistic Core, UCLA Department of Medicine Statistics Core, Los Angeles, CA, 7University of Michigan Health System, Ann Arbor, MI

Meeting: 2013 ACR/ARHP Annual Meeting

Keywords: Gout and outcome measures

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Session Information

Title: Metabolic and Crystal Arthropathies II

Session Type: Abstract Submissions (ACR)

Background/Purpose: Tophaceous gout is a chronic inflammatory arthritis that causes debilitating acute attacks and associated with exponential resource utilization. Our objective was to define predictors of tophaceous gout in a prospective cohort.

Methods: 112 veterans with gout were recruited from rheumatology and primary care clinics at a single VA facility and followed for a total of 4 visits 3 months apart.  Joint counts and presence of tophus was assessed by providers. HRQOL was evaluated with SF-36 v2, Health assessment questionnaire-disability index (HAQ-DI), and Gout Impact Scale (GIS) of GAQ2.0. Patient demographics, duration of gout, Charlson comorbidities (CCI), serum urate (sUA), and patient and physician rating of the severity of gout on a 0-10 scale were assessed. Comparisons were made using the student’s t test or the chi-square, Wilcoxon rank sum test or Fisher exact test, as appropriate, p-value < 0.5 was considered statistically significant. Age, race, physician severity score, functional class, disease duration, alcohol use, and number of comorbidities were considered as predictors of having tophaceous gout in univariate and multivariate logistic regression models.

Results: Patients diagnosed with tophaceous gout (N=35) were similar to patients without tophaceous gout (N=74) with respect to age, gender, race, alcohol use, duration of gout, polyarticular involvement, sUA and number of Charlson comorbidities, serum creatinine, and sUA (Table). Physician gout severity scores were significantly greater among patients with tophaceous gout; however, there was no difference in patient severity scores between groups. SF-36 scores indicated that the tophaceous group had worse physical functioning (p =0.04), bodily pain (p=0.07), total PCS scores (p=0.07), and gout concern overall domain of GIS (p=0.07). Physician severity score was the only significant predictor of outcomes identified after controlling for age, race, physician severity score, functional class, disease duration, alcohol use, and number of comorbidities.

Conclusion: Physicians rated tophaceous gout patients as having more severe disease. Surprisingly, conventional predictors of tophaceous gout such as disease duration, kidney disease, and sUA were similar in tophaceous and non-tophaceous groups. This may be reflective of the VA population that has a higher burden of urate even in the non-tophaceous patients.

Table 1. Patient Characteristics, Non-Tophaceous and Tophaceous

Total Cohort

N=112

Non-Tophaceous

N=74

Tophaceous

N=35

p-value

Age (Years)

Mean (SD)

65.7 (11.2)

65.5 (12.1)

66.5 (9.8)

0.68 α

Gender (Male)

N (%)

106 (97.3)

72 (97.3)

34 (97.1)

0.99 β

Race

Caucasian

N (%)

76 (67.86)

47(63.51)

26 (74.29)

0.29 β

African American

N (%)

17 (15.18)

15 (20.27)

2 (5.71)

Other

N (%)

19 (16.96)

12 (16.22)

7 (20.00)

Alcohol Use

N (%)

39 (35.1)

27 (36.5)

11 (32.4)

0.75 ε

Duration of Gout

Mean (SD)

13.9 (12.9)

12.7 (12.3)

15.7 (14.0)

0.31 γ

Polyarticular Involvement (>3 joints)

N (%)

37 (36.3)

22 (32.4)

14 (45.2)

0.22 ε

# of Comorbidities (CCI)

Mean (SD)

3.9 (2.5)

3.6 (2.3)

4.5 (2.6)

0.12 γ

Physician Severity Score

Mean (SD)

3.0 (2.5)

2.3 (2.1)

4.4 (2.9)

<0.0001 α

Patient Severity Score

Mean (SD)

6.0 (2.9)

6.5 (3.4)

0.44 α

Radiographic evidence of erosion or tophi

N (%)

35 (70.0)

16 (53.3)

19 (95.0)

0.002 β

Serum Urate

Mean (SD)

7.5 (1.9)

7.8 (2.0)

7.1 (1.6)

0.09 γ

Serum Creatinine

Mean (SD)

1.4 (0.9)

1.5 (0.9)

1.3 (0.5)

0.60 γ

α=T-test; β=Fisher Exact test; γ=Wilcoxon test;ε=Chi-square test


Disclosure:

P. Khanna,

NIH,

2;

C. Aquino-Beaton,
None;

J. A. Singh,

Takeda, Savient,

2,

Savient, Takeda, Ardea, Regeneron, Allergan,

5,

URL pharmaceuicals Novartis,

5;

E. Duffy,
None;

D. Elashoff,
None;

D. Khanna,

NIH,

2,

Scleroderma Foundation,

2.

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