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Abstract Number: 1544

Good Agreement Between The Ankylosing Spondylitis Disease Activity Scores Based On C-Reactive Protein and Erythrocyte Sedimentation Rate

Dilek Solmaz, Pinar Cetin, Ismail Sari, Merih Birlik, Servet Akar, Fatos Onen and Nurullah Akkoc, Rheumatology, Dokuz Eylul University School of Medicine, Izmir, Turkey

Meeting: 2013 ACR/ARHP Annual Meeting

Keywords: Disease Activity and ankylosing spondylitis (AS)

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Session Information

Title: Spondylarthropathies and Psoriatic Arthritis: Clinical Aspects and Treatment: II

Session Type: Abstract Submissions (ACR)

Background/Purpose:

Recently, ASDAS has been developed as a disease activity measuring tool for ankylosing spondylitis (AS), using a similar methodology to that used for the development of the Disease Activity Score (DAS) in rheumatoid arthritis. Two versions of ASDAS have been proposed, one based on CRP (preferred) and the other based on ESR (alternative).In the light of recent reports showing substantial difference between the two versions of DAS28, it is of interest to assess the agreement between the two ASDAS versions at individual level. Our aim is to assess the agreement between the ESR and CRP-based ASDAS scores in AS patients.

Methods:

Data were obtained from the local clinical database which contains slightly over 500 AS patients .Patients with full data at baseline were included in this analysis. Mean ASDAS-CRP and ASDAS-ESR values were compared by Spearman correlation and scatter plot with linear regression analysis. Bland-Altman analysis and kappa statistics were used to assess the agreement between the two ASDAS definitions in the whole group as well as in different gender and age groups.

Results:

396 patients (291 M; 44 ±12.0 years) were identified with complete data at baseline for this analysis. Mean (±SD) disease duration was 9.4 (±8.2) years.  Mean (±SD) BASDAI, BASFI and BASMI scores were 3.5 (±2.2), 2.9 (±2.6), 3.9 (±1.9), respectively.  HLA B27 was positive in 65% of the patients of whom 83.7% were using NSAIDs and 20.7% were using TNF inhibitors. Mean (±SD) ASDAS scores, based on CRP and ESR were 2.9 (± 1.1), and 2.8 (± 1.0), respectively. There was a strong correlation between the two definitions by Spearman’s correlation test (r=0.9, p<0.001) and linear regression analysis (R²=0.82, p<0.001). The agreement  was good for both genders  and all age groups with weighted kappa values ranging from  0.680  to 0.876 (Table 1). Similar number of patients was classified into the defined categories of disease activity with ASDAS-CRP and ASDAS-ESR(Table 2). Bland-Altman analysis showed excellent agreement between the two scores (ASDAS-CRP – ASDAS-ESR) with a mean difference (bias) of −0.0 ± 0.48 (95% CI −0.04, −0.047). Upper and lower limits of agreement were 0.95 (95% CI 0.87, 1.03) and −0.95 (95% CI −1.03, −0.87), respectively. Mean difference was 0.20 ± 0.49 in females and -0.10 ± 0.44 in males.

Conclusion:

The results suggest a good agreement between ASDAS-ESR and ASDAS-CRP for both genders and all age groups. 

Table 1: The correlation and agreement between ASDAS-CRP and ASDAS-ESR values in different gender and age groups

Patient group

Mean ASDAS-CRP

Mean ASDAS-ESR

Spearman correlation coeficient

Agreement rate

Kappa value

Weighted kappa value

r

P

Females (n=104)

2.8±1.1

3.1±1.0

0.906

<0.001

64.4%

0.455

0.680

Males (n=292)

2.9±1.1

2.7±1.0

0.923

<0.001

73.6%

0.618

0.803

≤40 years  old (n=163)

3.0±1.1

2.9±1.0

0.918

<0.001

69.7%

0.549

0.790

41-60 years old (n=193)

2.7±1.1

2.8±1.0

0.888

<0.001

70.5%

0.561

0.740

≥61 years old (n=40)

3.0±1.2

3.0±1.0

0.954

<0.001

74.4%

0.672

0.876

Overall (n=396 )

2.9 ±1.1

2.8 ±1.0

0.906

<0.001

70.0%

0.567

0.760

Table 2: Agreement between ASDAS-CRP and ASDAS-ESR on the classification of the patients into different categories of disease activity

 

 

ASDAS CRP

ASDAS ESR

 

<1.3

1.3-2.0

2.1-3.5

>3.5

Total

<1.3

13

5

2

0

20

1.3-2.0

17

40

19

0

76

2.1-3.5

6

19

137

25

187

>3.5

0

0

22

91

113

Total

36

64

180

116

396


Disclosure:

D. Solmaz,
None;

P. Cetin,
None;

I. Sari,
None;

M. Birlik,
None;

S. Akar,
None;

F. Onen,
None;

N. Akkoc,
None.

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