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Abstract Number: 2472

Disease Burden Is Similar Between Non-Radiographic Axial Spondyloarthritis and Ankylosing Spondylitis and Independent Of Gender Influences

Salih Ozgocmen1, Erkan Kilic2, Gamze Kilic2 and Ozgur Akgul2, 1Division of Rheumatology, Dept.PRM, Erciyes University, Faculty of Medicine, Kayseri, Turkey, 2Division of Rheumatology, Dept. PRM, Erciyes University, Faculty of Medicine, Kayseri, Turkey

Meeting: 2013 ACR/ARHP Annual Meeting

Keywords: Ankylosing spondylitis (AS) and spondylarthritis

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Session Information

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

Session Type: Abstract Submissions (ACR)

Disease Burden is Similar between Non-Radiographic Axial Spondyloarthritis and Ankylosing Spondylitis and Independent of Gender Influences

Background/Purpose:

Axial spondyloarthritis (SpA) covers both ankylosing spondylitis (AS) with established radiographic changes and non-radiographic axial SpA (nr-axSpA) without definite radiographic sacroiliitis. Clinical characteristics and differences between women and men with nr-axSpA or AS have been documented; however comparison of patients with nr-axSpA and AS within the same genders may provide more data. Registry data revealed similar burden of disease, however baseline characteristics regarding gender distribution and HLA-B27 differ in nr-axSpA from AS. We compared nr-axSpA and AS within the same genders regarding the clinical characteristics in a cohort of patients with axial SpA.

Methods:

A total of 170 consecutive patients diagnosed with axial SpA were studied and clinical and laboratory results were compared between male and female patients in subgroups of nr-axSpA and AS. Standard clinical assessment tools (VAS-pain, global assessment, BASDAI, BASFI, ASQoL and SF-36, ASDAS), laboratory data, existence of inflammation on the sacroiliac and lower-thoracic and lumbar spine MR (blindly assessed), SpA features and comorbidities were used in the analysis.

Results:

 Patients with AS (n=96) were predominantly male (79.2%) whereas patients with nr-axSpA (n=74) were predominantly female (55.4%) (p=0.0001). Women with nr-axSpA and AS did not differ in clinical variables except family history for SpA and spinal inflammation on MR (16.7% vs 68.8%, p=0.0001, respectively). Men with nr-axSpA and AS did not differ in clinical variables, except HLA B27, peripheral arthritis, younger age and spinal inflammation of MR (25.0% vs 52.1%, p=0.014, respectively).   

Table 1. Comparison between groups for the measured parameters 

Women

Men

nr-axSpA (n=41)

AS (n=20)

p

nr-axSpA (n=33)

AS (n=76)

p

Age, y

34.7±9.6

38.3±7.1

0.142

29.7±7.6

37.5±8.7

0.0001

Age at symptom onset, y

29.5±7.8

28.1±8.2

0.454

24.1±7.7

26.9±7.4

0.07

VAS-pain

4.7±2.5

5.2±2.8

0.336

4.4±3.0

3.8±2.7

0.334

Physician’s global

3.7±1.3

4.4±1.8

0.195

3.5±2.3

3.4±2.0

0.728

Patient’s global

4.6±2.4

5.6±2.1

0.066

4.0±2.8

3.9±2.5

0.779

BASDAI

3.9±1.9

4.3±2.2

0.634

3.8±2.2

3.2±2.3

0.255

BASFI

2.2±1.9

3.5±2.8

0.122

1.8±1.9

2.6±2.3

0.085

SF-36 MCS

51.6±23.3

40.2±17.2

0.072

56.0±22.4

58.7±23.2

0.575

SF-36 PCS

49.9±22.1

42.1±19.9

0.213

54.7±21.6

55.5±23.2

0.869

ASQoL

7.7±4.7

10.1±6.0

0.118

5.7±4.9

6.6±5.4

0.399

ASDAS-CRP

2.7±0.9

2.9±0.9

0.509

2.5±0.9

2.7±1.0

0.452

HLA B27+ve, %

48.8

60.0

0.430

51.5

72.3

0.047

Smoking, %

29.3

15.0

0.224

54.5

44.7

0.346

Inflammation-SIJ MR, %

82.1

89.5

0.703

78.8

61.8

0.084

Uveitis, %

9.8

15.0

0.546

15.1

19.7

0.570

Psoriasis, %

2.4

10.0

0.248

9.1

3.9

0.261

Family history,%

12.2

35.0

0.035

18.8

26.7

0.382

Peripheral arthritis

24.4

15.0

0.400

28.1

11.8

0.038

Preceding infection, %

19.5

5.0

0.134

18.8

6.6

0.056

   

Conclusion:    

Results of our cohort confirm the earlier data showing that the burden of disease is similar between nr-axSpA and AS. Although disease burden seem to be independent of gender, men or women with nr-axSpA differ from AS in several clinical aspects including HLA B27, peripheral arthritis, positive family history for SpA and more prevalent inflammation on spinal MR.  


Disclosure:

S. Ozgocmen,
None;

E. Kilic,
None;

G. Kilic,
None;

O. Akgul,
None.

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