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OP0128 (2018)
The phenotype of axial psoriatic arthritis: is it dependent on hla-b27 status?
L. Coates1, E. Alonso2, X. Baraliakos3, F. Blanco Garcia4, J. Braun3, V. Chandran5, J.L. Fernandez-Sueiro2, O. FitzGerald6, P. Gallagher7, D. Gladman5, E. Gubar8, T. Korotaeva8, E. Loginova8, E. Lubrano9, J. Mulero10, J. Pinto-Tasende2, R. Queiro11, J. Sanz Sanz12, A. Szentpetery7, P. Helliwell13
1NDORMS, University of Oxford, Oxford, UK
2INIBIC, Complexo Hospitalario Universitario de A Coruña, A Coruna, Spain
3Ruhr-University Bochum, Bochum, Germany
4Department of Rheumatology, INIBIC, Complexo Hospitalario Universitario de A Coruña, A Coruna, Spain
5Toronto Western Hospital, Toronto, Canada
6Dept Rheumatology
7St Vincent’s University Hospital, Dublin, Ireland
8Nasonova Research Institute of Rheumatology, Moscow, Russian Federation
9Università degli Studi del Molise, Campobasso, Italy
10Hospital Puerta de Hierro, Majadahonda, Madrid
11Hospital Universitario Central de Asturias, Oviedo
12Hospital Universitario Puerta de Hierro, Majadahonda, Madrid, Spain
13University of Leeds, Leeds, UK

 

Background: Up to 50% of patients with psoriatic arthritis (PsA) have associated spinal involvement similar to ankylosing spondylitis (AS). HLA-B27 positivity is lower in PsA compared to other SpA which may affect the disease phenotype.

Objectives: Our aim was to compare axial phenotype in PsA patients with and without HLA-B27 with AS patients.

Methods: A large international collaboration collected BASDAI, CRP, HLA-B27 status and sacroiliac joints (SIJ) and spine radiographs. These were read centrally by two blinded readers using consensus on the modified New York criteria, mSASSS and PASRI. AP spine radiographs were examined for symmetry (score difference ≥2 between sides) and morphology of syndesmophytes (typical marginal vs atypical chunky/non-marginal) were compared.

Results: Eight sites contributed 244 (25% HLA-B27+) PsA patients and 198 (75% HLA-B27+) AS patients. Mean BASDAI, mSASSS and PASRI were higher in AS. When categorised by diagnosis and HLA-B27 there were significant differences for age, sex, disease duration, mSASSS, PASRI and syndesmophyte symmetry. Regression analysis, with mSASSS and PASRI as dependent variables revealed significant associations with age, sex, duration of disease, and group (HLA-B27 and diagnosis).

Binary multivariate logistic regression was used to investigate associations of age, sex, HLA-B27 status, diagnosis (PsA v AS) and concomitant diabetes with radiographic features. Sacroiliac symmetry showed no significant associations, whilst syndesmophyte symmetry was associated with increasing age and HLA-B27 positivity. Typical marginal syndesmophytes were associated with age, HLA-B27 status and disease duration: in the cervical spine significant associations with age, sex and HLA-B27 status; in the lumbar spine with age, HLA-B27 and diagnosis. Atypical chunky syndesmophytes were associated only with increasing age and male sex.

Abstract OP0128 – Table 1

Psoriatic arthritis

Ankylosing spondylitis

Statistic

p (2 way)

B27- (n=184)

B27+ (n=60)

B27- (n=50)

B27+ (n=148)

Age, y mean (sd)

55.3 (13.4)

50.5 (13.70

48.5 (14.1)

48.5 (14.3)

7.7*

0.0001

Males n (%)

106 (58)

38 (63)

32 (64)

114 (77)

13.9+

0.003

Duration of disease, y mean (sd)

11.8 (10.3)

14.2 (11.0)

8.4 (9.5)

13.3 (12.3)

3.3*

0.02

Symmetry at SIJ n (%)

165 (90)

54 (90)

43 (86)

132 (89)

7.1+

Ns

Symmetry in spine n/N (%)

36/62 (58)

21/29 (72)

14/24 (58)

67/84 (80)

9.5+

0.02

Marginal syndesmophytes, n (%)

94 (51)

39 (65)

25 (50)

89 (60)

5.5+

Ns

Atypical syndesmophytes, n (%)

41 (22)

17 (28)

12 (24)

29 (20)

1.9+

Ns

* F statistic from one way analysis of variance. +chi squared statistic

Conclusions: This analysis suggests less difference in radiographic phenotype between AS and axial PsA than previously thought. HLA-B27 negative PsA patients have less severe disease as measured by mSASSS and PASRI with less typical marginal syndesmophytes and symmetry, whilst HLA-B27 positive PsA appears similar to AS.

Disclosure of Interest: None declared

DOI: 10.1136/annrheumdis-2018-eular.1832



Citation: Ann Rheum Dis, volume 77, supplement Suppl, year 2018, page A114
Session: The ‘A-B-C’ of PsA (Assessment, Biologicals, Co-morbidities)