Background: Clinical characteristics of nonradiographic axial spondyloarthritis (nr-ax-SpA) are highly variable across patients, and may potentially vary across patient populations, particularly due to differing distributions of human leukocyte antigens (HLA) and other genetic factors. The majority of nr-ax-SpA studies have been conducted in Europe, the United States, and small studies are reported from Asia [1].
Objectives: To delineate clinical characteristics of patients with nr-ax-SpA in Asian countries in comparison to other areas of the world.
Methods: Utilizing the ASAS-COMOSPA data, an international cross-sectional observational study of SpA patients, we analyzed information on demographics, disease characteristics, comorbidities, and risk factors. Patients were classified by region: Asia (China, Japan, Singapore, South Korea, and Taiwan), and non-Asian countries (Europe, Americas, and Africa); patient characteristics, including diagnosis and treatment, were compared.
Results: Among 3984 SpA patients included in the study, 1094 were from centers in Asian countries, and 2890 from other regions. 112/780 (14.4%) of axial SpA patients in Asian countries were nr-ax-SpA, substantially less than in other countries (486/1997, 24.3%). Nr-ax-SpA patients in Asian countries compared to nr-ax-SpA in other countries were more likely male (75.9 vs 47.1%), have onset (22.8 vs 27.8 years) and diagnosis (27.2 vs 34.5 years) at younger age, and experience less diagnostic delay (1.88 vs 2.92 years) (
Conclusion: Among axial SpA patients, substantially lower frequency of nr-ax-SpA was observed in Asian countries compared to other regions of the world. Nr-ax-SpA patients in Asian countries were predominantly male, and had younger disease onset with higher HLA-B27 positivity rate and less peripheral signs, and better response to NSAIDs. These results offer an opportunity to improve both early diagnosis and treatment of nr-ax-SpA patients in Asian countries.
Characteristics of nonradiographic axial SpA in Asia versus non-Asian regions
Variables | Asia | non-Asian regions | p value |
N | 112 | 486 | |
Age at disease diagnosis, yrs | 27.2 [21.1, 39.6] | 34.5 [27.7, 41.7] | <0.001 |
Diagnostic delay, yrs | 1.88 [0.27, 5.56] | 2.92 [0.59, 9.58] | 0.011 |
Male (%) | 85 (75.9) | 229 (47.1) | <0.001 |
Sacroiliitis on MRI among tested (%) | 49 (67.1) | 341 (82.2) | 0.005 |
HLA B27 positivity among measured (%) | 96 (90.6) | 273 (61.9) | <0.001 |
Inflammatory Back Pain (%) | 107 (95.5) | 478 (98.4) | 0.076 |
Arthritis, enthesitis, or dactylitis (%) | 60 (53.6) | 322 (66.3) | 0.016 |
Psoriasis (%) | 12 (10.7) | 82 (16.9) | 0.142 |
Uveitis (%) | 20 (17.9) | 81 (16.7) | 0.870 |
Inflammatory bowel disease (%) | 5 (4.5) | 27 (5.6) | 0.817 |
Elevated CRP (%) | 37 (33.0) | 213 (43.8) | 0.048 |
Physician global assessment (0-10) | 2.0 [1.0, 5.0] | 2.0 [1.0, 4.0] | 0.741 |
Patient global assessment (0-10) | 3.0 [1.0, 6.0] | 4.0 [2.0, 6.0] | 0.012 |
ASDAS-CRP | 1.40 [0.95, 2.08] | 1.97 [1.21, 2.78] | <0.001 |
BASFI | 0.8 [0.05, 2.65] | 2.9 [0.8, 5.6] | <0.001 |
Good response to NSAIDs (%) | 80 (71.4) | 272 (56.0) | 0.004 |
Methotrexate use (%) | 18 (16.1) | 134 (27.6) | 0.016 |
Biological DMARDs use (%) | 27 (24.1) | 191 (39.3) | 0.004 |
REFERENCES:
[1]López-Medina C, Ramiro S, van der Heijde D, et al. Characteristics and burden of disease in patients with radiographic and non-radiographic axial Spondyloarthritis: a comparison by systematic literature review and meta-analysis. RMD Open. 2019 Nov 21;5(2): e001108.
Acknowledgements: This study was conducted under the umbrella of the International Society for Spondyloarthritis Assessment (ASAS) and COMOSPA study was supported by unrestricted grants from Pfizer, AbbVie and UCB.
Disclosure of Interests: Keisuke Ono: None declared, Mitsumasa Kishimoto Speakers bureau: AbbVie, Amgen-Astellas BioPharma, Asahi-Kasei Pharma, Astellas, Ayumi Pharma, BMS, Chugai, Daiichi-Sankyo, Eisai, Eli Lilly, Gilead, Janssen, Kyowa Kirin, Novartis, Ono Pharma, Pfizer, Tanabe-Mitsubishi, Teijin Pharma, and UCB Pharma, Consultant of: AbbVie, Amgen-Astellas BioPharma, Asahi-Kasei Pharma, Astellas, Ayumi Pharma, BMS, Chugai, Daiichi-Sankyo, Eisai, Eli Lilly, Gilead, Janssen, Kyowa Kirin, Novartis, Ono Pharma, Pfizer, Tanabe-Mitsubishi, Teijin Pharma, and UCB Pharma, Sho Fukui: None declared, Satoshi Kawaai: None declared, Gautam A. Deshpande: None declared, Kazuki Yoshida Consultant of: OM1, Inc., Grant/research support from: Corrona, LLC, Naomi Ichikawa: None declared, Yuko Kaneko Speakers bureau: AbbVie, Astellas, Ayumi, Bristol-Myers Squibb, Chugai, Eisai, Eli Lilly, Hisamitsu, Jansen, Kissei, Pfizer, Sanofi, Takeda, Tanabe-Mitsubishi, and UCB, Taku Kawasaki: None declared, Kazuo Matsui: None declared, Mitsuhiro Morita: None declared, Kurisu Tada: None declared, Naoho Takizawa: None declared, Naoto Tamura: None declared, Atsuo Taniguchi: None declared, Yoshinori Taniguchi: None declared, Shigeyoshi Tsuji: None declared, Shigeto Kobayashi: None declared, Masato Okada: None declared, Clementina López-Medina: None declared, Anna Moltó Consultant of: AbbVie, Pfizer, MSD, Novartis, Gilead, Lilly and UCB, Grant/research support from: AbbVie, Pfizer, MSD, Novartis, Gilead, Lilly and UCB, Désirée van der Heijde Consultant of: AbbVie, Amgen, Astellas, AstraZeneca, Bayer, BMS, Boehringer Ingelheim, Celgene, Cyxone, Daiichi, Eisai, Eli-Lilly, Galapagos, Gilead, Glaxo-Smith-Kline, Janssen, Merck, Novartis, Pfizer, Regeneron, Roche, Sanofi, Takeda, UCB Pharma, Employee of: Imaging Rheumatology bv. (Director), Maxime Dougados: None declared, Yoshinori Komagata: None declared, Tetsuya Tomita: None declared, Shinya Kaname: None declared.