Journal List > J Rheum Dis > v.25(1) > 1064375

Kwon, Bang, and Kim: New Provisional Classification of Juvenile Idiopathic Arthritis Applying Rheumatoid Factor and Antinuclear Antibody

Abstract

Objective

Previous classification systems for juvenile idiopathic arthritis (JIA) were based on the number of joints involved and did not categorize homogenous disease entities. Therefore, JIA patients were reclassified retrospectively by applying rheumatoid factor (RF) and antinuclear antibody (ANA), which have been proven to constitute a homogenous disease entity.

Methods

The medical records of JIA patients were investigated retrospectively and reclassified into six categories using the new provisional classification. The nomenclature was based on Dr. Martini's proposal in the 23rd European Paediatric Rheumatology Congress (2016) at Genoa, Italy. New categories included systemic JIA (sJIA), RF-positive JIA (RF-JIA), early-onset ANA-positive JIA (eoANA-JIA), enthesitis/spondylitis-related JIA (ESR-JIA), “other JIA”, and “unclassified JIA”.

Results

Of a total of 262 JIA patients, 71 (27.1%) were reclassified as sJIA, 31 (11.8%) as RF-JIA, 22 (8.4%) as eoANA-JIA, 63 (24.0%) as ESR-JIA, 65 (24.8%) as “other JIA”, and 10 (3.8%) as “unclassified JIA”. A comparison of RF-JIA, eoANA-JIA, and ESR-JIA revealed significant differences in the gender ratio, age of disease onset, and the cumulative number and type of joints involved among the three groups. “Other JIA” comprised a significant proportion (24.8%) and warrants the need for further classification. The characteristics of the RF-positive patients were comparable to those of the anti-cyclic citrullinated peptide antibody-positive patients. The ANA positivity was lower (28.2%) than that in Western studies but showed similar clinical features.

Conclusion

This is the first study applying RF and ANA to classify JIA without considering the joint counts. The six new categories include sJIA, RF-JIA, eoANA-JIA, ESR-JIA, “other JIA,” and “unclassified JIA”.

REFERENCES

1. Fink CW. Proposal for the development of classification criteria for idiopathic arthritides of childhood. J Rheumatol. 1995; 22:1566–9.
2. Petty RE, Southwood TR, Baum J, Bhettay E, Glass DN, Manners P, et al. Revision of the proposed classification criteria for juvenile idiopathic arthritis: Durban, 1997. J Rheumatol. 1998; 25:1991–4.
3. Petty RE, Southwood TR, Manners P, Baum J, Glass DN, Goldenberg J, et al. International League of Associations for Rheumatology classification of juvenile idiopathic arthritis: second revision, Edmonton, 2001. J Rheumatol. 2004; 31:390–2.
4. Ravelli A, Martini A. Juvenile idiopathic arthritis. Lancet. 2007; 369:767–78.
crossref
5. Criteria for the classification of juvenile rheumatoid arthritis. Bull Rheum Dis. 1972; 23:712–9.
6. Brewer EJ Jr, Bass J, Baum J, Cassidy JT, Fink C, Jacobs J, et al. Current proposed revision of JRA Criteria. JRA Criteria subcommittee of the diagnostic and therapeutic criteria committee of the American rheumatism section of the arthritis foundation. Arthritis Rheum. 1977; 20(2 Suppl):195–9.
7. European League Against Rheumatism. EULAR Bulletin No. 4: Nomenclature and classification of arthritis in children. Basel: National Zeitung AG;1977.
8. Ravelli A, Varnier GC, Oliveira S, Castell E, Arguedas O, Magnani A, et al. Antinuclear antibody-positive patients should be grouped as a separate category in the classification of juvenile idiopathic arthritis. Arthritis Rheum. 2011; 63:267–75.
crossref
9. Martini A. Are the number of joints involved or the presence of psoriasis still useful tools to identify homogeneous disease entities in juvenile idiopathic arthritis? J Rheumatol. 2003; 30:1900–3.
10. Ravelli A, Felici E, Magni-Manzoni S, Pistorio A, Novarini C, Bozzola E, et al. Patients with antinuclear antibody-positive juvenile idiopathic arthritis constitute a homogeneous subgroup irrespective of the course of joint disease. Arthritis Rheum. 2005; 52:826–32.
crossref
11. Stoll ML, Zurakowski D, Nigrovic LE, Nichols DP, Sundel RP, Nigrovic PA. Patients with juvenile psoriatic arthritis comprise two distinct populations. Arthritis Rheum. 2006; 54:3564–72.
crossref
12. Martini A. It is time to rethink juvenile idiopathic arthritis classification and nomenclature. Ann Rheum Dis. 2012; 71:1437–9.
crossref
13. Hofer MF, Mouy R, Prieur AM. Juvenile idiopathic arthritides evaluated prospectively in a single center according to the Durban criteria. J Rheumatol. 2001; 28:1083–90.
14. Petty RE. Growing pains: the ILAR classification of juvenile idiopathic arthritis. J Rheumatol. 2001; 28:927–8.
15. Tsitsami E, Bozzola E, Magni-Manzoni S, Viola S, Pistorio A, Ruperto N, et al. Positive family history of psoriasis does not affect the clinical expression and course of juvenile idiopathic arthritis patients with oligoarthritis. Arthritis Rheum. 2003; 49:488–93.
crossref
16. Griffin TA, Barnes MG, Ilowite NT, Olson JC, Sherry DD, Gottlieb BS, et al. Gene expression signatures in polyarticular juvenile idiopathic arthritis demonstrate disease heterogeneity and offer a molecular classification of disease subsets. Arthritis Rheum. 2009; 60:2113–23.
crossref
17. Magni-Manzoni S, Epis O, Ravelli A, Klersy C, Veisconti C, Lanni S, et al. Comparison of clinical versus ultrasound-determined synovitis in juvenile idiopathic arthritis. Arthritis Rheum. 2009; 61:1497–504.
crossref
18. Stoll ML, Lio P, Sundel RP, Nigrovic PA. Comparison of Vancouver and international league of associations for rheumatology classification criteria for juvenile psoriatic arthritis. Arthritis Rheum. 2008; 59:51–8.
crossref
19. Barnes MG, Thompson SD, Griffin TA, Grom AA, Glass DN, Colbert RA. B-cell signature in patients with JIA is associated with age of onset suggesting biologically relevant classification criteria. Arthritis Rheum. 2009; 60(Suppl 10):620.
20. Prakken B, Albani S, Martini A. Juvenile idiopathic arthritis. Lancet. 2011; 377:2138–49.
crossref
21. Barnes MG, Grom AA, Thompson SD, Griffin TA, Luyrink LK, Colbert RA, et al. Biologic similarities based on age at onset in oligoarticular and polyarticular subtypes of juvenile idiopathic arthritis. Arthritis Rheum. 2010; 62:3249–58.
crossref
22. Borchers AT, Selmi C, Cheema G, Keen CL, Shoenfeld Y, Gershwin ME. Juvenile idiopathic arthritis. Autoimmun Rev. 2006; 5:279–98.
crossref
23. Aletaha D, Neogi T, Silman AJ, Funovits J, Felson DT, Bingham CO 3rd, et al. 2010 Rheumatoid arthritis classification criteria: an American College of Rheumatology/ European League Against Rheumatism collaborative initiative. Arthritis Rheum. 2010; 62:2569–81.
24. Rantapää-Dahlqvist S, de Jong BA, Berglin E, Hallmans G, Wadell G, Stenlund H, et al. Antibodies against cyclic citrullinated peptide and IgA rheumatoid factor predict the development of rheumatoid arthritis. Arthritis Rheum. 2003; 48:2741–9.
crossref
25. Kang M, Sohn TY, Kim SH, Lee HR, Kang HJ, Kim KN. The clinical significance of anti-cyclic citrullinated peptide anti-bodies in juvenile rheumatoid arthritis. J Rheum Dis. 2014; 21:236–40.
crossref
26. Omar A, Abo-Elyoun I, Hussein H, Nabih M, Atwa H, Gad S, et al. Anti-cyclic citrullinated peptide (anti-CCP) anti-body in juvenile idiopathic arthritis (JIA): correlations with disease activity and severity of joint damage (a multicenter trial). Joint Bone Spine. 2013; 80:38–43.
crossref
27. Ferucci ED, Majka DS, Parrish LA, Moroldo MB, Ryan M, Passo M, et al. Antibodies against cyclic citrullinated peptide are associated with HLA-DR4 in simplex and multiplex polyarticular-onset juvenile rheumatoid arthritis. Arthritis Rheum. 2005; 52:239–46.
crossref
28. Burgos-Vargas R. The assessment of the spondyloarthritis international society concept and criteria for the classification of axial spondyloarthritis and peripheral spondyloarthritis: A critical appraisal for the pediatric rheumatologist. Pediatr Rheumatol Online J. 2012; 10:14.
crossref
29. Helliwell PS, Hetthen J, Sokoll K, Green M, Marchesoni A, Lubrano E, et al. Joint symmetry in early and late rheumatoid and psoriatic arthritis: comparison with a mathematical model. Arthritis Rheum. 2000; 43:865–71.
crossref
30. Shin JI, Kim KH, Chun JK, Lee TJ, Kim KJ, Kim HS, et al. Prevalence and patterns of anti-nuclear antibodies in Korean children with juvenile idiopathic arthritis according to ILAR criteria. Scand J Rheumatol. 2008; 37:348–51.
crossref
31. Lee JH, Ryu JM, Park YS. Clinical observations of juvenile rheumatoid arthritis. Korean J Pediatr. 2006; 49:424–30.
crossref
32. Saurenmann RK, Rose JB, Tyrrell P, Feldman BM, Laxer RM, Schneider R, et al. Epidemiology of juvenile idiopathic arthritis in a multiethnic cohort: ethnicity as a risk factor. Arthritis Rheum. 2007; 56:1974–84.
crossref
33. Arguedas O, Fasth A, Andersson-Gäre B, Porras O. Juvenile chronic arthritis in urban San José, Costa Rica: a 2 year prospective study. J Rheumatol. 1998; 25:1844–50.
34. Aggarwal A, Misra R. Juvenile chronic arthritis in India: is it different from that seen in Western countries? Rheumatol Int. 1994; 14:53–6.
crossref
35. Colbert RA. Classification of juvenile spondyloarthritis: Enthesitis-related arthritis and beyond. Nat Rev Rheumatol. 2010; 6:477–85.
crossref
36. van Rossum M, van Soesbergen R, de Kort S, ten Cate R, Zwinderman AH, de Jong B, et al. Anti-cyclic citrullinated peptide (anti-CCP) antibodies in children with juvenile idiopathic arthritis. J Rheumatol. 2003; 30:825–8.
37. Guzmán J, Burgos-Vargas R, Duarte-Salazar C, Gómez-Mora P. Reliability of the articular examination in children with juvenile rheumatoid arthritis: interobserver agreement and sources of disagreement. J Rheumatol. 1995; 22:2331–6.
38. Nielen MM, van Schaardenburg D, Reesink HW, van de Stadt RJ, van der Horst-Bruinsma IE, de Koning MH, et al. Specific autoantibodies precede the symptoms of rheumatoid arthritis: a study of serial measurements in blood donors. Arthritis Rheum. 2004; 50:380–6.
crossref
39. Kroot EJ, de Jong BA, van Leeuwen MA, Swinkels H, van den Hoogen FH, van't Hof M, et al. The prognostic value of anticyclic citrullinated peptide antibody in patients with recent-onset rheumatoid arthritis. Arthritis Rheum. 2000; 43:1831–5.
crossref
40. Bracaglia C, de Graaf K, Pires Marafon D, et al. Elevated circulating levels of interferon-γ and interferon-γ-induced chemokines characterise patients with macrophage activation syndrome complicating systemic juvenile idiopathic arthritis. Ann Rheum Dis. 2017; 76:166–72.
crossref

Figure 1.
Comparison of sub-types between the ILAR classification and the new provisional classification. ILAR: International League of Associations for Rheumatology, RF: rheumatoid factor, ESR: enthesitis/ spondylitis-related, JIA: juvenile idiopathic arthritis, ANA: anti-nuclear antibody.
jrd-25-34f1.tif
Table 1.
Demographic and patient characteristics of JIA patients classified by the ILAR classification
Variable Systemic arthritis Oligoarthritis
RF-negative polyarthritis RF-positive polyarthritis Psoriatic arthritis ERA Undifferentiated arthritis Total
PE EX
Patient 73 (27.9) 39 (14.9) 16 (6.1) 37 (14.1) 15 (5.7) 1 (0.4) 63 (24.0) 18 (6.9) 262 (100)
Male: Female (female, %) 38:35 (47.9) 11:28 (71.8) 5:11 (68.8) 11:26 (70.3) 4:11 (73.3) 0:1 (100) 57:6 (9.5) 6:12 (66.7) 132:130 (49.6)
Disease onset, median (IQR) (yr) 6.0 (3.8∼9.4) 3.5 (2.3∼5.4 ) 3.5 (2.1∼11.3 ) 7.3 (3.3∼10.9 9) 7.7 (5.9∼11.9 9) 11.8 9.8 (7.8∼11.8 8) 6.7 (4.5∼9.5) 7.3 (3.9∼10.5)
RF 0 (0) 0 (0) 0 (0) 0 (0) 15 (100) 0 (0) 0 (0) 14 (77.8) 29 (11.1)
Anti-CCP Ab 2 (2.7) 0 (0) 2 (12.5) 3 (8.1) 13 (86.7) 0 (0) 1 (1.6) 10 (55.6) 31 (11.8)
ANA 12 (16.4) 15 (38.5) 4 (25.0) 15 (40.5) 11 (73.3) 0 (0) 8 (12.7) 9 (50.0) 74 (28.2)
HLA-B27 5 (6.8) 4 (10.3) 2 (12.5) 8 (21.6) 1 (6.7) 0 (0) 58 (92.1) 6 (33.3) 84 (32.1)
Uveitis 7 (9.6) 8 (20.5) 4 (25.0) 2 (5.4) 1 (6.7) 0 (0) 9 (14.3) 1 (5.6) 32 (12.2)
Enthesitis 1 (1.4) 1 (2.6) 0 (0) 2 (5.4) 0 (0) 0 (0) 32 (50.8) 1 (5.6) 37 (14.1)
Symmetricity 35 (47.9) 7 (17.9) 8 (50.0) 30 (81.1) 13 (86.7) 0 (0) 15 (23.8) 9 (50.0) 117 (44.7)
Cumulative number of joints involved, mean±SD 7.3±9.2 2.1±1.1 9.4±3.9 13.4±7.4 15.5±8.4 4 6.0±6.2 11.4±8.9 8.0±8.0
Upper large joint 36 (49.3) 7 (17.9) 15 (93.8) 29 (78.4) 14 (93.3) 0 (0) 17 (27.0) 16 (88.9) 134 (51.1)
Upper small joint 21 (28.8) 3 (7.7) 7 (43.8) 29 (78.4) 15 (100.0) 1 (100) 17 (27.0) 9 (50.0) 102 (38.9)
Lower large joint 60 (82.2) 35 (89.7) 15 (93.8) 33 (89.2) 11 (73.3) 0 (0) 59 (93.7) 17 (94.4) 230 (87.8)
Lower small joint 13 (17.8) 2 (5.1) 3 (18.8) 18 (48.6) 11 (73.3) 0 (0) 26 (41.3) 5 (27.8) 78 (29.8)
Axial joint 20 (27.4) 4 (10.3) 8 (50.0) 21 (56.8) 9 (60.0) 1 (100) 34 (54.0) 8 (44.4) 105 (40.1)

Except where indicated otherwise, values are the number (%). JIA: juvenile idiopathic arthritis, ILAR: International League of Associations for Rheumatology, PE: persistent, EX: extended, RF: rheumatoid factor, ERA: enthesitis-related arthritis, IQR: interquartile range, Anti-CCP Ab: anti-cyclic citrullinated peptide antibody, ANA: antinuclear antibody, HLA: human leukocyte antigen, SD: standard deviation.

Table 2.
Demographic and patient characteristics of subtypes in new provisional classification
Variable sJIA RF-JIA eoANA-JIA ESR-JIA Other JIA Unclassified JIA Total p-value Comparisons significant on post-hoc tests
Patient ILAR subtypes (n) 71 (27.1) 31 (11.8) 22 (8.4) 63 (24.0) 65 (24.8) 10 (3.8) 262 (100)    
Systemic arthritis 71 0 0 0 0 2 73    
Oligoarthritis PE 0 0 12 0 27 0 39    
Oligoarthritis EX 0 2 3 0 11 0 16    
Polyarthritis RF (−) 0 3 7 0 27 0 37    
Polyarthritis RF (+) Psoriatic arthritis 0 0 15 0 0 0 0 1 0 0 0 0 15 1    
ERA 0 0 0 62 0 1 63    
Undifferentiated 0 11 0 0 0 7 18    
Male: Female (female, %) 38:33 (46.5) 7:24 (77.4) 5:17 (77.3) 56:7 (11.1) 20:45 (69.2) 6:4 (40.0) 132:130 (49.6) <0.00001 RF vs. ESR ANA vs. ESR
Disease onset, median (IQR) (yr) 6.0 (3.8∼9.3) 7.0 (4.0∼9.6) 2.4 (2.1∼4.2) ) 9.8 (7.8∼11.8) 5.6 (3.0∼10.9) 9.0 (5.2∼12.2) 7.3 (3.9∼10.5) <0.00001 ANA vs. RF RF vs. ESR
                  ANA vs. ESR
RF 0 (0) 26 (83.9) 0 (0) 0 (0) 0 (0) 3 (30.0) 29 (11.1)    
Anti-CCP Ab 0 (0) 27 (87.1) 0 (0) 0 (0) 0 (0) 4 (40.0) 31 (12.7)    
ANA 12 (16.9) 19 (61.3) 22 (100) 8 (12.7) 11 (16.9) 2 (20.0) 74 (28.2)    
HLA-B27 5 (7.4) 5 (17.2) 4 (20.0) 57 (90.5) 7 (10.8) 6 (60.0) 84 (32.9) <0.00001 RF vs. ESR
                  ANA vs. ESR
Uveitis 7 (9.9) 2 (6.5) 7 (31.8) 9 (14.3) 7 (10.8) 0 (0) 32 (12.2) 0.039  
Enthesitis 1 (1.4) 0 (0) 0 (0) 31 (49.2) 3 (4.6) 2 (20.0) 37 (14.1) <0.00001 RF vs. ESR
Symmetricity 34 (47.9) 19 (61.3) 5 (22.7) 14 (22.2) 38 (58.5) 7 (70.0) 117 (44.7) 0.0004 ANA vs. ERA RF vs. ESR
Cumulative no. of joints involved, mean±SD 7.4±9.3 14.2±7.9 6.0±6.3 6.1±6.2 8.0±7.2 8.8±9.4 8.0±8.0 <0.00001 ANA vs. RF ANA vs. RF RF vs. ERA
Upper large joint 35 (49.3) 29 (93.5) 12 (54.5) 17 (27.0) 35 (53.8) 6 (60.0) 134 (51.1) <0.00001 RF vs. ESR
Upper small joint 20 (28.2) 25 (80.6) 9 (40.9) 18 (28.6) 26 (40.0) 4 (40.0) 102 (38.9) 0.00001 ANA vs. RF RF vs. ESR
Lower large joint 59 (83.1) 27 (87.1) 19 (86.4) 58 (92.1) 59 (90.8) 8 (80.0) 230 (87.8) 0.647 ANA vs. RF
Lower small joint 12 (16.9) 16 (51.6) 9 (27.3) 26 (41.3) 15 (23.1) 3 (30.0) 78 (29.8) 0.208  
Axial joint 20 (28.2) 16 (51.6) 3 (13.6) 35 (55.6) 27 (41.5) 4 (40.0) 105 (40.1) 0.003 ANA vs. ESR
                  ANA vs. RF
ASAS criteria 9 (12.7) 6 (19.4) 10 (45.5) 62 (98.4) 14 (21.5) 6 (60.0) 107 (40.8) <0.00001 RF vs. ESR
                  ANA vs. ESR
Axial SpA (n) 0 0 0 9 1 1 11    
Peripheral SpA (n) 9 6 10 53 13 5 96    

Except where indicated otherwise, values are the number (%). JIA: juvenile idiopathic arthritis, sJIA: systemic JIA, RF-JIA: Rheumatoid factor-positive JIA, eoANA-JIA: early-onset antinuclear antibody-positive JIA, ESR-JIA: enthesitis/spondylitis-related JIA, ILAR: International League of Associations for Rheumatology, PE: persistent, EX: extended, ERA: enthesitis-related arthritis, IQR: interquartile range, Anti-CCP Ab: anti-cyclic citrullinated peptide antibody, ANA: antinuclear antibody, HLA: human leukocyte antigen, SD: standard deviation, ASAS: Assessment of SpondyloArthritis International Society, SpA: spondyloarthritis.

* For overall comparisons. Following three subtypes were compared statistically—RF positive arthritis, ANA positive arthritis, and ERA/SpA. Comparisons of quantitative data were made by Mann-Whitney U test; comparisons of frequencies were made by chi-square test (or by Fishers exact test if expected frequencies were <5).

Pairs of comparisons that were statistically significant on post-hoc tests (Bonferroni adjustment). RF: RF-JIA, ANA: eoANA-JIA, ESR: ESR-JIA.

Table 3.
Joint involvement of RF-positive juvenile idiopathic arthritis (RF-JIA), early-onset ANA-positive JIA (eoANA-JIA) and Enthesitis/spondylitis related JIA (ESR-JIA)
Variable RF-JIA eoANA-JIA ESR-JIA p-value Comparisons significant on post-hoc test
Lower limbs Knee 23 (74.2) 18 (81.8) 51 (81.0) 0.711  
Ankle 25 (80.6) 11 (50.0) 37 (58.7) 0.045  
MTP joint 15 (48.4) 4 (18.2) 18 (28.6) 0.047  
Toe 8 (25.8) 3 (13.6) 16 (25.4) 0.493  
Upper limbs          
Elbow 14 (45.2) 8 (36.4) 7 (11.1) 0.001 RF vs. ESR
Wrist 28 (93.3) 7 (31.8) 13 (20.6) <0.00001 ANA vs. RF
MCP joint 14 (45.2) 5 (22.7) 13 (20.6) 0.037 RF vs. ESR RF vs. ESR
Finger 21 (67.7) 8 (36.4) 8 (12.7) <0.00001 RF vs. ESR
Axial joints          
TMJ 4 (12.9) 2 (9.1) 4 (6.3) 0.565  
Neck 1 (3.2) 1 (3.0) 8 (12.7) 0.087  
Shoulder 11 (35.5) 0 (0) 11 (17.5) 0.005 ANA vs. RF
Back 0 (0) 0 (0) 10 (15.9) 0.010  
Sacroiliac joint 1 (3.2) 0 (0) 9 (14.3) 0.055  
Hip 12 (38.7) 2 (9.1) 26 (41.3) 0.020 ANA vs. RF
          ANA vs. ESR

Except where indicated otherwise, values are the number (%). Comparisons of frequencies were made by chi-square test (or by Fisher's exact test if expected frequencies were <5). RF: rheumatoid factor, ANA: antinuclear antibody, MTP: metatarsophalangeal, MCP: metacarpophalangeal, TMJ: temporomandibular joint, ERA: enthesitis-related arthritis, SpA: spondyloarthritis.

* For overall comparisons. Following three subtypes were compared statistically― RF positive arthritis, ANA positive arthritis, and ERA/SpA. Comparisons of quantitative data were made by Mann-Whitney U test; comparisons of frequencies were made by chi-square test (or by Fisher's exact test if expected frequencies were <5).

Pairs of comparisons that were statistically significant on post-hoc tests (Bonferroni adjustment). RF: RF-JIA, ANA: eoANA-JIA, ESR: ESR-JIA

Table 4.
Univariate logistic regression analysis on rheumatoid factor (RF) and anti-cyclic citrullinated peptide antibody (anti-CCP Ab)
Variable RF Anti-CCP Ab
p-value Exp(β) (95% CI) p-value Exp(β) (95% CI)
Female 0.002 4.514 (1.773∼11.495) 0.005 3.332 (1.431∼7.757)
Age (>6 yr) 0.743 0.879 (0.406∼1.903) 0.662 1.183 (0.557∼2.512)
Uveitis 0.363 0.501 (0.113∼2.216) 0.137 0.215 (0.028∼1.634)
Enthesitis 0.998 0.000 (not available) 0.104 0.187 (0.025∼1.414)
ANA 0.000 7.366 (3.169∼17.123) 0.000 4.327 (1.995∼9.385)
HLA-B27 0.018 0.227 (0.066∼0.776) 0.238 0.585 (0.240∼1.424)
Number of Joints involved (≥5) 0.001 5.885 (1.986∼17.440) 0.001 6.464 (2.192∼19.059)
Symmetricity 0.020 2.617 (1.166∼5.876) 0.051 2.149 (0.997∼4.633)

CI: confidence interval, ANA: antinuclear antibody, HLA: human leukocyte antigen.

Table 5.
Comparison of ANA-positive patients and ANA-negative patients
Variable ANA-positive patients ANA-negative patients p-value
Patient 35 (36.8) 60 (63.2)  
Male: Female 7:28 (80.0) 24:36 (60.0) 0.045
(female, %)      
Disease onset, median (IQR) (yr) 4.1 (2.3∼8.0) 5.1 (2.8∼11.3) 0.104
Uveitis 9 (25.7) 5 (8.3) 0.021
Enthesitis 1 (2.9) 4 (6.7) 0.649
HLA-B27 5 (15.2) 12 (20.0) 0.563
Symmetricity 14 (40.0) 35 (58.3) 0.085
Cumulative number of joints involved, mean±SD 8.9±9.1 7.0±5.9 0.623
Upper large joint 21 (60.0) 31 (51.7) 0.431
Upper small joint 18 (51.4) 20 (33.3) 0.082
Lower large joint 30 (85.7) 55 (91.7) 0.490
Lower small joint 10 (28.6) 13 (21.7) 0.449
Axial joint 11 (31.4) 23 (38.3) 0.498

Except where indicated otherwise, values are the number (%). Comparisons of quantitative data were made by Mann-Whitney U test; comparisons of frequencies were made by chi-square test (or by Fisher's exact test if expected frequencies were <5). ANA: antinuclear antibody, IQR: interquartile range, HLA: human leukocyte antigen, SD: standard deviation.

TOOLS
Similar articles