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. Author manuscript; available in PMC: 2018 Jan 6.
Published in final edited form as: J Proteome Res. 2016 Oct 20;16(1):355–365. doi: 10.1021/acs.jproteome.6b00617

Table 2.

Clinical Characteristics of RA Patients Grouped by PAD4 T Cell Statusa

total
(n = 19)
group 1 T cell negative
(n = 14)
group 2 T cell positive
(n = 5)
group 1 vs group 2
p-value
gender, % female 58 57 60 0.99
raceb, % caucasian 94 (n = 18) 92 (n = 13) 100 0.99
age, mean years ± SD 64 ±9 64 ± 10 65 ± 7 0.82
RA duration, years 18 (13−28) 17 (13−30) 19 (14−20) 0.59
DR1 positive, % 74 71 80 0.99
DR4 positive, % 63 50 100 0.11
DR1 and DR4 positive, % 42 29 80 0.11
anti-CCP, % 100 100 100 0.99
anti-CCPb, units 100 (64−160) (n = 18) 100 (64−160) (n = 13) 100 (96−122) 0.92
anti-PAD4, % 63 64 60 0.99
CRPb, mg/L 0.8 (0.4−1.6) (n = 17) 0.6 (0.4−1.0) (n = 13) 2.1 (1.2−3.2) (n = 4) 0.042
CDAI scoreb 6.0 (1.0−9.5) (n = 15) 5.6 (1.0−11.0) (n = 12) 6.0 (1.3−6.0) (n = 3) 0.77
prednisoneb, % 24 (n = 17) 23 (n = 13) 25 (n = 4) 0.99
nonbiologic DMARDsb, % 76 (n = 17) 77 (n = 13) 75 (n = 4) 0.99
biologic DMARDsb, % 76 (n = 17) 69 (n = 13) 100 (n = 4) 0.52
a

Median (interquartile range) depicted unless otherwise noted.

b

Only patients with available data were included; n is indicated.

Anti-CCP = anticyclic citrullinated peptide antibodies; CDAI = clinical disease activity index; CRP = C-reactive protein; DMARDs = disease-modifying antirheumatic drugs including nonbiologic (methotrexate, sulfasalazine, leflunomide, and/or hydroxychloroquine) and biologic (monoclonal antibody inhibitors of TNFα, IL-6, or T cell costimulation); SD = standard deviation.