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1 t predictors (hazard ratios) of failure were rheumatoid arthritis (2.36), late post-surgical infectio
3 .8; 95% confidence interval [CI] = 1.2-2.5), rheumatoid arthritis (adjusted OR = 1.7; 95% CI = 1.5-1.
6 8.41), or ever having been hospitalized for rheumatoid arthritis (OR = 7.36; 95% CI: 2.95, 18.38).
7 1.27); anemia (OR, 1.19; 95% CI, 1.15-1.25); rheumatoid arthritis (OR, 1.19; 95% CI, 1.10-1.29); coag
8 .58; 95% CI, 1.51-1.66), osteoarthritis with rheumatoid arthritis (OR, 1.58; 95% CI, 1.38-1.82), anti
9 portance of studying individuals at risk for rheumatoid arthritis (pre-RA) and those with early RA (e
14 ible correlation of periodontal disease with rheumatoid arthritis (RA) and ankylosing spondylitis (AS
16 ne dysfunction underlies the pathogenesis of rheumatoid arthritis (RA) and inflammatory bowel disease
17 t prevalent AD is a risk factor for incident rheumatoid arthritis (RA) and inflammatory bowel disease
18 ated TACE-mediated disease models of sepsis, rheumatoid arthritis (RA) and inflammatory bowel disease
19 e development of autoimmune diseases such as rheumatoid arthritis (RA) and is associated with the exp
28 d a large-scale MHC fine-mapping analysis of rheumatoid arthritis (RA) in a Japanese population (6,24
40 the increased risk of heart failure (HF) in rheumatoid arthritis (RA) is independent of ischemic hea
41 o suggest that autoimmunity in patients with rheumatoid arthritis (RA) is initiated outside the joint
44 revious studies suggest that pathogenesis of rheumatoid arthritis (RA) is similar in all affected joi
47 rs in healthy donors (HDs) and patients with rheumatoid arthritis (RA) or systemic lupus erythematosu
48 o treat auto-immune related diseases such as rheumatoid arthritis (RA) or systemic lupus erythematosu
50 uccinate is abundant in synovial fluids from rheumatoid arthritis (RA) patients, and these fluids eli
56 pirical data from a large-scale trans-ethnic rheumatoid arthritis (RA) study and showed that the func
58 TNF-alpha is a major cytokine implicated in rheumatoid arthritis (RA), and its expression is regulat
59 er for clinical improvement in patients with rheumatoid arthritis (RA), and macrophages are reduced i
60 arget therapy is effective for patients with rheumatoid arthritis (RA), but long-term results of cont
64 code a "shared epitope" (SE) associated with rheumatoid arthritis (RA), especially more severe cyclic
67 ts, and identified significant enrichment in rheumatoid arthritis (RA), kidney function, and adult he
68 tified over 100 genetic loci associated with rheumatoid arthritis (RA), our ability to translate thes
69 s specific for different forms of arthritis (rheumatoid arthritis (RA), psoriatic arthritis (PsA), os
95 the chronic inflammatory autoimmune disease rheumatoid arthritis (RA); however, controversial data a
96 cupation of farming has been associated with rheumatoid arthritis (RA); pesticides may account for th
99 , we identified largest-ever effect on Asian rheumatoid arthritis across human non-HLA regions at GTF
100 gible participants were patients with active rheumatoid arthritis aged at least 18 years, with four o
102 enrolled patients with active, seropositive rheumatoid arthritis and an inadequate response to synth
103 in the inflamed synovium from patients with rheumatoid arthritis and compared with synovium from hea
106 lammatory reflex to significantly ameliorate rheumatoid arthritis and inflammatory bowel disease prov
107 eases such as cancer, inflammatory diseases (rheumatoid arthritis and inflammatory bowel disease), me
108 of-concept is established for immune-related rheumatoid arthritis and inflammatory bowel disease, as
109 various inflammatory disease models, such as rheumatoid arthritis and inflammatory bowel disease.
110 ity, and deregulated PGRN is associated with rheumatoid arthritis and inflammatory bowel disease.
111 e IL-6 pathway, has been approved for use in rheumatoid arthritis and interest in transplantation has
113 bitor treatment in patients seropositive for rheumatoid arthritis and naive to treatment with biologi
115 eting IL-20 is effective in the treatment of rheumatoid arthritis and psoriasis, both with strong GWA
117 nically approved agents for the treatment of rheumatoid arthritis and renal transplantation, respecti
118 Apoptotic CD4(+) T cells from patients with rheumatoid arthritis and systemic lupus erythematosus we
119 viously been implicated in severity of human rheumatoid arthritis and systemic lupus erythematosus, i
120 nd, more common autoimmune diseases, such as rheumatoid arthritis and systemic lupus erythematosus, s
121 ts who required NSAIDs for osteoarthritis or rheumatoid arthritis and were at increased cardiovascula
122 of pleiotropy was observed between PTSD and rheumatoid arthritis and, to a lesser extent, psoriasis.
123 nective tissue diseases (CTD) like lupus and rheumatoid arthritis associate with cardiovascular risk,
124 e aged 18 years or older with a diagnosis of rheumatoid arthritis at screening, as defined by the 201
125 control of inflammation optimise outcomes in rheumatoid arthritis but these approaches have not yet b
126 s) and European (n = 45,790; 11 collections) rheumatoid arthritis case-control cohorts with Immunochi
127 core in 28 joints (DAS28) was calculated and rheumatoid arthritis classification criteria applied.
128 D-naive, aged 18 years or older, met current rheumatoid arthritis classification criteria, and had a
130 shock protein 90 (HSP90) are associated with rheumatoid arthritis complicated by interstitial lung di
132 nt genetic studies in the KRN mouse model of rheumatoid arthritis demonstrate that the immunomodulato
133 ding TNF inhibitors, in patients with active rheumatoid arthritis despite methotrexate therapy are la
135 medication (OR = 3.98; 95% CI: 2.08, 7.62), rheumatoid arthritis duration of 6-20 years (OR = 3.80;
136 channel expressed at the plasma membrane of rheumatoid arthritis fibroblast-like synoviocytes (RA-FL
138 es of treatment response in the Biologics in Rheumatoid Arthritis Genetics and Genomics Study Syndica
141 ess the efficacy and safety of sirukumab for rheumatoid arthritis in a phase 3 study (SIRROUND-T).
143 drug or gene delivery and novel therapy for rheumatoid arthritis in an in situ forming gel formulati
144 with distinct effects on the development of rheumatoid arthritis in Asian and European populations.
145 mumab plus methotrexate for the treatment of rheumatoid arthritis in patients with a previous inadequ
146 xate combination therapy in the treatment of rheumatoid arthritis in patients with an inadequate resp
161 or tofacitinib's success in the treatment of rheumatoid arthritis led to biopharma's abandonment of i
162 rthritis, such as ever having received daily rheumatoid arthritis medication (OR = 3.98; 95% CI: 2.08
164 nd observational studies involved those with rheumatoid arthritis or inflammatory bowel disease.
167 e formation, while DCs from CTLA4-Ig-treated rheumatoid arthritis patients displayed diminished LC3B
168 torial staining approach to demonstrate that rheumatoid arthritis patients on therapy can mount effec
169 of platelets with synovial fluid cells from rheumatoid arthritis patients reduced inflammatory cytok
170 diovascular events in psoriasis patients and rheumatoid arthritis patients treated with tumor necrosi
171 ces to inhibit cytokines and inflammation in rheumatoid arthritis patients, and provided a mosaic vie
174 nclusions and Relevance: Among patients with rheumatoid arthritis previously treated with anti-TNF dr
179 subset of late phase genes was expressed in rheumatoid arthritis synovial macrophages, confirming th
181 ritical for the induction and progression of rheumatoid arthritis through its pivotal role in the dev
184 r, reduced disease activity in patients with rheumatoid arthritis who had not previously received tre
185 A 54-year-old white woman with a history of rheumatoid arthritis who was taking glucocorticoids and
186 INTERPRETATION: In patients with active rheumatoid arthritis who were refractory or intolerant t
187 risk of serious infections in patients with rheumatoid arthritis who were treated with biological dr
188 ncluded patients who had been diagnosed with rheumatoid arthritis within 1 year before inclusion, wer
189 o systemic (systemic lupus erythematosus and rheumatoid arthritis) and two organ-specific (multiple s
191 characterized in autoimmune disorders (e.g., rheumatoid arthritis), but there are some exceptional lo
195 Inclusion criteria were (i) patients with rheumatoid arthritis, (ii) adult population age >/=16yea
196 ; median [range] age, 59.5 [30-80] y), 6 had rheumatoid arthritis, 5 had psoriasis, 6 had inflammator
197 We included 16 studies (9 of patients with rheumatoid arthritis, 8 of patients with inflammatory bo
198 d T cells in joint tissue from patients with rheumatoid arthritis, a chronic immune-mediated arthriti
199 en periodontitis and cardiovascular disease, rheumatoid arthritis, Alzheimer's disease, pulmonary dis
200 re profoundly protected in several models of rheumatoid arthritis, and Ab blockade of G-CSF also prot
202 act of AMDs on systemic lupus erythematosus, rheumatoid arthritis, and devastating monogenic disorder
203 infections, allergies, autoimmune diseases, rheumatoid arthritis, and inflammatory bowel disease.
204 this system has been noted in patients with rheumatoid arthritis, and its pathogenic role has been c
205 teers, phase 3 trials involved patients with rheumatoid arthritis, and observational studies involved
207 plied our method to data on gene expression, rheumatoid arthritis, and type 2 diabetes and overwhelmi
209 therapies, however, which are effective for rheumatoid arthritis, are either ineffective for psorias
211 n are highly effective treatments for active rheumatoid arthritis, but so far no randomised controlle
212 ion covering gene DSC3 being associated with rheumatoid arthritis, but the GCP provides smaller P-val
213 diabetes, Crohn disease, ulcerative colitis, rheumatoid arthritis, celiac disease, psoriasis, and mul
214 es the severity of various illnesses such as rheumatoid arthritis, diabetes, and liver diseases.
215 ons (i.e. psoriasis, ankylosing spondylitis, rheumatoid arthritis, fibromyalgia) than those with NWU
217 ed cytokines in autoimmune diseases, such as rheumatoid arthritis, inflammatory bowel disease, and sy
218 emonstrated to provide a therapeutic role in rheumatoid arthritis, inflammatory intestinal disease, c
219 to chronic autoimmune inflammation, such as rheumatoid arthritis, is ill defined and probably requir
220 ddison's disease, primary biliary cirrhosis, rheumatoid arthritis, juvenile idiopathic arthritis, and
221 ed CRP levels with psoriatic osteoarthritis, rheumatoid arthritis, knee osteoarthritis, systolic bloo
222 ring the complex role of IL-33 in a model of rheumatoid arthritis, namely, collagen-induced arthritis
223 enous IL-1 receptor antagonist used to treat rheumatoid arthritis, normalizes hippocampal neurotransm
224 wn to be effective in managing patients with rheumatoid arthritis, patient outcomes sensitive to nurs
225 chronic conditions such as atherosclerosis, rheumatoid arthritis, psoriasis, and Crohn's disease.
226 cancers and increased risks for lung cancer, rheumatoid arthritis, Sjogren syndrome, and Raynaud synd
227 he development of autoimmunity, particularly rheumatoid arthritis, still needs extensive exploration.
229 sk was higher when we used proxies of severe rheumatoid arthritis, such as ever having received daily
230 sue disorders: systemic lupus erythematosus, rheumatoid arthritis, systemic sclerosis, and anti-neutr
232 ge 1) and Crohn disease, ulcerative colitis, rheumatoid arthritis, type 1 diabetes, celiac disease, a
233 jacent to GAK, HLA-DRB5, LRRK2, and MAPT for rheumatoid arthritis, ulcerative colitis and Crohn disea
234 patients (conducted between 2009-2012) with rheumatoid arthritis, with persistent disease activity (
235 Comparison groups included patients with rheumatoid arthritis-associated ILD (RA-ILD; n = 33), pa
236 l-length sgp130 and the shorter forms sgp130-rheumatoid arthritis-associated peptide (RAPS) and sgp13
282 ent types of CTD were analyzed individually (rheumatoid arthritis; lupus; scleroderma; Sjogren Syndro
283 were suppressed in macrophages isolated from rheumatoid-arthritis patients, revealing a disease-assoc
287 an biomarkers for the classification of both rheumatoid factor (RF)-positive and negative RA patients
288 profile, level of alanine aminotransferase, rheumatoid factor activity, C4 fraction of complement, a
289 t circulating autoantibodies, including both rheumatoid factor and anti-citrullinated protein antibod
291 adjustment for CVD risk factors, joint pain, rheumatoid factor positivity, and inflammatory markers (
292 n non-B cells, we transferred anti-self-IgG (rheumatoid factor) B cells and their physiologic target
293 otein, erythrocyte sedimentation rate (ESR), rheumatoid factor, anticitrullinated protein antibodies
294 re disease progression, including a positive rheumatoid factor, or anti-cyclic citrullinated peptide
295 In 358 children with oligoarthritis and rheumatoid factor-negative polyarthritis, erythrocyte se
296 pendent autoreactive EF response elicited in rheumatoid-factor B cells by DNA-containing immune compl
298 tance of periodontal pathogenic bacteria and rheumatoid parameters in the interrelationship between p
300 anscription analysis of ICBP90 shRNA-treated rheumatoid synoviocytes uncovered a subset of proinflamm
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