Abstract
Background
The aim of our study was to investigate the influence of conventional synthetic disease-modifying anti-rheumatic drugs (csDMARDs) and body mass index (BMI) on circulating drug levels and clinical response to tumour necrosis factor inhibitor (TNFi) therapy in axial spondyloarthritis (axSpA) patients.
Methods
Prospective observational study during 1 year with 2 cohorts (Madrid and Amsterdam) including 180 axSpA patients treated with standard doses of infliximab or adalimumab. Patients were stratified by BMI, being 78 (43%) normal weight (18.5–24.9 kg/m2) and 102 (57%) overweight/obese (≥ 25.0 kg/m2). After the first year of treatment, TNFi trough levels were measured by capture ELISA. Clinical response to TNFi was defined as ∆BASDAI ≥ 2 and clinical remission as BASDAI < 2 and CRP ≤ 5 mg/L. Logistic regression models were employed to analyse the association between concomitant csDMARDs and BMI with drug levels and clinical response.
Results
Seventy-nine patients (44%) received concomitant csDMARDs. The administration of concomitant csDMARDs (OR 3.82; 95% CI 1.06–13.84) and being normal weight (OR 18.38; 95% CI 2.24–150.63) were independently associated with serum TNFi drug persistence. Additionally, the use of concomitant csDMARDs contributed positively to achieve clinical response (OR 7.86; 95% CI 2.39–25.78) and remission (OR 4.84; 95% CI 1.09–21.36) in overweight/obese patients, but no association was found for normal-weight patients (OR 1.10; 0.33–3.58).
Conclusions
The use of concomitant csDMARDs with TNFi may increase the probability of achieving clinical response in overweight/obese axSpA patients. Further research studies including larger cohorts of patients need to be done to confirm it.
Electronic supplementary material
The online version of this article (10.1186/s13075-019-1849-3) contains supplementary material, which is available to authorized users.
Keywords: Axial spondyloarthritis, TNF inhibitors, Concomitant csDMARDs, Body mass index, Clinical response
Introduction
In patients suffering from spondyloarthritis (SpA), conventional synthetic disease-modifying anti-rheumatic drugs (csDMARDs), such as methotrexate (MTX) and sulfasalazine (SSZ), can be useful for treating peripheral joint manifestations. However, they have not shown to be efficient for axial manifestations and therefore are not recommended by ASAS-EULAR to control axial disease [1].
Nevertheless, it has been described that the phenomenon of immunogenicity, an immune response that may hamper the efficacy of TNF inhibitor (TNFi) monoclonal antibodies [2, 3], can be modulated by co-administration of csDMARDs. To this regard, concomitant use of certain csDMARDs, especially MTX, may ameliorate the immunogenicity of infliximab and adalimumab by reducing anti-drug antibody (ADA) formation and therefore maintaining serum drug circulating levels and prolonging drug survival [4, 5].
However, immunogenicity is not the only cause for losing response to TNFi therapy. Other factors may be of influence. Currently, obesity is being considered as a risk factor for worsening clinical parameters of disease activity in patients with ankylosing spondylitis (AS). The increase of pro-inflammatory adipokines during obesity, such as vinfastin, correlates with the progression of radiographic damage in AS [6]. Furthermore, an increased body mass index (BMI) has been recently found to be associated with significantly lower response rates to TNFi in patients with axial (axSpA) [7, 8]. Some studies have furthermore demonstrated that high BMI is negatively associated with TNFi serum drug levels [9, 10].
In summary, both BMI and csDMARDs are associated with serum TNFi level persistence, but only BMI seems to be associated on clinical response to this therapy. To extent the knowledge on the relationship of these factors, the aim of this study was to investigate the influence of both BMI and concomitant csDMARDs on serum TNFi persistence as well as on the clinical response in patients with axSpA [7, 8].
Methods
Study design and patients
This was a prospective observational study. Data from two different cohorts including patients diagnosed of axSpA treated with standard doses of infliximab or adalimumab (infliximab 5 mg/kg at 0, 2, 6 weeks and later every 8 weeks; adalimumab 40 mg/2 weeks) according to the clinical practice guidelines were analysed. No modifications in the dose or interval of administration were carried out. Patients were included from June 2000 to June 2015. All included patients were diagnosed as axSpA according to physician criteria. The adherence to ASAS criteria was verified before including them into the study [11, 12]. When the datasets were locked (November 2016), a total of 246 patients had been enrolled in these cohorts: 166 from a Spanish inception cohort at the Department of Rheumatology of La Paz University Hospital (Madrid) and 80 from a Netherland cohort at the Department of Rheumatology of Reade Center (Amsterdam). For this study, only patients who had baseline BMI data available and serum drug levels measured or disease activity assessment during the first year of TNFi therapy after 1 year of starting infliximab or adalimumab were selected (n = 180). Out of these, 81% were naïve to biological therapy. It was described in a flowchart in Additional file 1. Non-radiographic axSpA and radiographic axSpA were defined according to physician and clinical practice, but imaging was not systematically read for this study. The study was conducted according to the guidelines of the 1975 Declaration of Helsinki. Approval was obtained from the Institutional Ethics Committee from both centres.
Clinical disease activity assessment
Disease activity was assessed by Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) and Ankylosing Spondylitis Disease Activity Score (ASDAS) at baseline (before starting TNFi treatment) and after 1 year of treatment. Clinical response to TNFi was defined as ΔBASDAI ≥ 2 and as ΔASDAS ≥ 1.1. Clinical remission was defined as BASDAI < 2 and CRP ≤ 5 mg/L and as ASDAS < 1.3. For all analyses, BASDAI was considered as the main variable due to the later development of the ASDAS in 2010, which explained why fewer patients from both cohorts were evaluated by this score (n = 170 patients with BASDAI score and n = 141 patients with ASDAS).
Determination of drug levels and anti-drug antibodies
Blood samples were collected at 24 h maximum before drug administration for adalimumab or immediately before intravenous infusions for infliximab.
Serum drug concentrations were determined by a capture enzyme-linked immunosorbent assay (ELISA), as described previously [13], using specific biotin-conjugated anti-idiotype antibodies to infliximab and adalimumab. Threshold values for positive drug levels were 10 ng/mL for infliximab and 5 ng/mL for adalimumab.
Serum anti-drug antibody (ADA) levels were analysed by radioimmunoassay (RIA), as described previously [14], using 125I-infliximab F(ab’)2 or 125I-adalimumab F(ab’)2. Threshold values for positive ADA levels were 12 AU/mL.
Statistical analyses
First, descriptive analysis was employed. According to BMI, patients were classified as normal weight (18.5–24.9 kg/m2) and overweight/obese (≥ 25.0 kg/m2). Differences between the groups were assessed using the unpaired t test or Mann-Whitney U test for continuous variables depending on the distribution and Fisher’s exact test for ordinal variables. Second, the association between concomitant csDMARDs and BMI with drug persistence and clinical response to TNFi at 1 year was analysed through univariate and multivariate logistic regression models. Interactions with age, gender, HLA-B27, BMI, csDMARDs and symptom duration were tested. If relevant interactions were found, analyses were stratified. If not, variables were entered as covariates. Additionally, the type of TNFi for drug persistence outcome and baseline disease activity (BASDAI and CRP) for clinical response outcome were included as covariates. Results are shown as odds ratio (OR) and 95% confidence interval (CI).
For TNFi levels, the last observation carried forward method (LOCF) was performed to include patients who dropped out before 1 year of follow-up (n = 43). Statistical significance was calculated considering p value < 0.05 statistically significant. The Statistical Package for the Social Sciences version 24 (SPSS, Chicago, IL, USA) was used for the analyses.
Results
Baseline characteristics
From a total of 246 patients, 180 patients with axSpA starting infliximab (n = 74) or adalimumab (n = 106) were included in the study. Patient and disease characteristics at baseline are shown in Table 1. There were no differences between the total group of patients and the patients included in the study. A total of 79 (44%) patients received concomitant csDMARD distributed as follows: MTX (25; 14%), SSZ (36; 20%) and MTX+SSZ (18; 10%). According to BMI, 78 (43%) patients were normal weight (18.5–24.9 kg/m2) and 102 (57%) were overweight/obese (≥ 25.0 kg/m2). Overall, no differences between both groups of BMI were found, except for age, sex, disease duration, TNFi type and concomitant sulfasalazine.
Table 1.
Baseline characteristics of patients included in the study
| Characteristics | Total patients (n = 246) | Included patients (n = 180) | Included patients BMI ≤ 25 (n = 78) | Included patients BMI > 25 (n = 102) |
|---|---|---|---|---|
| Age (years) | 47.6 ± 13.1 | 47.0 ± 12.7 | 42.9 ± 11.7 | 50.1 ± 12.6*** |
| Male | 146 (59) | 107 (59) | 39 (50) | 68 (67)* |
| Disease duration (years) | 10 (5–16) | 8 (5–16) | 7 (3–13) | 9 (6–18)** |
| SpA subtype | ||||
| Ankylosing spondylitis | 179 (78) | 140 (78) | 64 (82) | 76 (74) |
| Non-radiographic SpA | 49 (22) | 40 (22) | 14 (18) | 26 (26) |
| HLA-B27 | 174 (74) | 131 (73) | 61 (78) | 70 (69) |
| Psoriasis/IBD/uveitis | 71 (29) | 58 (32) | 27 (35) | 31 (30) |
| Peripheral arthritis | 97 (40) | 86 (48) | 38 (49) | 48 (47) |
| BASDAI | 5.8 ± 2.0 | 5.8 ± 2.0 | 5.5 ± 2.1 | 6.0 ± 1.9 |
| ASDAS | 3.3 ± 0.9 | 3.3 ± 1.0 | 3.2 ± 1.0 | 3.4 ± 1.0 |
| ESR (mmHg) | 17 (7–33) | 17 (7–31) | 19 (6–34) | 16 (7–31) |
| CRP (mg/L) | 5 (2–15) | 6 (3–17) | 7 (2–20) | 5 (3–15) |
| Previous TNFi | 43 (18) | 35 (19) | 13 (17) | 22 (21) |
| TNFi type | ||||
| Infliximab | 107 (43) | 74 (41) | 25 (32) | 49 (48)* |
| Adalimumab | 139 (57) | 106 (59) | 53 (68) | 53 (52)* |
| csDMARD | ||||
| Any csDMARD | 102 (42) | 79 (44) | 31 (40) | 48 (47) |
| MTX | 34 (15) | 25 (14) | 12 (15) | 13 (13) |
| SSZ | 46 (21) | 36 (20) | 10 (13) | 26 (25)* |
| MTX and SSZ | 22 (9) | 18 (10) | 9 (11) | 9 (9) |
| Prednisone | 22 (9) | 20 (11) | 11 (14) | 9 (9) |
The table shows mean ± SD, median (IQR) or absolute number (percentage) for all patients included (n = 180). The results are also stratified by body mass index (BMI). p value < 0.05 was considered statistically significant. Significant statistical differences between the groups of included patients, stratified by BMI: *p < 0.05, **p < 0.01, ***p < 0.001. SpA spondyloarthritis, HLA-B27 human leucocyte antigen B27, ESR erythrocyte sedimentation rate, CRP C-reactive protein, IBD inflammatory bowel disease, BASDAI Bath Ankylosing Spondylitis Disease Activity Index, ASDAS Ankylosing Spondylitis Disease Activity Index, TNFi tumour necrosis factor inhibitors, csDMARD conventional synthetic disease-modifying anti-rheumatic drug, MTX methotrexate, SSZ sulfasalazine
Effect of concomitant csDMARDs and BMI on persistence of TNFi in serum
A total of 157 patients (87%) had detectable circulating TNFi levels after 1 year of treatment. For this outcome, no significant interaction with other variables was found. Univariable analyses were performed to analyse the association between the persistence of serum TNFi and each variable included in Table 1. A significant association was found for being male (OR 0.32; 95% CI 0.11–0.89), disease duration (OR 0.94; 95% CI 0.90–0.98), being normal weight (OR 9.85; 95% CI 2.23–43.44) and concomitant csDMARDs (OR 2.71; 95% CI 1.03–7.14). In the multivariable logistic regression model, disease duration (OR 0.93; 95% CI 0.88–0.99), concomitant csDMARDs (OR 3.82; 95% CI 1.06–13.84) and especially being normal weight (OR 18.38; 95% CI 2.24–150.63) remained independently associated with serum TNFi persistence after 1 year of treatment (Table 2). Specifically, all the patients concomitantly treated with MTX [± SSZ] showed detectable TNFi levels after 1 year of treatment. At the same time, lower percentages of patients showing detectable TNFi levels after 1 year of treatment were found in the groups under TNFi monotherapy (83/101; 82%) or concomitantly treated with SSZ alone (31/36; 86%).
Table 2.
Association between csDMARDs and BMI with the presence of serum TNFi after 1 year of treatment
| OR | 95% CI | |
|---|---|---|
| Age | 1.04 | 0.98–1.11 |
| Male | 0.59 | 0.17–2.14 |
| Disease duration | 0.93 | 0.88–0.99* |
| TNFi type (ref: infliximab) | 0.46 | 0.15–1.39 |
| csDMARD (ref: use of any csDMARD) | 3.82 | 1.06–13.84* |
| BMI (ref: normal weight) | 18.38 | 2.24–150.63* |
The adjusted multivariable logistic regression analysis included 161 patients. Odds ratio (OR) and 95% confidence interval (CI) were calculated. *p value < 0.05 was considered statistically significant. TNFi tumour necrosis factor inhibitors, csDMARD conventional synthetic disease-modifying anti-rheumatic drug, BMI body mass index
These results were similar, regardless of the TNFi type. Patients receiving TNFi as monotherapy showed a higher percentage of undetectable drug levels than patients treated with MTX [± SSZ] after 1 year of treatment, regardless of the TNFi type (28% for infliximab, 17% for adalimumab; p = 0.2).
Concerning the association with BMI, patients who showed undetectable TNFi presented mainly overweight/obese (n = 21/23; 91%), regardless of the TNFi type.
Effect of concomitant csDMARDs and BMI on ADA development
Thirty-eight out of 180 patients (21%) developed ADA at 1 year of TNFi treatment. The development of ADA for each therapeutic group was as follows: 30/101 (30%) patients under TNFi monotherapy, 7/36 (19%) patients treated with SSZ (p = 1.0) and 1/43 (2%) patients treated with MTX [± SSZ] (p = 0.03). The provided p values were obtained by comparison with TNFi monotherapy. ADA development was significantly negatively associated with TNFi persistence (β − 3.94; OR 0.02; 95% CI 0.005–0.72).
Moreover, a higher BMI was associated with the development of ADA (p = 0.002). Forty-five percent of obese patients (15/35) were ADA positive at 1 year of treatment. On the other hand, ADA development was lower in overweight (11/69; 16%) as well as normal-weight (12/78; 15%) patients. No statistical differences were observed between the overweight and normal-weight groups.
Effect of concomitant csDMARDs and BMI on clinical outcomes
Effect on clinical response
Patients had active disease at baseline, as indicated by a mean BASDAI of 5.8 and a mean ASDAS of 3.3. After 1 year of TNFi treatment, 48% (n = 68) of the patients achieved BASDAI clinical response. For this outcome, a relevant interaction between csDMARDs and BMI with clinical response was found (Wald chi-square value 3.63; p = 0.057), and therefore, the results were stratified according to BMI. The results showed that the use of concomitant csDMARDs contributed positively to achieve BASDAI clinical response in overweight/obese patients (OR 7.86; 95% CI 2.39–25.78); however, no association was found for normal-weight patients (OR 1.10; 95% CI 0.33–3.58) (Table 3).
Table 3.
Association between csDMARDs and clinical response (∆BASDAI ≥ 2.0) or remission (BASDAI < 2 and CRP ≤ 5 mg/L) at 1 year, stratified for body mass index
| BMI ≤ 25 (n = 60; 42%) | BMI > 25 (n = 81; 58%) | |||
|---|---|---|---|---|
| OR | 95% CI | OR | 95% CI | |
| Clinical response | ||||
| Any csDMARD | 1.10 | 0.33–3.58 | 7.86 | 2.39–25.78* |
| MTX [± SSZ] | 1.04 | 0.25–4.25 | 9.82 | 2.13–45.20* |
| SSZ | 1.18 | 0.25–5.63 | 6.86 | 1.85–25.40* |
| Remission | ||||
| Any csDMARD | 0.76 | 0.20–2.86 | 4.84 | 1.09–21.36* |
| MTX [± SSZ] | 0.60 | 0.11–3.18 | 5.56 | 0.84–36.52 |
| SSZ | 0.99 | 0.17–5.64 | 4.35 | 0.77–24.54 |
The adjusted multivariable logistic regression analysis included 141 patients. Two different models are presented for the following outcomes: clinical response and remission. Odds ratio (OR) and 95% confidence interval (CI) were calculated. All models were adjusted for age, gender, disease duration, HLA-B27, baseline BASDAI and CRP. *p value < 0.05 was considered statistically significant. BMI body mass index, HLA-B27 human leucocyte antigen B27, CRP C-reactive protein, BASDAI Bath Ankylosing Spondylitis Disease Activity Index, csDMARD conventional synthetic disease-modifying anti-rheumatic drug, MTX methotrexate, SSZ sulfasalazine
Furthermore, the influence of csDMARD type on these associations was also investigated. Concomitant MTX [± SSZ] (OR 9.82; 95% CI 2.13–45.20) as well as concomitant SSZ alone (OR 6.86; 95% CI 1.85–25.40) contributed to achieve BASDAI clinical response in overweight/obese patients.
Effect on clinical remission
After 1 year of treatment with TNFi, 25% (n = 35) of patients achieved clinical remission. Similarly to the results observed for clinical response, the analysis revealed that the use of csDMARDs contributes to achieve BASDAI clinical remission in overweight/obese patients (OR 4.84; 95% CI 1.09–21.36) (Table 3). The individual results for csDMARD type were analysed, but neither concomitant MTX [± SSZ] (OR 5.56; 95% CI 0.84–36.52) nor concomitant SSZ (OR 4.35; 0.77–24.54) showed significant results.
Sensitivity analyses
Finally, sensitivity analyses were performed employing ASDAS definition for clinical response using data from 119 patients in which ASDAS was available. Out of these, 45% (n = 53) of patients achieved clinical response and 29% (n = 34) remission. The results found were consistent with the evaluation with BASDAI, being the probability of achieving clinical response in overweight/obese patients increased by the use of concomitant csDMARD (Additional file 1). However, these results were not statistically significant, due to the smaller sample size.
Discussion
This study investigates the influence of concomitant csDMARDs and BMI on circulating drug levels as well as on the clinical response to TNFi therapy in axSpA patients. The observed results show that both concomitant csDMARDs and especially BMI were associated with TNFi drug persistence. Furthermore, the concomitant treatment with csDMARDs (MTX and/or SSZ) was also associated with good clinical response in overweight/obese axSpA patients receiving TNFi but not in normal-weight patients.
According to previous data, BMI and csDMARDs were found to have an influence on TNFi clearance [8]. Particularly, MTX was more effective in reducing immunogenicity. However, the effect of BMI seems to be more relevant. Different studies have suggested that higher BMI is associated with a higher volume of distribution in the central compartment and therefore with increased TNFi clearance [7–10].
Up to date, there are no clear data about the clinical superiority of co-therapy csDMARDs+TNFi vs. TNFi in monotherapy for the treatment of axSpA [1]. Recently, Sepriano et al. indicated that co-medication with csDMARDs do not prolong TNFi retention in axSpA [15]. To this regard, we observed that the use of concomitant csDMARDs have no influence on the clinical response for normal-weight patients and therefore support previous data. However, csDMARDs were associated with a higher probability of having both BASDAI clinical response and clinical remission in patients being overweight or obese. An explanation for this association could be the fact that obesity might be considered as additional inflammation where pro-inflammatory adipokines, such as TNFα, IL1β, IL6 or MCP1, are segregated by adipose tissue and macrophages [16]. Therefore, the concomitant treatment with immunomodulators (csDMARDs) would allow decreasing the production of these adipokines helping to restore inflammation balance [17, 18]. TNFi would achieve the clinical outcome, once decreased the effect of the overweight/obese pro-inflammatory environment.
Nevertheless, the results of this study need to be interpreted with caution. It is well known that studies testing treatment effects without blinded and random treatment allocation are at risk for confounding by indication. In our study, csDMARD prescription was not randomised and was done according to the clinical criteria by the treating physician. Patients who were prescribed csDMARDs may be inherently different from those who did not take these drugs, and such differences can drive the positive association rather than the treatment itself. So, confounding by indication needs to be considered as the main limitation of this study. On the other hand, we are convinced that the reason to prescribe concomitant csDMARDs were not based on BMI because this is not the clinical practice in the participant centres.
This study presents other limitations that need to be kept in mind when interpreting the results: (i) Statistical analyses could not be adjusted for smoking habit because it was not registered. (ii) Some patients were included before 2010, when ASDAS was not available, and therefore, the sample size for these analyses was reduced; the results obtained for this analysis showed a similar trend to that of BASDAI clinical response but were not statistically significant. The lower number of patients with ASDAS registered may be an explanation. Furthermore, a different explanation could be that ASDAS was not really influenced by BMI. In this regard, it has recently been published that it would not be necessary to take BMI into account when assessing disease activity by ASDAS in axSpA patients with high BMI [19]. (iii) LOCF was employed for patients who dropped out before 1 year of follow-up (n = 43). (iv) csDMARD prescription was not randomised, although prescription followed clinical criteria. (v) Patients are included from two different centres with some differences in the therapeutic strategy. (vi) BMI and csDMARD information was collected only at baseline, and therefore, the possible change on these over the study period was not taken into account. (vii) The compliance in adalimumab, SSZ and MTX administrations could not be ensured in all patients.
Conclusions
In conclusion, our study suggests that the use of concomitant csDMARDs with TNFi would not be justified in axSpA patients with normal weight as it would not increase the probability of achieving clinical response. Moreover, in agreement with previous data, it also suggests that BMI is associated with lower TNFi serum drug persistence. Therefore, obese patients should be encouraged to achieving normal weight. Nevertheless, based on the results of this study, if losing weight is proven impossible, it can be hypothesised that the co-medication with csDMARDs (MTX or SSZ) could be of additional value to increase treatment success in overweight/obese patients. However, before implementing the results of this study, further research studies with better methodological design including larger cohorts of patients need to confirm them.
Additional file
(i) Association between csDMARDs and clinical response (∆ASDAS≥1.1) or remission (ASDAS<1.3) at one year, stratified for body mass index; (ii) Flowchart of patients included in the present study. (DOCX 46 kb)
Acknowledgements
Authors thank the nurses from the Department of Rheumatology and the laboratory technicians of the Immunology Unit for their help and for contributing to a good working environment.
Funding
No funding was received to perform this research.
Availability of data and materials
All data generated or analysed during this study are included in this published article.
Abbreviations
- ADA
Anti-drug antibodies
- ASDAS
Ankylosing Spondylitis Disease Activity Score
- axSpA
Axial spondyloarthritis
- BASDAI
Bath Ankylosing Spondylitis Disease Activity Index
- BMI
Body mass index
- CI
Confidence interval
- CRP
C-reactive protein
- csDMARD
Conventional synthetic disease-modifying anti-rheumatic drug
- ELISA
Enzyme-linked immunosorbent assay
- ESR
Erythrocyte sedimentation rate
- HLA-B27
Human leucocyte antigen B27
- IBD
Inflammatory bowel disease
- IL1β
Interleukin-1β
- IL6
Interleukin-6
- LOCF
Last observation carried forward
- MCP1
Monocyte chemoattractant protein 1
- MTX
Methotrexate
- OR
Odds ratio
- RIA
Radioimmunoassay
- SSZ
Sulfasalazine
- TNF
Tumour necrosis factor
- TNFi
TNF inhibitor
Authors’ contributions
CP-R was the main contributor to the study conception and design. AB and DP-S made a substantial contribution to the study conception and design. BH-B, CP-R, AM-F and AJ completed and revised the patient’s database. CP-R, ELK, GJW and AB were involved in obtaining the clinical data. BH-B performed the statistical analysis. VN-C supervised the statistical analysis. CD actively participated in processing the samples and performing the experiments to measure drug and anti-drug antibody levels. DP-S and TR supervised the drug and anti-drug antibody level measurements. BH-B drafted the manuscript. CP-R, VN-C, AM-F, TR, DP-S and AB critically reviewed the manuscript. All authors read and approved the final manuscript.
Ethics approval and consent to participate
The study was conducted according to the guidelines of the 1975 Declaration of Helsinki. Approval was obtained from the Institutional Ethics Committee from the participant Institutions (La Paz University Hospital and READE centre).
Consent for publication
All authors have read and approved the manuscript for publication.
Competing interests
VN-C has received speaker fees and grants from Abbvie, BMS, Lilly, MSD, Novartis, Pfizer, Roche and UCB. DP-S has received grants and speaker fees from Pfizer, MSD, Abbvie, Novartis, Grifols and Menarini. CP-R has received grants and speaker fees from Pfizer and MSD. TR reports grants from Pfizer during the conduct of the study, grants from Genmab, consultancy fees from Genmab and payment for lectures from Pfizer, Abbvie and Regeneron outside the submitted work. GJW has received research funding from Pfizer and honoraria for lectures and in advisory boards of Pfizer, UCB, BMS, AbbVie, Novartis and Biogen. AB has received grants, consultancies and speaker fees from Abbvie, Pfizer, MSD, Roche, UCB, Celltrion, Novartis and Lilly. The other authors declare that they have no competing interests.
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Contributor Information
Borja Hernández-Breijo, Phone: +34 912071460, Email: borja.hernandez@idipaz.es.
Chamaida Plasencia-Rodríguez, Email: chamiplaro@gmail.com.
Victoria Navarro-Compán, Email: mvictoria.navarroc@gmail.com.
Ana Martínez-Feito, Email: amartinezf@salud.madrid.org.
Andrea Jochems, Email: andreajochems8@gmail.com.
Eva L. Kneepkens, Email: e.l.kneepkens@olvg.nl
Gerrit J. Wolbink, Email: wolbink@gmail.com
Theo Rispens, Email: T.Rispens@sanquin.nl.
Cristina Diego, Email: cristinadiego83@gmail.com.
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
(i) Association between csDMARDs and clinical response (∆ASDAS≥1.1) or remission (ASDAS<1.3) at one year, stratified for body mass index; (ii) Flowchart of patients included in the present study. (DOCX 46 kb)
Data Availability Statement
All data generated or analysed during this study are included in this published article.