Introduction
Randomized controlled trials (RCTs) have demonstrated that the tumor necrosis factor alpha (TNF-α) blocking agents infliximab, etanercept, and adalimumab are effective in the treatment of Ankylosing Spondylitis (AS). However, a significant proportion of patients has to withdraw from TNF-α blocking therapy due to inefficacy or adverse events [
1‐
3]. Identifying patients who are likely to benefit from TNF-α blocking therapy is important, especially in view of the costs and potential side effects of these agents.
Several studies using clinical data from RCTs have focused on the identification of predictors of response to anti-TNF-α treatment in AS [
4‐
6]. However, many patients who are treated with TNF-α blocking therapy in daily clinical practice would have been excluded in RCTs. Until now, three population based registries have investigated predictors of response and/or continuation of TNF-α blocking therapy. These registries showed that raised inflammatory markers, lower Bath Ankylosing Spondylitis Functional Index (BASFI), and younger age at baseline were associated with clinical response [
7,
8], whereas male gender, raised inflammatory markers, low visual analogue scale (VAS) fatigue, and presence of peripheral arthritis were baseline predictors of longer drug survival [
7,
9].
Disease activity in AS encompasses a wide range of concepts and is therefore difficult to measure. Recently, the Ankylosing Spondylitis Disease Activity Score (ASDAS) has been developed [
10,
11]. This new index is a composite score of patient-reported measures and acute phase reactants developed in order to capture both subjective and objective aspects of AS disease activity. Currently, information about the predictive value of the ASDAS with respect to response to TNF-α blocking therapy or drug survival is lacking due to the absence of ASDAS data in previous studies. The aim of the present study was to identify baseline predictors of response and discontinuation of TNF-α blocking therapy in AS patients in daily clinical practice.
Results
Between November 2004 and April 2010, a total of 220 patients (MCL:
n = 163; UMCG:
n = 57) started treatment with a first TNF-α blocking agent; 32 receiving infliximab, 137 etanercept, and 51 adalimumab. Mean age of all patients was 42.9 years (SD ± 11.9), median disease duration was 15 years (range 1 to 53), and 69% were male. The three treatment groups were comparable for age, gender, HLA-B27 status, BASDAI, ASDAS, patient's GDA, CRP, ESR, concomitant medication, and presence of peripheral arthritis at baseline. In the infliximab group, time since diagnosis was significantly longer, the percentage of patients with a history of inflammatory bowel disease (IBD) was significantly higher, and occiput to wall distance was significantly larger compared to the etanercept and adalimumab groups. In the adalimumab group, the percentage of patients with a history of uveitis and physician's GDA were significantly lower and chest expansion was significantly higher compared to the infliximab and/or etanercept group (Table
1).
Table 1
Baseline characteristics of the AS study population
Number of patients | 220 | 32 | 137 | 51 |
Age (yrs) | 42.9 ± 11.9 | 45.8 ± 10.1 | 41.9 ± 11.6 | 43.7 ± 13.3 |
Gender (male) (n, %) | 152 (69) | 20 (63) | 96 (70) | 36 (71) |
Duration of symptoms (yrs) | 15 (1 to 53) | 21 (2 to 49) | 15 (1 to 47) | 11 (1 to 53) |
Time since diagnosis (yrs) | 7 (0 to 45) | 16 (0 to 35)* | 7 (0 to 44) | 6 (0 to 45) |
HLA-B27+ (n, %) | 174 (81) | 24 (75) | 108 (82) | 42 (82) |
History of IBD (n, %) | 20 (9) | 8 (26)† | 7 (5) | 4 (8) |
History of uveitis (n, %) | 64 (29) | 13 (40) | 44 (32) | 7 (14)‡ |
History of psoriasis (n, %) | 13 (6) | 3 (9) | 8 (6) | 13 (6) |
Peripheral arthritis (n, %) | 37 (17) | 5 (16) | 27 (20) | 5 (10) |
Current NSAID use (n, %) | 158 (72) | 24 (75) | 102 (75) | 32 (63) |
Current DMARD use (n, %) | 45 (21) | 10 (31) | 28 (20) | 7 (14) |
BASDAI (range 0 to 10) | 6.1 ± 1.7 | 6.1 ± 1.4 | 6.2 ± 1.7 | 5.9 ± 1.7 |
ASDAS | 3.8 ± 0.8 | 3.8 ± 0.6 | 3.8 ± 0.8 | 3.7 ± 0.9 |
Physician's GDA (range 0-10) | 5 (0 to 9) | 5 (0 to 8) | 5 (0 to 9) | 3 (0 to 9)‡ |
Patient's GDA (range 0 to 10) | 7 (1 to 10) | 6 (1 to 9) | 7 (1 to 10) | 6 (1 to 10) |
ESR (mm/h) | 21 (2 to 101) | 24 (2 to 90) | 20 (2 to 101) | 23 (2 to 74) |
CRP (mg/l) | 13 (2 to 99) | 15 (2 to 74) | 12 (2 to 99) | 14 (2 to 92) |
BASFI (range 0 to 10) | 6.1 (0.3 to 9.7) | 6.3 (1.9 to 9.6) | 5.9 (0.3 to 9.7) | 6.3 (0.4 to 9.5) |
Chest expansion (cm) | 3.0 (0.5 to 43.0) | 2.5 (0.5 to 7.0) | 3.0 (0.5 to 22.0) | 3.5 (0.0 to 43.0)§ |
Modified Schober test (cm) | 2.9 (0.0 to 7.0) | 2.4 (0.5 to 6.0) | 2.8 (0.1 to 7.0) | 3.2 (0.0 to 5.5) |
Occiput to wall distance (cm) | 4.9 (0.0 to 34.5) | 9.0 (0.0 to 26.0)^ | 4.5 (0.0 to 34.5) | 3.5 (0.0 to 30.0) |
Lateral lumbar flexion L (cm) | 8.0 (0.0 to 30.0) | 7.0 (2.0 to 15.0) | 9.0 (0.0 to 30.0) | 8.0 (1.0 to 20.5) |
Lateral lumbar flexion R (cm) | 8.0 (0.0 to 29.0) | 8.0 (0.5 to 17.0) | 8.0 (0.0 to 29.0) | 7.5 (1.0 to 20.0) |
ASAS20 response
The percentage of ASAS20 responders to TNF-α blocking therapy was 68% and 63% at three and six months, respectively. No significant differences were found in the percentage of ASAS20 responders between the three TNF-α blocking agents at three or six months (
P = 0.297 and
P = 0.128, respectively) (Table
2).
Table 2
Response and drug survival rate in AS patients treated with TNF-α blocking therapy
Number of patients | 220 | 32 | 137 | 51 |
ASAS20 responders at three months | 68% | 80% | 66% | 65% |
(number of patients) | (145 of 214) | (24 of 30) | (88 of 133) | (33 of 51) |
ASAS20 responders at six months | 63% | 71% | 66% | 51% |
(number of patients) | (132 of 209) | (22 of 31) | (86 of 131) | (24 of 47) |
ASAS40 responders at three months | 49% | 63% | 47% | 45% |
(number of patients) | (104 of 214) | (19 of 30) | (62 of 133) | (23 of 51) |
ASAS40 responders at six months | 46% | 52% | 48% | 38% |
(number of patients) | (97 of 209) | (16 of 31) | (63 of 131) | (18 of 47) |
BASDAI50 responders at three months | 49% | 60% | 46% | 51% |
(number of patients) | (105 of 214) | (18 of 30) | (61 of 133) | (26 of 51) |
BASDAI50 responders at six months | 50% | 48% | 51% | 47% |
(number of patients) | (104 of 209) | (15 of 31) | (67 of 131) | (22 of 47) |
One-year drug survival | 71% | 76% | 72% | 65% |
(number of patients) | (136 of 192) | (22 of 29) | (88 of 123) | (26 of 40) |
Two-year drug survival | 66% | 70% | 69% | 48% |
(number of patients) | (97 of 148) | (19 of 27) | (66 of 96) | (12 of 25) |
Results of univariate and multivariate logistic regression analysis for ASAS20 response at three and six months of anti-TNF-α treatment are presented in Tables
3 and
4, respectively. Male gender (OR: 2.166) was identified as a significant baseline predictor of ASAS20 response in univariate logistic regression analysis. Therefore, variables that significantly differed between men and women at baseline were included in multivariate analysis: age, patient's GDA, ESR, chest expansion, and occiput to wall distance. Multivariate logistic regression analysis showed that younger age (OR: 0.972), male gender (OR: 3.151), and higher ESR level (OR: 1.023) or alternatively, higher CRP level (OR: 1.024) or higher ASDAS score (OR: 1.728), were independent baseline predictors of ASAS20 response at three months of anti-TNF-α treatment (Table
3).
Table 3
Baseline predictors of ASAS20 response at three months of anti-TNF-α treatment
Age (yr)†a | | 0.982 (0.959 to 1.006) | 0.150 | 0.972 (0.947 to 0.998) | 0.035 |
Gender | Female | 1 | - | | - |
| Male | 2.166 (1.185 to 3.958) | 0.012 | 3.151 (1.580 to 6.285) | 0.001 |
Duration of symptoms (yr)† | | 1.001 (0.976 to 1.028) | 0.914 | | *** |
HLA-B27 | Negative | 1 | - | | - |
| Positive | 0.779 (0.363 to 1.675) | 0.523 | | *** |
Peripheral arthritis | Absent | 1 | - | | - |
| Present | 2.120 (0.876 to 5.129) | 0.096 | | ** |
BASDAI (range 0 to 10)‡ | | 0.946 (0.793 to 1.129) | 0.538 | | *** |
ASDAS‡ | | 1.458 (0.992 to 2.144) | 0.055 | | * |
Physician's GDA (range 0 to 10)‡ | | 1.122 (0.983 to 1.282) | 0.089 | | ** |
Patient's GDA (range 0 to 10)‡a | | 1.029 (0.882 to 1.201) | 0.714 | | ** |
ESR (mm/h)‡a | | 1.016 (1.000 to 1.032) | 0.049 | 1.023 (1.005 to 1.041) | 0.014 |
CRP (mg/l)‡ | | 1.021 (1.003 to 1.040) | 0.025 | | * |
BASFI (range 0 to 10)‡ | | 0.939 (0.816 to 1.081) | 0.382 | | *** |
Chest expansion (cm)‡a | | 1.081 (0.948 to 1.233) | 0.243 | | ** |
Modified Schober test (cm)‡ | | 1.026 (0.861 to 1.224) | 0.773 | | *** |
Occiput to wall distance (cm)‡a | | 0.981 (0.942 to 1.022) | 0.364 | | ** |
Lateral lumbar flexion L (cm)‡ | | 1.027 (0.965 to 1.092) | 0.402 | | *** |
Lateral lumbar flexion R (cm)‡ | | 1.029 (0.968 to 1.094) | 0.352 | | *** |
TNF-α blocking agent | ETA | 1 | - | | - |
| IFX | 2.045 (0.780 to 5.364) | 0.146 | | ** |
| ADA | 0.938 (0.476 to 1.846) | 0.852 | | ** |
At six months of anti-TNF-α treatment, younger age (OR: 0.960), male gender (OR: 2.991), and higher ASDAS score (OR: 1.573) or alternatively, presence of peripheral arthritis (OR: 2.518) and higher patient's GDA (OR: 1.173), were independent baseline predictors of ASAS20 response (Table
4).
Table 4
Baseline predictors of ASAS20 response at six months of anti-TNF-α treatment
Age (yr)†a | | 0.977 (0.954 to 1.002) | 0.069 | 0.960 (0.934 to 0.987) | 0.004 |
Gender | Female | 1 | - | | - |
| Male | 1.995 (1.087 to 3.659) | 0.026 | 2.991 (1.519 to 5.890) | 0.002 |
Duration of symptoms (yr)† | | 0.997 (0.972 to 1.023) | 0.821 | | *** |
HLA-B27 | Negative | 1 | - | | - |
| Positive | 1.086 (0.520 to 2.266) | 0.827 | | *** |
Peripheral arthritis | Absent | 1 | - | | - |
| Present | 2.218 (0.952 to 5.165) | 0.065 | | * |
BASDAI (range 0 to 10)‡ | | 1.031 (0.873 to 1.219) | 0.717 | | *** |
ASDAS‡ | | 1.356 (0.945 to 1.946) | 0.099 | 1.573 (1.051 to 2.354) | 0.028 |
Physician's GDA (range 0 to 10)‡ | | 1.087 (0.955 to 1.239) | 0.207 | | ** |
Patient's GDA (range 0 to 10)‡a | | 1.124 (0.973 to 1.300) | 0.113 | | * |
ESR (mm/h)‡a | | 1.005 (0.991 to 1.019) | 0.499 | | ** |
CRP (mg/l)‡ | | 1.009 (0.993 to 1.024) | 0.281 | | ** |
BASFI (range 0 to 10)‡ | | 0.989 (0.861 to 1.135) | 0.872 | | *** |
Chest expansion (cm)‡a | | 1.108 (0.953 to 1.289) | 0.183 | | ** |
Modified Schober test (cm)‡ | | 0.900 (0.755 to 1.074) | 0.243 | | ** |
Occiput to wall distance (cm)‡a | | 0.989 (0.950 to 1.030) | 0.591 | | ** |
Lateral lumbar flexion L (cm)‡ | | 0.985 (0.928 to 1.044) | 0.606 | | *** |
Lateral lumbar flexion R (cm)‡ | | 1.018 (0.960 to 1.079) | 0.557 | | *** |
TNF-α blocking agent | ETA | 1 | - | | - |
| IFX | 1.279 (0.544 to 3.008) | 0.573 | | ** |
| ADA | 0.546 (0.278 to 1.076) | 0.079 | | ** |
ASAS40 response
The percentage of ASAS40 responders to TNF-α blocking therapy was 49% and 46% at three and six months, respectively. No significant differences were found in the percentage of responders between the three TNF-α blocking agents at three or six months (
P = 0.216 and
P = 0.421, respectively) (Table
2).
Multivariate logistic regression analysis showed that younger age (OR: 0.970, 95% CI: 0.946 to 0.994) was the only independent baseline predictor of ASAS40 response at three months of anti-TNF-α treatment.
At six months of anti-TNF-α treatment, younger age (OR: 0.961, 95% CI: 0.935 to 0.987), male gender (OR: 2.488, 95% CI: 1.235 to 5.014), and higher patient's GDA (OR: 1.258, 95% CI: 1.067 to 1.483) or alternatively, higher ASDAS score (OR: 1.721, 95% CI: 1.159 to 2.555), were independent baseline predictors of ASAS40 response.
BASDAI50 response
The percentage of BASDAI50 responders to TNF-α blocking therapy was 49% and 50% at three and six months, respectively. No significant differences were found in the percentage of responders between the three TNF-α blocking agents at three or six months (
P = 0.358 and
P = 0.866, respectively) (Table
2).
Multivariate logistic regression analysis showed that younger age (OR: 0.975, 95% CI: 0.951 to 0.999), male gender (OR: 2.572, 95% CI: 1.346 to 4.913), and higher CRP level (OR: 1.025, 95% CI: 1.008 to 1.042) or alternatively, higher ESR level (OR: 1.026, 95% CI: 1.009 to 1.042), were independent baseline predictors of BASDAI50 response at three months of anti-TNF-α treatment.
At six months of anti-TNF-α treatment, younger age (OR: 0.957, 95% CI: 0.929 to 0.985), male gender (OR: 2.598, 95% CI: 1.302 to 5.186), presence of peripheral arthritis (OR: 4.991, 95% CI: 2.054 to 12.124), and lower modified Schober test (OR: 0.751, 95% CI: 0.610 to 0.924) were independent baseline predictors of BASDAI50 response.
Treatment discontinuation
In August 2010, 141 (64%) patients were still using their TNF-α blocking agent with a median follow-up of 33.1 months (range 2.4 to 68.2). The remaining 79 (36%) patients discontinued TNF-α blocking therapy after median treatment duration of 7.0 months (range 0.2 to 55.6). Reasons for discontinuation of TNF-α blocking therapy were inefficacy (n = 40, 51%), adverse events (n = 21, 27%: infection (n = 8); allergic reaction (n = 4); diarrhea or IBD (n = 5); cardio-vascular disease (n = 2); demyelization problems (n = 1); bladder cancer (n = 1)), both inefficacy and adverse events (n = 8, 10%: recurrent infections (n = 3); allergic reaction (n = 1); diarrhea or IBD (n = 2); uveitis (n = 1); malaise (n = 1)), or other reasons (n = 10, 13%: good initial response, own choice (n = 3); pregnancy wish (n = 5); lost to follow up (n = 2)).
Antibodies to TNF-α blocking agents were measured in patients who discontinued infliximab (n = 7) or adalimumab (n = 14) treatment due to inefficacy. Antibody data were missing for one adalimumab patient. Antibodies against infliximab and adalimumab were detected in 5 of 7 (71%) and in 8 of 13 (62%) patients who discontinued treatment due to inefficacy, respectively. In total, 5 of 13 (38%) patients with antibodies to TNF-α blocking agents were primary non-responders and 8 of 13 (62%) patients were secondary non-responders.
The one-year and two-year TNF-α blocking therapy survival rates were 71% and 66%, respectively. No significant differences were found in one-year or two-year survival rates between the three TNF-α blocking agents (
P = 0.593 and
P = 0.127, respectively) (Table
2).
Results of univariate and multivariate Cox regression analysis for discontinuation of anti-TNF-α treatment are presented in Table
5. Since female gender (HR: 0.503) and absence of peripheral arthritis (HR: 0.382) were significantly associated with treatment discontinuation in univariate Cox regression analysis, baseline variables that significantly differed between men and women (age, patient's GDA, ESR, chest expansion, and occiput to wall distance) or between patients with and without peripheral arthritis (BASDAI, ASDAS, physician's GDA, and CRP) were included in multivariate analysis. Multivariate Cox regression analysis showed that female gender (HR: 0.406), absence of peripheral arthritis (HR: 0.320), higher BASDAI score (HR: 1.225), and lower ESR level (HR: 0.983) or alternatively, lower CRP level (HR: 0.984), were independent baseline predictors of discontinuation of anti-TNF-α treatment (Table
5).
Table 5
Baseline predictors of anti-TNF-α treatment discontinuation
Age (yr)†a | | 0.994 (0.975 to 1.014) | 0.561 | | ** |
Gender | Female | 1 | - | | - |
| Male | 0.503 (0.321 to 0.787) | 0.003 | 0.406 (0.251 to 0.657) | 0.000 |
Duration of symptoms (yr)† | | 0.981 (0.959 to 1.002) | 0.082 | | ** |
HLA-B27 | Negative | 1 | - | | - |
| Positive | 0.823 (0.468 to 1.448) | 0.500 | | *** |
Peripheral arthritis | Absent | 1 | - | | - |
| Present | 0.382 (0.176 to 0.830) | 0.015 | 0.320 (0.144 to 0.712) | 0.005 |
BASDAI (range 0 to 10)‡b | | 1.162 (1.016 to 1.329) | 0.028 | 1.225 (1.053 to 1.424) | 0.008 |
ASDAS‡b | | 1.005 (0.759 to 1.330) | 0.974 | | ** |
Physician's GDA (range 0 to 10)‡b | | 0.907 (0.816 to 1.008) | 0.070 | | ** |
Patient's GDA (range 0 to 10)‡a | | 1.075 (0.958 to 1.208) | 0.219 | | ** |
ESR (mm/h)‡a | | 0.987 (0.974 to 0.999) | 0.039 | 0.983 (0.969 to 0.997) | 0.018 |
CRP (mg/l)‡b | | 0.986 (0.972 to 1.000) | 0.049 | | * |
BASFI (range 0 to 10)‡ | | 1.045 (0.935 to 1.168) | 0.438 | | *** |
Chest expansion (cm)‡a | | 0.986 (0.903 to 1.076) | 0.753 | | ** |
Modified Schober test (cm)‡ | | 1.189 (1.036 to 1.365) | 0.014 | | ** |
Occiput to wall distance (cm)‡a | | 0.971 (0.938 to 1.006) | 0.971 | | ** |
Lateral lumbar flexion L (cm)‡ | | 1.018 (0.973 to 1.066) | 0.434 | | *** |
Lateral lumbar flexion R (cm)‡ | | 1.016 (0.971 to 1.062) | 0.498 | | *** |
TNF-α blocking agent | ETA | 1 | - | | - |
| IFX | 0.847 (0.441 to 1.627) | 0.618 | | *** |
| ADA | 1.334 (0.769 to 2.314) | 0.305 | | *** |
Discussion
In this prospective longitudinal observational cohort study, ASAS20 and ASAS40 response was reached by 51% to 80% and 38% to 63% of AS patients at three to six months of anti-TNF-α treatment, respectively. These results from daily practice are in line with the findings in RCTs [
1‐
3]. Although TNF-α blocking therapy is effective in the majority of AS patients, identifying patients who are likely to benefit from TNF-α blocking therapy is important, especially in view of the potential side effects and financial burden of these agents. Data from observational studies are necessary, since inclusion criteria of RCTs are very strict and, therefore, not completely comparable to the criteria for starting TNF-α blocking therapy in daily clinical practice. Our finding that younger AS patients respond significantly better to anti-TNF-α treatment is in line with previous studies using data from RCTs and population based registries [
5‐
7]. Previous studies in rheumatoid arthritis (RA) also found that females were less likely to achieve remission on anti-TNF-α treatment [
19,
20]. Furthermore, female gender was significantly associated with discontinuation of TNF-α blocking therapy in registries of arthritic rheumatic diseases [
21,
22] and AS [
7,
9]. Unfortunately, it is still unclear why male patients respond better to TNF-α blocking therapy.
Multiple studies have shown the importance of raised inflammatory markers with regard to achieving clinical response [
4‐
7] or treatment continuation [
7]. This study also confirms the predictive value of high ESR or CRP levels. Our finding that absence of peripheral arthritis is associated with treatment discontinuation is in accordance with Kristensen
et al., who reported that patients with peripheral arthritis are more likely to continue TNF-α blocking therapy [
9]. In the present study, presence of peripheral arthritis was also independently related to ASAS20 and BASDAI50 response at six months in the presence of age and gender, indicating that concomitant peripheral arthritis is a predictor of both response and continuation of anti-TNF-α treatment.
Recently, the ASDAS has been developed to assess a broader spectrum of disease activity [
10,
11]. A new and interesting finding is that higher ASDAS score was identified as a significant baseline predictor of ASAS20 and ASAS40 response to TNF-α blocking therapy in this study. Until now, in clinical practice, starting and continuation TNF-α blocking therapy is mainly based on BASDAI response, which is solely based on the opinion of the patient. In this study, more objective variables such as higher inflammatory markers and higher ASDAS score were identified as independent baseline predictors of response and/or continuation of anti-TNF-α treatment. In contrast, a higher baseline BASDAI score was independently associated with treatment discontinuation. Based on these results, it seems clinically relevant to include more objective variables in the evaluation of anti-TNF-α treatment.
Our finding that the majority of AS patients discontinued TNF-α blocking therapy because of inefficacy is in accordance with Glintborg
et al. [
7], but other registries found an almost equal distribution between treatment withdrawal due to adverse events and inefficacy [
9,
23] or even a higher discontinuation rate because of adverse events [
21,
22]. These differences may be explained by variation in the classification of reasons for stopping TNF-α blocking therapy.
Since previous studies in AS patients treated with etanercept have reported that no antibodies against etanercept could be detected [
24,
25], antibodies were only measured in patients who discontinued infliximab and adalimumab due to inefficacy in this study. Antibody formation seems to be related to inefficacy of infliximab and adalimumab since these antibodies were detected in almost two third of patients (13 out of 20) who discontinued infliximab or adalimumab treatment due to inefficacy. This is in line with our previous findings in a smaller group of AS patients. In this study, patients with antibodies had significantly lower serum TNF-α blocker levels compared to patients without antibodies and significant negative correlations between serum levels of TNF-α blocking agents and assessments of disease activity were found [
24]. Based on these results, it seems useful to determine antibody formation to TNF-α blocking agents in non-responsive AS patients.
In the present study, we did not find significant differences in the percentage of ASAS20, ASAS40, or BASDAI50 responders at three and six months or in one-year and two-year drug survival rates between the three TNF-α blocking agents. Furthermore, the type of anti-TNF-α treatment (infliximab, etanercept, or adalimumab) was not significantly associated with achieving response or discontinuation of treatment. However, these findings should be interpreted with caution since there were differences in disease duration, the percentage of patients with extra-articular manifestations, physician's GDA, and spinal mobility measures at baseline and there was an uneven distribution of patients among the different treatment groups.
Conclusions
This prospective longitudinal observational cohort study identified higher ASDAS score, higher ESR or CRP level, presence of peripheral arthritis, younger age, male gender, lower modified Schober test, higher patient's GDA, and lower BASDAI as independent baseline predictors of response and/or continuation of TNF-α blocking therapy in AS patients. These findings may help clinicians to identify AS patients who are more likely to benefit from TNF-α blocking therapy in daily clinical practice.
Acknowledgements
The authors wish to acknowledge Mrs. L. Bulstra, Mrs. A. Krol, Mrs. J. Vierdag-Loth, and Mrs. J. Bulthuis-Kuiper for their contribution to clinical data collection. The GLAS study was supported by an unrestricted grant from Wyeth pharmaceuticals received by EB and AS. Wyeth had no role in the design, conduct, interpretation, or publication of this study.
Competing interests
EB has received unrestricted research grants from Abbott, Schering-Plough, and Wyeth. AS has received unrestricted research grants from Abbott and Wyeth. The other authors declare that they have no competing interests.
Authors' contributions
SA performed the statistical analysis and interpretation of data and drafted the manuscript; EB and AS participated in the design of the study, performed the acquisition of data, and critically revised the manuscript. EV and HG contributed to the statistical analysis and interpretation of data and critically revised the manuscript. ML, PH and TJ contributed to the acquisition of clinical data and critically revised the manuscript. CK participated in the design of the study and critically revised the manuscript. All authors read and approved the final manuscript.