Ankylosing Spondylitis, Psoriatic Arthritis
Conditions
Keywords
Post-marketing observational study (PMOS) Protocol, Effectiveness of Adalimumab (HUMIRA®), Psoriatic Arthritis, Ankylosing Spondylitis
Brief summary
This 12-month postmarketing observational study (PMOS) was a prospective, single-arm, multicenter, multi-country study, with follow-up visits at 3, 6, 9, and 12 months after the initial baseline visit. The study was conducted to determine the long-term effectiveness of treatment with adalimumab in routine clinical use in participants with Ankylosing Spondylitis (AS) and Psoriatic Arthritis (PsA) in Central and Eastern European Countries.
Detailed description
Additional study objectives were to evaluate AS and PsA with regard to extra-articular manifestations (EAMs), functional status, the use of concomitant nonsteroidal anti-inflammatory medication, and work productivity impairment. In addition, the Ankylosing Spondylitis Disease Activity Score (ASDAS), a new disease activity index in AS, was measured in parallel with the standard Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) score to assess the effectiveness of adalimumab in treating axial symptoms.
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
Patients will be enrolled in this Postmarketing observational study PMOS if they fulfill all of the below criteria: 1. Adult patients with diagnosis of Ankylosing Spondylitis (AS) or Psoriatic Arthritis (PsA). 2. Eligible for adalimumab therapy according to the local product label and prescription/reimbursement guidelines. 3. Have been prescribed adalimumab within a maximum of one (1) month prior to the study enrolment. 4. Have negative result of Tuberculosis (TB) screening test or TB prophylaxis as per local guidelines. 5. Are willing to provide Authorization to the investigator to use and/or disclose personal and/or health data, or to provide Informed Consent if requested by the Local Regulations, before entry into the study.
Exclusion criteria
Patients fulfilling below
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Percentage of Participants With a 50% or More Decrease in Bath Ankylosing Spondylitis Daily Activity Index (BASDAI) Score at 12 Months Relative to Baseline | Baseline (Visit 0) to 12 months | The BASDAI score was calculated using a questionnaire with 6 questions that the participants completed by marking responses on a 10-centimeter visual analog scale ranging from 0 (none) to 10 (very severe) regarding severity of fatigue, spinal and peripheral joint pain, localized tenderness and morning stiffness. The final BASDAI score ranges from 0 to 10. A positive response was defined as a 50% or more decrease in the BASDAI score at 12 months as compared to baseline. |
| Percentage of Participants With a Disease Activity Score 28 (DAS28) Decrease ≥1.2 at 12 Months Relative to Baseline | Baseline (Visit 0) to 12 months | The DAS28 is a validated index of rheumatoid arthritis disease activity. Twenty-eight tender joint counts, 28 swollen joint counts, C-reactive protein, and general health are included in the DAS28 score. Scores on the DAS28 range from 0 to 10. A DAS28 score \>5.1 indicates high disease activity, a DAS28 score \<3.2 indicates low disease activity, and a DAS28 score \<2.6 indicates clinical remission. |
| Percentage of Participants With Active Axial Symptoms in Remission | Baseline (Visit 0) to 12 months | The Ankylosing Spondylitis Disease Score (ASDAS) tool is a self-administered questionnaire plus an objective laboratory evaluation. The questionnaire covers disease activity, back pain, duration of morning stiffness and peripheral pain/swelling assessed on a visual analogue scale (from 0 to 10 cm) or on a numerical rating scale (from 0 to 10). The laboratory parameter is a measurement of C-reactive protein (mg/L) or erythrocyte sedimentation rate (mm/h). Remission was defined as ASDAS \<1.3 at 12 months. |
| Percentage of Participants With Peripheral Symptoms in Remission | Baseline (Visit 0) to 12 months | The DAS28 is a validated index of rheumatoid arthritis disease activity. Twenty-eight tender joint counts, 28 swollen joint counts, C-reactive protein, and general health are included in the DAS28 score. Scores on the DAS28 range from 0 to 10. A DAS28 score \>5.1 indicates high disease activity, a DAS28 score \<3.2 indicates low disease activity, and a DAS28 score \<2.6 indicates clinical remission. Remission was defined as DAS28 ≤2.6 at 12 months. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Mean Change in Health Assessment Questionnaire Disability Index (HAQ-DI) Score (in Case of Peripheral Symptoms) or Bath Ankylosing Spondylitis Functional Index (BASFI) Score (in Case of Axial Symptoms) in Participants With Ankylosing Spondylitis | Baseline (Visit 0) to 12 months | HAQ-DI consists of 20 questions referring to 8 domains: dressing/grooming, arising, eating, walking, hygiene, reach, grip, and daily activities. Participants assessed their ability to do each task over the past week using the following categories: without any difficulty (0); with some difficulty (1); with much difficulty (2); and unable to do (3). Scores on each task were summed and averaged to provide an overall score ranging from 0 to 3, with a higher score representing a high-dependency disability. The minimal clinically important difference defined for the HAQ-DI is ≥0.22. HAQ-DI remission, indicating normal physical function, is defined as HAQ-DI \< 0.5. The BASFI is a set of 10 questions designed to determine the degree of functional limitation in those with AS. A visual analogue scale (with 0 being easy and 10 impossible) is used. The BASFI score ranges from 0 to 10 and is derived as the mean of the single items. A higher score indicates a higher impairment of functioning. |
| Mean Frequency of Extra-articular Manifestations (EAMs) | Baseline (Visit 0) to 12 months | Extra-articular manifestations (EAMs) are symptoms and diseases that occur in parts of the body other than joints. The number of EAMs was determined at each study visit. These included the presence of enthesitis (inflammation of ligaments and/or tendons at the site of insertion into bones), uveitis (inflammation of the middle layer of the eye), psoriasis (a skin condition that causes itchy or sore patches of thick, red skin with silvery scales), and Inflammatory bowel disease (Crohn's disease or ulcerative colitis). |
| Duration of Treatment With Adalimumab | Baseline (Visit 0) to 12 months | The duration of treatment with adalimumab was calculated separately for participants who discontinued the medication during the study and for those who did not. |
| Percentage of Participants Whose Co-medication With Nonsteroidal Anti-inflammatory Drugs (NSAIDs) Was Stopped During the Study | Baseline (Visit 0) to 12 months | Participants were surveyed at each study visit for their use of NSAID medication. |
| Mean Change in Individual Components of the Work Productivity and Activity Impairment Specific Health Problem Questionnaire in Participants With Ankylosing Spondylitis | Baseline (Visit 0) to 12 months | Work Productivity and Activity Impairment (WPAI) Questionnaire is a quantitative assessment of the amount of absenteeism, presenteeism, total work productivity impairment, and total activity impairment attributable to a specific health problem (WPAI-SHP), expressed as a percentage. Participants were queried regarding their current employment status, hours missed from work because of problems associated with their AS, hours missed from work because of any other reason, number of hours worked, how much AS affected work productivity (0=AS had no effect,10= AS completely prevented me from working), and how much AS affected ability to do regular daily activities, other than work at a job (0= AS had no effect, 10= AS completely prevented me from doing my daily activities) in the past 7 days. |
| Change in the Percentage of Ankylosing Spondylitis Participants Who Have Paid Work | Baseline (Visit 0) to 12 months | Working status (Working full-time, working part-time, working at home, unemployed but seeking work, work disabled, retired, student) was documented at each study visit. |
| Mean Change in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) Score (in Case of Axial Symptoms) and/or Disease Activity Score/28 Joints (DAS28) (in Case of Peripheral Symptoms) in Participants With Ankylosing Spondylitis | Baseline (Visit 0) to 12 months | The BASDAI score was calculated using a questionnaire with 6 questions that the participants completed by marking responses on a 10-centimeter visual analog scale ranging from 0 (none) to 10 (very severe) regarding severity of fatigue, spinal and peripheral joint pain, localized tenderness and morning stiffness. The final BASDAI score ranges from 0 to 10. A positive response was defined as a 50% or more decrease in the BASDAI score at 12 months as compared to baseline. The DAS28 is a validated index of rheumatoid arthritis disease activity. Twenty-eight tender joint counts, 28 swollen joint counts, C- reactive protein, and general health are included in the DAS28 score. Scores on the DAS28 range from 0 to 10. A DAS28 score \>5.1 indicates high disease activity, a DAS28 score \<3.2 indicates low disease activity, and a DAS28 score \<2.6 indicates clinical remission. |
| Correlation Between Change in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) and Ankylosing Spondylitis Disease Activity Score (ASDAS) in Participants With Psoriatic Arthritis | Baseline (Visit 0) to 12 months | BASDAI score (ranging from 0 to 10) was calculated using a questionnaire. Participants marked responses on a 10 cm visual analog scale ranging from 0 (none) to 10 (very severe) regarding fatigue, spinal and peripheral joint pain, localized tenderness and morning stiffness. A positive response was defined as a 50% or more decrease in the BASDAI score at 12 months as compared to baseline. ASDAS score consists of a self-administered questionnaire plus an objective laboratory evaluation. The questionnaire covers disease activity, back pain, duration of morning stiffness and peripheral pain/swelling assessed on a visual analogue scale (from 0 to 10 cm) or on a numerical rating scale (from 0 to 10). The laboratory parameter is a measurement of C-reactive protein (mg/L) or erythrocyte sedimentation rate (mm/h). Spearman's rank correlation coefficient (CC) was calculated for BASDAI vs. ASDAS(subscript)CRP(subscript) and BASDAI vs. ASDAS(subscript)ESR(subscript). |
| Predictors of Maintained Treatment Response and Remission in Participants With Psoriatic Arthritis | Baseline (Visit 0) to 12 months | A mathematical technique called logistic regression was performed to identify factors that could be used to predict maintained treatment response and remission. The following baseline variables were used in the logistic regression analyses: age, gender, disease of interest, result of tuberculosis screening, time since diagnosis and extra-articular manifestations (symptoms and diseases that occur in parts of the body other than joints) at baseline. The BASDAI score at baseline was forced to serve as a predictor in each model. |
| Mean Change in Health Assessment Questionnaire Disability Index ( HAQ-DI) Score (in Case of Peripheral Symptoms) or Bath Ankylosing Spondylitis Functional Index (BASFI) Score (in Case of Axial Symptoms) in Participants With Psoriatic Arthritis | Baseline (Visit 0) to 12 months | HAQ-DI consists of 20 questions referring to 8 domains: dressing/grooming, arising, eating, walking, hygiene, reach, grip, and daily activities. Participants assessed their ability to do each task over the past week using the following categories: without any difficulty (0); with some difficulty (1); with much difficulty (2); and unable to do (3). Scores on each task were summed and averaged to provide an overall score ranging from 0 to 3, with a higher score representing a high-dependency disability. The minimal clinically important difference defined for the HAQ-DI is ≥0.22. HAQ-DI remission, indicating normal physical function, is defined as HAQ-DI \< 0.5. The BASFI is a set of 10 questions designed to determine the degree of functional limitation in those with AS. A visual analogue scale (with 0 being easy and 10 impossible) is used. The BASFI score ranges from 0 to 10 and is derived as the mean of the single items. A higher score indicates a higher impairment of functioning. |
| Mean Change in Individual Components of the Work Productivity and Activity Impairment Specific Health Problem Questionnaire in Participants With Psoriatic Arthritis | Baseline (Visit 0) to 12 months | The Work Productivity and Activity Impairment (WPAI) Questionnaire is a quantitative assessment of the amount of absenteeism, presenteeism, total work productivity impairment, and total activity impairment attributable to a specific health problem (WPAI-SHP), expressed as a percentage. Participants were queried regarding their current employment status, hours missed from work because of problems associated with their PsA, hours missed from work because of any other reason, number of hours worked, how much PsA affected work productivity (0= PsA had no effect,10= PsA completely prevented me from working), and how much PsA affected ability to do regular daily activities, other than work at a job (0= PsA had no effect, 10= PsA completely prevented me from doing my daily activities) in the past 7 days. |
| Change in the Percentage of Psoriatic Arthritis Participants Who Have Paid Work | Baseline (Visit 0) to 12 months | Working status (Working full-time, working part-time, working at home, unemployed but seeking work, work disabled, retired, student) was documented at each study visit. |
| Mean Change in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) Score (in Case of Axial Symptoms) and/or Disease Activity Score/28 Joints (DAS28) (in Case of Peripheral Symptoms) in Participants With Psoriatic Arthritis | Baseline (Visit 0) to 12 months | The BASDAI score was calculated using a questionnaire with 6 questions that the participants completed by marking responses on a 10-centimeter visual analog scale ranging from 0 (none) to 10 (very severe) regarding severity of fatigue, spinal and peripheral joint pain, localized tenderness and morning stiffness. The final BASDAI score ranges from 0 to 10. A positive response was defined as a 50% or more decrease in the BASDAI score at 12 months as compared to baseline. The DAS28 is a validated index of rheumatoid arthritis disease activity. Twenty-eight tender joint counts, 28 swollen joint counts, C- reactive protein, and general health are included in the DAS28 score. Scores on the DAS28 range from 0 to 10. A DAS28 score \>5.1 indicates high disease activity, a DAS28 score \<3.2 indicates low disease activity, and a DAS28 score \<2.6 indicates clinical remission. |
| Mean Change in Ankylosing Spondylitis Disease Activity Score (ASDAS) | Baseline (Visit 0) to 12 months | The ASDAS tool is a self-administered questionnaire plus an objective laboratory evaluation. The questionnaire covers disease activity, back pain, and peripheral pain/swelling assessed on a visual analogue scale (from 0 (normal) to 10 (extreme pain or disability) cm) and duration of morning stiffness on a numerical rating scale (from 0 to 10, with 0 being none and 10 representing a duration of 2 hours or longer). The laboratory parameter is a measurement of C-reactive protein (mg/L) (CRP) or erythrocyte sedimentation rate (mm/h) (ESR). Data from five variables (disease activity, back pain, duration of morning stiffness, peripheral pain/swelling, and either CRP or ESR values) are combined to yield a score ranging from 0 to no defined upper limit. Remission is defined as ASDAS score \<1.3. Clinically important improvement is defined as a change ≥ 1.1 units, and major improvement is defined as a change ≥ 2.0 units. |
| Correlation Between Change in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) and Ankylosing Spondylitis Disease Activity Score (ASDAS) in Participants With Ankylosing Spondylitis | Baseline (Visit 0) to 12 months | BASDAI score (ranging from 0 to 10) was calculated using a questionnaire. Participants marked responses on a 10 cm visual analog scale ranging from 0 (none) to 10 (very severe) regarding fatigue, spinal and peripheral joint pain, localized tenderness and morning stiffness. A positive response was defined as a 50% or more decrease in the BASDAI score at 12 months as compared to baseline. ASDAS is a self-administered questionnaire plus an objective laboratory evaluation. The questionnaire covers disease activity, back pain, duration of morning stiffness and peripheral pain/swelling assessed on a visual analogue scale (from 0 to 10 cm) or on a numerical rating scale (from 0 to 10). The laboratory parameter is a measurement of C-reactive protein (mg/L) or erythrocyte sedimentation rate (mm/h). Spearman's rank correlation coefficient (CC) was calculated for BASDAI vs. ASDAS(subscript)CRP(subscript) and BASDAI vs. ASDAS(subscript)ESR(subscript ). |
| Predictors of Maintained Treatment Response and Remission in Participants With Ankylosing Spondylitis | Baseline (Visit 0) to 12 months | A mathematical technique called logistic regression was performed to identify factors that could be used to predict maintained treatment response and remission. The following baseline variables were used in the logistic regression analyses: age, gender, disease of interest, result of tuberculosis screening, time since diagnosis and extra-articular manifestations (symptoms and diseases that occur in parts of the body other than joints) at baseline. The BASDAI score at baseline was forced to serve as a predictor in each model. |
Participant flow
Pre-assignment details
A total of 566 participants were enrolled, and 11 participants were lost to follow-up after the baseline visit. According to the pre-specified analysis strategy in the statistical analysis plan, these participants were excluded from the full analysis set, which consisted of 555 participants.
Participants by arm
| Arm | Count |
|---|---|
| Ankylosing Spondylitis Participants with a diagnosis of ankylosing spondylitis | 403 |
| Psoriatic Arthritis Participants with a diagnosis of psoriatic arthritis | 151 |
| Disease State Unknown For one participant, information regarding the underlying disease was not available | 1 |
| Total | 555 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 | FG002 |
|---|---|---|---|---|
| Overall Study | Adverse Event | 11 | 5 | 0 |
| Overall Study | Investigator's decision | 28 | 6 | 0 |
| Overall Study | Investigator's decision and pt request | 1 | 0 | 0 |
| Overall Study | Lost to Follow-up | 5 | 4 | 0 |
| Overall Study | Patient's request | 19 | 5 | 0 |
| Overall Study | Serious Adverse Event | 2 | 3 | 0 |
Baseline characteristics
| Characteristic | Ankylosing Spondylitis | Psoriatic Arthritis | Disease State Unknown | Total |
|---|---|---|---|---|
| Age, Continuous | 44.0 years STANDARD_DEVIATION 12.8 | 49.7 years STANDARD_DEVIATION 12.1 | 40 years | 45.6 years STANDARD_DEVIATION 12.9 |
| Sex: Female, Male Female | 109 Participants | 65 Participants | 0 Participants | 174 Participants |
| Sex: Female, Male Male | 294 Participants | 86 Participants | 1 Participants | 381 Participants |
Adverse events
| Event type | EG000 affected / at risk |
|---|---|
| deaths Total, all-cause mortality | — / — |
| other Total, other adverse events | 0 / 0 |
| serious Total, serious adverse events | 26 / 555 |
Outcome results
Percentage of Participants With a 50% or More Decrease in Bath Ankylosing Spondylitis Daily Activity Index (BASDAI) Score at 12 Months Relative to Baseline
The BASDAI score was calculated using a questionnaire with 6 questions that the participants completed by marking responses on a 10-centimeter visual analog scale ranging from 0 (none) to 10 (very severe) regarding severity of fatigue, spinal and peripheral joint pain, localized tenderness and morning stiffness. The final BASDAI score ranges from 0 to 10. A positive response was defined as a 50% or more decrease in the BASDAI score at 12 months as compared to baseline.
Time frame: Baseline (Visit 0) to 12 months
Population: Participants with active axial symptoms (a baseline value of the BASDAI \> 4).
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Ankylosing Spondylitis | Percentage of Participants With a 50% or More Decrease in Bath Ankylosing Spondylitis Daily Activity Index (BASDAI) Score at 12 Months Relative to Baseline | 76.5 Percentage of participants |
| Psoriatic Arthritis | Percentage of Participants With a 50% or More Decrease in Bath Ankylosing Spondylitis Daily Activity Index (BASDAI) Score at 12 Months Relative to Baseline | 73.1 Percentage of participants |
Percentage of Participants With Active Axial Symptoms in Remission
The Ankylosing Spondylitis Disease Score (ASDAS) tool is a self-administered questionnaire plus an objective laboratory evaluation. The questionnaire covers disease activity, back pain, duration of morning stiffness and peripheral pain/swelling assessed on a visual analogue scale (from 0 to 10 cm) or on a numerical rating scale (from 0 to 10). The laboratory parameter is a measurement of C-reactive protein (mg/L) or erythrocyte sedimentation rate (mm/h). Remission was defined as ASDAS \<1.3 at 12 months.
Time frame: Baseline (Visit 0) to 12 months
Population: Participants with active axial symptoms (a baseline value of BASDAI \> 4)
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Ankylosing Spondylitis | Percentage of Participants With Active Axial Symptoms in Remission | 34.3 Percentage of participants |
| Psoriatic Arthritis | Percentage of Participants With Active Axial Symptoms in Remission | 28.8 Percentage of participants |
Percentage of Participants With a Disease Activity Score 28 (DAS28) Decrease ≥1.2 at 12 Months Relative to Baseline
The DAS28 is a validated index of rheumatoid arthritis disease activity. Twenty-eight tender joint counts, 28 swollen joint counts, C-reactive protein, and general health are included in the DAS28 score. Scores on the DAS28 range from 0 to 10. A DAS28 score \>5.1 indicates high disease activity, a DAS28 score \<3.2 indicates low disease activity, and a DAS28 score \<2.6 indicates clinical remission.
Time frame: Baseline (Visit 0) to 12 months
Population: Participants with peripheral symptoms (DAS28 \> 5.1 at baseline)
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Ankylosing Spondylitis | Percentage of Participants With a Disease Activity Score 28 (DAS28) Decrease ≥1.2 at 12 Months Relative to Baseline | 83.3 Percentage of participants |
| Psoriatic Arthritis | Percentage of Participants With a Disease Activity Score 28 (DAS28) Decrease ≥1.2 at 12 Months Relative to Baseline | 83.6 Percentage of participants |
Percentage of Participants With Peripheral Symptoms in Remission
The DAS28 is a validated index of rheumatoid arthritis disease activity. Twenty-eight tender joint counts, 28 swollen joint counts, C-reactive protein, and general health are included in the DAS28 score. Scores on the DAS28 range from 0 to 10. A DAS28 score \>5.1 indicates high disease activity, a DAS28 score \<3.2 indicates low disease activity, and a DAS28 score \<2.6 indicates clinical remission. Remission was defined as DAS28 ≤2.6 at 12 months.
Time frame: Baseline (Visit 0) to 12 months
Population: Participants with peripheral symptoms (DAS28 \> 5.1 at baseline)
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Ankylosing Spondylitis | Percentage of Participants With Peripheral Symptoms in Remission | 11.1 Percentage of participants |
| Psoriatic Arthritis | Percentage of Participants With Peripheral Symptoms in Remission | 14.8 Percentage of participants |
Change in the Percentage of Ankylosing Spondylitis Participants Who Have Paid Work
Working status (Working full-time, working part-time, working at home, unemployed but seeking work, work disabled, retired, student) was documented at each study visit.
Time frame: Baseline (Visit 0) to 12 months
Population: Participants with ankylosing spondylitis who received adalimumab treatment
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Ankylosing Spondylitis | Change in the Percentage of Ankylosing Spondylitis Participants Who Have Paid Work | Working at Baseline (Visit 0), n=403 | 56.6 Percentage of participants |
| Ankylosing Spondylitis | Change in the Percentage of Ankylosing Spondylitis Participants Who Have Paid Work | Working at last visit- valid data, n=351 | 56.1 Percentage of participants |
Change in the Percentage of Psoriatic Arthritis Participants Who Have Paid Work
Working status (Working full-time, working part-time, working at home, unemployed but seeking work, work disabled, retired, student) was documented at each study visit.
Time frame: Baseline (Visit 0) to 12 months
Population: Participants with psoriatic arthritis who received adalimumab treatment
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Ankylosing Spondylitis | Change in the Percentage of Psoriatic Arthritis Participants Who Have Paid Work | Working at Baseline (Visit 0), n=151 | 55.6 Percentage of participants |
| Ankylosing Spondylitis | Change in the Percentage of Psoriatic Arthritis Participants Who Have Paid Work | Working at last visit- valid data, n=140 | 54.3 Percentage of participants |
Correlation Between Change in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) and Ankylosing Spondylitis Disease Activity Score (ASDAS) in Participants With Ankylosing Spondylitis
BASDAI score (ranging from 0 to 10) was calculated using a questionnaire. Participants marked responses on a 10 cm visual analog scale ranging from 0 (none) to 10 (very severe) regarding fatigue, spinal and peripheral joint pain, localized tenderness and morning stiffness. A positive response was defined as a 50% or more decrease in the BASDAI score at 12 months as compared to baseline. ASDAS is a self-administered questionnaire plus an objective laboratory evaluation. The questionnaire covers disease activity, back pain, duration of morning stiffness and peripheral pain/swelling assessed on a visual analogue scale (from 0 to 10 cm) or on a numerical rating scale (from 0 to 10). The laboratory parameter is a measurement of C-reactive protein (mg/L) or erythrocyte sedimentation rate (mm/h). Spearman's rank correlation coefficient (CC) was calculated for BASDAI vs. ASDAS(subscript)CRP(subscript) and BASDAI vs. ASDAS(subscript)ESR(subscript ).
Time frame: Baseline (Visit 0) to 12 months
Population: Participants with ankylosing spondylitis and active axial symptoms (a baseline value of BASDAI \> 4)
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Ankylosing Spondylitis | Correlation Between Change in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) and Ankylosing Spondylitis Disease Activity Score (ASDAS) in Participants With Ankylosing Spondylitis | Correlation BASDAI and ASDAS-CRP, n=299 | 0.62 Correlation coefficient |
| Ankylosing Spondylitis | Correlation Between Change in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) and Ankylosing Spondylitis Disease Activity Score (ASDAS) in Participants With Ankylosing Spondylitis | Correlation BASDAI and ASDAS-ESR, n=358 | 0.71 Correlation coefficient |
Correlation Between Change in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) and Ankylosing Spondylitis Disease Activity Score (ASDAS) in Participants With Psoriatic Arthritis
BASDAI score (ranging from 0 to 10) was calculated using a questionnaire. Participants marked responses on a 10 cm visual analog scale ranging from 0 (none) to 10 (very severe) regarding fatigue, spinal and peripheral joint pain, localized tenderness and morning stiffness. A positive response was defined as a 50% or more decrease in the BASDAI score at 12 months as compared to baseline. ASDAS score consists of a self-administered questionnaire plus an objective laboratory evaluation. The questionnaire covers disease activity, back pain, duration of morning stiffness and peripheral pain/swelling assessed on a visual analogue scale (from 0 to 10 cm) or on a numerical rating scale (from 0 to 10). The laboratory parameter is a measurement of C-reactive protein (mg/L) or erythrocyte sedimentation rate (mm/h). Spearman's rank correlation coefficient (CC) was calculated for BASDAI vs. ASDAS(subscript)CRP(subscript) and BASDAI vs. ASDAS(subscript)ESR(subscript).
Time frame: Baseline (Visit 0) to 12 months
Population: Participants with psoriatic arthritis and active axial symptoms (a baseline value of BASDAI \> 4)
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Ankylosing Spondylitis | Correlation Between Change in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) and Ankylosing Spondylitis Disease Activity Score (ASDAS) in Participants With Psoriatic Arthritis | Correlation BASDAI and ASDAS-CRP, n=45 | 0.75 Correlation coefficient |
| Ankylosing Spondylitis | Correlation Between Change in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) and Ankylosing Spondylitis Disease Activity Score (ASDAS) in Participants With Psoriatic Arthritis | Correlation BASDAI and ASDAS-ESR, n=51 | 0.84 Correlation coefficient |
Duration of Treatment With Adalimumab
The duration of treatment with adalimumab was calculated separately for participants who discontinued the medication during the study and for those who did not.
Time frame: Baseline (Visit 0) to 12 months
Population: Participants who received adalimumab treatment
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Ankylosing Spondylitis | Duration of Treatment With Adalimumab | No discontinuation of treatment, n=315, 117 | 11.8 Months | Standard Deviation 1.2 |
| Ankylosing Spondylitis | Duration of Treatment With Adalimumab | Discontinuation of treatment, n=66, 23 | 4.8 Months | Standard Deviation 3 |
| Psoriatic Arthritis | Duration of Treatment With Adalimumab | No discontinuation of treatment, n=315, 117 | 11.6 Months | Standard Deviation 1.1 |
| Psoriatic Arthritis | Duration of Treatment With Adalimumab | Discontinuation of treatment, n=66, 23 | 5.0 Months | Standard Deviation 3.2 |
Mean Change in Ankylosing Spondylitis Disease Activity Score (ASDAS)
The ASDAS tool is a self-administered questionnaire plus an objective laboratory evaluation. The questionnaire covers disease activity, back pain, and peripheral pain/swelling assessed on a visual analogue scale (from 0 (normal) to 10 (extreme pain or disability) cm) and duration of morning stiffness on a numerical rating scale (from 0 to 10, with 0 being none and 10 representing a duration of 2 hours or longer). The laboratory parameter is a measurement of C-reactive protein (mg/L) (CRP) or erythrocyte sedimentation rate (mm/h) (ESR). Data from five variables (disease activity, back pain, duration of morning stiffness, peripheral pain/swelling, and either CRP or ESR values) are combined to yield a score ranging from 0 to no defined upper limit. Remission is defined as ASDAS score \<1.3. Clinically important improvement is defined as a change ≥ 1.1 units, and major improvement is defined as a change ≥ 2.0 units.
Time frame: Baseline (Visit 0) to 12 months
Population: Participants with active axial symptoms (a baseline value of BASDAI \> 4)
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Ankylosing Spondylitis | Mean Change in Ankylosing Spondylitis Disease Activity Score (ASDAS) | Mean change in ASDAS-CRP, n=299 and 45 | -2.6 Units on a scale | Standard Deviation 1.2 |
| Ankylosing Spondylitis | Mean Change in Ankylosing Spondylitis Disease Activity Score (ASDAS) | Mean change in ASDAS-ESR, n=358 and 51 | -2.3 Units on a scale | Standard Deviation 1.1 |
| Psoriatic Arthritis | Mean Change in Ankylosing Spondylitis Disease Activity Score (ASDAS) | Mean change in ASDAS-CRP, n=299 and 45 | -1.9 Units on a scale | Standard Deviation 1.7 |
| Psoriatic Arthritis | Mean Change in Ankylosing Spondylitis Disease Activity Score (ASDAS) | Mean change in ASDAS-ESR, n=358 and 51 | -1.9 Units on a scale | Standard Deviation 1.4 |
Mean Change in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) Score (in Case of Axial Symptoms) and/or Disease Activity Score/28 Joints (DAS28) (in Case of Peripheral Symptoms) in Participants With Ankylosing Spondylitis
The BASDAI score was calculated using a questionnaire with 6 questions that the participants completed by marking responses on a 10-centimeter visual analog scale ranging from 0 (none) to 10 (very severe) regarding severity of fatigue, spinal and peripheral joint pain, localized tenderness and morning stiffness. The final BASDAI score ranges from 0 to 10. A positive response was defined as a 50% or more decrease in the BASDAI score at 12 months as compared to baseline. The DAS28 is a validated index of rheumatoid arthritis disease activity. Twenty-eight tender joint counts, 28 swollen joint counts, C- reactive protein, and general health are included in the DAS28 score. Scores on the DAS28 range from 0 to 10. A DAS28 score \>5.1 indicates high disease activity, a DAS28 score \<3.2 indicates low disease activity, and a DAS28 score \<2.6 indicates clinical remission.
Time frame: Baseline (Visit 0) to 12 months
Population: Participants with ankylosing spondylitis with peripheral symptoms (DAS28 \> 5.1 at baseline) and/or active axial symptoms (a baseline value of BASDAI \> 4)
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Ankylosing Spondylitis | Mean Change in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) Score (in Case of Axial Symptoms) and/or Disease Activity Score/28 Joints (DAS28) (in Case of Peripheral Symptoms) in Participants With Ankylosing Spondylitis | Mean change in BASDAI score, n=366 | -4.6 Units on a scale | Standard Deviation 2.3 |
| Ankylosing Spondylitis | Mean Change in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) Score (in Case of Axial Symptoms) and/or Disease Activity Score/28 Joints (DAS28) (in Case of Peripheral Symptoms) in Participants With Ankylosing Spondylitis | Mean change in DAS28 score, n=18 | -1.9 Units on a scale | Standard Deviation 1.3 |
Mean Change in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) Score (in Case of Axial Symptoms) and/or Disease Activity Score/28 Joints (DAS28) (in Case of Peripheral Symptoms) in Participants With Psoriatic Arthritis
The BASDAI score was calculated using a questionnaire with 6 questions that the participants completed by marking responses on a 10-centimeter visual analog scale ranging from 0 (none) to 10 (very severe) regarding severity of fatigue, spinal and peripheral joint pain, localized tenderness and morning stiffness. The final BASDAI score ranges from 0 to 10. A positive response was defined as a 50% or more decrease in the BASDAI score at 12 months as compared to baseline. The DAS28 is a validated index of rheumatoid arthritis disease activity. Twenty-eight tender joint counts, 28 swollen joint counts, C- reactive protein, and general health are included in the DAS28 score. Scores on the DAS28 range from 0 to 10. A DAS28 score \>5.1 indicates high disease activity, a DAS28 score \<3.2 indicates low disease activity, and a DAS28 score \<2.6 indicates clinical remission.
Time frame: Baseline (Visit 0) to 12 months
Population: Participants with psoriatic arthritis with peripheral symptoms (DAS28 \> 5.1 at baseline) and/or active axial symptoms (a baseline value of BASDAI \> 4)
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Ankylosing Spondylitis | Mean Change in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) Score (in Case of Axial Symptoms) and/or Disease Activity Score/28 Joints (DAS28) (in Case of Peripheral Symptoms) in Participants With Psoriatic Arthritis | Mean change in BASDAI score, n=52 | -4.2 Units on a scale | Standard Deviation 2.4 |
| Ankylosing Spondylitis | Mean Change in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) Score (in Case of Axial Symptoms) and/or Disease Activity Score/28 Joints (DAS28) (in Case of Peripheral Symptoms) in Participants With Psoriatic Arthritis | Mean change in DAS28 score, n=61 | -2.4 Units on a scale | Standard Deviation 1.3 |
Mean Change in Health Assessment Questionnaire Disability Index (HAQ-DI) Score (in Case of Peripheral Symptoms) or Bath Ankylosing Spondylitis Functional Index (BASFI) Score (in Case of Axial Symptoms) in Participants With Ankylosing Spondylitis
HAQ-DI consists of 20 questions referring to 8 domains: dressing/grooming, arising, eating, walking, hygiene, reach, grip, and daily activities. Participants assessed their ability to do each task over the past week using the following categories: without any difficulty (0); with some difficulty (1); with much difficulty (2); and unable to do (3). Scores on each task were summed and averaged to provide an overall score ranging from 0 to 3, with a higher score representing a high-dependency disability. The minimal clinically important difference defined for the HAQ-DI is ≥0.22. HAQ-DI remission, indicating normal physical function, is defined as HAQ-DI \< 0.5. The BASFI is a set of 10 questions designed to determine the degree of functional limitation in those with AS. A visual analogue scale (with 0 being easy and 10 impossible) is used. The BASFI score ranges from 0 to 10 and is derived as the mean of the single items. A higher score indicates a higher impairment of functioning.
Time frame: Baseline (Visit 0) to 12 months
Population: Participants with ankylosing spondylitis with peripheral symptoms (DAS28 \> 5.1 at baseline) and/or active axial symptoms (a baseline value of BASDAI \> 4)
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Ankylosing Spondylitis | Mean Change in Health Assessment Questionnaire Disability Index (HAQ-DI) Score (in Case of Peripheral Symptoms) or Bath Ankylosing Spondylitis Functional Index (BASFI) Score (in Case of Axial Symptoms) in Participants With Ankylosing Spondylitis | Mean change in HAQ-DI, n=30 | -0.9 Units on a scale | Standard Deviation 0.6 |
| Ankylosing Spondylitis | Mean Change in Health Assessment Questionnaire Disability Index (HAQ-DI) Score (in Case of Peripheral Symptoms) or Bath Ankylosing Spondylitis Functional Index (BASFI) Score (in Case of Axial Symptoms) in Participants With Ankylosing Spondylitis | Mean change in BASFI, n=346 | -4.1 Units on a scale | Standard Deviation 2.5 |
Mean Change in Health Assessment Questionnaire Disability Index ( HAQ-DI) Score (in Case of Peripheral Symptoms) or Bath Ankylosing Spondylitis Functional Index (BASFI) Score (in Case of Axial Symptoms) in Participants With Psoriatic Arthritis
HAQ-DI consists of 20 questions referring to 8 domains: dressing/grooming, arising, eating, walking, hygiene, reach, grip, and daily activities. Participants assessed their ability to do each task over the past week using the following categories: without any difficulty (0); with some difficulty (1); with much difficulty (2); and unable to do (3). Scores on each task were summed and averaged to provide an overall score ranging from 0 to 3, with a higher score representing a high-dependency disability. The minimal clinically important difference defined for the HAQ-DI is ≥0.22. HAQ-DI remission, indicating normal physical function, is defined as HAQ-DI \< 0.5. The BASFI is a set of 10 questions designed to determine the degree of functional limitation in those with AS. A visual analogue scale (with 0 being easy and 10 impossible) is used. The BASFI score ranges from 0 to 10 and is derived as the mean of the single items. A higher score indicates a higher impairment of functioning.
Time frame: Baseline (Visit 0) to 12 months
Population: Participants with psoriatic arthritis with peripheral symptoms (DAS28 \> 5.1 at baseline) and/or active axial symptoms (a baseline value of BASDAI \> 4)
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Ankylosing Spondylitis | Mean Change in Health Assessment Questionnaire Disability Index ( HAQ-DI) Score (in Case of Peripheral Symptoms) or Bath Ankylosing Spondylitis Functional Index (BASFI) Score (in Case of Axial Symptoms) in Participants With Psoriatic Arthritis | Mean change in HAQ-DI, n=88 | -0.7 Units on a scale | Standard Deviation 0.6 |
| Ankylosing Spondylitis | Mean Change in Health Assessment Questionnaire Disability Index ( HAQ-DI) Score (in Case of Peripheral Symptoms) or Bath Ankylosing Spondylitis Functional Index (BASFI) Score (in Case of Axial Symptoms) in Participants With Psoriatic Arthritis | Mean change in BASFI, n=47 | -3.8 Units on a scale | Standard Deviation 2.8 |
Mean Change in Individual Components of the Work Productivity and Activity Impairment Specific Health Problem Questionnaire in Participants With Ankylosing Spondylitis
Work Productivity and Activity Impairment (WPAI) Questionnaire is a quantitative assessment of the amount of absenteeism, presenteeism, total work productivity impairment, and total activity impairment attributable to a specific health problem (WPAI-SHP), expressed as a percentage. Participants were queried regarding their current employment status, hours missed from work because of problems associated with their AS, hours missed from work because of any other reason, number of hours worked, how much AS affected work productivity (0=AS had no effect,10= AS completely prevented me from working), and how much AS affected ability to do regular daily activities, other than work at a job (0= AS had no effect, 10= AS completely prevented me from doing my daily activities) in the past 7 days.
Time frame: Baseline (Visit 0) to 12 months
Population: For presenteeism, absenteeism, and total work productivity impairment endpoints: participants with ankylosing spondylitis who were employed at the time of the documentation. For the total activity impairment endpoint: participants with ankylosing spondylitis who received adalimumab treatment.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Ankylosing Spondylitis | Mean Change in Individual Components of the Work Productivity and Activity Impairment Specific Health Problem Questionnaire in Participants With Ankylosing Spondylitis | Mean change in absenteeism, n=170 | -9.7 Percentage change | Standard Deviation 24.4 |
| Ankylosing Spondylitis | Mean Change in Individual Components of the Work Productivity and Activity Impairment Specific Health Problem Questionnaire in Participants With Ankylosing Spondylitis | Mean change in presenteeism, n=160 | -37.3 Percentage change | Standard Deviation 28 |
| Ankylosing Spondylitis | Mean Change in Individual Components of the Work Productivity and Activity Impairment Specific Health Problem Questionnaire in Participants With Ankylosing Spondylitis | Mean change in work productivity impairment, n=160 | -38.6 Percentage change | Standard Deviation 28.8 |
| Ankylosing Spondylitis | Mean Change in Individual Components of the Work Productivity and Activity Impairment Specific Health Problem Questionnaire in Participants With Ankylosing Spondylitis | Mean change in total activity impairment, n=342 | -36.5 Percentage change | Standard Deviation 26.7 |
Mean Change in Individual Components of the Work Productivity and Activity Impairment Specific Health Problem Questionnaire in Participants With Psoriatic Arthritis
The Work Productivity and Activity Impairment (WPAI) Questionnaire is a quantitative assessment of the amount of absenteeism, presenteeism, total work productivity impairment, and total activity impairment attributable to a specific health problem (WPAI-SHP), expressed as a percentage. Participants were queried regarding their current employment status, hours missed from work because of problems associated with their PsA, hours missed from work because of any other reason, number of hours worked, how much PsA affected work productivity (0= PsA had no effect,10= PsA completely prevented me from working), and how much PsA affected ability to do regular daily activities, other than work at a job (0= PsA had no effect, 10= PsA completely prevented me from doing my daily activities) in the past 7 days.
Time frame: Baseline (Visit 0) to 12 months
Population: For presenteeism, absenteeism, and total work productivity impairment endpoints: participants with psoriatic arthritis who were employed at the time of the documentation. For the total activity impairment endpoint: participants with psoriatic arthritis who received adalimumab treatment.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Ankylosing Spondylitis | Mean Change in Individual Components of the Work Productivity and Activity Impairment Specific Health Problem Questionnaire in Participants With Psoriatic Arthritis | Mean change in absenteeism, n=57 | -6.0 Percentage change | Standard Deviation 29 |
| Ankylosing Spondylitis | Mean Change in Individual Components of the Work Productivity and Activity Impairment Specific Health Problem Questionnaire in Participants With Psoriatic Arthritis | Mean change in presenteeism, n=54 | -32.8 Percentage change | Standard Deviation 24.9 |
| Ankylosing Spondylitis | Mean Change in Individual Components of the Work Productivity and Activity Impairment Specific Health Problem Questionnaire in Participants With Psoriatic Arthritis | Mean change in work productivity impairment, n=54 | -33.6 Percentage change | Standard Deviation 25.4 |
| Ankylosing Spondylitis | Mean Change in Individual Components of the Work Productivity and Activity Impairment Specific Health Problem Questionnaire in Participants With Psoriatic Arthritis | Mean change in total activity impairment, n=119 | -34.7 Percentage change | Standard Deviation 25.7 |
Mean Frequency of Extra-articular Manifestations (EAMs)
Extra-articular manifestations (EAMs) are symptoms and diseases that occur in parts of the body other than joints. The number of EAMs was determined at each study visit. These included the presence of enthesitis (inflammation of ligaments and/or tendons at the site of insertion into bones), uveitis (inflammation of the middle layer of the eye), psoriasis (a skin condition that causes itchy or sore patches of thick, red skin with silvery scales), and Inflammatory bowel disease (Crohn's disease or ulcerative colitis).
Time frame: Baseline (Visit 0) to 12 months
Population: Participants who received adalimumab treatment
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Ankylosing Spondylitis | Mean Frequency of Extra-articular Manifestations (EAMs) | Visit 3, n=339, 124 | 0.1 Mean EAMs per participant | Standard Deviation 0.3 |
| Ankylosing Spondylitis | Mean Frequency of Extra-articular Manifestations (EAMs) | Visit 1 , n=400, 150 | 0.2 Mean EAMs per participant | Standard Deviation 0.4 |
| Ankylosing Spondylitis | Mean Frequency of Extra-articular Manifestations (EAMs) | Visit 4, n=324, 124 | 0.1 Mean EAMs per participant | Standard Deviation 0.3 |
| Ankylosing Spondylitis | Mean Frequency of Extra-articular Manifestations (EAMs) | Baseline (Visit 0), n=403, 151 | 0.5 Mean EAMs per participant | Standard Deviation 0.6 |
| Ankylosing Spondylitis | Mean Frequency of Extra-articular Manifestations (EAMs) | Visit 4-LOCF, n=401, 151 | 0.1 Mean EAMs per participant | Standard Deviation 0.3 |
| Ankylosing Spondylitis | Mean Frequency of Extra-articular Manifestations (EAMs) | Visit 2, n=357, 137 | 0.1 Mean EAMs per participant | Standard Deviation 0.3 |
| Psoriatic Arthritis | Mean Frequency of Extra-articular Manifestations (EAMs) | Visit 4-LOCF, n=401, 151 | 0.5 Mean EAMs per participant | Standard Deviation 0.5 |
| Psoriatic Arthritis | Mean Frequency of Extra-articular Manifestations (EAMs) | Baseline (Visit 0), n=403, 151 | 1.1 Mean EAMs per participant | Standard Deviation 0.6 |
| Psoriatic Arthritis | Mean Frequency of Extra-articular Manifestations (EAMs) | Visit 1 , n=400, 150 | 0.6 Mean EAMs per participant | Standard Deviation 0.6 |
| Psoriatic Arthritis | Mean Frequency of Extra-articular Manifestations (EAMs) | Visit 3, n=339, 124 | 0.5 Mean EAMs per participant | Standard Deviation 0.5 |
| Psoriatic Arthritis | Mean Frequency of Extra-articular Manifestations (EAMs) | Visit 4, n=324, 124 | 0.5 Mean EAMs per participant | Standard Deviation 0.5 |
| Psoriatic Arthritis | Mean Frequency of Extra-articular Manifestations (EAMs) | Visit 2, n=357, 137 | 0.5 Mean EAMs per participant | Standard Deviation 0.6 |
Percentage of Participants Whose Co-medication With Nonsteroidal Anti-inflammatory Drugs (NSAIDs) Was Stopped During the Study
Participants were surveyed at each study visit for their use of NSAID medication.
Time frame: Baseline (Visit 0) to 12 months
Population: Participants who were receiving NSAID medication at baseline
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Ankylosing Spondylitis | Percentage of Participants Whose Co-medication With Nonsteroidal Anti-inflammatory Drugs (NSAIDs) Was Stopped During the Study | 96.6 Percentage of participants |
| Psoriatic Arthritis | Percentage of Participants Whose Co-medication With Nonsteroidal Anti-inflammatory Drugs (NSAIDs) Was Stopped During the Study | 94.9 Percentage of participants |
Predictors of Maintained Treatment Response and Remission in Participants With Ankylosing Spondylitis
A mathematical technique called logistic regression was performed to identify factors that could be used to predict maintained treatment response and remission. The following baseline variables were used in the logistic regression analyses: age, gender, disease of interest, result of tuberculosis screening, time since diagnosis and extra-articular manifestations (symptoms and diseases that occur in parts of the body other than joints) at baseline. The BASDAI score at baseline was forced to serve as a predictor in each model.
Time frame: Baseline (Visit 0) to 12 months
Population: Participants with ankylosing spondylitis and active axial symptoms (a baseline value of BASDAI \> 4)
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Ankylosing Spondylitis | Predictors of Maintained Treatment Response and Remission in Participants With Ankylosing Spondylitis | Response (BASDAI at V0), n=361 | 1.18 Odds Ratio |
| Ankylosing Spondylitis | Predictors of Maintained Treatment Response and Remission in Participants With Ankylosing Spondylitis | Response (Age), n=361 | 0.98 Odds Ratio |
| Ankylosing Spondylitis | Predictors of Maintained Treatment Response and Remission in Participants With Ankylosing Spondylitis | Response (Enthesitis at V0), n=361 | 2.47 Odds Ratio |
| Ankylosing Spondylitis | Predictors of Maintained Treatment Response and Remission in Participants With Ankylosing Spondylitis | Remission (Age), n=356 | 0.96 Odds Ratio |
| Ankylosing Spondylitis | Predictors of Maintained Treatment Response and Remission in Participants With Ankylosing Spondylitis | Remission (TB positive at V0), n=356 | 0.57 Odds Ratio |
| Ankylosing Spondylitis | Predictors of Maintained Treatment Response and Remission in Participants With Ankylosing Spondylitis | Remission (Male gender), n=356 | 1.77 Odds Ratio |
| Ankylosing Spondylitis | Predictors of Maintained Treatment Response and Remission in Participants With Ankylosing Spondylitis | Remission (BASDAI at V0), n=356 | 0.94 Odds Ratio |
Predictors of Maintained Treatment Response and Remission in Participants With Psoriatic Arthritis
A mathematical technique called logistic regression was performed to identify factors that could be used to predict maintained treatment response and remission. The following baseline variables were used in the logistic regression analyses: age, gender, disease of interest, result of tuberculosis screening, time since diagnosis and extra-articular manifestations (symptoms and diseases that occur in parts of the body other than joints) at baseline. The BASDAI score at baseline was forced to serve as a predictor in each model.
Time frame: Baseline (Visit 0) to 12 months
Population: Participants with psoriatic arthritis and active axial symptoms (a baseline value of BASDAI \> 4)
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Ankylosing Spondylitis | Predictors of Maintained Treatment Response and Remission in Participants With Psoriatic Arthritis | Remission (BASDAI score at Visit 0) | 0.87 Odds Ratio |
| Ankylosing Spondylitis | Predictors of Maintained Treatment Response and Remission in Participants With Psoriatic Arthritis | Treatment response (Enthesitis at Visit 0) | 0.23 Odds Ratio |
| Ankylosing Spondylitis | Predictors of Maintained Treatment Response and Remission in Participants With Psoriatic Arthritis | Treatment response (BASDAI score at Visit 0) | 1.35 Odds Ratio |
| Ankylosing Spondylitis | Predictors of Maintained Treatment Response and Remission in Participants With Psoriatic Arthritis | Remission (Psoriasis at Visit 0) | 0.21 Odds Ratio |