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Multi-country Post-Marketing Observational Study on Maintenance of Effectiveness of Adalimumab (Humira®) in Patients With Ankylosing Spondylitis and Psoriatic Arthritis

Multicountry Post-Marketing Observational Study on Maintenance of Effectiveness of Adalimumab in Patients With Ankylosing Spondylitis and Psoriatic Arthritis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01474876
Enrollment
566
Registered
2011-11-18
Start date
2011-11-30
Completion date
2014-05-31
Last updated
2015-07-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ankylosing Spondylitis, Psoriatic Arthritis

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

AbbVie (prior sponsor, Abbott)
Lead SponsorINDUSTRY

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

MeasureTime frameDescription
Percentage of Participants With a 50% or More Decrease in Bath Ankylosing Spondylitis Daily Activity Index (BASDAI) Score at 12 Months Relative to BaselineBaseline (Visit 0) to 12 monthsThe 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 BaselineBaseline (Visit 0) to 12 monthsThe 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 RemissionBaseline (Visit 0) to 12 monthsThe 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 RemissionBaseline (Visit 0) to 12 monthsThe 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

MeasureTime frameDescription
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 SpondylitisBaseline (Visit 0) to 12 monthsHAQ-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 monthsExtra-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 AdalimumabBaseline (Visit 0) to 12 monthsThe 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 StudyBaseline (Visit 0) to 12 monthsParticipants 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 SpondylitisBaseline (Visit 0) to 12 monthsWork 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 WorkBaseline (Visit 0) to 12 monthsWorking 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 SpondylitisBaseline (Visit 0) to 12 monthsThe 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 ArthritisBaseline (Visit 0) to 12 monthsBASDAI 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 ArthritisBaseline (Visit 0) to 12 monthsA 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 ArthritisBaseline (Visit 0) to 12 monthsHAQ-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 ArthritisBaseline (Visit 0) to 12 monthsThe 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 WorkBaseline (Visit 0) to 12 monthsWorking 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 ArthritisBaseline (Visit 0) to 12 monthsThe 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 monthsThe 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 SpondylitisBaseline (Visit 0) to 12 monthsBASDAI 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 SpondylitisBaseline (Visit 0) to 12 monthsA 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

ArmCount
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
Total555

Withdrawals & dropouts

PeriodReasonFG000FG001FG002
Overall StudyAdverse Event1150
Overall StudyInvestigator's decision2860
Overall StudyInvestigator's decision and pt request100
Overall StudyLost to Follow-up540
Overall StudyPatient's request1950
Overall StudySerious Adverse Event230

Baseline characteristics

CharacteristicAnkylosing SpondylitisPsoriatic ArthritisDisease State UnknownTotal
Age, Continuous44.0 years
STANDARD_DEVIATION 12.8
49.7 years
STANDARD_DEVIATION 12.1
40 years45.6 years
STANDARD_DEVIATION 12.9
Sex: Female, Male
Female
109 Participants65 Participants0 Participants174 Participants
Sex: Female, Male
Male
294 Participants86 Participants1 Participants381 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
— / —
other
Total, other adverse events
0 / 0
serious
Total, serious adverse events
26 / 555

Outcome results

Primary

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).

ArmMeasureValue (NUMBER)
Ankylosing SpondylitisPercentage of Participants With a 50% or More Decrease in Bath Ankylosing Spondylitis Daily Activity Index (BASDAI) Score at 12 Months Relative to Baseline76.5 Percentage of participants
Psoriatic ArthritisPercentage of Participants With a 50% or More Decrease in Bath Ankylosing Spondylitis Daily Activity Index (BASDAI) Score at 12 Months Relative to Baseline73.1 Percentage of participants
Primary

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)

ArmMeasureValue (NUMBER)
Ankylosing SpondylitisPercentage of Participants With Active Axial Symptoms in Remission34.3 Percentage of participants
Psoriatic ArthritisPercentage of Participants With Active Axial Symptoms in Remission28.8 Percentage of participants
Primary

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)

ArmMeasureValue (NUMBER)
Ankylosing SpondylitisPercentage of Participants With a Disease Activity Score 28 (DAS28) Decrease ≥1.2 at 12 Months Relative to Baseline83.3 Percentage of participants
Psoriatic ArthritisPercentage of Participants With a Disease Activity Score 28 (DAS28) Decrease ≥1.2 at 12 Months Relative to Baseline83.6 Percentage of participants
Primary

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)

ArmMeasureValue (NUMBER)
Ankylosing SpondylitisPercentage of Participants With Peripheral Symptoms in Remission11.1 Percentage of participants
Psoriatic ArthritisPercentage of Participants With Peripheral Symptoms in Remission14.8 Percentage of participants
Secondary

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

ArmMeasureGroupValue (NUMBER)
Ankylosing SpondylitisChange in the Percentage of Ankylosing Spondylitis Participants Who Have Paid WorkWorking at Baseline (Visit 0), n=40356.6 Percentage of participants
Ankylosing SpondylitisChange in the Percentage of Ankylosing Spondylitis Participants Who Have Paid WorkWorking at last visit- valid data, n=35156.1 Percentage of participants
Secondary

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

ArmMeasureGroupValue (NUMBER)
Ankylosing SpondylitisChange in the Percentage of Psoriatic Arthritis Participants Who Have Paid WorkWorking at Baseline (Visit 0), n=15155.6 Percentage of participants
Ankylosing SpondylitisChange in the Percentage of Psoriatic Arthritis Participants Who Have Paid WorkWorking at last visit- valid data, n=14054.3 Percentage of participants
Secondary

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)

ArmMeasureGroupValue (NUMBER)
Ankylosing SpondylitisCorrelation Between Change in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) and Ankylosing Spondylitis Disease Activity Score (ASDAS) in Participants With Ankylosing SpondylitisCorrelation BASDAI and ASDAS-CRP, n=2990.62 Correlation coefficient
Ankylosing SpondylitisCorrelation Between Change in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) and Ankylosing Spondylitis Disease Activity Score (ASDAS) in Participants With Ankylosing SpondylitisCorrelation BASDAI and ASDAS-ESR, n=3580.71 Correlation coefficient
Secondary

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)

ArmMeasureGroupValue (NUMBER)
Ankylosing SpondylitisCorrelation Between Change in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) and Ankylosing Spondylitis Disease Activity Score (ASDAS) in Participants With Psoriatic ArthritisCorrelation BASDAI and ASDAS-CRP, n=450.75 Correlation coefficient
Ankylosing SpondylitisCorrelation Between Change in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) and Ankylosing Spondylitis Disease Activity Score (ASDAS) in Participants With Psoriatic ArthritisCorrelation BASDAI and ASDAS-ESR, n=510.84 Correlation coefficient
Secondary

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

ArmMeasureGroupValue (MEAN)Dispersion
Ankylosing SpondylitisDuration of Treatment With AdalimumabNo discontinuation of treatment, n=315, 11711.8 MonthsStandard Deviation 1.2
Ankylosing SpondylitisDuration of Treatment With AdalimumabDiscontinuation of treatment, n=66, 234.8 MonthsStandard Deviation 3
Psoriatic ArthritisDuration of Treatment With AdalimumabNo discontinuation of treatment, n=315, 11711.6 MonthsStandard Deviation 1.1
Psoriatic ArthritisDuration of Treatment With AdalimumabDiscontinuation of treatment, n=66, 235.0 MonthsStandard Deviation 3.2
Secondary

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)

ArmMeasureGroupValue (MEAN)Dispersion
Ankylosing SpondylitisMean Change in Ankylosing Spondylitis Disease Activity Score (ASDAS)Mean change in ASDAS-CRP, n=299 and 45-2.6 Units on a scaleStandard Deviation 1.2
Ankylosing SpondylitisMean Change in Ankylosing Spondylitis Disease Activity Score (ASDAS)Mean change in ASDAS-ESR, n=358 and 51-2.3 Units on a scaleStandard Deviation 1.1
Psoriatic ArthritisMean Change in Ankylosing Spondylitis Disease Activity Score (ASDAS)Mean change in ASDAS-CRP, n=299 and 45-1.9 Units on a scaleStandard Deviation 1.7
Psoriatic ArthritisMean Change in Ankylosing Spondylitis Disease Activity Score (ASDAS)Mean change in ASDAS-ESR, n=358 and 51-1.9 Units on a scaleStandard Deviation 1.4
Secondary

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)

ArmMeasureGroupValue (MEAN)Dispersion
Ankylosing SpondylitisMean 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 SpondylitisMean change in BASDAI score, n=366-4.6 Units on a scaleStandard Deviation 2.3
Ankylosing SpondylitisMean 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 SpondylitisMean change in DAS28 score, n=18-1.9 Units on a scaleStandard Deviation 1.3
Secondary

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)

ArmMeasureGroupValue (MEAN)Dispersion
Ankylosing SpondylitisMean 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 ArthritisMean change in BASDAI score, n=52-4.2 Units on a scaleStandard Deviation 2.4
Ankylosing SpondylitisMean 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 ArthritisMean change in DAS28 score, n=61-2.4 Units on a scaleStandard Deviation 1.3
Secondary

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)

ArmMeasureGroupValue (MEAN)Dispersion
Ankylosing SpondylitisMean 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 SpondylitisMean change in HAQ-DI, n=30-0.9 Units on a scaleStandard Deviation 0.6
Ankylosing SpondylitisMean 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 SpondylitisMean change in BASFI, n=346-4.1 Units on a scaleStandard Deviation 2.5
Secondary

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)

ArmMeasureGroupValue (MEAN)Dispersion
Ankylosing SpondylitisMean 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 ArthritisMean change in HAQ-DI, n=88-0.7 Units on a scaleStandard Deviation 0.6
Ankylosing SpondylitisMean 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 ArthritisMean change in BASFI, n=47-3.8 Units on a scaleStandard Deviation 2.8
Secondary

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.

ArmMeasureGroupValue (MEAN)Dispersion
Ankylosing SpondylitisMean Change in Individual Components of the Work Productivity and Activity Impairment Specific Health Problem Questionnaire in Participants With Ankylosing SpondylitisMean change in absenteeism, n=170-9.7 Percentage changeStandard Deviation 24.4
Ankylosing SpondylitisMean Change in Individual Components of the Work Productivity and Activity Impairment Specific Health Problem Questionnaire in Participants With Ankylosing SpondylitisMean change in presenteeism, n=160-37.3 Percentage changeStandard Deviation 28
Ankylosing SpondylitisMean Change in Individual Components of the Work Productivity and Activity Impairment Specific Health Problem Questionnaire in Participants With Ankylosing SpondylitisMean change in work productivity impairment, n=160-38.6 Percentage changeStandard Deviation 28.8
Ankylosing SpondylitisMean Change in Individual Components of the Work Productivity and Activity Impairment Specific Health Problem Questionnaire in Participants With Ankylosing SpondylitisMean change in total activity impairment, n=342-36.5 Percentage changeStandard Deviation 26.7
Secondary

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.

ArmMeasureGroupValue (MEAN)Dispersion
Ankylosing SpondylitisMean Change in Individual Components of the Work Productivity and Activity Impairment Specific Health Problem Questionnaire in Participants With Psoriatic ArthritisMean change in absenteeism, n=57-6.0 Percentage changeStandard Deviation 29
Ankylosing SpondylitisMean Change in Individual Components of the Work Productivity and Activity Impairment Specific Health Problem Questionnaire in Participants With Psoriatic ArthritisMean change in presenteeism, n=54-32.8 Percentage changeStandard Deviation 24.9
Ankylosing SpondylitisMean Change in Individual Components of the Work Productivity and Activity Impairment Specific Health Problem Questionnaire in Participants With Psoriatic ArthritisMean change in work productivity impairment, n=54-33.6 Percentage changeStandard Deviation 25.4
Ankylosing SpondylitisMean Change in Individual Components of the Work Productivity and Activity Impairment Specific Health Problem Questionnaire in Participants With Psoriatic ArthritisMean change in total activity impairment, n=119-34.7 Percentage changeStandard Deviation 25.7
Secondary

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

ArmMeasureGroupValue (MEAN)Dispersion
Ankylosing SpondylitisMean Frequency of Extra-articular Manifestations (EAMs)Visit 3, n=339, 1240.1 Mean EAMs per participantStandard Deviation 0.3
Ankylosing SpondylitisMean Frequency of Extra-articular Manifestations (EAMs)Visit 1 , n=400, 1500.2 Mean EAMs per participantStandard Deviation 0.4
Ankylosing SpondylitisMean Frequency of Extra-articular Manifestations (EAMs)Visit 4, n=324, 1240.1 Mean EAMs per participantStandard Deviation 0.3
Ankylosing SpondylitisMean Frequency of Extra-articular Manifestations (EAMs)Baseline (Visit 0), n=403, 1510.5 Mean EAMs per participantStandard Deviation 0.6
Ankylosing SpondylitisMean Frequency of Extra-articular Manifestations (EAMs)Visit 4-LOCF, n=401, 1510.1 Mean EAMs per participantStandard Deviation 0.3
Ankylosing SpondylitisMean Frequency of Extra-articular Manifestations (EAMs)Visit 2, n=357, 1370.1 Mean EAMs per participantStandard Deviation 0.3
Psoriatic ArthritisMean Frequency of Extra-articular Manifestations (EAMs)Visit 4-LOCF, n=401, 1510.5 Mean EAMs per participantStandard Deviation 0.5
Psoriatic ArthritisMean Frequency of Extra-articular Manifestations (EAMs)Baseline (Visit 0), n=403, 1511.1 Mean EAMs per participantStandard Deviation 0.6
Psoriatic ArthritisMean Frequency of Extra-articular Manifestations (EAMs)Visit 1 , n=400, 1500.6 Mean EAMs per participantStandard Deviation 0.6
Psoriatic ArthritisMean Frequency of Extra-articular Manifestations (EAMs)Visit 3, n=339, 1240.5 Mean EAMs per participantStandard Deviation 0.5
Psoriatic ArthritisMean Frequency of Extra-articular Manifestations (EAMs)Visit 4, n=324, 1240.5 Mean EAMs per participantStandard Deviation 0.5
Psoriatic ArthritisMean Frequency of Extra-articular Manifestations (EAMs)Visit 2, n=357, 1370.5 Mean EAMs per participantStandard Deviation 0.6
Secondary

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

ArmMeasureValue (NUMBER)
Ankylosing SpondylitisPercentage of Participants Whose Co-medication With Nonsteroidal Anti-inflammatory Drugs (NSAIDs) Was Stopped During the Study96.6 Percentage of participants
Psoriatic ArthritisPercentage of Participants Whose Co-medication With Nonsteroidal Anti-inflammatory Drugs (NSAIDs) Was Stopped During the Study94.9 Percentage of participants
Secondary

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)

ArmMeasureGroupValue (NUMBER)
Ankylosing SpondylitisPredictors of Maintained Treatment Response and Remission in Participants With Ankylosing SpondylitisResponse (BASDAI at V0), n=3611.18 Odds Ratio
Ankylosing SpondylitisPredictors of Maintained Treatment Response and Remission in Participants With Ankylosing SpondylitisResponse (Age), n=3610.98 Odds Ratio
Ankylosing SpondylitisPredictors of Maintained Treatment Response and Remission in Participants With Ankylosing SpondylitisResponse (Enthesitis at V0), n=3612.47 Odds Ratio
Ankylosing SpondylitisPredictors of Maintained Treatment Response and Remission in Participants With Ankylosing SpondylitisRemission (Age), n=3560.96 Odds Ratio
Ankylosing SpondylitisPredictors of Maintained Treatment Response and Remission in Participants With Ankylosing SpondylitisRemission (TB positive at V0), n=3560.57 Odds Ratio
Ankylosing SpondylitisPredictors of Maintained Treatment Response and Remission in Participants With Ankylosing SpondylitisRemission (Male gender), n=3561.77 Odds Ratio
Ankylosing SpondylitisPredictors of Maintained Treatment Response and Remission in Participants With Ankylosing SpondylitisRemission (BASDAI at V0), n=3560.94 Odds Ratio
Comparison: Treatment response and participant agep-value: 0.0164Regression, Logistic
Comparison: Treatment response and presence of enthesitis at Visit 0p-value: 0.02Regression, Logistic
Comparison: Treatment response and BASDAI score at Visit 0p-value: 0.0867Regression, Logistic
Comparison: Remission and participant agep-value: 0.0001Regression, Logistic
Comparison: Remission and positive tuberculosis screening at Visit 0p-value: 0.0734Regression, Logistic
Comparison: Remission and male genderp-value: 0.0438Regression, Logistic
Comparison: Remission and BASDAI score at Visit 0p-value: 0.503Regression, Logistic
Secondary

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)

ArmMeasureGroupValue (NUMBER)
Ankylosing SpondylitisPredictors of Maintained Treatment Response and Remission in Participants With Psoriatic ArthritisRemission (BASDAI score at Visit 0)0.87 Odds Ratio
Ankylosing SpondylitisPredictors of Maintained Treatment Response and Remission in Participants With Psoriatic ArthritisTreatment response (Enthesitis at Visit 0)0.23 Odds Ratio
Ankylosing SpondylitisPredictors of Maintained Treatment Response and Remission in Participants With Psoriatic ArthritisTreatment response (BASDAI score at Visit 0)1.35 Odds Ratio
Ankylosing SpondylitisPredictors of Maintained Treatment Response and Remission in Participants With Psoriatic ArthritisRemission (Psoriasis at Visit 0)0.21 Odds Ratio
Comparison: Treatment response and presence of enthesitis at Visit 0p-value: 0.0576Regression, Logistic
Comparison: Treatment response and BASDAI score at Visit 0p-value: 0.1739Regression, Logistic
Comparison: Remission and Psoriasis at Visit 0p-value: 0.0733Regression, Logistic
Comparison: Remission and BASDAI at Visit 0p-value: 0.5Regression, Logistic

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026