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Abstract Number: 2533

Current Psa Therapy Impacts the Relationship between the Degree of Skin Invlovment and Joint Activity

Philip J Mease1, Carol J. Etzel2, Jeffrey Lisse3, April W Armstrong4, William J Huster3, Sabrina Rebello2, Rhiannon Dodge2, Talia M Muram3, Sarah Al Sawah3, Mwangi J Murage3, Jeffrey D Greenberg2 and William Malatestinic3, 1Swedish Medical Center and University of Washington, Seattle, WA, 2Corrona, LLC, Southborough, MA, 3Eli Lilly and Company, Indianapolis, IN, 4Keck School of Medicine, University of Southern California, Los Angeles, CA

Meeting: 2017 ACR/ARHP Annual Meeting

Date of first publication: September 18, 2017

Keywords: Clinical practice, Disease Activity, psoriasis, psoriatic arthritis and skin

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Session Information

Date: Tuesday, November 7, 2017

Title: Spondyloarthropathies and Psoriatic Arthritis – Clinical Aspects and Treatment Poster III: Outcomes, Outcome Measures, and Comorbidities

Session Type: ACR Poster Session C

Session Time: 9:00AM-11:00AM

Background/Purpose: Simultaneous control of joint symptoms and degree of skin involvement has been linked to improvement in health-related quality of life in patients with coexistent PsA and psoriasis (PsO). The objective of this analysis was to understand how the relationship between skin and joint severity is impacted by PsA therapy.

Methods: Enrollment visit data from Corrona PsA/SpA registry were obtained from 3/21/2013-9/30/2016. To be included in the analysis, patients had to have a diagnosis of PsA and history of PsO. Patients were subsequently stratified into three subgroups based on therapy at enrollment: a) not on DMARD therapy, b) on csDMARDS, or c) on anti-TNFs. Patient demographic and disease characteristics were compared.

The relationship of skin severity (BSA) and joint activity (CDAI) was evaluated using linear regression. To evaluate whether factors modified the relationship between CDAI and BSA, multiple linear regression was performed.

Results: 1,542 patients met inclusion criteria and 1484 had known therapy status. 266 (18%) patients were on no DMARD therapy, 430 (29%) were on csDMARDs only, and 765 (52%) were on anti-TNFs at time of enrollment. Patients on no DMARD therapy were more likely to be female, younger, have shorter PsA duration, more likely to have dactylitis, enthesitis and higher levels of joint activity, skin severity, and HAQ, and less likely to have MDA. (Table). Patients on TNFi therapy had better disease control (CDAI and BSA) than other therapy subgroups, but proportion of patients with MDA was similar to those on csDMARDS.

In the no DMARD therapy group, no variables tested resulted in a significant impact on the relationship. In both csDMARD and TNFi groups, age, BMI, SPARCC, HAQ, patient reported pain and fatigue significantly impacted the relationship between joint activity and skin severity. In csDMARDs group, dactylitis modified the relationship and in TNFi group, PsO onset and MDA modified the relationship.

Table: Descriptive statistics for patient characteristics, disease characteristics and PROs stratified by current drug therapy

 

No DMARDs

N=266

csDMARDs only

N=430

1st or 2nd Line TNF

N=765

P-value

Age (yrs):                                                  Mean (SD)

51.9 ±14.0

57.5 ±14.1

52.7 ±12.0

<0.0001

Sex:                                                        n(%) Female

157 (59.5)

237 (55.5)

361 (47.6)

0.0001

Insurance Type:                                        No

266

430

765

Private

209 (78.6)

310 (72.1)

645 (84.3)

<0.0001

Medicare

58 (21.8)

127 (29.5)

127 (16.6)

Medicaid

7 (2.6)

24 (5.6)

31 (4.1)

None

6 (2.3)

8 (1.9)

12 (1.6)

Smoking Status:                      No

257

420

753

Never: n(%)

131 (51.0)

222 (52.9)

402 (53.4)

0.359

Former: n(%)

90 (35.0)

160 (38.1)

269 (35.7)

Current: n(%)

36 (14.0)

38 (9.0)

82 (10.9)

BMI:                                                           Mean (SD)

31.5 ±7.8

31.4 ±7.3

31.5 ±6.9

0.995

PsA Disease Duration (years):            Median (IQR)

6.0(2.0,13.0)

7.0(3.0,14.5)

10.0(5.0,18.0)

<0.0001

PsO Disease Duration (years):           Median (IQR)

15.0(8.0,27.0)

16.0(9.0,29.0)

18.0(10.0,28.0)

0.435

Work Status: No

266

423

756

Full or Part-time: n(%)

174 (65.4)

233 (55.1)

502 (66.4)

<0.0001

Student/Not Working Outside Home: n(%)

15 (5.6)

25 (5.9)

56 (7.4)

Retired: n(%o)

52 (19.5)

131 (31.0)

133 (17.6)

Disabled: n(%)

25 (9.4)

34 (8.0)

65 (8.6)

CDAI:                                                         Mean (SD)

14.9 ±8.9

11.9 ±9.3

10.5 ±7.2

<0.0001

BSA:                                                          Mean (SD)

7.5 ±14.3

5.2 ±10.0

5.2 ±10.3

0.008

Enthesitis SPARCC Score:                  Mean (SD)

3.9 ±2.9

4.8 ±3.5

4.0 ±2.9

0.156

Dactylitis: No

266

430

765

 

Mean (SD)

2.2 ±1.5

2.7 ±2.2

1.9 ±1.5

0.083

Minimal Disease Activity:                                n(%)

57 (22.9)

172 (43.8)

343 (48.4)

<0.0001

28 Tender Joints Count:                          Mean (SD)

4.0 ±5.3

2.6 ±4.8

2.2 ±4.5

<0.0001

28 Swollen Joints Count: Mean (SD)

2.7 ±3.7

2.0 ±3.7

1.1 ±2.4

<0.0001

Nail Pso VAS (0-100):              Mean (SD)

9.1 ±16.0

8.1 ±21.4

6.2 ±13.6

0.023

HAQ (0-3): Mean (SD)

0.7 ±0.7

0.6 ±0.7

0.5 ±0.6

0.0001

Patient Pain VAS (0-100): Mean (SD)

46.0 ±29.0

37.4 ±28.7

34.0 ±28.7

<0.0001

Patient Reported Fatigue (0-100): Mean (SD)

45.3 ±29.0

39.3 ±29.0

38.2 ±28.9

0.003

Proportions are calculated among patients with non-missing response. Enthesiits SPARCC Score and Dactylitis Counts are among patients with enthesitis and dactylitis, respectively

Conclusion: There were significant differences in disease characteristics and patient reported outcomes in PsA patients with PsO history when stratified by type of therapy. The relationship between joint activity and skin severity is influenced by age, SPARCC, patient reported pain, fatigue, and HAQ among patients on DMARDs and TNFi therapies. Dactylitis and PsO onset also modified the relationship among csDMARD and TNFi therapy groups, respectively. For improved disease management of PsA patients with a history of PsO, consideration of these factors is important when determining type of therapy.


Disclosure: P. J. Mease, AbbVie, Amgen, BMS, Celgene, Janssen, Lilly, Novartis, Pfizer, Sun, UCB, 2,AbbVie, Amgen, BMS, Celgene, Janssen, Lilly, Novartis, Pfizer, Sun, UCB, 5,AbbVie, Amgen, BMS, Celgene, Genentech, Janssen, Novartis, Pfizer, UCB, 8; C. J. Etzel, Corrona, LLC, 3,Merck Human Health, 9; J. Lisse, Eli Lilly and Company, 1,Eli Lilly and Company, 3; A. W. Armstrong, AbbVie, Amgen, Janssen, Merck, Lilly, Celgene, Novartis, and Pfizer, 5,AbbVie, Janssen, Lilly, 2,AbbVie, Lilly, 8; W. J. Huster, Eli Lilly and Company, 1,Eli Lilly and Company, 3; S. Rebello, Corrona, LLC, 3; R. Dodge, Corrona, LLC, 3; T. M. Muram, Eli Lilly and Company, 1,Eli Lilly and Company, 3; S. Al Sawah, Eli Lilly and Company, 1,Eli Lilly and Company, 3; M. J. Murage, Eli Lilly and Company, 1,Eli Lilly and Company, 3; J. D. Greenberg, corrona, LLC, 1,Corrona, LLC, 3,Genentech, Janssen, Novartis, Pfizer, Eli Lilly, 5; W. Malatestinic, Eli Lilly and Company, 1,Eli Lilly and Company, 3.

To cite this abstract in AMA style:

Mease PJ, Etzel CJ, Lisse J, Armstrong AW, Huster WJ, Rebello S, Dodge R, Muram TM, Al Sawah S, Murage MJ, Greenberg JD, Malatestinic W. Current Psa Therapy Impacts the Relationship between the Degree of Skin Invlovment and Joint Activity [abstract]. Arthritis Rheumatol. 2017; 69 (suppl 10). https://acrabstracts.org/abstract/current-psa-therapy-impacts-the-relationship-between-the-degree-of-skin-invlovment-and-joint-activity/. Accessed .
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