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Abstract Number: 1570

Relationship Between Psoriatic Arthritis Severity, Duration, and Comorbidities

Stacy Tanner1, Molly McFadden2, Daniel Clegg3 and Jessica Walsh4, 1Internal Medicine, University of Utah, Salt Lake City, UT, 2Internal Medicine-Division of Epidemiology, University of Utah, SLC, UT, 3Division of Rheumatology, University of Utah Medical Ctr, Salt Lake City, UT, 4Rheumatology Room 4B200 School of Medicine, University of Utah, Salt Lake City, UT

Meeting: 2014 ACR/ARHP Annual Meeting

Keywords: Comorbidity, Psoriatic arthritis and severity

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Session Information

Title: Spondyloarthropathies and Psoriatic Arthritis - Clinical Aspects and Treatment II

Session Type: Abstract Submissions (ACR)

Background/Purpose

People with psoriatic arthritis (PsA) have an increased risk for several comorbidities that negatively impact quality of life and survival.  Defining the relationships between comorbidities and PsA characteristics may help identify subsets of PsA patients at high risk for comorbidities.  The objective of this study was to determine if PsA severity or duration associated with the number of comorbidities.

Methods

This was a cross-sectional study of PsA participants in the Utah Psoriasis Initiative Arthritis Registry.  Data were collected with questionnaires, interviews, and examinations between 1/22/2010 and 4/21/2014.  Disease severity measures included a functional assessment [BASFI], a quality of life instrument [Psoriatic Arthritis Quality of Life (PsAQOL)], and disease activity measures, [68 tender joint count (TJC), 66 swollen joint count (SJC), BASDAI, Physician Global, Patient Global, and a cutaneous physician global assessment multiplied by the body surface area (PGAxBSA)].  To analyze PsA duration, a proportional odds logistic regression model was used to test for an association between PsA duration (<5 years, 5-15 years, and >15 years) and number of comorbidities (0, 1-2, or ≥3 comorbidities), after adjustment for age, gender, race, body mass index (BMI), TJC, and SJC.  For severity assessments, a general linear model was used to test for differences in the mean score for each instrument after adjusting for age, gender, race, BMI, and PsA duration.

­­Results

PsA was diagnosed and phenotyped by a rheumatologist in 190 participants (Table 1). Compared to participants with PsA duration <5 years, participants with durations of 5-15 years and >15 years had higher mean numbers of comorbidities, but the difference was statistically significant only in the group with duration of 5-15 years (Table 2).  The number of comorbidities was associated with BASFI (Table 3), but not with measures of quality of life or disease activity (data not shown).

Conclusion

Higher numbers of comorbidities may be associated with longer PsA duration and functional limitations as measured by BASFI.  Anticipated analysis of a larger number of participants in a multi-center comorbidity project will provide a better understanding of the relationships between comorbidities, PsA duration, and PsA severity.

 

Table 1. Demographics, disease characteristics, and comorbidities (n=170-190)

                                                                         

Number of participants (%) or mean (SD)

PsA duration

<5 years

5-15 years

>15 years

Number

76

55

58

Demographics

Age,  yrs

46.0 (12.3)

49.0 (14.0)

54.7 (12.8)

Female

43 (56.6)

27 (49.1)

30 (51.7)

Caucasian Race

71 (93.4)

54 (98.2)

55 (94.8)

BMI > 30

30.3 (8.7)

30.5 (8.8)

30.4 (8.9)

Disease severity

BASFI

3.7 (2.6)

4.8 (2.7)

4.3 (2.7)

BASDAI

5.3 (2.2)

6.0 (2.4)

4.7 (2.1)

PsAQOL

7.0 (5.6)

11.1 (9.0)

6.6 (5.8)

Tender joint count

3.4(4.3)

4.2 (5.3)

3.7 (6.0)

Swollen joint count

2.8(3.3)

4.6 (7.3)

2.9 (5.5)

PGAxBSA

5.5 (10.0)

14.7 (52.2)

5.0 (13.1)

Physician Global

3.8 (1.5)

4.3 (1.9)

3.4 (1.8)

Comorbidities

Number of comorbidities

1.8 (2.0)

2.7 (2.0)

2.6 (2.1)

Uveitis

2 (2.6)

0

4 (6.9)

Inflammatory Bowel Disease

0

2 (3.6)

5 (8.6)

Hypertension

18 (23.7)

25 (45.5)

21 (36.2)

Myocardial Infarction

2 (2.6)

1 (1.8)

1 (1.7)

Congestive Heart Failure

3 (3.9)

3 (5.5)

0

Angina

1 (1.3)

2 (3.6)

2 (3.4)

Stroke

3 (3.9)

2 (3.6)

2 (3.4)

Dyslipidemia

13 (17.1)

17 (30.9)

20 (34.5)

Chronic kidney disease

2 (2.6)

4 (7.3)

2 (3.4)

COPD/emphysema

1 (1.3)

0

3 (5.2)

Cancer

5 (6.6)

1 (1.8)

6 (10.3)

Diabetes

5 (6.6)

7 (12.7)

11 (19.0)

Osteoporosis/osteopenia

5 (6.6)

8 (14.5)

7 (12.1)

Seizure disorder

1 (1.3)

1 (1.8)

0

Multiple sclerosis

0

0

2 (3.4)

Restless leg syndrome

5 (6.6)

2(3.6)

7 (12.1)

Insomnia

6 (7.9)

10 (18.2)

7 (12.1)

Sleep apnea

12 (15.8)

11 (20.0)

14 (24.1)

Chronic heartburn/reflux

13 (17.1)

14 (25.5)

15 (25.9)

Thyroid disease

8 (10.5)

7 (12.7)

8 (13.8)

Hepatitis B

1 (1.3)

2 (3.6)

0

Hepatitis C

1 (1.3)

3 (5.5)

0

Depression

17 (22.4)

18 (32.7)

12 (20.7)

 

 

Table 2. Number of comorbidities and PsA duration (n=190)

Duration(years)

n

Unadjusted OR (95% CI)

p value

before adjustment

Adjusted* OR (95% CI)

p value

after adjustment

<5

76

Reference

Reference

Reference

Reference

5-15

55

2.54 (1.36-4.73)

0.003

2.63 (1.29-5.36)

0.008

>15

58

2.39 (1.30-4.42]

0.003

1.73 (0.86-3.48)

0.128

* Adjusted for age, gender, race, body mass index, tender joint count, & swollen joint count

 

Table 3. Number of comorbidities and BASFI (n=170)

Number of comorbidities

n

BASFI

LS* mean

(95% Confidence Limits)

p value

(Compared to ≥5 comorbidities)

0

47

2.33 (0.46-4.29)

0.04

1

34

2.51 (0.57-4.46)

0.10

2

31

2.18 (0.32-4.14)

0.03

3

27

3.84 (1.83-5.85)

0.99

4

21

4.20 (2.11-6.30)

1.00

≥5

29

4.26 (2.42-6.11)

Reference

LS = least squares


Disclosure:

S. Tanner,
None;

M. McFadden,
None;

D. Clegg,
None;

J. Walsh,
None.

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