Session Information
Session Type: Abstract Submissions (ACR)
Background/Purpose: Few clinical studies describe psoriasis (PSO) and psoriatic arthritis (PsA) in ethnic minority groups. Previous patient-reported data show PSO/PsA to be less frequent in African Americans (AA) compared to Caucasians, but of equal severity. We describe the clinical characteristics of a diverse ethnic cohort of patients with PSO and PsA in an urban setting.
Methods: IRB consented patients with PSO diagnosed by a dermatologist and PsA satisfying CASPAR criteria, were enrolled from 4 academic outpatient clinics. Socio-demographic data, disease duration, time to diagnosis, disease phenotype and activity, quality of life measures, comorbidities, use of disease modifying anti-rheumatic drugs (DMARD) and biologic therapies were recorded.
Results: There were 160 PSO/PsA patients enrolled; 41.9% were non-Caucasian, 90% of whom were AA (Table). Mean PSO and PsA disease duration was 18.1 (SD14.3) and 13.3 (SD10.9) years, respectively. Mean BMI was 30.3 (SD5.7) kg/m2 and PsA patients had a mean DAS28 of 2.7 (SD1.7). Non-Caucasians had worse PASI scores. Compared to Caucasians, AA had a lower frequency of PsA, worse SF-36 mental component and psoriasis related quality of life scores, received less years of education, had lower frequencies of private insurance coverage, DMARD and biologic use, and lower Vitamin D levels. AA also had higher frequencies of tobacco use, hypertension, diabetes, hyperlipidemia and cerebrovascular accidents. There were no differences in alcohol use, uric acid levels or other psoriatic disease-related parameters.
Conclusion: Compared to Caucasians, African Americans had less frequent PsA but experienced greater impact on quality of life from psoriatic disease. Improved implementation and evaluation of disease activity and quality of life measures are needed in psoriatic disease, particularly in African American patients. Ours is the first study to use validated clinical measures to describe psoriatic disease in a diverse ethnic cohort.
Variable, n (%) |
Cohort |
Caucasian |
Non Caucasian** |
African American |
p-value |
Cohort |
160 (100) |
93 (60.8) |
67 (41.9) |
60 (39.2) |
— |
PSO Only |
75 (49.0) |
33 (35.5) |
44 (65.7) |
42 (70.0) |
<0.001 |
PSA |
78 (51.0) |
60 (64.5) |
23 (34.3) |
18 (30.0) |
<0.001 |
Age (Mean ± SD) |
56.7 ± 13.3 |
55.6 ± 13.4 |
56.8 ± 14.7 |
58.7 ± 13.2 |
0.18 |
Male |
120 (78.4) |
77 (82.8) |
48 (71.6) |
43 (71.7) |
— |
Education Years (Mean ± SD) |
14.5 ± 3.3 |
15.1 ± 3.2 |
13.6 ± 3.2 |
13.4 ± 3.3* |
0.0025* |
Private Insurance |
71 (46.4) |
51 (54.8) |
8 (11.9) |
20 (33.3)* |
0.009* |
Tobacco Use |
39 (26.4) |
19 (20.7) |
21 (33.3) |
20 (35.7) |
0.044 |
Dactylitis |
15 (9.8) |
13 (14.0) |
2(11.1) |
2 (3.3) |
0.034 |
Oligoarthritis |
42 (53.8) |
32 (53.3) |
10 (43.5) |
7 (38.9) |
— |
Symmetric |
14 (17.9) |
12 (20) |
2 (8.7) |
2 (11.1) |
— |
PASI (Mean ± SD) |
6.6 ± 8.1 |
5.5 ± 6.4 |
8.6± 10.4 |
8.4± 10.0 |
0.04 |
SF36 Physical |
40.5 ± 11.9 |
41.0 ± 12.3 |
40.1 ± 11.1 |
39.7 ± 11.4 |
0.54 |
SF36 Mental |
45.8 ± 12.0 |
47.7 ± 11.7 |
43.5 ±12.2 |
42.8 ± 12.1* |
0.02* |
PSAQOL |
5.5 ± 5.8 |
5.2 ±5.7 |
5.81 ± 6.23 |
6.3 ± 6.4 |
0.56 |
PSOQOL |
7.5 ± 6.8 |
6.1 ± 6.6 |
9.32 ±6.6 |
9.9 ± 6.7* |
0.02* |
DMARD |
31 20.3) |
26 (28.0) |
7 (10.5) |
4 (8.3)* |
0.044* |
Biologic |
51 (33.3) |
43 (46.2) |
9 (13.4) |
8 (13.3)* |
0.014* |
Diabetes |
28 (18.3) |
14 (15.0) |
14(25.5) |
14 (23.3) |
0.05 |
Hypertension |
68 (44.4) |
33 (35.5) |
36(65.5) |
35 (58.3)* |
<0.001* |
Hyperlipidemia |
51 (33.3) |
28 (30.1) |
25(45.5) |
23 (38.3) |
0.046 |
Cerebrovascular Accident |
7 (4.6) |
2 (2.2) |
5(8.8) |
5 (8.3) |
0.045 |
Vitamin D (Mean ± SD) |
28.3 ± 13.8 |
31.2 ± 13.9 |
21.8 ± 10.8 |
21.6 ± 11.0* |
0.02* |
*Indicates corresponding p-value **Includes African American, Hispanic and Asian |
Disclosure:
G. S. Kerr,
Amgen, Abbott,
2;
S. Qaiyumi,
None;
J. S. Richards,
None;
C. Kindred,
None;
S. A. Whelton,
None;
F. M. Constantinescu,
None.
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