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Abstract Number: 2176

Comorbidities and DMARD, NSAID and Steroid Use in a Real Life Cohort of 8,981 Patients with Psoriatic Arthritis

Elena Generali1, Greta Carrara2, Carlo Alberto Scirè3 and Carlo Selmi4,5, 1Rheumatology and Clinical Immunology, Humanitas Research Hospital, Rozzano (MI), Italy, 2Epidemiology Unit, Italian Society for Rheumatology, Milano, Italy, 3Epidemiology Unit, Italian Society for Rheumatology, Milan, Italy, 4Rheumatology and Clinical Immunology, Humanitas Research Hospital, Rozzano, Italy, 5BIOMETRA Department, University of Milan, Milan, Italy

Meeting: ACR/ARHP Annual Meeting 2016

Date of first publication: September 28, 2016

Keywords: Methotrexate (MTX) and sex bias

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Session Information

Date: Tuesday, November 15, 2016

Title: Epidemiology and Public Health - Poster III

Session Type: ACR Poster Session C

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

Background/Purpose: Psoriatic arthritis (PsA) treatment options are based on the use of DMARDs and NSAID but their use may vary widely, despite international recommendations and guidelines. We aimed at determining the prevalence of comorbidities and prescription patterns of synthetic DMARDs, NSAIDs, and other drugs in a real-life cohort of patients and to determine if sex influences the use and retention rates of therapeutic options.

Methods: We performed a retrospective cohort analysis of administrative health databases of Lombardia region (>10 million population) through the RECORD study of the Italian Society of Rheumatology. PsA and comorbidities were identified using specific copayment exemptions (045.696.0 for PsA) from January 1st 2005 to December 31st 2015 and then linked to DMARD, NSAID, steroid, and other prescriptions. The influence of sex on prescriptions and retention rates was evaluated using Cox regression analyses and the results presented as hazard ratios (HR) and 95% confidence intervals (95%CI).

Results: We identified 8,981 PsA cases (Table 1) and the prescribed DMARDs, NSAIDs and steroids are reported in Table 2. Among clinical features, most comorbidities were found in significantly different proportions in men and women. Of note, 0.8% of patients had a diagnosis of depression while 20.5% received anti-depressants (both being more frequent in women). Methotrexate (MTX) was used in 59% of patients, almost equally in its oral and parenteral formulation, with the latter most commonly prescribed at 10 mg weekly dose. MTX was most frequently prescribed to men, while sulfasalazine and hydroxychloroquine (HCQ) to women. Of note, women received more steroids while men received more NSAIDs. A higher risk for MTX discontinuation was found in women (HR1.06,95%CI1-1.1,p-value0.047), who retained HCQ more commonly (HR0.83,95%CI0.72-0.96, p-value0.012); no differences were observed for other DMARDs retention rates.

Conclusion: In our real-life cohort of patients with PsA anti-depressants are largely used, especially in women. Among DMARDs, MTX is most frequently prescribed but appears to be largely used in its oral formulation and at low dose. Off-label treatments for PsA such as HCQ and steroids are used more frequently in women. In general terms, women and men with PsA have different comorbidities and may underlie different treatment choices. Table 1.

Total n 8,981 Men n 4,478 (49.9%) Women n 4,503 (50.1%) p value
Age, years median (IQR) 51.9 (42-61) 51.2 (41.5-61.1) 52.6 (42.6-61) 0.0158
Disease duration, years median (IQR) 4.7 (2.2-7.6) 4.9 (2.3-7.7) 4.6 (2.1-7.6) 0.0012
Crohn, n 26 (0.3%) 14 (0.3%) 12 (0.3%) 0.684
Hypertension, n 1,428 (15.9%) 704 (15.7%) 724 (16.1%) 0.644
Dyslipidemia, n 256 (2.9%) 127 (2.8%) 129 (2.9%) 0.935
Diabetes, n 730 (8.1%) 397 (8.9%) 333 (7.4%) 0.011
Liver disease, n 132 (1.5%) 77 (1.7%) 55 (1.2%) 0.050
Liver cirrhosis, n 41 (0.5%) 30 (0.7%) 11 (0.2%) 0.003
Chronic kidney disease, n 89 (1%) 54 (1.2%) 35 (0.8%) 0.040
Depression, n 73 (0.8%) 23 (0.5%) 50 (1.1%) 0.002
Prescription of anti-depressants, n 1,840 (20.5%) 648 (14.5%) 1,192 (26.5%) <0.001

Table 2.

Total n 8,981 Men n 4,478 (49.9%) Women n 4,503 (50.1%) p value
Methotrexate, n 5,301 (59%) 2,740 (61.2%) 2,561 (56.9%) <0.001
Oral methotrexate, n 2,164 (24.1%) 1,151 (25.7%) 1,013 (22.5%) <0.001
Parenteral methotrexate, n
  7.5 mg/week, n 433 (4.8%) 199 (4.4%) 234 (5.2%) NS
  10 mg/week, n 1,510 (16.8%) 730 (16.3%) 780 (17.3%) NS
  15 mg/week, n 1,035 (11.5%) 561 (12.5%) 474 (10.5%) 0.003
  20 mg/week, n 142 (1.6%) 90 (2%) 52 (1.2%) 0.001
  25 mg/week, n 17 (0.2%) 9 (0.2%) 8 (0.2%) NS
Cyclosporine, n 1,238 (13.8%) 653 (14.6%) 585 (13%) 0.029
Leflunomide, n 600 (6.7%) 275 (6.1%) 325 (7.22%) 0.041
Sulfasalazine, n 2,192 (24.4%) 982 (21.9%) 1,210 (26.9%) <0.001
Hydroxychloroquine, n 1,117 (12,4%) 340 (7.6%) 777 (17.3%) <0.001
Oral steroids, n 5,196 (57.9%) 2,519 (56.3%) 2,677 (59.5%) 0.002
NSAIDs, n 4,034 (44.9%) 2,127 (47.5%) 1,907 (42.4%) <0.001

Disclosure: E. Generali, None; G. Carrara, None; C. A. Scirè, None; C. Selmi, None.

To cite this abstract in AMA style:

Generali E, Carrara G, Scirè CA, Selmi C. Comorbidities and DMARD, NSAID and Steroid Use in a Real Life Cohort of 8,981 Patients with Psoriatic Arthritis [abstract]. Arthritis Rheumatol. 2016; 68 (suppl 10). https://acrabstracts.org/abstract/comorbidities-and-dmard-nsaid-and-steroid-use-in-a-real-life-cohort-of-8981-patients-with-psoriatic-arthritis/. Accessed .
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