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Abstract Number: 2443

Pregnancy Comorbidities and Outcomes in Psoriasis and Psoriatic Arthritis: A Prospective Cohort Study

Neda Amiri1, Gretchen Bandoli2 and Christina Chambers2, 1Division of Rheumatology, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada, 2Pediatrics, University of California, San Diego, La Jolla, CA

Meeting: 2016 ACR/ARHP Annual Meeting

Date of first publication: September 28, 2016

Keywords: pregnancy, psoriasis and psoriatic arthritis

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Session Information

Date: Tuesday, November 15, 2016

Title: Reproductive Issues in Rheumatic Disorders - Poster

Session Type: ACR Poster Session C

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

Pregnancy Comorbidities and Outcomes in Psoriasis and Psoriatic Arthritis: A Prospective Cohort Study

Background/Purpose: While there is some evidence that women with psoriasis (Pso) and psoriatic arthritis (PsA) are at increased risk of various comorbidities, this has not been well described in pregnancy.  In addition, there are limited data on the risks of adverse pregnancy outcomes in women with these conditions.  

Methods: Individuals were selected (enrolled 2005-2015) from the Organization of Teratology Information Specialists (OTIS) Autoimmune Diseases in Pregnancy project, a North American prospective cohort study of pregnancy outcome. The ÒexposedÓ were defined as women with singleton live births and PsA (with or without Pso) or psoriasis (Pso) alone. ÒUnexposedÓ were non-diseased pregnant women without exposure to known human teratogens or underlying chronic conditions. The outcomes of interest were baseline differences among the three groups (PsA, Pso, unexposed) and maternal comorbidities. As a secondary objective, we compared selected adverse birth outcomes in the exposed (PsA/Pso) and unexposed groups.   

Results:  A total of 180 exposed women were identified (91 with PsA and 89 with Pso alone). These were compared to 379 non-diseased unexposed women. Except for greater use of biologics in women with PsA, there were no baseline differences between women with PsA and Pso. However, compared to the unexposed group, the PsA/Pso women had a higher prevalence of unplanned pregnancies, pre-pregnancy overweight or obesity, smoking, and illicit drug use. Moreover, compared to the unexposed, Pso/PsA women had higher rates of pre-existing depression (19.4% vs. 9.4%) and hypertension (6.7% vs. 2.1%) (Table 1). In terms of pregnancy outcomes, there were no differences comparing women with PsA to those with Pso. However, pregnant women with either PsA or Pso were at increased risk for cesarean section (RR 1.42 (95% CI 1.10,1.83)) and preterm birth (RR 1.81 (95% CI 1.02,3.23)) compared to the unexposed (Table 2). There was no increased risk for preeclampsia/pregnancy-induced hypertension or small for gestational age infants in exposed.

Conclusion: In this prospective study, pregnant women with PsA (with or without Pso) and Pso alone were similar in their baseline demographics, comorbidities and frequency of adverse pregnancy outcomes. However, compared to healthy controls, PsA/Pso women had more risk factors for adverse pregnancy outcomes (tobacco use, increased pre-pregnancy BMI, and pre-existing depression and hypertension). After adjusting for covariates, PsA/Pso women had increased risks for cesarean section delivery and preterm birth compared to healthy controls.

Table 1. Baseline characteristics in PsA/Pso exposed compared to unexposed pregnant women
Characteristic – mean (SD) or n (%)

Exposed (N=180)

Unexposed (N=379)

P value

Maternal Age, years

32.29 (4.52)

31.80 (4.86)

0.26

Race/Ethnicity
–       Non-Hispanic White

147 (81.67)

287 (75.73)

0.09

–       Hispanic

13 (7.22)

49 (12.93)

–       African American

7 (3.89)

14 (3.69)

–       Asian/Pacific Islander

6 (3.33)

8 (2.11)

–       American Indian/Native American

3 (1.67)

2 (0.53)

–       Other/Missing

4 (2.22)

19 (5.01)

Primi-Gravida

68 (37.78)

148 (39.05)

0.77

Prepregnancy BMI
–       <24.9

83 (46.11)

251 (66.23)

<0.05

–       >=25

96 (53.33)

126 (33.25)

Socioeconomic Status (SES)
–       Low

18 (10.00)

31 (8.18)

0.46

–       High

155 (86.11)

325 (85.75)

–       Missing

7 (3.89)

23 (6.07)

Household Income
–       <$10,000

10 (5.56)

11 (2.90)

0.19

–       $10,000-$49,9999

43 (23.89)

80 (21.11)

–       >$50,000

119 (66.11)

273 (72.03)

–       Missing

8 (4.44)

15 (3.96)

Planned pregnancy

105 (58.33)

282 (74.41)

<0.001

Tobacco use

36 (20.00)

8 (2.10)

<0.001

Alcohol use

89 (49.44)

171 (45.12)

0.39

Illicit drug use

7 (3.89)

2 (0.53)

<0.05

Folic acid supplementation

179 (99.44)

376 (99.21)

1

Disease modifying anti-rheumatic drug (DMARD) use*

18 (10.00)

2 (0.53)

<0.001

Biologic use$

121 (67.22)

0

–

Glucocorticoid use#

51 (28.33)

14 (3.69)

<0.001

*DMARD was defined as use of any of the following medications: apremilast , azathioprine, chloroquine, cyclosporine, cyclophosphamide, gold, hydroxychloroquine, leflunomide, mepacrine, methotrexate, mycophenolate mofetil, sulfasalazine, tacrolimus, tofacitinib $Biologics were defined as any of the following drugs: abatacept, adalimumab, anakinra, belimumab, certolizumab, etanercept, golimumab, infliximab, rituximab, tocilizumab, ustekinumab #Glucocorticoid use was defined as any orally administered glucocorticoids.
Table 2. Pregnancy outcomes in the PsA/Pso exposed compared unexposed pregnant women  

Exposed (N=180)

Unexposed (N=379)

RR (95% CI)

aRR* (95% CI)

Cesarean section  – n (%)

77 (42.78)

98 (25.86)

1.65 (1.30,2.10)

1.421 (1.10,1.83)

Preterm birth – n (%)

25 (13.89)

23 (6.07)

2.29 (1.33,3.95)

1.81 (1.02,3.23)

Small for gestational age – n (%)

18 (10.00)

26 (3.86)

1.46 (0.81,2.58)

1.492 (0.78,2.77)

Pregnancy induced Hypertension/Pre-eclampsia – n(%)

20 (11.11)

25 (6.60)

1.69 (0.95,2.95)

1.40 (0.77,2.48)

*Adjusted for BMI, SES, tobacco use unless otherwise stated. 1Adjusted for BMI, SES, race (Caucasian vs. other). 2Adjusted for BMI, SES, tobacco use and race (Caucasian vs. other).

Disclosure: N. Amiri, None; G. Bandoli, None; C. Chambers, Contract Apotex, Inc., Barr Labs, Inc., 2,Contract Bristol Myers/Squibb, 2,Contract Hoffman La Roche Genentech, 2,Contract Genzyme (Sanofi-Aventis), 2,Contract UCB Pharma, 2,Contract Janssen Biotech, Inc., 2,Contract Pfizer, 2,Contract AAAAI VAMPSS Post marketing Surveillance of Afluria, 2,Contract Celgene, 2,Contract Takeda, 2,ournal Birth Defects Research Part A: Clinical and Molecular Teratology, 3.

To cite this abstract in AMA style:

Amiri N, Bandoli G, Chambers C. Pregnancy Comorbidities and Outcomes in Psoriasis and Psoriatic Arthritis: A Prospective Cohort Study [abstract]. Arthritis Rheumatol. 2016; 68 (suppl 10). https://acrabstracts.org/abstract/pregnancy-comorbidities-and-outcomes-in-psoriasis-and-psoriatic-arthritis-a-prospective-cohort-study/. Accessed .
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