Pregnancy complications and new-onset maternal autoimmune disease

Author:

Scime Natalie V12ORCID,Grandi Sonia M34ORCID,Ray Joel G245,Dennis Cindy-Lee56,De Vera Mary A789ORCID,Banack Hailey R4ORCID,Vigod Simone N21011,Boblitz Alexa2,Brown Hilary K12411ORCID

Affiliation:

1. Department of Health and Society, University of Toronto Scarborough , Toronto, Ontario, Canada

2. ICES , Toronto, Ontario, Canada

3. Child Health Evaluative Sciences, The Hospital for Sick Children , Toronto, Ontario, Canada

4. Dalla Lana School of Public Health, University of Toronto , Toronto, Ontario, Canada

5. Li Ka Shing Knowledge Institute, St Michael’s Hospital , Toronto, Ontario, Canada

6. Lawrence S. Bloomberg Faculty of Nursing, University of Toronto , Toronto, Ontario, Canada

7. Faculty of Pharmaceutical Sciences, University of British Columbia , Vancouver, British Columbia, Canada

8. Collaboration for Outcomes Research and Evaluation, University of British Columbia , Vancouver, British Columbia, Canada

9. Centre for Health Evaluation & Outcome Science, St. Paul’s Hospital , Vancouver, British Columbia, Canada

10. Department of Psychiatry, University of Toronto , Toronto, Ontario, Canada

11. Women’s College Research Institute, Women’s College Hospital , Toronto, Ontario, Canada

Abstract

Abstract Background Autoimmune diseases disproportionately impact women and female-specific aspects of reproduction are thought to play a role. We investigated the time-varying association between pregnancy complications and new-onset autoimmune disease in females during the reproductive and midlife years. Methods We conducted a population-based cohort study of 1 704 553 singleton births to 1 072 445 females in Ontario, Canada (2002–17) with no pre-existing autoimmune disease. Pregnancy complications were preeclampsia, stillbirth, spontaneous preterm birth and severe small for gestational age (SGA). Royston-Parmar models were used to estimate the time-varying association between pregnancy complications and a composite of 25 autoimmune diseases from date of delivery to date of autoimmune disease diagnosis or censoring at death, loss of health insurance, or 31 March 2021. Models were adjusted for baseline socio-demographics, parity and comorbidities. Results At 19 years (median = 10.9 years of follow-up), cumulative incidence of autoimmune disease was 3.1% in those with a pregnancy complication and 2.6% in those without complications. Adjusted hazard ratio (AHR) curves as a function of time since birth were generally L-shaped. Universally, risks were most elevated within the first 3 years after birth [at 1 year: preeclampsia AHR 1.22, 95% confidence interval (CI) 1.09–1.36; stillbirth AHR 1.36, 95% CI 0.99–1.85; spontaneous preterm birth AHR 1.30, 95% CI 1.18–1.44; severe SGA AHR 1.14, 95% CI 0.99–1.31] and plateaued but remained elevated thereafter. Conclusions Prior history of pregnancy complications may be an important female-specific risk factor to consider during clinical assessment of females for possible autoimmune disease to facilitate timely detection and treatment.

Funder

Canadian Institutes of Health Research

Publisher

Oxford University Press (OUP)

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