Characterising the effects of genetic liability to autoimmune conditions on pregnancy outcomes using Mendelian Randomization
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Background
Autoimmune conditions are common in women of reproductive age. They are associated with increased risk of adverse pregnancy outcomes; whether this is causal is unclear. Our aim was to explore the effects of autoimmune condition liability on pregnancy outcomes.
Methods
We conducted two-sample Mendelian randomization (MR) to estimate effects of liability to ten autoimmune conditions on nine primary and seven secondary pregnancy outcomes. We used data from the MR-PREG collaboration including up to 934,566 pregnancies. Main analyses used the inverse variance weighted method; sensitivity analyses were used to explore bias due to pleiotropic variants and fetal genetics.
Findings
We found evidence for 14 effects of autoimmune condition liability on primary pregnancy outcomes that were robust across sensitivity analyses. Higher liability to Hashimoto’s thyroiditis was protective against large for gestational age and increased risks of hypertensive disorders of pregnancy (HDP), preterm birth (PTB), and neonatal intensive care unit (NICU) admission. For instance, risk of PTB increased by 6% (OR=1.06 (95%CI: 1.02, 1.11)) per doubling in log odds of Hashimoto’s thyroiditis. Liability to type 1 diabetes increased risks of HDP and NICU admission, as well as gestational diabetes mellitus (GDM) and stillbirth.
Liability to rheumatoid arthritis increased risks of NICU admission, HDP, and GDM. Higher ankylosing spondylitis liability reduced risks of HDP and increased risks of low Apgar score, while systemic lupus erythematosus liability increased risks of PTB only. For multiple sclerosis, systemic sclerosis, coeliac disease, inflammatory bowel disease, and psoriasis, we did not detect any robust effects of increased liability.
Interpretation
We observed higher liability to Hashimoto’s thyroiditis, type 1 diabetes, and rheumatic conditions cause increased risks of adverse pregnancy outcomes, suggesting the need for enhanced antenatal monitoring of women with these conditions.
Funding
Wellcome Trust, UK Medical Research Council
