Evidence map›Paper›PMID 42552644›Full record

ArticlePaediatric and perinatal epidemiology2026

Infertility and Risk of Congenital Anomalies: A Population-Based Cohort Study.

Bailey Milne, Susan B Brogly, Jonas Shellenberger, Maria P Velez

Abstract read
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Article in Paediatric and perinatal epidemiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Bailey MilneDepartment of Public Health Sciences, Queen's University, Kingston, Ontario, Canada.ORCID https://orcid.org/0009-0007-6840-0405
Susan B BroglyDepartment of Surgery, Queen's University, Kingston, Ontario, Canada.ORCID https://orcid.org/0000-0002-2339-3287
Jonas ShellenbergerICES, Toronto, Ontario, Canada.ORCID https://orcid.org/0000-0002-8676-6650
Maria P VelezICES, Toronto, Ontario, Canada.ORCID https://orcid.org/0000-0003-4834-8279

Funding

Canadian Institutes of Health Research Institute of Human Development, Child & Youth Health, Clinician - Investigator Teams in Obstetrics and Maternal-Fetal Medicine MFM-146444Queen's University
6 · The paper itself

Abstract

backgroundFertility treatments have been associated with an increased risk of congenital anomalies. Most studies have compared births conceived through fertility treatment with unassisted conceptions; consequently, these estimates reflect the combined effects of fertility treatment and the underlying infertility, potentially resulting in confounding by indication.

objectivesTo estimate the association between infertility, independent of fertility treatment, and the risk of congenital anomalies.

methodsThis population-based cohort study included all live births and stillbirths at ≥ 20 weeks' gestation to women aged 15-50 in Ontario, Canada, 2006-2021. Infertility without treatment was defined as a history of one or more infertility consultations with a physician within 2 years before conception, in the absence of fertility treatment. Modified Poisson regression generated relative risks (RR) adjusted for maternal age, income quintile, rurality, pre-existing comorbidities, and smoking, alcohol use, and substance use during pregnancy.

resultsOf the 1,415,324 deliveries, the prevalence of congenital anomalies was 5.3% in unassisted conception and 5.9% among births to women with infertility who did not use fertility treatment. A small increase in risk was observed for any congenital anomaly (RR 1.12, 95% confidence interval [CI] 1.09, 1.14). Among organ system anomalies, the highest relative risks were observed for eye anomalies (0.11% vs 0.14%; RR 1.22, 95% CI 1.03, 1.45) and ear, face, and neck anomalies (0.06% vs 0.08%; RR 1.19, 95% CI 1.05, 1.35). Among specific anomalies, the highest relative risk was observed for other penile malformations (0.03% vs 0.04%; RR 1.41, 95% CI 1.09, 1.83).

conclusionsAlthough the overall risk of congenital anomalies was low, infants born to women with infertility who did not use fertility treatment had small increased risks of any congenital anomaly, selected organ system anomalies, and specific anomalies compared with infants born from unassisted conceptions.

Indexed as

Congenital AbnormalitiesInfertility, FemaleReproductive Techniques, AssistedAdolescentAdultCohort StudiesFemaleHumansInfant, NewbornMiddle AgedOntarioPregnancyPrevalenceRisk FactorsYoung Adultconfoundingcongenital anomaliesepidemiologyinfertilitysubfertility

Identifiers

PMID42552644
PMCPMC13522657

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.