Evidence map›Paper›PMID 40932552›Full record

ArticleJournal of assisted reproduction and genetics2025

Does assisted reproductive technology influence the complexity and associated malformations in esophageal atresia?

Federica Pederiva, Nigel Hall, Tuktu Soyer, Francesco Morini, Esophageal atresia registry participants

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Article in Journal of assisted reproduction and genetics, 2025. 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

What it found

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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

5 authors.

Federica PederivaPediatric Surgery, "F. Del Ponte" Hospital, ASST Settelaghi, Via Filippo del Ponte 19, Varese, 21100, Italy. federica_pederiva@yahoo.it.ORCID http://orcid.org/0000-0002-2792-1550
Nigel HallDepartment of Paediatric Surgery and Urology, Southampton Children Hospital, Southampton, UK.
Tuktu SoyerDepartment of Pediatric Surgery, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Francesco MoriniDepartment of Maternal, Child Health and Urological Sciences, Sapienza University of Rome, Rome, Italy.
Esophageal atresia registry participants

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAssisted reproductive technology (ART) has been associated with increased risks of congenital anomalies and preterm birth. However, its role in influencing the complexity of specific malformations, such as esophageal atresia (EA), remains unclear. This study aimed to assess whether ART impacts the phenotypic complexity of EA, including associated anomalies and VACTERL (vertebral, anal, cardiac, tracheoesophageal, renal, and limb anomalies) association.

methodsData from 374 EA patients enrolled in the European Pediatric Surgeons' Association (EUPSA) Esophageal Atresia Registry were analyzed. Patients were grouped based on mode of conception (28 ART and 346 natural conception) and compared for demographics, gestational age, birth weight, associated malformations, VACTERL association, and genetic disorders.

resultsGestational age and birth weight were comparable between groups (36.5 ± 3.3 vs. 36.4 ± 3.3 weeks, p = 0.42; 2412.3 ± 761.6 g vs. 2601.3 ± 744.3 g, p = 0.24). Maternal age was significantly higher in the ART group. The prevalence of cardiac, gastrointestinal, renal, musculoskeletal, and vertebral anomalies did not differ significantly. All cardiac anomalies in ART patients were minor. VACTERL association rates (25.0% vs. 18.5%, p = 0.398) and genetic disorder prevalence (7.1% vs. 4.9%, p = 0.605) were comparable.

conclusionsART does not appear to increase the complexity of EA in terms of associated malformations, VACTERL spectrum disorders, or genetic abnormalities. Further studies with larger cohorts and detailed ART subtype data are warranted to confirm these findings.

Indexed as

Abnormalities, MultipleEsophageal AtresiaHeart Defects, CongenitalLimb Deformities, CongenitalReproductive Techniques, AssistedTracheaAdultAnal CanalBirth WeightEsophagusFemaleGestational AgeHumansInfant, NewbornKidneyMaleARTAssisted reproductive technologyCongenital malformationEsophageal atresiaVACTERL

Identifiers

PMID40932552
PMCPMC12602759

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