Postnatal genetic and neurodevelopmental assessment in infants born at term with severely low birth weight of non‐placental origin

Author:

Paz y Miño M. F.1,Pauta M.2ORCID,Meler E.1ORCID,Matas I.1,Mazarico E.1,Camacho A.3,Segura M.4,Figueras F.125,Borrell A.125ORCID

Affiliation:

1. BCNatal ‐ Barcelona Center for Maternal–Fetal and Neonatal Medicine Hospital Clínic Barcelona and Hospital Sant Joan de Déu Barcelona Catalonia Spain

2. IDIBAPS, University of Barcelona, Fetal i+D Fetal Medicine Research Barcelona Catalonia Spain

3. Mental Health and Perinatal Nursing Hospital Clínic Barcelona Barcelona Catalonia Spain

4. qGenomics, Esplugues de Llobregat Catalonia Spain

5. Departament de Cirurgia i Especialitats Medicoquirúrgiques, Facultat de Medicina i Ciències de la Salut Universitat de Barcelona Barcelona Catalonia Spain

Abstract

ABSTRACTObjectiveTo determine the frequency of genetic syndromes and childhood neurodevelopmental impairment in non‐malformed infants born at term with severely low birth weight and no evidence of placental insufficiency.MethodsThis case series was constructed from the data of infants delivered at term between 2013 and 2018 with severely low birth weight, defined as birth weight more than 2.5 SD below the mean, with normal maternal and fetal Doppler (umbilical artery, fetal middle cerebral artery, cerebroplacental ratio and uterine artery) and no maternal hypertensive disorder during pregnancy or fetal structural anomaly on prenatal ultrasound examination. Clinical exome sequencing and copy number variation (CNV) analysis were performed using DNA extracted from the children's saliva. Cognitive and psychomotor development was evaluated using the Bayley Scales of Infant and Toddler Development, 3rd edition or the Wechsler Intelligence Scale for Children, 5th edition tests, according to the child's age at testing.ResultsAmong the 36 405 infants born within the study period, 274 (0.75%) had a birth weight below –2.5 SD, of whom 98 met the inclusion criteria. Among the 63 families contacted, seven (11%) reported a postnatal diagnosis of a genetic syndrome and a further 18 consented to participate in the study. Median gestational age at delivery was 38.0 (interquartile range (IQR), 37.3–38.5) weeks and median birth weight was 2020 (IQR, 1908–2248) g. All 18 children showed a normal result on clinical exome sequencing and CNV analysis, but six (33%) obtained a low score on neurodevelopmental testing.ConclusionNon‐malformed severely small term infants with no clinical or Doppler signs of placental insufficiency present a high rate of genetic syndromes and neurodevelopmental impairment during childhood. © 2023 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology.

Funder

Instituto de Salud Carlos III

Publisher

Wiley

Subject

Obstetrics and Gynecology,Radiology, Nuclear Medicine and imaging,Reproductive Medicine,General Medicine,Radiological and Ultrasound Technology

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Reply;Ultrasound in Obstetrics & Gynecology;2023-08-30

2. Born small‐for‐gestational age: not just smaller;Ultrasound in Obstetrics & Gynecology;2023-08-30

3. Placental and genetic origins of fetal growth restriction are independent and may overlap;Ultrasound in Obstetrics & Gynecology;2023-08-30

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