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Ultrasound features in early pregnancy for predicting abnormal karyotype in first‐trimester miscarriage

Setty, T; Kastora, SL; Tellum, T; Farren, J; Jauniaux, E; Jurkovic, D; (2026) Ultrasound features in early pregnancy for predicting abnormal karyotype in first‐trimester miscarriage. Ultrasound in Obstetrics & Gynecology , Article uog.70159. 10.1002/uog.70159. (In press). Green open access

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Abstract

Objective To investigate whether combining abnormal morphological features observed on ultrasound in live pregnancies that ended in a first‐trimester miscarriage can predict an abnormal karyotype. Methods This retrospective observational cohort study was conducted at the early‐pregnancy assessment unit at University College London Hospital, London, UK, between January 2017 and February 2024. Cytogenetic testing was offered routinely to patients experiencing recurrent miscarriage (at least two miscarriages) or was made available through self‐funding. Eligible participants had a singleton, normally sited pregnancy with evidence of cardiac activity on at least one ultrasound scan, and were subsequently diagnosed with a first‐trimester miscarriage, with successful cytogenetic testing of pregnancy tissue. Crude ultrasound measurements of gestational sac mean diameter (GSMD), yolk sac mean diameter (YSMD), crown–rump length (CRL) and embryonic heart rate from the last live ultrasound scan were converted to centiles according to established biometric reference data. Univariable and multivariable logistic regression analysis was used to assess associations between sonographic features and karyotype result. Results Among 158 cases included in the final analysis, 46 (29.1%) had a normal karyotype and 112 (70.9%) had an abnormal karyotype. Those with an abnormal karyotype had a significantly higher median maternal age at conception (38 (interquartile range (IQR), 34–41) years vs 35 (IQR, 33–38) years; P  = 0.0005). Median GSMD centile ( P  = 0.005) and median CRL centile ( P  = 0.003) were lower in pregnancies with an abnormal karyotype, while bradycardia (heart rate < 5 th  centile) ( P  = 0.04) and enlarged YSMD (≥ 95 th  centile) ( P  = 0.03) were more common in this group. A combination of four abnormal morphological features (GSMD < 5 th  centile + YSMD ≥ 95 th  centile + CRL < 5 th  centile + bradycardia), termed the ‘tetrad of aneuploidy’, predicted an abnormal karyotype (odds ratio, 7.51 (95% CI, 2.41–140.22); P  < 0.001), with a specificity of 100% (95% CI, 92.29–100%), for cases last examined sonographically ≤ 10 weeks' gestation. Conclusions The presence of a specific combination of abnormal early‐pregnancy ultrasound markers, termed the tetrad of aneuploidy, is a strong predictor of chromosomal abnormality in pregnancies presenting initially with a live embryo. Recognition of this pattern could improve patient counseling and inform clinical decision‐making in early pregnancy. © 2026 The Author(s). Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology.

Type: Article
Title: Ultrasound features in early pregnancy for predicting abnormal karyotype in first‐trimester miscarriage
Open access status: An open access version is available from UCL Discovery
DOI: 10.1002/uog.70159
Publisher version: https://doi.org/10.1002/uog.70159
Language: English
Additional information: Published online in Wiley Online Library (wileyonlinelibrary.com). DOI: 10.1002/uog.70159. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Keywords: chromosomal aberration; crown–rump length; cytogenetic analysis; early diagnosis; first trimester; gestational sac; live pregnancy; maternal age; miscarriage; ultrasonography; yolk sac
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL EGA Institute for Womens Health
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL EGA Institute for Womens Health > Reproductive Health
URI: https://discovery.ucl.ac.uk/id/eprint/10219583
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