First-trimester ultrasound measurements and maternal serum biomarkers as prognostic factors in monochorionic twins: a cohort study.

AFP Monochorionic PlGF Prediction Prognostic factor Twin pregnancy Twin-twin transfusion syndrome sFlt-1

Journal

Diagnostic and prognostic research
ISSN: 2397-7523
Titre abrégé: Diagn Progn Res
Pays: England
ID NLM: 101718985

Informations de publication

Date de publication:
2019
Historique:
received: 19 12 2018
accepted: 20 03 2019
entrez: 17 5 2019
pubmed: 17 5 2019
medline: 17 5 2019
Statut: epublish

Résumé

Monochorionic twin pregnancies are at high risk of adverse outcomes, but it is not possible to predict which pregnancies will develop complications. The aim of the study was to evaluate, in monochorionic twin pregnancies, whether first-trimester ultrasound (nuchal translucency [NT], crown-rump length [CRL]), and maternal serum biomarkers (alpha-fetoprotein [AFP], soluble fms-like tyrosine kinase-1 [sFlt-1] and placental growth factor [PlGF]), are prognostic factors for fetal adverse outcome composite, twin-twin transfusion syndrome (TTTS), growth restriction, and intrauterine fetal death (IUFD). A cohort study of 177 monochorionic diamniotic twin pregnancies. Independent prognostic ability of each factor was assessed by multivariable logistic regression, adjusting for standard prognostic factors. Factors were analysed as continuous data; thus, the reported ORs relate to either 1% change in NT or CRL inter-twin percentage discordance or one unit of measure in each serum biomarker. The odds of the fetal adverse outcome composite were significantly associated with increased NT inter-twin percentage discordance (adjusted OR 1.03 [95% CI 1.01, 1.06]) and CRL inter-twin percentage discordance (adjusted OR 1.17 [95% CI 1.07, 1.29]). TTTS was significantly associated with increased NT discordance (adjusted OR 1.06 [95% CI 1.03, 1.10]) and decreased PlGF (adjusted OR 0.42 [95% CI 0.19, 0.93]). Antenatal growth restriction was significantly associated with increased CRL discordance (adjusted OR 1.20 [95% CI 1.08, 1.34]). Single and double IUFD were associated with decreased PlGF (adjusted OR 0.34 [95% CI 0.12, 0.98]) and (adjusted OR 0.18 [95%CI 0.05, 0.58]) respectively. This study has identified potential individual prognostic factors in the first trimester (fetal biometric and maternal serum biomarkers) that show promise but require further robust evaluation in a larger, prospective series of MC twin pregnancies, so that their usefulness both individually and in combination can be defined. ISRCTN 13114861 (retrospectively registered).

Sections du résumé

BACKGROUND BACKGROUND
Monochorionic twin pregnancies are at high risk of adverse outcomes, but it is not possible to predict which pregnancies will develop complications. The aim of the study was to evaluate, in monochorionic twin pregnancies, whether first-trimester ultrasound (nuchal translucency [NT], crown-rump length [CRL]), and maternal serum biomarkers (alpha-fetoprotein [AFP], soluble fms-like tyrosine kinase-1 [sFlt-1] and placental growth factor [PlGF]), are prognostic factors for fetal adverse outcome composite, twin-twin transfusion syndrome (TTTS), growth restriction, and intrauterine fetal death (IUFD).
METHODS METHODS
A cohort study of 177 monochorionic diamniotic twin pregnancies. Independent prognostic ability of each factor was assessed by multivariable logistic regression, adjusting for standard prognostic factors. Factors were analysed as continuous data; thus, the reported ORs relate to either 1% change in NT or CRL inter-twin percentage discordance or one unit of measure in each serum biomarker.
RESULTS RESULTS
The odds of the fetal adverse outcome composite were significantly associated with increased NT inter-twin percentage discordance (adjusted OR 1.03 [95% CI 1.01, 1.06]) and CRL inter-twin percentage discordance (adjusted OR 1.17 [95% CI 1.07, 1.29]). TTTS was significantly associated with increased NT discordance (adjusted OR 1.06 [95% CI 1.03, 1.10]) and decreased PlGF (adjusted OR 0.42 [95% CI 0.19, 0.93]). Antenatal growth restriction was significantly associated with increased CRL discordance (adjusted OR 1.20 [95% CI 1.08, 1.34]). Single and double IUFD were associated with decreased PlGF (adjusted OR 0.34 [95% CI 0.12, 0.98]) and (adjusted OR 0.18 [95%CI 0.05, 0.58]) respectively.
CONCLUSIONS CONCLUSIONS
This study has identified potential individual prognostic factors in the first trimester (fetal biometric and maternal serum biomarkers) that show promise but require further robust evaluation in a larger, prospective series of MC twin pregnancies, so that their usefulness both individually and in combination can be defined.
TRIAL REGISTRATION BACKGROUND
ISRCTN 13114861 (retrospectively registered).

Identifiants

pubmed: 31093579
doi: 10.1186/s41512-019-0054-9
pii: 54
pmc: PMC6507122
doi:

Types de publication

Journal Article

Langues

eng

Pagination

9

Déclaration de conflit d'intérêts

This study received ethical approval from East Midlands Research Ethics Committee (15/EM/0240) in June 2015 and the Royal Prince Alfred Hospital Research and Ethics Governance Office (HREC/11/RPAH/472) in January 2016.Not applicableThe authors declare that they have no competing interests.Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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Auteurs

Fiona L Mackie (FL)

1Centre for Women's and Newborn Health, Institute of Metabolism and Systems Research, University of Birmingham, Birmingham, B15 2TT UK.
2Fetal Medicine Department, Birmingham Women's and Children's NHS Foundation Trust, Edgbaston, Birmingham, B15 2TG UK.

Rebecca Whittle (R)

3Centre for Prognosis Research, Research Institute for Primary Care & Health Sciences, Keele University, Keele, Staffordshire ST5 5BG UK.

R Katie Morris (RK)

1Centre for Women's and Newborn Health, Institute of Metabolism and Systems Research, University of Birmingham, Birmingham, B15 2TT UK.
2Fetal Medicine Department, Birmingham Women's and Children's NHS Foundation Trust, Edgbaston, Birmingham, B15 2TG UK.

Jon Hyett (J)

4Department of Women and Babies, Royal Alfred Hospital, University of Sydney, Sydney, Australia.

Richard D Riley (RD)

3Centre for Prognosis Research, Research Institute for Primary Care & Health Sciences, Keele University, Keele, Staffordshire ST5 5BG UK.

Mark D Kilby (MD)

1Centre for Women's and Newborn Health, Institute of Metabolism and Systems Research, University of Birmingham, Birmingham, B15 2TT UK.
2Fetal Medicine Department, Birmingham Women's and Children's NHS Foundation Trust, Edgbaston, Birmingham, B15 2TG UK.

Classifications MeSH