Adrenal volumes in fetuses delivering prior to 32 weeks' gestation: An MRI pilot study.

adrenal gland chorioamnionitis fetal MRI fetal inflammatory response syndrome preterm birth preterm prelabor rupture of the membranes

Journal

Acta obstetricia et gynecologica Scandinavica
ISSN: 1600-0412
Titre abrégé: Acta Obstet Gynecol Scand
Pays: United States
ID NLM: 0370343

Informations de publication

Date de publication:
Mar 2024
Historique:
revised: 07 11 2023
received: 11 07 2023
accepted: 09 11 2023
medline: 16 2 2024
pubmed: 27 11 2023
entrez: 27 11 2023
Statut: ppublish

Résumé

Spontaneous preterm birth prior to 32 weeks' gestation accounts for 1% of all deliveries and is associated with high rates of morbidity and mortality. A total of 70% are associated with chorioamnionitis which increases the incidence of morbidity, but for which there is no noninvasive antenatal test. Fetal adrenal glands produce cortisol and dehydroepiandosterone-sulphate which upregulate prior to spontaneous preterm birth. Ultrasound suggests that adrenal volumes may increase prior to preterm birth, but studies are limited. This study aimed to: (i) demonstrate reproducibility of magnetic resonance imaging (MRI) derived adrenal volumetry; (ii) derive normal ranges of total adrenal volumes, and adrenal: body volume for normal; (iii) compare with those who have spontaneous very preterm birth; and (iv) correlate with histopathological chorioamnionitis. Patients at high risk of preterm birth prior to 32 weeks were prospectively recruited, and included if they did deliver prior to 32 weeks; a control group who delivered an uncomplicated pregnancy at term was also recruited. T2 weighted images of the entire uterus were obtained, and a deformable slice-to-volume method was used to reconstruct the fetal abdomen. Adrenal and body volumes were obtained via manual segmentation, and adrenal: body volume ratios generated. Normal ranges were created using control data. Differences between groups were investigated accounting for the effect of gestation by use of regression analysis. Placental histopathology was reviewed for pregnancies delivering preterm. A total of 56 controls and 26 cases were included in the analysis. Volumetry was consistent between observers. Adrenal volumes were not higher in the case group (p = 0.2); adrenal: body volume ratios were higher (p = 0.011), persisting in the presence of chorioamnionitis (p = 0.017). A cluster of three pairs of adrenal glands below the fifth centile were noted among the cases all of whom had a protracted period at risk of preterm birth prior to MRI. Adrenal: body volume ratios are significantly larger in fetuses who go on to deliver preterm than those delivering at term. Adrenal volumes were not significantly larger, we hypothesize that this could be due to an adrenal atrophy in fetuses with fulminating chorioamnionitis. A straightforward relationship of adrenal size being increased prior to preterm birth should not be assumed.

Identifiants

pubmed: 38009386
doi: 10.1111/aogs.14733
pmc: PMC10867361
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

512-521

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/T018119/1
Pays : United Kingdom
Organisme : NICHD NIH HHS
ID : U01 HD087202
Pays : United States
Organisme : Wellcome Trust
ID : 201374/Z/16/Z
Pays : United Kingdom

Informations de copyright

© 2023 The Authors. Acta Obstetricia et Gynecologica Scandinavica published by John Wiley & Sons Ltd on behalf of Nordic Federation of Societies of Obstetrics and Gynecology (NFOG).

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Auteurs

Megan Hall (M)

Center for the Developing Brain, St Thomas' Hospital, King's College London, London, UK.
Department of Women and Children's Health, St Thomas' Hospital, King's College London, London, UK.

Jana Hutter (J)

Center for the Developing Brain, St Thomas' Hospital, King's College London, London, UK.

Alena Uus (A)

Center for the Developing Brain, St Thomas' Hospital, King's College London, London, UK.

Elise du Crest (E)

Department of Women and Children's Health, St Thomas' Hospital, King's College London, London, UK.

Alexia Egloff (A)

Center for the Developing Brain, St Thomas' Hospital, King's College London, London, UK.

Natalie Suff (N)

Department of Women and Children's Health, St Thomas' Hospital, King's College London, London, UK.

Mudher Al Adnani (M)

Department of Cellular Pathology, St Thomas' Hospital, Guy's and St Thomas' NHS Foundation Trust, London, UK.

Paul T Seed (PT)

Department of Women and Children's Health, St Thomas' Hospital, King's College London, London, UK.

Deena Gibbons (D)

Department of Immunobiology, King's College London, London, UK.

Maria Deprez (M)

Center for the Developing Brain, St Thomas' Hospital, King's College London, London, UK.

Rachel M Tribe (RM)

Department of Women and Children's Health, St Thomas' Hospital, King's College London, London, UK.

Andrew Shennan (A)

Department of Women and Children's Health, St Thomas' Hospital, King's College London, London, UK.

Mary Rutherford (M)

Center for the Developing Brain, St Thomas' Hospital, King's College London, London, UK.

Lisa Story (L)

Center for the Developing Brain, St Thomas' Hospital, King's College London, London, UK.
Department of Women and Children's Health, St Thomas' Hospital, King's College London, London, UK.

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