Evidence map›Paper›PMID 32865812›Full record

ArticleActa obstetricia et gynecologica Scandinavica2021

Antenatal thymus volumes in fetuses that delivered <32 weeks' gestation: An MRI pilot study.

Lisa Story, Tong Zhang, Alena Uus, Jana Hutter, Alexia Egloff, Deena Gibbons, Alison Ho, Mudher Al-Adnani, Caroline L Knight, Iakovos Theodoulou and 5 more

Abstract read
In one paragraph

Article in Acta obstetricia et gynecologica Scandinavica, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Article
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  7. Observational
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  11. Review
  12. Assessment of the fetal thymus gland: Comparing MRI-acquired thymus volumes with 2D ultrasound measurements.European journal of obstetrics, gynecology, and reproductive biology · 2021
    Article
  13. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Lisa StoryDepartment of Women and Children's Health, School of Life Sciences, King's College London, London, UK.ORCID 0000-0001-9328-9592
Tong ZhangArtificial Intelligence Research Center, Peng Cheng Laboratory, Shenzhen, China.
Alena UusCentre for the Developing Brain and Centre for Medical Engineering, King's College London, London, UK.
Jana HutterCentre for the Developing Brain and Centre for Medical Engineering, King's College London, London, UK.
Alexia EgloffCentre for the Developing Brain and Centre for Medical Engineering, King's College London, London, UK.ORCID 0000-0002-2005-8328
Deena GibbonsDepartment of Immunobiology, King's College London, London, UK.
Alison HoDepartment of Women and Children's Health, School of Life Sciences, King's College London, London, UK.
Mudher Al-AdnaniCellular Pathology Department, St Thomas' Hospital, London, UK.
Caroline L KnightDepartment of Women and Children's Health, School of Life Sciences, King's College London, London, UK.
Iakovos TheodoulouKing's College London Medical School, London, UK.ORCID 0000-0002-2799-6077
Maria DeprezArtificial Intelligence Research Center, Peng Cheng Laboratory, Shenzhen, China.
Paul T SeedDepartment of Women and Children's Health, School of Life Sciences, King's College London, London, UK.
Rachel M TribeDepartment of Women and Children's Health, School of Life Sciences, King's College London, London, UK.
Andrew H ShennanDepartment of Women and Children's Health, School of Life Sciences, King's College London, London, UK.ORCID 0000-0001-5273-3132
Mary RutherfordCentre for the Developing Brain and Centre for Medical Engineering, King's College London, London, UK.

Funding

Medical Research Council MC_PC_17164Medical Research Council MR/T018119/1Wellcome TrustWellcome Trust 102431
6 · The paper itself

Abstract

introductionInfection and inflammation have been implicated in the etiology and subsequent morbidity associated with preterm birth. At present, there are no tests to assess for fetal compartment infection. The thymus, a gland integral in the fetal immune system, has been shown to involute in animal models of antenatal infection, but its response in human fetuses has not been studied. This study aims: (a) to generate magnetic resonance imaging (MRI) -derived fetal thymus volumes standardized for fetal weight; (b) to compare standardized thymus volumes from fetuses that delivered before 32 weeks of gestation with fetuses that subsequently deliver at term; (c) to assess thymus size as a predictor of preterm birth; and (d) to correlate the presence of chorioamnionitis and funisitis at delivery with thymic volumes in utero in fetuses that subsequently deliver preterm. MATERIAL AND

methodsWomen at high-risk of preterm birth at 20-32 weeks of gestation were recruited. A control group was obtained from existing data sets acquired as part of three research studies. A fetal MRI was performed on a 1.5T or 3T MRI scanner: T2 weighted images were obtained of the entire uterine content and specifically the fetal thorax. A slice-to-volume registration method was used for reconstruction of three-dimensional images of the thorax. Thymus segmentations were performed manually. Body volumes were calculated by manual segmentation and thymus:body volume ratios were generated. Comparison of groups was performed using multiple regression analysis. Normal ranges were created for thymus volume and thymus:body volume ratios using the control data. Receiver operating curves (ROC) curves were generated for thymus:body volume ratio and gestation-adjusted thymus volume centiles as predictors of preterm birth. Placental histology was analyzed where available from pregnancies that delivered very preterm and the presence of chorioamnionitis/funisitis was noted.

resultsNormative ranges were created for thymus volume, and thymus volume was standardized for fetal size from fetuses that subsequently delivered at term, but were imaged at 20-32 weeks of gestation. Image data sets from 16 women that delivered <32 weeks of gestation (ten with ruptured membranes and six with intact membranes) and 80 control women that delivered >37 weeks were included. Mean gestation at MRI of the study group was 28

conclusionsWe have produced MRI-derived normal ranges for fetal thymus and thymus:body volume ratios between 20 and 32 weeks of gestation. Fetuses that deliver very preterm had reduced thymus volumes when standardized for fetal size. A reduced thymus volume was also a predictor of spontaneous preterm delivery. Thymus volume may be a suitable marker of the fetal inflammatory response, although further work is needed to assess this, increasing the sample size to correlate the extent of chorioamnionitis with thymus size.

Indexed as

AdultCase-Control StudiesFemaleGestational AgeHumansInfant, NewbornMagnetic Resonance ImagingOrgan SizePilot ProjectsPregnancyPregnancy, High-RiskPremature BirthPremature Rupture of Fetal MembranesThymus GlandUltrasonography, Prenatalfetal thymusinfectionmagnetic resonance imagingpreterm birththymusvolume

Identifiers

PMID32865812
PMCPMC7614117

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.