Evidence map›Paper›PMID 39869487›Full record

ArticleExperimental physiology2025

In utero exposure to experimental maternal asthma alters fetal airway development in sheep.

Sarah J Hammond, Andrea J Roff, Joshua L Robinson, Jack R T Darby, Ashley S Meakin, Vicki L Clifton, Robert J Bischof, Michael J Stark, Megan J Wallace, Andrew Tai and 2 more

Abstract read
In one paragraph

Article in Experimental physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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

12 authors.

Sarah J HammondRobinson Research Institute, University of Adelaide, Adelaide, South Australia, Australia.
Andrea J RoffRobinson Research Institute, University of Adelaide, Adelaide, South Australia, Australia.ORCID https://orcid.org/0000-0003-2560-7629
Joshua L RobinsonRobinson Research Institute, University of Adelaide, Adelaide, South Australia, Australia.ORCID https://orcid.org/0000-0001-5267-1496
Jack R T DarbyEarly Origins of Adult Health Research Group, Health and Biomedical Innovation and Health Sciences, University of South Australia, Adelaide, Australia.ORCID https://orcid.org/0000-0001-7114-3920
Ashley S MeakinEarly Origins of Adult Health Research Group, Health and Biomedical Innovation and Health Sciences, University of South Australia, Adelaide, Australia.
Vicki L CliftonMater Medical Research Institute, University of Queensland, South Brisbane, Queensland, Australia.
Robert J BischofInstitute of Innovation, Science and Sustainability, Federation University Australia, Berwick, Victoria, Australia.
Michael J StarkRobinson Research Institute, University of Adelaide, Adelaide, South Australia, Australia.ORCID https://orcid.org/0000-0003-1835-8679
Megan J WallaceDepartment of Obstetrics and Gynaecology, Monash University, Clayton, Victoria, Australia.
Andrew TaiRobinson Research Institute, University of Adelaide, Adelaide, South Australia, Australia.
Janna L MorrisonEarly Origins of Adult Health Research Group, Health and Biomedical Innovation and Health Sciences, University of South Australia, Adelaide, Australia.ORCID https://orcid.org/0000-0002-8602-8519
Kathryn L GatfordRobinson Research Institute, University of Adelaide, Adelaide, South Australia, Australia.ORCID https://orcid.org/0000-0002-2823-3004

Funding

Australian Research Council Future Fellowship FT170100431Channel 7 Children's Research Foundation of South Australia 20190628Robinson Research Institute
6 · The paper itself

Abstract

The mechanisms linking maternal asthma (MA) exposure in utero and subsequent risk of asthma in childhood are not fully understood. Pathological airway remodelling, including reticular basement membrane thickening, has been reported in infants and children who go on to develop asthma later in childhood. This suggests altered airway development before birth as a mechanism underlying increased risk of asthma in children exposed in utero to MA. We hypothesised that in utero MA exposure would reduce airway diameter and increase airway-associated smooth muscle area and reticular basement membrane thickness in neonatal offspring. Experimental MA was induced by maternal sensitisation followed by airway challenges with house dust mite before and during pregnancy. Lambs from control (n = 16) or MA (n = 26) ewes were delivered at ∼140 days gestation (term = 150 days), ventilated for 45 min, then humanely killed. Left lungs were inflation-fixed, and cross-sections of generation 2-5 airways were collected. Airway sections were stained with Haematoxylin and Eosin, Masson's Trichrome and Gordon and Sweet's histological stains for morphological analysis. Lamb body and lung weights were similar between groups (P > 0.5 and P > 0.7, respectively). Lambs that were exposed to MA had narrower airway diameters (P = 0.019) and thinner reticular basement membrane (P = 0.016) but similar airway-associated smooth muscle area (P = 0.152) compared with unexposed control lambs. Our results demonstrate a potential mechanism for increased risk of asthma in children of mothers with asthma, independent of genetic risk or behavioural changes during pregnancy.

Indexed as

AsthmaFetal DevelopmentLungPrenatal Exposure Delayed EffectsAirway RemodelingAnimalsBasement MembraneFemaleMaternal ExposureMuscle, SmoothPregnancySheepairway remodellingasthma susceptibilitymaternal asthmapregnancyrespiratory developmentsheep

Identifiers

PMID39869487
PMCPMC12128463

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Registered trials

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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.