Evidence map›Paper›PMID 40312554›Full record

ArticleScientific reports2025

Systemic heparin administration impairs lung development in neonatal mice.

Thomas I Hirsch, Savas T Tsikis, Scott C Fligor, Amy Shei Pan, Sarah Z Wang, Mikayla Quigley, Srujan Dadi, Hiroko Kishikawa, Paul D Mitchell, Colin Niaudet and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Thomas I HirschVascular Biology Program, Boston Children's Hospital, Harvard Medical School, Boston, MA, 02115, USA.
Savas T TsikisVascular Biology Program, Boston Children's Hospital, Harvard Medical School, Boston, MA, 02115, USA.
Scott C FligorVascular Biology Program, Boston Children's Hospital, Harvard Medical School, Boston, MA, 02115, USA.
Amy Shei PanVascular Biology Program, Boston Children's Hospital, Harvard Medical School, Boston, MA, 02115, USA.
Sarah Z WangVascular Biology Program, Boston Children's Hospital, Harvard Medical School, Boston, MA, 02115, USA.
Mikayla QuigleyVascular Biology Program, Boston Children's Hospital, Harvard Medical School, Boston, MA, 02115, USA.
Srujan DadiVascular Biology Program, Boston Children's Hospital, Harvard Medical School, Boston, MA, 02115, USA.
Hiroko KishikawaVascular Biology Program, Boston Children's Hospital, Harvard Medical School, Boston, MA, 02115, USA.
Paul D MitchellBiostatistics and Research Design Center, Boston Children's Hospital, Boston, MA, 02115, USA.
Colin NiaudetVascular Biology Program, Boston Children's Hospital, Harvard Medical School, Boston, MA, 02115, USA.
Diane R BielenbergVascular Biology Program, Boston Children's Hospital, Harvard Medical School, Boston, MA, 02115, USA.
Mark PuderVascular Biology Program, Boston Children's Hospital, Harvard Medical School, Boston, MA, 02115, USA. Mark.Puder@childrens.harvard.edu.

Funding

HARVARD-LONGWOOD RESEARCH TRAINING IN VASCULAR SURGERYT32HL007734 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI FERRAN, CHRISTIANE, LOGERFO, FRANK W · 1993 to 2023
$10.5M
RESEARCH TRAINING IN ALIMENTARY TRACT SURGERYT32DK007754 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI HODIN, RICHARD A. · 1997 to 2025
$6.5M
Harvard-Longwood Short-Term Research Training in Vascular SurgeryT35HL110843 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI CHRISTIANE FERRAN, FRANK W LOGERFO · 2013 to 2026
$609k
NHLBI NIH HHS T32 HL007734NHLBI NIH HHS T35 HL110843NIDDK NIH HHS T32 DK007754NIH HHS 2T32DK007754-22NIH HHS 5T32HL007734NIH HHS 5T35HL110843
6 · The paper itself

Abstract

Preterm infants born in the saccular stage of lung development are at risk for developing bronchopulmonary dysplasia (BPD). Oxygen toxicity and volutrauma are identified as major contributors of BPD. Despite mitigation of these risks preterm infants continue to be affected by chronic lung disease. Heparin is commonly administered to preterm infants and is known to interfere with angiogenesis, a critical element of lung development. We previously demonstrated, in a murine model, that compensatory lung growth after left pneumonectomy is inhibited by heparin administration. Based on these results, we hypothesized that heparin would interfere with lung development in neonatal mice, which are born during the saccular phase of lung development. Newborn C57BL/6J mice received either therapeutic unfractionated heparin (UFH), low molecular weight heparin (LMWH) or normal saline (control) for the first week of life. At one month, both UFH and LMWH produced an emphysematous lung phenotype. Late administration of heparin, after the saccular phase did not impact lung function or growth. This data establishes the negative effects of UFH and LMWH during the critical period of postnatal lung development. Based on this work, clinical studies on the impact of heparin on lung development of newborn and preterm infants are warranted.

Indexed as

HeparinHeparin, Low-Molecular-WeightLungAnimalsAnimals, NewbornBronchopulmonary DysplasiaDisease Models, AnimalFemaleMaleMiceMice, Inbred C57BLHeparinHeparin, Low-Molecular-Weight

Identifiers

PMID40312554
PMCPMC12046039

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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.