Evidence map›Paper›PMID 39971745›Full record

ArticleBJOG : an international journal of obstetrics and gynaecology2026

Free Fetal Haemoglobin in Severe Early-Onset Fetal Growth Restriction: A Prospective Multi-Centre Study.

Adam Brook, Georgia Baynes, Jonathan Scargill, Angelos Evangelinos, Charlotte Brennan-Richardson, Freya Dow, Yuval Ginsberg, Tal Weissbach, Jana Brodszki, Eva Hansson and 8 more

Abstract readMulticenter Study
In one paragraph

Article in BJOG : an international journal of obstetrics and gynaecology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

18 authors.

Adam BrookMaternal and Fetal Health Research Centre, University of Manchester, Manchester, UK.
Georgia BaynesMaternal and Fetal Health Research Centre, University of Manchester, Manchester, UK.ORCID https://orcid.org/0009-0008-0659-3851
Jonathan ScargillNorthern Care Alliance NHS Group, Royal Oldham Hospital, Manchester, UK.
Angelos EvangelinosMaternal and Fetal Health Research Centre, University of Manchester, Manchester, UK.
Charlotte Brennan-RichardsonMaternal and Fetal Health Research Centre, University of Manchester, Manchester, UK.
Freya DowMaternal and Fetal Health Research Centre, University of Manchester, Manchester, UK.
Yuval GinsbergDepartment of Obstetrics and Gynecology, Rambam Medical Centre, Haifa, Israel.
Tal WeissbachDepartment of Obstetrics and Gynecology, Sheba Medical Center, Tel Aviv, Israel.ORCID https://orcid.org/0000-0001-5558-7871
Jana BrodszkiDepartment of Obstetrics and Gynecology, Institute of Clinical Sciences Lund, Lund University and Skåne University Hospital, Malmö, Sweden.
Eva HanssonDepartment of Obstetrics and Gynecology, Institute of Clinical Sciences Lund, Lund University and Skåne University Hospital, Malmö, Sweden.
Anke DiemertDepartment of Obstetrics and Fetal Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Kurt HecherDepartment of Obstetrics and Fetal Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Katarzyna MaksymElizabeth Garrett Anderson Institute for Women's Health, 2nd Floor Medical School Building, University College London, London, UK.
Neil MarlowElizabeth Garrett Anderson Institute for Women's Health, 2nd Floor Medical School Building, University College London, London, UK.ORCID https://orcid.org/0000-0001-5890-2953
Rebecca N SpencerElizabeth Garrett Anderson Institute for Women's Health, 2nd Floor Medical School Building, University College London, London, UK.
Anna L DavidElizabeth Garrett Anderson Institute for Women's Health, 2nd Floor Medical School Building, University College London, London, UK.ORCID https://orcid.org/0000-0002-0199-6140
Stefan R HanssonDepartment of Obstetrics and Gynecology, Institute of Clinical Sciences Lund, Lund University and Skåne University Hospital, Malmö, Sweden.
Paul BrownbillMaternal and Fetal Health Research Centre, University of Manchester, Manchester, UK.ORCID https://orcid.org/0000-0002-8328-7072

Funding

Regional Skane FoundationSeventh Framework ProgrammeSwedish Research CouncilWellbeing of Women
6 · The paper itself

Abstract

objectiveTo assess fetal circulating free fetal haemoglobin (fHbF) levels and heme defences, correlated to fetal circulatory biometry and fetal sex in severe early-onset fetal growth restriction (FGR). DESIGN, SETTING AND POPULATION: A prospective study severe early-onset fetal growth restriction pregnancies with close clinical management (estimated fetal weight (EFW) < 3rd centile and < 600 g at 20-26 + 6 weeks; N = 20). METHOD &

main outcome measuresTemporal fetal vascular obstetric biometry was recorded. Cord blood fHbF and key heme-scavenger defences were measured and compared with normal term births (N = 26) and births with late-onset FGR (N = 12).

resultsfHbF was elevated in early-onset FGR compared with normal pregnancy: 0.437(0.337/0.753) mg/mL; and 0.098 (0.045/0.264) mg/mL, respectively (p < 0.0001); whilst hemopexin was downregulated in early- (p < 0.001) and late-onset FGR (p < 0.0001), compared to normal pregnancy: 36(14/81) μg/mL, 25(19/40) μg/mL, and 155(132/219) μg/mL, respectively; median (interquartile ranges). Early-onset FGR male fetuses had higher HbF compared with the normal males: 0.710(0.433/0.857) mg/mL; (p < 0.001); 0.099(0.043/0.246) mg/mL, respectively; median (interquartile ranges). In early-onset FGR, ratios of mid-cerebral artery and umbilical artery pulsatility indices correlated positively with heme-scavenger levels (hemopexin and a heme-handling composite measure: p < 0.05, r = 0.672; and p < 0.01, r = 0.620; respectively), indicating lower levels are associated with cerebral vascular redistribution. These heme handling measures also positively correlated with gestational age at delivery (r = 0.713 and r = 0.642, respectively, p < 0.01, both) and birthweight (r = 0.742, p < 0.001; and r = 0.523, p < 0.05; respectively).

conclusionOverproduction of fHbF and an inadequate heme defence may contribute to fetal distress and poor umbilical arterial Dopplers in early onset FGR due to elevated placental vascular resistance and vascular inflammation.

Indexed as

Fetal BloodFetal Growth RetardationFetal HemoglobinAdultFemaleFetal WeightGestational AgeHemopexinHumansInfant, NewbornMalePregnancyProspective StudiesUltrasonography, PrenatalUmbilical ArteriesFetal HemoglobinHemopexinalpha 1 microglobulinfetal growth restrictionhaemoglobinhemopexin

Identifiers

PMID39971745
PMCPMC12770088

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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.