Evidence map›Paper›PMID 37432936›Full record

ArticleThe Journal of physiology2024

Circadian patterns of heart rate variability in fetal sheep after hypoxia-ischaemia: A biomarker of evolving brain injury.

Christopher A Lear, Yoshiki Maeda, Victoria J King, Simerdeep K Dhillon, Michael J Beacom, Mark I Gunning, Benjamin A Lear, Joanne O Davidson, Peter R Stone, Tomoaki Ikeda and 2 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of physiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
6.4field-weighted citation impact, top 4% of its field
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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Dysmaturation of sleep state and electroencephalographic activity after hypoxia-ischaemia in preterm fetal sheep.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2024
    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 at 2 institutions in 2 countries.

Christopher A LearDepartment of Physiology, Fetal Physiology and Neuroscience Group, The University of Auckland, Auckland, New Zealand.ORCID 0000-0002-8937-0846
Yoshiki MaedaDepartment of Physiology, Fetal Physiology and Neuroscience Group, The University of Auckland, Auckland, New Zealand.
Victoria J KingDepartment of Physiology, Fetal Physiology and Neuroscience Group, The University of Auckland, Auckland, New Zealand.
Simerdeep K DhillonDepartment of Physiology, Fetal Physiology and Neuroscience Group, The University of Auckland, Auckland, New Zealand.
Michael J BeacomDepartment of Physiology, Fetal Physiology and Neuroscience Group, The University of Auckland, Auckland, New Zealand.
Mark I GunningDepartment of Physiology, Fetal Physiology and Neuroscience Group, The University of Auckland, Auckland, New Zealand.
Benjamin A LearDepartment of Physiology, Fetal Physiology and Neuroscience Group, The University of Auckland, Auckland, New Zealand.ORCID 0000-0003-0970-3063
Joanne O DavidsonDepartment of Physiology, Fetal Physiology and Neuroscience Group, The University of Auckland, Auckland, New Zealand.ORCID 0000-0002-6781-4258
Peter R StoneThe Department of Obstetrics and Gynaecology, The University of Auckland, Auckland, New Zealand.ORCID 0000-0003-1546-752X
Tomoaki IkedaThe Department of Obstetrics and Gynaecology, Mie University, Mie, Japan.
Alistair J GunnDepartment of Physiology, Fetal Physiology and Neuroscience Group, The University of Auckland, Auckland, New Zealand.ORCID 0000-0003-0656-7035
Laura BennetDepartment of Physiology, Fetal Physiology and Neuroscience Group, The University of Auckland, Auckland, New Zealand.ORCID 0000-0002-4336-7596
University of Auckland · NZMie University · JP

Funding

Auckland Medical Research Foundation 1122002Health Research Council of New Zealand 17/601Health Research Council of New Zealand 20/437Health Research Council of New Zealand 22/559
6 · The paper itself

Abstract

Hypoxia-ischaemia (HI) before birth is a key risk factor for stillbirth and severe neurodevelopmental disability in survivors, including cerebral palsy, although there are no reliable biomarkers to detect at risk fetuses that may have suffered a transient period of severe HI. We investigated time and frequency domain measures of fetal heart rate variability (FHRV) for 3 weeks after HI in preterm fetal sheep at 0.7 gestation (equivalent to preterm humans) until 0.8 gestation (equivalent to term humans). We have previously shown that this is associated with delayed development of severe white and grey matter injury, including cystic white matter injury (WMI) resembling that observed in human preterm infants. HI was associated with suppression of time and frequency domain measures of FHRV and reduced their circadian rhythmicity during the first 3 days of recovery. By contrast, circadian rhythms of multiple measures of FHRV were exaggerated over the final 2 weeks of recovery, mediated by a greater reduction in FHRV during the morning nadir, but no change in the evening peak. These data suggest that the time of day at which FHRV measurements are taken affects their diagnostic utility. We further propose that circadian changes in FHRV may be a low-cost, easily applied biomarker of antenatal HI and evolving brain injury. KEY POINTS: Hypoxia-ischaemia (HI) before birth is a key risk factor for stillbirth and probably for disability in survivors, although there are no reliable biomarkers for antenatal brain injury. In preterm fetal sheep, acute HI that is known to lead to delayed development of severe white and grey matter injury over 3 weeks, was associated with early suppression of multiple time and frequency domain measures of fetal heart rate variability (FHRV) and loss of their circadian rhythms during the first 3 days after HI. Over the final 2 weeks of recovery after HI, exaggerated circadian rhythms of frequency domain FHRV measures were observed. The morning nadirs were lower with no change in the evening peak of FHRV. Circadian changes in FHRV may be a low-cost, easily applied biomarker of antenatal HI and evolving brain injury.

Indexed as

BiomarkersCircadian RhythmHypoxia-Ischemia, BrainAnimalsBrain InjuriesFemaleHeart Rate, FetalPregnancySheepBiomarkersbiomarkerfetal heart rate variabilityfetushypoxia‐ischaemiapreterm

Identifiers

PMID37432936
PMCPMC11607889
OpenAlexW4383898663

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.