Evidence map›Paper›PMID 39684715›Full record

ReviewInternational journal of molecular sciences2024

Chronic Inflammation Offers Hints About Viable Therapeutic Targets for Preeclampsia and Potentially Related Offspring Sequelae.

Jaya Prasad, Juliette Van Steenwinckel, Alistair J Gunn, Laura Bennet, Steven J Korzeniewski, Pierre Gressens, Justin M Dean

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. 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. Relationships Between HAntioxidants (Basel, Switzerland) · 2025
    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

7 authors.

Jaya PrasadDepartment of Physiology, Faculty of Medical and Health Sciences, University of Auckland, Auckland 1142, New Zealand.
Juliette Van SteenwinckelInserm, Neurodiderot, Université de Paris, 75019 Paris, France.
Alistair J GunnDepartment of Physiology, Faculty of Medical and Health Sciences, University of Auckland, Auckland 1142, New Zealand.ORCID 0000-0003-0656-7035
Laura BennetDepartment of Physiology, Faculty of Medical and Health Sciences, University of Auckland, Auckland 1142, New Zealand.
Steven J KorzeniewskiC.S. Mott Center for Human Growth and Development, Department of Emergency Medicine, Wayne State University School of Medicine, Detroit, MI 48202, USA.ORCID 0000-0002-8895-6052
Pierre GressensInserm, Neurodiderot, Université de Paris, 75019 Paris, France.ORCID 0000-0002-0909-4221
Justin M DeanDepartment of Physiology, Faculty of Medical and Health Sciences, University of Auckland, Auckland 1142, New Zealand.ORCID 0000-0002-1377-0878

Funding

ACHIEVE P3 - CHDP50MD017351 · NIMHD · WAYNE STATE UNIVERSITY · PI BROOK, ROBERT DANIEL · 2021 to 2025
$21.1M
Translational Research Support CoreP30ES036084 · NIEHS · WAYNE STATE UNIVERSITY · PI Melissa A Runge-Morris · 2024 to 2026
$5.2M
NIEHS NIH HHS P30 ES036084NIMHD NIH HHS P50 MD017351the Auckland Medical Research Foundation 1116008the Health Research Council of New Zealand 17/076; 22/559the Neurological Foundation of New Zealand 1522-PG
6 · The paper itself

Abstract

The combination of hypertension with systemic inflammation during pregnancy is a hallmark of preeclampsia, but both processes also convey dynamic information about its antecedents and correlates (e.g., fetal growth restriction) and potentially related offspring sequelae. Causal inferences are further complicated by the increasingly frequent overlap of preeclampsia, fetal growth restriction, and multiple indicators of acute and chronic inflammation, with decreased gestational length and its correlates (e.g., social vulnerability). This complexity prompted our group to summarize information from mechanistic studies, integrated with key clinical evidence, to discuss the possibility that sustained or intermittent systemic inflammation-related phenomena offer hints about viable therapeutic targets, not only for the prevention of preeclampsia, but also the neurobehavioral and other developmental deficits that appear to be overrepresented in surviving offspring. Importantly, we feel that carefully designed hypothesis-driven observational studies are necessary if we are to translate the mechanistic evidence into child health benefits, namely because multiple pregnancy disorders might contribute to heightened risks of neuroinflammation, arrested brain development, or dysconnectivity in survivors who exhibit developmental problems later in life.

Indexed as

InflammationPre-EclampsiaAnimalsChronic DiseaseFemaleFetal Growth RetardationHumansPregnancyautismcerebral palsychorioamnionitisdisabilityhypertensionintrauterine growth restrictionneurodevelopmentalsmall for gestational agesocial vulnerability

Identifiers

PMID39684715
PMCPMC11640791

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.