Evidence map›Paper›PMID 40738637›Full record

Observational studyBMJ open2025

Identification of novel genetic, neurobiological and radio-anatomical biomarkers for risk stratification of sudden unexpected death in infancy and early childhood: the BIOMINRISK study protocol.

Mathilde Ducloyer, Alban-Elouen Baruteau, Patricia Franco, Aurore Guyon, Vincent Sapin, Matilde Karakachoff, Frédéric Savall, Jean-Jacques Schott, Loïc de Pontual, Sophie De Visme and 5 more

Registry-linked trialAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in BMJ open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06244433 (Risk Stratification of Sudden Unexpected Death in Infant Based on Biomarkers - Identification of Genetic Variants Associated With Unexpected Infant Death Syndrome), which is not on this 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.

NCT06244433 recruitingnot on this map

Risk Stratification of Sudden Unexpected Death in Infant Based on Biomarkers - Identification of Genetic Variants Associated With Unexpected Infant Death Syndrome

TypeobservationalSponsorNantes University HospitalRan2024 to 2027Enrolled650ConditionsSudden Infant Death, Sudden Unexplained Infant DeathArmswhole genome sequencing
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

15 authors.

Mathilde DucloyerCHU Nantes, Forensic Department, Nantes University, Nantes, France mathilde.ducloyer@chu-nantes.fr.ORCID http://orcid.org/0000-0003-1116-4943
Alban-Elouen BaruteauCHU Nantes, Department of Pediatric Cardiology and Pediatric Cardiac Surgery, FHU PreciCare, CIC1413, Nantes Université, Nantes, France.ORCID http://orcid.org/0000-0003-2548-7858
Patricia FrancoPediatric Sleep Unit, Hôpital Femme-Mère Enfant, Hospices Civils de Lyon, INSERM U1028/CNRS UMR 5292, Lyon Neuroscience Research Center, Lyon, France.
Aurore GuyonPediatric Sleep Unit, Hôpital Femme-Mère Enfant, Hospices Civils de Lyon, INSERM U1028/CNRS UMR 5292, Lyon Neuroscience Research Center, Lyon, France.
Vincent SapinBiochemistry and Molecular Genetics Department, University Hospital of Clermont-Ferrand, Clermont-Ferrand, France.
Matilde KarakachoffClinique des données, CIC 1413, INSERM, Pôle Hospitalo-Universitaire 11: Santé Publique, Centre Hospitalier Universitaire Nantes, Nantes University, Nantes, France.
Frédéric SavallCentre for Anthropobiology and Genomics of Toulouse, UMR 5288 (CNRS/UT3), Toulouse III University-Paul Sabatier, Toulouse, France.
Jean-Jacques SchottCHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes University, Nantes, France.
Loïc de PontualDepartment of Pediatrics, Assistance Publique - Hôpitaux de Paris, Paris, France.
Sophie De VismeCHU Nantes, INSERM, UIC Femme-Enfant-Adolescent, CIC 1413, Nantes University, Nantes, France.
Léa FerrandCHU Nantes, INSERM, UIC Femme-Enfant-Adolescent, CIC 1413, Nantes University, Nantes, France.
Bérengère JarryCHU Nantes, INSERM, UIC Femme-Enfant-Adolescent, CIC 1413, Nantes University, Nantes, France.
Didier BeudinCHU Nantes, Research and Innovation Department, Promotion Department, INSERM, UIC Femme-Enfant-Adolescent, CIC 1413, Nantes University, Nantes, France.
Pauline ScherdelCHU Nantes, INSERM, UIC Femme-Enfant-Adolescent, CIC 1413, Nantes University, Nantes, France.ORCID http://orcid.org/0000-0003-4517-9430
Fleur LortonCHU Nantes, INSERM, Paediatric Emergency Department, CIC 1413, Nantes University, Nantes, France.ORCID http://orcid.org/0000-0003-0921-4622

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe BIOMINRISK project is a national French study aimed at identifying novel biomarkers associated with sudden unexpected death in infancy (SUDI) through a multidisciplinary approach encompassing three key components of intrinsic vulnerability to SUDI: genetic, neurobiological and radio-anatomical. A better understanding of the pathophysiological mechanisms underlying SUDI may enhance the personalisation of prevention strategies and contribute to reducing its incidence. METHODS AND ANALYSIS: We will analyse data from 250 children under the age of 2 included in the national SUDI registry (the OMIN registry) since 2020 for which biological samples and medical imaging data will have been collected from 15 participating French hospitals. Our investigations will focus on three axes: (1) genetic: we will conduct whole genome sequencing family trio analyses to identify novel variants and genes associated with sudden infant death syndrome (SIDS) by examining SIDS cases along with their two parents; (2) neurobiological: a case-control study will be performed to investigate the roles of various neuromodulators-including serum serotonin, blood butyrylcholinesterase and cerebrospinal fluid orexin-in the arousal regulation in children who have died from SUDI. We will recruit 250 living age-matched and sex-matched controls who will undergo blood tests and lumbar punctures as part of their routine care and (3) radio-anatomical: a case-control study will explore the potential anatomical predisposition to SUDI by assessing upper airway narrowness. We will compare the osseous structures of the upper airways (nasal fossae, hard palate) using geometric morphometrics on CT images. Recruitment of 250 living age-matched and sex-matched controls who have undergone brain CT scans, including facial bones, will be conducted. ETHICS AND DISSEMINATION: The study has received ethics approval for all three axes. Results will be published in international peer-reviewed journals and presented at national and international conferences. TRIAL REGISTRATION NUMBER: NCT06244433.

Indexed as

Sudden Infant DeathBiomarkersCase-Control StudiesChild, PreschoolFemaleFranceHumansInfantInfant, NewbornMaleOrexinsRegistriesResearch DesignRisk AssessmentWhole Genome SequencingBiomarkersOrexinsCot deathDeath, Sudden, CardiacGENETICSNeurobiologyPaediatric radiologyPUBLIC HEALTH

Identifiers

PMID40738637
PMCPMC12314952

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Registered trials

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.