Evidence map›Paper›PMID 38323418›Full record

ArticleJournal of neuropathology and experimental neurology2024

Altered 5-HT2A/C receptor binding in the medulla oblongata in the sudden infant death syndrome (SIDS): Part II. Age-associated alterations in serotonin receptor binding profiles within medullary nuclei supporting cardiorespiratory homeostasis.

Kevin J Cummings, James C Leiter, Felicia L Trachtenberg, Benjamin W Okaty, Robert A Darnall, Elisabeth A Haas, Ronald M Harper, Eugene E Nattie, Henry F Krous, Othon J Mena and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of neuropathology and experimental neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Platelet Pathophysiology: Unexpected New Research Directions.Seminars in thrombosis and hemostasis · 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

14 authors at 8 institutions in 1 country.

Kevin J CummingsDepartment of Biomedical Sciences, Dalton Cardiovascular Research Center, University of Missouri, Columbia, Missouri, USA.ORCID 0000-0002-4100-8856
James C LeiterDepartment of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, USA.
Felicia L TrachtenbergClinical Research, Carelon Research, Newton, Massachusetts, USA.
Benjamin W OkatyDepartment of Genetics, Harvard Medical School, Boston, Massachusetts, USA.
Robert A DarnallDepartment of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, USA.
Elisabeth A HaasDepartment of Research, Rady's Children's Hospital, San Diego, California, USA.
Ronald M HarperDepartment of Neurobiology and the Brain Research Institute, David Geffen School of Medicine at UCLA, Los Angeles, California, USA.
Eugene E NattieDepartment of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, USA.
Henry F KrousDepartment of Pediatrics, University of California San Diego, San Diego, California, USA.
Othon J MenaSan Diego County Medical Examiner Office, San Diego, California, USA.
George B RichersonDepartments of Neurology and Molecular Physiology & Biophysics, University of Iowa, Iowa City, Iowa, USA.
Susan M DymeckiDepartment of Genetics, Harvard Medical School, Boston, Massachusetts, USA.
Hannah C KinneyDepartment of Pathology, CJ Murphy Laboratory for SIDS Research, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Robin L HaynesDepartment of Pathology, CJ Murphy Laboratory for SIDS Research, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Dartmouth College · USBoston Children's Hospital · USHarvard University · USDade County Medical Examiner Department · USRady Children's Hospital-San Diego · USUniversity of California San Diego · USUniversity of Iowa · USUniversity of Missouri · US

Funding

VENTRAL MEDULLA, BREATHING, AND CENTRAL CHEMORECEPTIONP01HD036379 · NICHD · HARVARD MEDICAL SCHOOL · PI COMMONS, KATHRYN G · 1998 to 2017
$32.2M
Genetic Analysis and Manipulation Core (GAEC)P50HD105351 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI Hisashi Umemori · 2021 to 2026
$9.4M
BRAINSTEM MATURATION IN THE SUDDEN INFANT DEATH SYNDROMER01HD020991 · NICHD · CHILDREN'S HOSPITAL BOSTON · PI HAYNES, ROBIN LYNN, KINNEY, HANNAH CHASE · 1986 to 2015
$3.3M
Does neurotransmitter plasticity of para-serotonergic neurons augment autoresuscitation following perinatal stress and buffer SIDS risk?R01HD100823 · NICHD · HARVARD MEDICAL SCHOOL · PI DYMECKI, SUSAN M., HAYNES, ROBIN LYNN · 2020 to 2024
$3.2M
The Hippocampus and Brainstem in the Sudden Infant Death SyndromeR01HD090064 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI HAYNES, ROBIN LYNN · 2017 to 2021
$3.2M
Inflammatory stressors in serotonergic brainstem dysfunction and SIDSR01HD107060 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI ROBIN Lynn HAYNES · 2023 to 2026
$2.9M
Prevention of SUDEP by milk whey: Role of CO2 chemoreception and serotoninR01NS123155 · NINDS · UNIVERSITY OF IOWA · PI RICHERSON, GEORGE B · 2021 to 2025
$2.9M
NICHD NIH HHS P01 HD036379NICHD NIH HHS P50 HD105351NICHD NIH HHS R01 HD020991NICHD NIH HHS R01 HD090064NICHD NIH HHS R01 HD100823NICHD NIH HHS R01 HD107060NINDS NIH HHS R01 NS123155
6 · The paper itself

Abstract

The failure of chemoreflexes, arousal, and/or autoresuscitation to asphyxia may underlie some sudden infant death syndrome (SIDS) cases. In Part I, we showed that some SIDS infants had altered 5-hydroxytryptamine (5-HT)2A/C receptor binding in medullary nuclei supporting chemoreflexes, arousal, and autoresuscitation. Here, using the same dataset, we tested the hypotheses that the prevalence of low 5-HT1A and/or 5-HT2A/C receptor binding (defined as levels below the 95% confidence interval of controls-a new approach), and the percentages of nuclei affected are greater in SIDS versus controls, and that the distribution of low binding varied with age of death. The prevalence and percentage of nuclei with low 5-HT1A and 5-HT2A/C binding in SIDS were twice that of controls. The percentage of nuclei with low 5-HT2A/C binding was greater in older SIDS infants. In >80% of older SIDS infants, low 5-HT2A/C binding characterized the hypoglossal nucleus, vagal dorsal nucleus, nucleus of solitary tract, and nuclei of the olivocerebellar subnetwork (important for blood pressure regulation). Together, our findings from SIDS infants and from animal models of serotonergic dysfunction suggest that some SIDS cases represent a serotonopathy. We present new hypotheses, yet to be tested, about how defects within serotonergic subnetworks may lead to SIDS.

Indexed as

Sudden Infant DeathAgedAnimalsHumansInfantMedulla OblongataReceptors, SerotoninSerotoninReceptors, SerotoninSerotoninAutoradiographyBlood pressure recoveryGaspingHypoxiaInferior oliveNucleus of the solitary tractRaphe

Identifiers

PMID38323418
PMCPMC10880067
OpenAlexW4391592209

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.