Evidence map›Paper›PMID 31995186›Full record

ArticleJournal of neuropathology and experimental neurology2020

Neuropathologic Changes in Sudden Unexplained Death in Childhood.

Declan McGuone, Dominique Leitner, Christopher William, Arline Faustin, Nalin Leelatian, Ross Reichard, Timothy M Shepherd, Matija Snuderl, Laura Crandall, Thomas Wisniewski and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of neuropathology and experimental neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 24% 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

15 citing papers in PubMed, 19 citations in OpenAlex.

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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

11 authors at 6 institutions in 1 country.

Declan McGuoneFrom the Department of Pathology, Yale School of Medicine, New haven, Connecticut.
Dominique LeitnerComprehensive Epilepsy Center, New York University School of Medicine, New York, New York.
Christopher WilliamDepartment of Neurology.
Arline FaustinDepartment of Neurology.
Nalin LeelatianFrom the Department of Pathology, Yale School of Medicine, New haven, Connecticut.
Ross ReichardDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.
Timothy M ShepherdDepartment of Radiology.
Matija SnuderlDepartment of Pathology, NYU Langone Health and School of Medicine, New York, New York.
Laura CrandallComprehensive Epilepsy Center, New York University School of Medicine, New York, New York.
Thomas WisniewskiDepartment of Neurology.
Orrin DevinskyComprehensive Epilepsy Center, New York University School of Medicine, New York, New York.
New York University · USNYU Langone Health · USYale University · USCenter for Neuro-Oncology · USMayo Clinic · USThomas Cole Historic House · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
PSYCHOSOCIAL COREP30AG008051 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SHAO, YONGZHAO · 1990 to 2019
$36.1M
Research Education ComponentP30AG066512 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Mary Sherman Mittelman · 2020 to 2026
$28.4M
Transgenic/Behavior CoreP01AG060882 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI WISNIEWSKI, THOMAS M · 2020 to 2024
$12.0M
NCATS NIH HHS UL1 TR001863NIA NIH HHS P01 AG060882NIA NIH HHS P30 AG008051NIA NIH HHS P30 AG066512
6 · The paper itself

Abstract

Sudden unexplained death in childhood (SUDC) affects children >1-year-old whose cause of death remains unexplained following comprehensive case investigation and is often associated with hippocampal abnormalities. We prospectively performed systematic neuropathologic investigation in 20 SUDC cases, including (i) autopsy data and comprehensive ancillary testing, including molecular studies, (ii) ex vivo 3T MRI and extensive histologic brain samples, and (iii) blinded neuropathology review by 2 board-certified neuropathologists. There were 12 girls and 8 boys; median age at death was 33.3 months. Twelve had a history of febrile seizures, 85% died during apparent sleep and 80% in prone position. Molecular testing possibly explained 3 deaths and identified genetic mutations in TNNI3, RYR2, and multiple chromosomal aberrations. Hippocampal abnormalities most often affected the dentate gyrus (altered thickness, irregular configuration, and focal lack of granule cells), and had highest concordance between reviewers. Findings were identified with similar frequencies in cases with and without molecular findings. Number of seizures did not correlate with hippocampal findings. Hippocampal alterations were the most common finding on histological review but were also found in possibly explained deaths. The significance and specificity of hippocampal findings is unclear as they may result from seizures, contribute to seizure pathogenesis, or be an unrelated phenomenon.

Indexed as

BrainChildChild, PreschoolDeath, SuddenFemaleHippocampusHumansInfantMaleSudden Infant DeathDentate gyrusHippocampal abnormalitiesNeuropathologyPediatricSeizureSudden unexplained death in childhood

Identifiers

PMID31995186
PMCPMC7036658
OpenAlexW3003475740

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.