Evidence map›Paper›PMID 38151596›Full record

ArticleJournal of perinatology : official journal of the California Perinatal Association2024

Modulation of intestinal TLR4 expression in infants with neonatal opioid withdrawal syndrome.

Rebecca C Barnett, Angela N Lewis, Qingqing Gong, Deborah L Preston, Lauren C Frazer, Joseph W Werthammer, Misty Good

Open access · hybridAbstract read
In one paragraph

Article in Journal of perinatology : official journal of the California Perinatal Association, 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
0.5field-weighted citation impact, top 39% 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, 3 citations in OpenAlex.

  1. Prenatal Opioid Exposure and Neonatal Opioid Withdrawal Syndrome.Advances in experimental medicine and biology · 2026
    Review
  2. Article
  3. 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 at 3 institutions in 2 countries.

Rebecca C BarnettDepartment of Pediatrics, Marshall University, Joan C. Edwards School of Medicine, Huntington, WV, USA.
Angela N LewisDivision of Neonatal-Perinatal Medicine, Department of Pediatrics, Saint Louis University, Cardinal Glennon Children's Hospital, St. Louis, MO, USA.
Qingqing GongDivision of Newborn Medicine, Department of Pediatrics, Washington University School of Medicine, St. Louis Children's Hospital, St. Louis, MO, USA.
Deborah L PrestonDepartment of Pediatrics, Marshall University, Joan C. Edwards School of Medicine, Huntington, WV, USA.
Lauren C FrazerDivision of Newborn Medicine, Department of Pediatrics, Washington University School of Medicine, St. Louis Children's Hospital, St. Louis, MO, USA.
Joseph W WerthammerDepartment of Pediatrics, Marshall University, Joan C. Edwards School of Medicine, Huntington, WV, USA.
Misty GoodDivision of Newborn Medicine, Department of Pediatrics, Washington University School of Medicine, St. Louis Children's Hospital, St. Louis, MO, USA. mistygood@unc.edu.ORCID 0000-0002-0264-5721
Marshall University · USSt. Louis Children's Hospital · USCardinal Glennon Children’s Medical Center · US

Funding

Point of Care maternal milk concentration device to optimize neonatal growth with targeted nutrition supportR44HD110306 · NICHD · MOTHER'S MILK IS BEST, INC. · PI Elizabeth Randall Nelson · 2023 to 2026
$4.2M
Non-invasive analysis of methylated cell free DNA in necrotizing enterocolitisR01DK124614 · NIDDK · WASHINGTON UNIVERSITY · PI GOOD, MISTY L, PETERS, DAVID GERARD · 2021 to 2024
$2.5M
Neonatal gut-on-a-chip platform for high content drug testing and precision medicineR01HD105301 · NICHD · WASHINGTON UNIVERSITY · PI GOOD, MISTY L, MAGNESS, SCOTT T · 2021 to 2024
$2.4M
Modulation of the Intestinal Immune Response in Necrotizing EnterocolitisR01DK118568 · NIDDK · WASHINGTON UNIVERSITY · PI GOOD, MISTY L · 2018 to 2022
$1.8M
NICHD NIH HHS R01 HD105301NICHD NIH HHS R44 HD110306NIDDK NIH HHS R01 DK118568NIDDK NIH HHS R01 DK124614U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01DK124614U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01HD105301U.S. Department of Health & Human Services | National Institutes of Health (NIH) R44HD110306
6 · The paper itself

Abstract

objectiveNeonatal Opioid Withdrawal Syndrome (NOWS) has been associated with the development of necrotizing enterocolitis (NEC) in term and late-preterm neonates. In this study, we used stool gene expression to determine if an increase in baseline inflammation in the intestine of infants with NOWS is associated with these findings. STUDY

designStool samples were prospectively collected between days 1-3 and days 4-9 after delivery for opioid-exposed ( n = 9) or non-exposed neonates (n = 8). Stool gene expression for TLR4 and HMGB1 was determined via real-time PCR.

resultsTLR4 expression was higher in the stool of the non-exposed group in both time periods, between days 1-3 (P < 0.0001) and days 4-9 (P < 0.05) after delivery. No significant difference in HMGB1 expression was found at either time point (P > 0.05).

conclusionThese findings point to an important interplay between opioid exposure and/or NOWS and the inflammatory milieu of the neonatal intestine.

Indexed as

Analgesics, OpioidEnterocolitis, NecrotizingHMGB1 ProteinNeonatal Abstinence SyndromeToll-Like Receptor 4Case-Control StudiesFecesFemaleHumansInfant, NewbornIntestinal MucosaIntestinesMaleProspective StudiesReal-Time Polymerase Chain ReactionAnalgesics, OpioidHMGB1 ProteinHMGB1 protein, humanTLR4 protein, humanToll-Like Receptor 4

Identifiers

PMID38151596
PMCPMC11209831
OpenAlexW4390274170

What OpenQuestion 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 OpenQuestion graph.