Evidence map›Paper›PMID 36975847›Full record

ArticleInternational journal of neonatal screening2023

Immunoreactive Trypsinogen in Infants Born to Women with Cystic Fibrosis Taking Elexacaftor-Tezacaftor-Ivacaftor.

Payal Patel, Jana Yeley, Cynthia Brown, Melissa Wesson, Barbara G Lesko, James E Slaven, James F Chmiel, Raksha Jain, Don B Sanders

Open access · goldAbstract read
In one paragraph

Article in International journal of neonatal screening, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 5% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Guideline
  2. Maternal and fetal outcomes associated with CFTR modulator use during pregnancy: a scoping review.European respiratory review : an official journal of the European Respiratory Society · 2026
    Article
  3. Article
  4. Cystic fibrosis year in review 2023.Pediatric pulmonology · 2024
    Review
  5. Review
  6. Review
  7. Review
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

9 authors at 2 institutions in 1 country.

Payal PatelIndiana University School of Medicine, Indianapolis, IN 46202, USA.ORCID 0000-0002-3521-3124
Jana YeleyDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Cynthia BrownDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Melissa WessonDepartment of Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Barbara G LeskoDepartment of Pathology, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
James E SlavenDepartment of Biostatistics and Health Data Science, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
James F ChmielDepartment of Pediatrics, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Raksha JainDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Don B SandersDepartment of Pediatrics, Indiana University School of Medicine, Indianapolis, IN 46202, USA.ORCID 0000-0001-6265-6249
Indiana University School of MedicineThe University of Texas Southwestern Medical Center · US

Funding

Quality Assurance and Quality Control Project Management: Improving Submissions and Study Conduct in the Human Subjects Research Prior Approval ProcessUL1TR002529 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI MOE, SHARON M, WIEHE, SARAH ELIZABETH · 2018 to 2022
$27.2M
NIH HHS UL1TR002529
6 · The paper itself

Abstract

Most people with cystic fibrosis (CF) are diagnosed following abnormal newborn screening (NBS), which begins with measurement of immunoreactive trypsinogen (IRT) values. A case report found low concentrations of IRT in an infant with CF exposed to the CF transmembrane conductance regulator (CFTR) modulator, elexacaftor-tezacaftor-ivacaftor (ETI), in utero. However, IRT values in infants born to mothers taking ETI have not been systematically assessed. We hypothesized that ETI-exposed infants have lower IRT values than newborns with CF, CFTR-related metabolic syndrome/CF screen positive, inconclusive diagnosis (CRMS/CFSPID), or CF carriers. IRT values were collected from infants born in Indiana between 1 January 2020, and 2 June 2022, with ≥1 CFTR mutation. IRT values were compared to infants born to mothers with CF taking ETI followed at our institution. Compared to infants identified with CF (

Indexed as

cystic fibrosisimmunoreactive trypsinogennewborn screening

Identifiers

PMID36975847
PMCPMC10056483
OpenAlexW4321456886

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.