Evidence mapPaperPMID 41277678Full record

ArticleJournal of genetic counseling2025

Experiences of parents who receive a false-positive CK-MM screening for their newborn.

Janice P Tzeng, Allyson M Corbo, Heidi L Cope, Emily Cheves, Sara M Andrews, Samantha Scott, Beth Lincoln Boyea, Sean N Halpin, Holly L Peay

Abstract read
In one paragraph

Article in Journal of genetic counseling, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Janice P TzengCenter for Communication and Engagement Research, RTI International, Research Triangle Park, North Carolina, USA.ORCID 0000-0003-3915-5811
Allyson M CorboCenter for Communication and Engagement Research, RTI International, Research Triangle Park, North Carolina, USA.ORCID 0000-0002-5862-0216
Heidi L CopeGenOmics and Translational Research Center, RTI International, Research Triangle Park, North Carolina, USA.ORCID 0000-0003-0586-9277
Emily ChevesGenOmics and Translational Research Center, RTI International, Research Triangle Park, North Carolina, USA.ORCID 0000-0001-8801-0411
Sara M AndrewsGenOmics and Translational Research Center, RTI International, Research Triangle Park, North Carolina, USA.ORCID 0000-0003-0218-0976
Samantha ScottGenOmics and Translational Research Center, RTI International, Research Triangle Park, North Carolina, USA.
Beth Lincoln BoyeaGenOmics and Translational Research Center, RTI International, Research Triangle Park, North Carolina, USA.
Sean N HalpinGenOmics and Translational Research Center, RTI International, Research Triangle Park, North Carolina, USA.ORCID 0000-0001-5624-6083
Holly L PeayGenOmics and Translational Research Center, RTI International, Research Triangle Park, North Carolina, USA.ORCID 0000-0002-3053-7453

Funding

North Carolina Translational and Clinical Sciences Institute (NC TraCS)UM1TR004406 · UNIV OF NORTH CAROLINA CHAPEL HILL · 2025 to 2025
$8.6M
Foundation for the National Institutes of Health UL1TR002489John Merck FundMuscular Dystrophy AssociationNCATS NIH HHS UL1 TR002489NCATS NIH HHS UM1 TR004406Sarepta Therapeutics
6 · The paper itself

Abstract

Duchenne muscular dystrophy (DMD) is a rare inherited, X-linked neuromuscular disorder that leads to a progressive decline in physical mobility, muscle atrophy, and premature death. Newborn screening (NBS) offers the potential for earlier diagnosis and earlier intervention, although NBS using the creatine kinase isoenzyme (CK-MM) assay may detect conditions other than DMD and lead to initial false-positive results. Early Check, a voluntary supplemental newborn screening study in North Carolina, screened 16,566 newborns for DMD over nearly 3 years. Parents and legal guardians of infants who received an initial false-positive screen result for DMD (n = 20) were interviewed about their experiences. Data were coded in NVivo using directed content analysis. Participants described feelings of stress, shock, and concern associated with receiving the initial positive screening result, and varying levels of stress and anxiety while waiting for confirmatory genomic panel testing during the follow-up period. The study genetic counselor played a critical role in sharing the initial false-positive results, answering parents'/guardians' questions, and informing them of factors other than DMD that can cause elevated CK-MM levels. Despite the stressful experience of receiving a false-positive result, parents/guardians found value in participating in Early Check, as it provided knowledge about their child's health and the opportunity for earlier intervention, if needed.

Indexed as

Creatine KinaseMuscular Dystrophy, DuchenneNeonatal ScreeningParentsAdultFalse Positive ReactionsFemaleHumansInfant, NewbornMaleCreatine KinasecommunicationDuchenne muscular dystrophyfalse‐positivegenetic counselingnewborn screeningpsychosocial outcomes

Identifiers

PMID41277678
PMCPMC12798709

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.