Evidence map›Paper›PMID 38920848›Full record

ArticleInternational journal of neonatal screening2024

Age-Related Blood Levels of Creatine Kinase-MM in Newborns and Patients with Duchenne Muscular Dystrophy: Considerations for the Development of Newborn Screening Algorithms.

Sarah Nelson Potter, Brooke Migliore, Javan Carter, Veronica R Copeland, Edward C Smith, Holly L Peay, Katerina S Kucera

Abstract read
In one paragraph

Article in International journal of neonatal screening, 2024. 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

7 authors.

Sarah Nelson PotterRTI International, Research Triangle Park, Durham, NC 22709, USA.ORCID 0000-0002-8640-8992
Brooke MiglioreRTI International, Research Triangle Park, Durham, NC 22709, USA.ORCID 0000-0003-0991-8371
Javan CarterRTI International, Research Triangle Park, Durham, NC 22709, USA.ORCID 0000-0001-5104-9283
Veronica R CopelandRTI International, Research Triangle Park, Durham, NC 22709, USA.
Edward C SmithDepartment of Pediatrics, Duke University, Durham, NC 27710, USA.ORCID 0000-0003-0073-9377
Holly L PeayRTI International, Research Triangle Park, Durham, NC 22709, USA.ORCID 0000-0002-3053-7453
Katerina S KuceraRTI International, Research Triangle Park, Durham, NC 22709, USA.ORCID 0000-0003-4148-6599

Funding

Re-Entry Supplement: Investigation of Oral Microbial Enzymes for the Detection and Treatment of Periodontal DiseaseUL1TR002489 · NCATS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BUSE, JOHN BERNARD, SHAHEEN, NICHOLAS J · 2018 to 2022
$48.6M
North Carolina Translational & Clinical Sciences Institute (NC TraCS)UL1TR001111 · NCATS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BUSE, JOHN BERNARD, CAREY, TIMOTHY S · 2013 to 2017
$43.9M
North Carolina Translational and Clinical Sciences Institute (NC TraCS)UM1TR004406 · NCATS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI NICHOLAS J SHAHEEN · 2023 to 2026
$37.5M
Early Check: A Collaborative Innovation to Facilitate Pre-Symptomatic Clinical Trials in NewbornsU01TR001792 · NCATS · RESEARCH TRIANGLE INSTITUTE · PI BAILEY, DONALD B, COTTEN, CHARLES MICHAEL · 2016 to 2020
$7.8M
NCATS NIH HHS U01TR001792NCATS NIH HHS UL1TR001111NCATS NIH HHS UL1TR002489NCATS NIH HHS UM1 TR004406
6 · The paper itself

Abstract

Duchenne muscular dystrophy (DMD) is an X-linked progressive disorder and the most common type of muscular dystrophy in children. As newborn screening (NBS) for DMD undergoes evaluation for the Recommended Uniform Screening Panel and is already mandated in multiple states, refining NBS algorithms is of utmost importance. NBS for DMD involves measuring creatine kinase-MM (CK-MM) concentration-a biomarker of muscle damage-in dried blood spots. The current test is FDA-approved for samples obtained less than 72 h after birth. Separate reference ranges are needed for samples collected later than 72 h after birth. In this study, we investigated the relationship between age and CK-MM in presumed healthy newborns to inform NBS algorithm designs. In patients with DMD, CK-MM is persistently elevated in childhood and adolescence, while it may be transiently elevated for other reasons in healthy newborns. CK-MM decrease over time was demonstrated by a population sample of 20,306 presumed healthy newborns tested between 0 and 60 days of life and repeat testing of 53 newborns on two separate days. In the population sample, CK-MM concentration was highest in the second 12 h period of life (median = 318 ng/mL) when only 57.6% of newborns tested below 360 ng/mL, the lowest previously published cutoff. By 72 h of age, median CK-MM concentration was 97 ng/mL, and 96.0% of infants had concentrations below 360 ng/mL. Between 72 h and 60 days, median CK-MM concentration ranged from 32 to 37 ng/mL. Establishing age-related cutoffs is crucial for optimizing the sensitivity and specificity of NBS for DMD.

Indexed as

creatine kinase-MMdried blood spotDuchenne muscular dystrophyneuromuscular disordernewborn screening

Identifiers

PMID38920848
PMCPMC11203585

What Socratic holds

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LicenceCC BY
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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 Socratic graph.