Evidence map›Paper›PMID 42201228›Full record

ArticleInternational journal of neonatal screening2026

Comparison of Four Screening Markers [(C16 + C18:1)/C2, C14/C3, C12/C0, and C12/C2] for Carnitine Palmitoyltransferase II Deficiency in the Nationwide Newborn Screening Program in Japan.

Go Tajima, Nobuyuki Ishige, Junji Hanai, Keiko Konomura

Abstract read
In one paragraph

Article in International journal of neonatal screening, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Go TajimaDivision of Neonatal Screening, Research Institute, National Center for Child Health and Development, 2-10-1 Okura, Setagaya 157-8535, Japan.ORCID 0000-0002-2398-0748
Nobuyuki IshigeDivision of Newborn Screening, Tokyo Health Service Association, 1-2-59 Ichiga-Sadohara, Shinjuku 162-8460, Japan.ORCID 0000-0002-1386-2705
Junji HanaiHokkaido Pharmaceutical Association Public Health Examination Center, 8-6-6 Hiragishi 1-jo, Toyohira 062-0931, Japan.
Keiko KonomuraCenter for Outcomes Research and Economic Evaluation for Health (C2H), National Institute of Public Health, 2-3-6 Minami, Wako 351-0197, Japan.ORCID 0000-0002-9457-5969

Funding

the Health and Labour Sciences Research Grants for Research on Rare and Intractable Diseases 23FC1033the Practical Research Project for Rare / Intractable Diseases from the Japan Agency for Medical Research and Development JP23ek0109636the Practical Research Project for Rare / Intractable Diseases from the Japan Agency for Medical Research and Development JP26ek0109873
6 · The paper itself

Abstract

False-positive results are known to occur frequently in newborn screening (NBS) for carnitine palmitoyltransferase II (CPT II) deficiency, highlighting the need to identify appropriate screening markers. The present study aimed to compare the performance of two markers currently used in NBS for CPT II deficiency, (C16 + C18:1)/C2 and C14/C3, with two promising alternative markers, C12/C0 and C12/C2. We analyzed non-patient data from the 2023 fiscal year NBS program together with patient data for CPT II deficiency and very-long-chain acyl-CoA dehydrogenase deficiency derived from previously reported case series. Marker performance was assessed using precision-recall curves, including an analysis in which patients with the myopathic form of CPT II deficiency who passed NBS using (C16 + C18:1)/C2 and C14/C3 were reclassified as true positives. The area under the precision-recall curve values for C12/C2 and C14/C3 were 0.711 (95% confidence interval, 0.492-0.923) and 0.569 (0.341-0.779), respectively, indicating superior performance compared with the other markers. When cases with the myopathic form of CPT II deficiency were included as true positives, the performance of all markers decreased markedly. Although some patients with the myopathic form are still likely to be missed, C12/C2 appears to be an effective marker for reducing false-positive results.

Indexed as

carnitine palmitoyltransferase IICPT IIdodecanoylcarnitine (C12)false positivenewborn screening

Identifiers

PMID42201228
PMCPMC13214869

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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 OpenQuestion graph.