Evidence map›Paper›PMID 40843903›Full record

ArticleInternational journal of neonatal screening2025

Prediction of Congenital Portosystemic Shunt in Neonatal Hypergalactosemia Using Gal-1-P/Gal Ratio, Bile Acid, and Ammonia.

Sayaka Suzuki-Ajihara, Ikuma Musha, Masato Arao, Koki Mori, Shunsuke Fujibayashi, Ihiro Ryo, Tomotaka Kono, Asako Tajima, Hiroshi Mochizuki, Atsuko Imai-Okazaki and 3 more

Abstract read
In one paragraph

Article in International journal of neonatal screening, 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

13 authors.

Sayaka Suzuki-AjiharaDepartment of Pediatrics, Saitama Medical University, Saitama 350-0495, Japan.ORCID 0000-0002-4369-8379
Ikuma MushaDepartment of Pediatrics, Saitama Medical University, Saitama 350-0495, Japan.ORCID 0000-0001-6108-7312
Masato AraoDepartment of Pediatrics, Saitama Medical University, Saitama 350-0495, Japan.
Koki MoriDepartment of Clinical Laboratory, Saitama Children's Medical Center, Saitama 330-8777, Japan.
Shunsuke FujibayashiDivision of Endocrinology and Metabolism, Saitama Children's Medical Center, Saitama 330-8777, Japan.
Ihiro RyoDivision of Endocrinology and Metabolism, Saitama Children's Medical Center, Saitama 330-8777, Japan.
Tomotaka KonoDivision of Endocrinology and Metabolism, Saitama Children's Medical Center, Saitama 330-8777, Japan.
Asako TajimaDivision of Endocrinology and Metabolism, Saitama Children's Medical Center, Saitama 330-8777, Japan.ORCID 0009-0008-8135-130X
Hiroshi MochizukiDivision of Endocrinology and Metabolism, Saitama Children's Medical Center, Saitama 330-8777, Japan.
Atsuko Imai-OkazakiDiagnosis and Therapeutics of Intractable Diseases, Intractable Disease Research Center, Juntendo University Graduate School of Medicine, Tokyo 113-8421, Japan.
Ryuichiro ArakiMedical Education Center, Saitama Medical University, Saitama 350-0495, Japan.ORCID 0000-0003-4846-2418
Chikahiko NumakuraDepartment of Pediatrics, Saitama Medical University, Saitama 350-0495, Japan.
Akira OhtakeDepartment of Pediatrics, Saitama Medical University, Saitama 350-0495, Japan.ORCID 0000-0003-1147-3113

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital portosystemic shunts (CPSSs) are often associated with life-threatening systemic complications, which may be detected by identifying hypergalactosemia in newborn screening (NBS). However, diagnosing CPSS at an early stage is not easy. The purpose of this study was to predict CPSS early using screening values and general blood tests. The medical records of 153 patients with hypergalactosemia who underwent NBS in Saitama Prefecture between 1 December 1997 and 31 October 2023 were retrospectively analyzed. We provided the final diagnosis of the analyzed patients. Of the 153 patients, 44 (29%) were in the CPSS group and 83 (54%) were in the transient galactosemia group. Using the initial screening items and the six blood test items, we attempted to extract a CPSS group from the transient galactosemia group. Finally, a model for CPSS prediction was established. From multiple logistic regression analysis, filtered blood galactose-1 phosphate/galactose, serum total bile acid, and ammonia were adopted as explanatory variables for the prediction model. If the cut-off value for predicted disease probability value (P) was >0.357, CPSS was identified with 86.4% sensitivity (95%CI 72.6-94.8%) and 81.9% specificity (95%CI 72.0-89.5%). This predictive model might allow prediction of CPSS and early intervention.

Indexed as

ammoniacongenital portosystemic shuntgalactose-1 phosphate/galactosehypergalactosemianewborn screeningtotal bile acid

Identifiers

PMID40843903
PMCPMC12372138

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.