Evidence map›Paper›PMID 41816002›Full record

ArticleOpen forum infectious diseases2026

Proteomic Analysis of Serum and Cerebrospinal Fluid in Children with Encephalopathy Associated with Human Betaherpesvirus 6B.

Yoshiki Kawamura, Hisateru Yamaguchi, Tomoki Nishioka, Mao Kiribuchi, Ayano Yun, Hiroki Miura, Yotaro Kondo, Masato Itano, Yuki Higashimoto, Masaru Ihira and 2 more

Abstract read
In one paragraph

Article in Open forum infectious diseases, 2026. 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

12 authors.

Yoshiki KawamuraDepartment of Pediatrics, Fujita Health University School of Medicine, Toyoake, Japan.ORCID https://orcid.org/0000-0003-3942-7098
Hisateru YamaguchiDepartment of Medical Technology, School of Nursing and Medical Care, Yokkaichi Nursing and Medical Care University, Yokkaichi, Japan.ORCID https://orcid.org/0000-0002-4507-9598
Tomoki NishiokaDivision of Cell Biology, International Center for Brain Science, Fujita Health University, Toyoake, Japan.ORCID https://orcid.org/0000-0001-8472-8311
Mao KiribuchiDepartment of Pediatrics, Fujita Health University School of Medicine, Toyoake, Japan.
Ayano YunDepartment of Pediatrics, Fujita Health University School of Medicine, Toyoake, Japan.
Hiroki MiuraDepartment of Pediatrics, Fujita Health University School of Medicine, Toyoake, Japan.ORCID https://orcid.org/0000-0002-2847-3374
Yotaro KondoDepartment of Pediatrics, Fujita Health University School of Medicine, Toyoake, Japan.ORCID https://orcid.org/0009-0007-6168-8063
Masato ItanoDepartment of Pediatrics, Fujita Health University School of Medicine, Toyoake, Japan.
Yuki HigashimotoDepartment of Clinical Microbiology, Fujita Health University School of Medical Sciences, Toyoake, Japan.
Masaru IhiraDepartment of Clinical Science for Biological Monitoring, Fujita Health University School of Medical Sciences, Toyoake, Japan.
Jun-Ichi KawadaDepartment of Pediatrics, Fujita Health University School of Medicine, Toyoake, Japan.ORCID https://orcid.org/0000-0003-1553-2539
Tetsushi YoshikawaDepartment of Pediatrics, Fujita Health University School of Medicine, Toyoake, Japan.ORCID https://orcid.org/0000-0002-2847-7682

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Exanthem subitum (ES), a benign febrile exanthematous disease, is caused by primary human betaherpesvirus 6B (HHV-6B) infection. It may cause neurological complications, including complex febrile seizures (cFS), acute encephalopathy with biphasic seizures, and late reduced diffusion (AESD). cFS resolves spontaneously; however, AESD can pose severe sequelae. We aimed to elucidate AESD pathogenesis using a proteomic analysis. Methods: Using liquid chromatography-tandem mass spectrometry (LC-MS/MS), serum and cerebrospinal fluid (CSF) protein profiles were compared between patients with AESD and those with cFS ( Results: A total of 698 proteins were identified across all serum and CSF samples using LC-MS/MS. Nineteen serum proteins were differentially expressed in AESD and cFS during the acute phase. The glycolytic pathway was upregulated in AESD. Myristoylated alanine-rich C kinase substrate (MARCKS) and Golgi membrane protein 1 (GOLM1) were selected for validation using ELISA. Both proteins were upregulated during the acute phase ( Conclusions: Glycolysis and MARCKS pathways might be involved in HHV-6B-associated AESD pathogenesis.

Indexed as

encephalitisencephalopathyglycolysishuman herpesvirus 6BMARCKS

Identifiers

PMID41816002
PMCPMC12973172

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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.