Evidence map›Paper›PMID 41612503›Full record

ArticleInflammation and regeneration2026

Diagnostic potential of cryptic exon-derived peptides in serum extracellular vesicles for sporadic amyotrophic lateral sclerosis.

Koki Takahashi, Chris Kato, Koji Ueda, Shiho Nakamura, Fumiko Ozawa, Nobuko Moritoki, Shinsuke Shibata, Shinichi Takahashi, Satoru Morimoto, Hideyuki Okano

Abstract read
In one paragraph

Article in Inflammation and regeneration, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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

10 authors.

Koki Takahashi *Keio University Regenerative Medicine Research Center, Kanagawa, 210-0821, Japan.
Chris Kato *Keio University Regenerative Medicine Research Center, Kanagawa, 210-0821, Japan.
Koji UedaCancer Proteomics Group, Cancer Precision Medicine Center, Japanese Foundation for Cancer Research, Tokyo, 135-8550, Japan.
Shiho NakamuraKeio University Regenerative Medicine Research Center, Kanagawa, 210-0821, Japan.
Fumiko OzawaKeio University Regenerative Medicine Research Center, Kanagawa, 210-0821, Japan.
Nobuko MoritokiElectron Microscope Laboratory, Keio University School of Medicine, Tokyo, 160-0082, Japan.
Shinsuke ShibataElectron Microscope Laboratory, Keio University School of Medicine, Tokyo, 160-0082, Japan.
Shinichi TakahashiKeio University Regenerative Medicine Research Center, Kanagawa, 210-0821, Japan.
Satoru MorimotoKeio University Regenerative Medicine Research Center, Kanagawa, 210-0821, Japan. morimoto.satoru@keio.jp.
Hideyuki OkanoKeio University Regenerative Medicine Research Center, Kanagawa, 210-0821, Japan. hidokano@keio.jp.ORCID http://orcid.org/0000-0001-7482-5935

Funding

Japan Agency for Medical Research and Development JP21wm0425009Japan Agency for Medical Research and Development JP22bm0804003Japan Agency for Medical Research and Development JP22ek0109616Japan Agency for Medical Research and Development JP23bm1123046Japan Agency for Medical Research and Development JP23bm1423002Japan Agency for Medical Research and Development JP23kk0305024Japan Agency for Medical Research and Development JP25ek0109811Japan Agency for Medical Research and Development JP25wm0625519Japan Intractable Diseases(Nanbyo)Research Foundation 2024A04Japan Society for the Promotion of Science JP21H05278Japan Society for the Promotion of Science JP22K15736Japan Society for the Promotion of Science JP25H00007
6 · The paper itself

Abstract

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by progressive degeneration and loss of upper and lower motor neurons, with approximately 90% of cases being sporadic (sporadic ALS, SALS). A reliable diagnostic biomarker remains an unmet clinical need in SALS, with misdiagnosis and diagnostic delay hindering early management. The mislocalization of the RNA-binding protein TDP-43 (encoded by TARDBP), a pathological hallmark of SALS, could lead to aberrant splicing that produces transcripts with cryptic exons and, consequently, cryptic peptides. This study proposes cryptic peptides in serum extracellular vesicles as a novel candidate diagnostic biomarker of SALS. We included 10 healthy controls and 20 patients with SALS and quantified cryptic peptides predicted from cryptic exon sequences using mass spectrometry-based proteomics. Cryptic peptides from four proteins (RANBP1, IGLON5, ACTN1, ALPK2) were detected in participants, with the IGLON5 cryptic peptide detected significantly more frequently in SALS than in HC (adjusted P = 0.044). The number of detected cryptic peptides classified SALS and healthy controls with acceptable performance (area under the curve = 0.82). In conclusion, cryptic peptides could have diagnostic performance for SALS, warranting further validation.

Indexed as

BiomarkerCryptic exonCryptic peptideProteomicsSporadic amyotrophic lateral sclerosisTDP-43

Identifiers

PMID41612503
PMCPMC12924518

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.