Evidence map›Paper›PMID 42824914›Full record

ReviewFrontiers in oncology2026

ApoA2 isoforms as blood-based biomarkers reflecting pancreatic exocrine dysfunction for risk stratification and perioperative management of pancreatic cancer.

Akira Matsushita, Takashi Ono, Takahiro Murokawa, Junji Ueda, Tetsuya Shimizu, Yoichi Kawano, Akihisa Matsuda, Yuta Hasegawa, Norio Itokawa, Keiko Takeuchi and 2 more

Abstract readReview
In one paragraph

Review in Frontiers in oncology, 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.

Akira MatsushitaDepartment of Gastroenterological Surgery, Nippon Medical School, Tokyo, Japan.
Takashi OnoDepartment of Gastroenterological Surgery, Nippon Medical School, Tokyo, Japan.
Takahiro MurokawaDepartment of Gastroenterological Surgery, Nippon Medical School, Tokyo, Japan.
Junji UedaDepartment of Gastroenterological Surgery, Nippon Medical School, Tokyo, Japan.
Tetsuya ShimizuDepartment of Gastroenterological Surgery, Nippon Medical School, Tokyo, Japan.
Yoichi KawanoDepartment of Gastroenterological Surgery, Nippon Medical School, Tokyo, Japan.
Akihisa MatsudaDepartment of Gastroenterological Surgery, Nippon Medical School, Tokyo, Japan.
Yuta HasegawaDepartment of Gastroenterology, Nippon Medical School, Tokyo, Japan.
Norio ItokawaDepartment of Gastroenterology, Nippon Medical School, Tokyo, Japan.
Keiko TakeuchiDepartment of Molecular Prevention, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
Ayumi KashiroDepartment of Molecular Prevention, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
Kazufumi HondaDepartment of Molecular Prevention, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Apolipoprotein A2 isoforms (apoA2‑i) are clinically validated blood‑based biomarkers for the auxiliary diagnosis of pancreatic cancer. Emerging evidence also suggests that apoA2‑i may contribute to the detection of early‑stage pancreatic cancer, particularly in cohorts where CA19‑9 shows limited sensitivity, although these applications remain investigational and require prospective validation. Beyond diagnostic applications, apoA2‑i reflect pancreatic exocrine physiology, linking biomarker biology with perioperative outcomes such as postoperative pancreatic fistula and steatotic liver disease. Because type 3c diabetes mellitus arises from exocrine dysfunction, emerging evidence suggests that exocrine‑based markers, including apoA2‑i,. may contribute to future approaches for stratifying new‑onset diabetes, although current evidence remains preliminary. By integrating validated diagnostic roles with developing translational and physiological applications, this review outlines the evolving relevance of apoA2‑i within pancreatic oncology while emphasizing the need for prospective, multi-center validation and real-world data integration.

Indexed as

apolipoprotein A2 isoformsintraductal papillary mucinous neoplasmsnew-onset diabetespancreatic adenocarcinomapancreatic exocrine insufficiencypancreatic fistulasteatotic liver diseasetype 3C diabetes mellitus

Identifiers

PMID42824914
PMCPMC13628349

What OpenQuestion holds

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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 OpenQuestion graph.