Evidence map›Paper›PMID 37925580›Full record

ArticleScientific reports2023

Improved artificial intelligence discrimination of minor histological populations by supplementing with color-adjusted images.

Satomi Hatta, Yoshihito Ichiuji, Shingo Mabu, Mauricio Kugler, Hidekata Hontani, Tadakazu Okoshi, Haruki Fuse, Takako Kawada, Shoji Kido, Yoshiaki Imamura and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
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.

Satomi HattaDivision of Molecular Pathology, Department of Pathological Sciences, University of Fukui, 23-3 Matsuoka-Shimoaizuki, Eiheiji, Fukui, 910-1193, Japan.
Yoshihito IchiujiGraduate School of Sciences and Technology for Innovation, Yamaguchi University, Yamaguchi, Japan.
Shingo MabuGraduate School of Sciences and Technology for Innovation, Yamaguchi University, Yamaguchi, Japan.
Mauricio KuglerDepartment of Computer Science, Nagoya Institute of Technology, Nagoya, Japan.
Hidekata HontaniDepartment of Computer Science, Nagoya Institute of Technology, Nagoya, Japan.
Tadakazu OkoshiDepartment of Pathology, Fukui Red Cross Hospital, Fukui, Japan.
Haruki FuseDepartment of Clinical Inspection, Maizuru Kyosai Hospital, Maizuru, Japan.
Takako KawadaDepartment of Clinical Inspection, Maizuru Kyosai Hospital, Maizuru, Japan.
Shoji KidoDepartment of Artificial Intelligence Diagnostic Radiology, Osaka University Graduate School of Medicine, Suita, Japan.
Yoshiaki ImamuraDivision of Diagnostic/Surgical Pathology, University of Fukui Hospital, Eiheiji, Japan.
Hironobu NaikiDivision of Molecular Pathology, Department of Pathological Sciences, University of Fukui, 23-3 Matsuoka-Shimoaizuki, Eiheiji, Fukui, 910-1193, Japan.
Kunihiro InaiDivision of Molecular Pathology, Department of Pathological Sciences, University of Fukui, 23-3 Matsuoka-Shimoaizuki, Eiheiji, Fukui, 910-1193, Japan. kinai@u-fukui.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the dedicated research of artificial intelligence (AI) for pathological images, the construction of AI applicable to histopathological tissue subtypes, is limited by insufficient dataset collection owing to disease infrequency. Here, we present a solution involving the addition of supplemental tissue array (TA) images that are adjusted to the tonality of the main data using a cycle-consistent generative adversarial network (CycleGAN) to the training data for rare tissue types. F1 scores of rare tissue types that constitute < 1.2% of the training data were significantly increased by improving recall values after adding color-adjusted TA images constituting < 0.65% of total training patches. The detector also enabled the equivalent discrimination of clinical images from two distinct hospitals and the capability was more increased following color-correction of test data before AI identification (F1 score from 45.2 ± 27.1 to 77.1 ± 10.3, p < 0.01). These methods also classified intraoperative frozen sections, while excessive supplementation paradoxically decreased F1 scores. These results identify strategies for building an AI that preserves the imbalance between training data with large differences in actual disease frequencies, which is important for constructing AI for practical histopathological classification.

Indexed as

Artificial IntelligenceCaffeineFrozen SectionsHistocompatibility TestingHospitalsCaffeine

Identifiers

PMID37925580
PMCPMC10625567

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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.