Evidence map›Paper›PMID 36553202›Full record

ArticleDiagnostics (Basel, Switzerland)2022

Automated Classification of Idiopathic Pulmonary Fibrosis in Pathological Images Using Convolutional Neural Network and Generative Adversarial Networks.

Atsushi Teramoto, Tetsuya Tsukamoto, Ayano Michiba, Yuka Kiriyama, Eiko Sakurai, Kazuyoshi Imaizumi, Kuniaki Saito, Hiroshi Fujita

Abstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2022. 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. Review
  2. Article
  3. Article
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

8 authors.

Atsushi TeramotoSchool of Medical Sciences, Fujita Health University, Toyoake 470-1192, Japan.ORCID 0000-0001-7613-5348
Tetsuya TsukamotoGraduate School of Medicine, Fujita Health University, Toyoake 470-1192, Japan.ORCID 0000-0002-7502-8724
Ayano MichibaGraduate School of Medicine, Fujita Health University, Toyoake 470-1192, Japan.
Yuka KiriyamaGraduate School of Medicine, Fujita Health University, Toyoake 470-1192, Japan.
Eiko SakuraiGraduate School of Medicine, Fujita Health University, Toyoake 470-1192, Japan.
Kazuyoshi ImaizumiGraduate School of Medicine, Fujita Health University, Toyoake 470-1192, Japan.ORCID 0000-0002-3790-8691
Kuniaki SaitoSchool of Medical Sciences, Fujita Health University, Toyoake 470-1192, Japan.
Hiroshi FujitaFaculty of Engineering, Gifu University, Gifu 501-1194, Japan.ORCID 0000-0002-2936-9296

Funding

Ministry of Education, Culture, Sports, Science and Technology 20K08060
6 · The paper itself

Abstract

Interstitial pneumonia of uncertain cause is referred to as idiopathic interstitial pneumonia (IIP). Among the various types of IIPs, the prognosis of cases of idiopathic pulmonary fibrosis (IPF) is extremely poor, and accurate differentiation between IPF and non-IPF pneumonia is critical. In this study, we consider deep learning (DL) methods owing to their excellent image classification capabilities. Although DL models require large quantities of training data, collecting a large number of pathological specimens is difficult for rare diseases. In this study, we propose an end-to-end scheme to automatically classify IIPs using a convolutional neural network (CNN) model. To compensate for the lack of data on rare diseases, we introduce a two-step training method to generate pathological images of IIPs using a generative adversarial network (GAN). Tissue specimens from 24 patients with IIPs were scanned using a whole slide scanner, and the resulting images were divided into patch images with a size of 224 × 224 pixels. A progressive growth GAN (PGGAN) model was trained using 23,142 IPF images and 7817 non-IPF images to generate 10,000 images for each of the two categories. The images generated by the PGGAN were used along with real images to train the CNN model. An evaluation of the images generated by the PGGAN showed that cells and their locations were well-expressed. We also obtained the best classification performance with a detection sensitivity of 97.2% and a specificity of 69.4% for IPF using DenseNet. The classification performance was also improved by using PGGAN-generated images. These results indicate that the proposed method may be considered effective for the diagnosis of IPF.

Indexed as

classificationconvolutional neural networkgenerative adversarial networksidiopathic interstitial pneumonias

Identifiers

PMID36553202
PMCPMC9777207

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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.