Evidence map›Paper›PMID 39038392›Full record

ArticleComputers in biology and medicine2024

Deep learning-based IDH1 gene mutation prediction using histopathological imaging and clinical data.

Riku Nakagaki, Shyam Sundar Debsarkar, Hiroharu Kawanaka, Bruce J Aronow, V B Surya Prasath

Abstract read
In one paragraph

Article in Computers in biology and medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 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

13 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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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

5 authors.

Riku NakagakiGraduate School of Engineering, Mie University, 1577 Kurima-machiya, Tsu, Mie 514-8507, Japan. Electronic address: 422m236@m.mie-u.ac.jp.
Shyam Sundar DebsarkarDepartment of Computer Science, University of Cincinnati, OH 45221, USA. Electronic address: debsarss@mail.uc.edu.
Hiroharu KawanakaGraduate School of Engineering, Mie University, 1577 Kurima-machiya, Tsu, Mie 514-8507, Japan. Electronic address: kawanaka@elec.mie-u.ac.jp.
Bruce J AronowDepartment of Computer Science, University of Cincinnati, OH 45221, USA; Division of Biomedical Informatics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA; Department of Pediatrics, University of Cincinnati, OH 45267, USA; Department of Biomedical Informatics, College of Medicine, University of Cincinnati, OH 45267, USA. Electronic address: bruce.aronow@cchmc.org.
V B Surya PrasathDepartment of Computer Science, University of Cincinnati, OH 45221, USA; Division of Biomedical Informatics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA; Department of Pediatrics, University of Cincinnati, OH 45267, USA; Department of Biomedical Informatics, College of Medicine, University of Cincinnati, OH 45267, USA. Electronic address: surya.prasath@cchmc.org.

Funding

The LungMAP Data Coordination Center for Next Gen Systems Biology of RespirationU24HL148865 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI Bruce J Aronow, Nathan G. Salomonis · 2019 to 2026
$12.4M
NHLBI NIH HHS U24 HL148865
6 · The paper itself

Abstract

In the field of histopathology, many studies on the classification of whole slide images (WSIs) using artificial intelligence (AI) technology have been reported. We have studied the disease progression assessment of glioma. Adult-type diffuse gliomas, a type of brain tumor, are classified into astrocytoma, oligodendroglioma, and glioblastoma. Astrocytoma and oligodendroglioma are also called low grade glioma (LGG), and glioblastoma is also called glioblastoma multiforme (GBM). LGG patients frequently have isocitrate dehydrogenase (IDH) mutations. Patients with IDH mutations have been reported to have a better prognosis than patients without IDH mutations. Therefore, IDH mutations are an essential indicator for the classification of glioma. That is why we focused on the IDH1 mutation. In this paper, we aimed to classify the presence or absence of the IDH1 mutation using WSIs and clinical data of glioma patients. Ensemble learning between the WSIs model and the clinical data model is used to classify the presence or absence of IDH1 mutation. By using slide level labels, we combined patch-based imaging information from hematoxylin and eosin (H & E) stained WSIs, along with clinical data using deep image feature extraction and machine learning classifier for predicting IDH1 gene mutation prediction versus wild-type across cohort of 546 patients. We experimented with different deep learning (DL) models including attention-based multiple instance learning (ABMIL) models on imaging data along with gradient boosting machine (LightGBM) for the clinical variables. Further, we used hyperparameter optimization to find the best overall model in terms of classification accuracy. We obtained the highest area under the curve (AUC) of 0.823 for WSIs, 0.782 for clinical data, and 0.852 for ensemble results using MaxViT and LightGBM combination, respectively. Our experimental results indicate that the overall accuracy of the AI models can be improved by using both clinical data and images.

Indexed as

Brain NeoplasmsDeep LearningGliomaIsocitrate DehydrogenaseMutationAdultFemaleHumansMaleMiddle AgedIDH1 protein, humanIsocitrate DehydrogenaseBrain gliomaClinical dataDeep learningDigital pathologyFusion modelGene mutationWeakly supervised

Identifiers

PMID39038392
PMCPMC13215039

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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.