Artificial Intelligence Detected the Relationship Between Nuclear Morphological Features and Molecular Abnormalities of Papillary Thyroid Carcinoma

IF 11.3 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Endocrine Pathology Pub Date : 2024-01-02 DOI:10.1007/s12022-023-09796-8
Toui Nishikawa, Ibu Matsuzaki, Ayata Takahashi, Iwamoto Ryuta, Fidele Yambayamba Musangile, Kanako Sagan, Mizuki Nishikawa, Yurina Mikasa, Yuichi Takahashi, Fumiyoshi Kojima, Shin-ichi Murata
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Abstract

Papillary thyroid carcinoma (PTC) is the most common type of thyroid carcinoma and has characteristic nuclear features. Genetic abnormalities of PTC affect recent molecular target therapeutic strategy towards RET-altered cases, and they affect clinical prognosis and progression. However, there has been insufficient objective analysis of the correlation between genetic abnormalities and nuclear features. Using our newly developed methods, we studied the correlation between nuclear morphology and molecular abnormalities of PTC with the aim of predicting genetic abnormalities of PTC. We studied 72 cases of PTC and performed genetic analysis to detect BRAF p.V600E mutation and RET fusions. Nuclear features of PTC, such as nuclear grooves, pseudo-nuclear inclusions, and glassy nuclei, were also automatically detected by deep learning models. After analyzing the correlation between genetic abnormalities and nuclear features of PTC, logistic regression models could be used to predict gene abnormalities. Nuclear features were accurately detected with over 0.90 of AUCs in every class. The ratio of glassy nuclei to nuclear groove and the ratio of pseudo-nuclear inclusion to glassy nuclei were significantly higher in cases that were positive for RET fusions (p = 0.027, p = 0.043, respectively) than in cases that were negative for RET fusions. RET fusions were significantly predicted by glassy nuclei/nuclear grooves, pseudo-nuclear inclusions/glassy nuclei, and age (p = 0.023). Our deep learning models could accurately detect nuclear features. Genetic abnormalities had a correlation with nuclear features of PTC. Furthermore, our artificial intelligence model could significantly predict RET fusions of classic PTC.

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人工智能检测甲状腺乳头状癌核形态特征与分子异常之间的关系
甲状腺乳头状癌(PTC)是最常见的甲状腺癌类型,具有特征性的核特征。PTC的基因异常会影响近期针对RET改变病例的分子靶向治疗策略,并影响临床预后和病情进展。然而,目前对基因异常与核特征之间的相关性还缺乏足够的客观分析。我们利用新开发的方法研究了 PTC 核形态与分子异常之间的相关性,旨在预测 PTC 的基因异常。我们研究了 72 例 PTC 病例,并进行了基因分析,以检测 BRAF p.V600E 突变和 RET 融合。深度学习模型还自动检测了 PTC 的核特征,如核沟、假性核内含物和玻璃样核。在分析了 PTC 基因异常与核特征之间的相关性后,逻辑回归模型可用于预测基因异常。核特征被准确检测出来,每一类的AUC都超过0.90。RET融合阳性病例中玻璃样核与核沟的比率以及假核包涵体与玻璃样核的比率(分别为p = 0.027和p = 0.043)明显高于RET融合阴性病例。玻璃样核/核沟、假性核内含物/玻璃样核和年龄(p = 0.023)对RET融合有明显的预测作用。我们的深度学习模型可以准确检测核特征。遗传异常与 PTC 的核特征具有相关性。此外,我们的人工智能模型可以显著预测典型PTC的RET融合。
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来源期刊
Endocrine Pathology
Endocrine Pathology 医学-病理学
CiteScore
12.30
自引率
20.50%
发文量
41
审稿时长
>12 weeks
期刊介绍: Endocrine Pathology publishes original articles on clinical and basic aspects of endocrine disorders. Work with animals or in vitro techniques is acceptable if it is relevant to human normal or abnormal endocrinology. Manuscripts will be considered for publication in the form of original articles, case reports, clinical case presentations, reviews, and descriptions of techniques. Submission of a paper implies that it reports unpublished work, except in abstract form, and is not being submitted simultaneously to another publication. Accepted manuscripts become the sole property of Endocrine Pathology and may not be published elsewhere without written consent from the publisher. All articles are subject to review by experienced referees. The Editors and Editorial Board judge manuscripts suitable for publication, and decisions by the Editors are final.
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