从解剖学到基因组学,使用多任务深度学习方法进行全面的胶质瘤分析。

IF 3.7 3区 医学 Q2 ENGINEERING, BIOMEDICAL
Akmalbek Abdusalomov, Sabina Umirzakova, Obidjon Bekmirzaev, Adilbek Dauletov, Abror Buriboev, Alpamis Kutlimuratov, Akhram Nishanov, Rashid Nasimov, Ryumduck Oh
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引用次数: 0

摘要

背景:胶质瘤是最复杂和致命的原发性脑肿瘤之一,需要精确评估解剖亚区和分子改变以有效的临床治疗。方法:为了解决当前生物图像分析管道的脱节性质,其中基于MRI的解剖分割和分子生物标志物预测是作为单独的任务完成的,我们在这里使用了分子基因组和多任务(MGMT-Net),这是一个深度学习方案,执行多模态MRI数据的任务而不进行任何转换。MGMT-Net采用了一种新颖的跨模态注意融合(CMAF)模块,该模块动态集成了各种成像序列,并将它们与混合变压器-卷积神经网络(CNN)编码器进行匹配,以捕获全局背景和局部解剖细节。该架构支持双任务解码器,支持并行体素肿瘤描述和主题水平的关键基因组标记分类,包括IDH基因突变、1p/19q共缺失和TERT基因启动子突变。结果:在脑肿瘤分割(BraTS 2024)数据集和癌症基因组图谱/伊拉斯姆斯胶质瘤数据库(TCGA/EGD)数据集上进行的广泛验证显示出高分割准确性和强大的生物标志物分类性能,具有很强的外部机构队列推广能力。消融研究进一步证实了每个架构组件在实现整体健壮性方面的重要性。结论:MGMT-Net提供了一种可扩展的、与临床相关的解决方案,它将放射成像和基因组学见解联系起来,有可能减少诊断延迟,提高神经肿瘤学决策的准确性。通过在单一模型中整合空间和遗传分析,这项工作代表了朝着全面的、人工智能驱动的胶质瘤评估迈出的重要一步。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
From Anatomy to Genomics Using a Multi-Task Deep Learning Approach for Comprehensive Glioma Profiling.

Background: Gliomas are among the most complex and lethal primary brain tumors, necessitating precise evaluation of both anatomical subregions and molecular alterations for effective clinical management.

Methods: To find a solution to the disconnected nature of current bioimage analysis pipelines, where anatomical segmentation based on MRI and molecular biomarker prediction are done as separate tasks, we use here Molecular-Genomic and Multi-Task (MGMT-Net), a one deep learning scheme that carries out the task of the multi-modal MRI data without any conversion. MGMT-Net incorporates a novel Cross-Modality Attention Fusion (CMAF) module that dynamically integrates diverse imaging sequences and pairs them with a hybrid Transformer-Convolutional Neural Network (CNN) encoder to capture both global context and local anatomical detail. This architecture supports dual-task decoders, enabling concurrent voxel-wise tumor delineation and subject-level classification of key genomic markers, including the IDH gene mutation, the 1p/19q co-deletion, and the TERT gene promoter mutation.

Results: Extensive validation on the Brain Tumor Segmentation (BraTS 2024) dataset and the combined Cancer Genome Atlas/Erasmus Glioma Database (TCGA/EGD) datasets demonstrated high segmentation accuracy and robust biomarker classification performance, with strong generalizability across external institutional cohorts. Ablation studies further confirmed the importance of each architectural component in achieving overall robustness.

Conclusions: MGMT-Net presents a scalable and clinically relevant solution that bridges radiological imaging and genomic insights, potentially reducing diagnostic latency and enhancing precision in neuro-oncology decision-making. By integrating spatial and genetic analysis within a single model, this work represents a significant step toward comprehensive, AI-driven glioma assessment.

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来源期刊
Bioengineering
Bioengineering Chemical Engineering-Bioengineering
CiteScore
4.00
自引率
8.70%
发文量
661
期刊介绍: Aims Bioengineering (ISSN 2306-5354) provides an advanced forum for the science and technology of bioengineering. It publishes original research papers, comprehensive reviews, communications and case reports. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. All aspects of bioengineering are welcomed from theoretical concepts to education and applications. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. There are, in addition, four key features of this Journal: ● We are introducing a new concept in scientific and technical publications “The Translational Case Report in Bioengineering”. It is a descriptive explanatory analysis of a transformative or translational event. Understanding that the goal of bioengineering scholarship is to advance towards a transformative or clinical solution to an identified transformative/clinical need, the translational case report is used to explore causation in order to find underlying principles that may guide other similar transformative/translational undertakings. ● Manuscripts regarding research proposals and research ideas will be particularly welcomed. ● Electronic files and software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material. ● We also accept manuscripts communicating to a broader audience with regard to research projects financed with public funds. Scope ● Bionics and biological cybernetics: implantology; bio–abio interfaces ● Bioelectronics: wearable electronics; implantable electronics; “more than Moore” electronics; bioelectronics devices ● Bioprocess and biosystems engineering and applications: bioprocess design; biocatalysis; bioseparation and bioreactors; bioinformatics; bioenergy; etc. ● Biomolecular, cellular and tissue engineering and applications: tissue engineering; chromosome engineering; embryo engineering; cellular, molecular and synthetic biology; metabolic engineering; bio-nanotechnology; micro/nano technologies; genetic engineering; transgenic technology ● Biomedical engineering and applications: biomechatronics; biomedical electronics; biomechanics; biomaterials; biomimetics; biomedical diagnostics; biomedical therapy; biomedical devices; sensors and circuits; biomedical imaging and medical information systems; implants and regenerative medicine; neurotechnology; clinical engineering; rehabilitation engineering ● Biochemical engineering and applications: metabolic pathway engineering; modeling and simulation ● Translational bioengineering
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