用可解释的生物学改进精准医疗的疗法:仅有人工智能是不够的

IF 4.5 2区 医学 Q1 RHEUMATOLOGY Best Practice & Research in Clinical Rheumatology Pub Date : 2024-09-26 DOI:10.1016/j.berh.2024.102006
I Jurisica
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引用次数: 0

摘要

技术进步和高通量生化检测正在迅速改变我们提出和检验生物学假设的方式,以及我们治疗病人的方式。大多数复杂疾病都是在遗传、生活方式和环境因素的基础上产生的,并表现为一系列症状。为了弄清复杂的生物过程及其从健康状态到疾病状态的变化,我们需要系统地整合和分析多组学数据集、本体论和各种注释。如果不能妥善管理这些复杂的生物和临床数据,仅靠人工智能(AI)算法是无法进行有效训练、验证和成功应用的,也就无法提供值得信赖的、以患者为中心的诊断、预后和治疗。精准医疗要求有效使用多组学方法,这为使用人工智能、"大数据 "分析和整合计算生物学工作流程提供了许多机会。光学和生化检测技术(包括测序、质谱分析和成像模式)的进步改变了研究工作,使我们有能力在单个细胞水平上同时查看所有表达的基因,识别整个蛋白质组的变化,并评估动态变化的生物系统中每个蛋白质的相互作用伙伴。虽然这种视图已经对我们了解健康和疾病状况产生了影响,但要从单项研究中全面系统地提取有用信息、确保信号与噪声分离、建立模型并为进一步研究提供假设,仍然具有挑战性。数据仍然不完整,而且往往利用支离破碎的生物网络进行连接。此外,统计和机器学习模型是在队列水平上开发的,往往没有在患者个体水平上进行验证。将综合性计算生物学与人工智能相结合,有可能通过识别生物标志物和建立可解释的模型来描述个体患者的特征,从而提高对疾病的理解和治疗。从系统数据分析到更具体的诊断、预后和预测生物标志物、药物作用机制和患者选择,此类分析影响着从预防到疾病特征描述、从预后到药物发现的多个步骤。数据挖掘、机器学习、图论和高级可视化可帮助确定诊断、预后和预测生物标志物,并创建疾病的因果模型。将计算预测和建模与生物实验相结合,可以更快、更多地发现生物和临床相关性。然而,计算分析结果和模型的准确性和实用性取决于用于构建这些结果和模型的网络、本体和数据集的正确性和全面性。高质量、经过整理的数据门户网站为转化研究提供了必要的基础。它们有助于确定更好的生物标志物、新药和精准治疗,并能改善患者的治疗效果和生活质量。将计算预测和建模与生物实验有效地结合起来,可以更快地获得更有用的发现。
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Explainable biology for improved therapies in precision medicine: AI is not enough.

Technological advances and high-throughput bio-chemical assays are rapidly changing ways how we formulate and test biological hypotheses, and how we treat patients. Most complex diseases arise on a background of genetics, lifestyle and environment factors, and manifest themselves as a spectrum of symptoms. To fathom intricate biological processes and their changes from healthy to disease states, we need to systematically integrate and analyze multi-omics datasets, ontologies, and diverse annotations. Without proper management of such complex biological and clinical data, artificial intelligence (AI) algorithms alone cannot be effectively trained, validated, and successfully applied to provide trustworthy and patient-centric diagnosis, prognosis and treatment. Precision medicine requires to use multi-omics approaches effectively, and offers many opportunities for using AI, "big data" analytics, and integrative computational biology workflows. Advances in optical and biochemical assay technologies including sequencing, mass spectrometry and imaging modalities have transformed research by empowering us to simultaneously view all genes expressed, identify proteome-wide changes, and assess interacting partners of each individual protein within a dynamically changing biological system, at an individual cell level. While such views are already having an impact on our understanding of healthy and disease conditions, it remains challenging to extract useful information comprehensively and systematically from individual studies, ensure that signal is separated from noise, develop models, and provide hypotheses for further research. Data remain incomplete and are often poorly connected using fragmented biological networks. In addition, statistical and machine learning models are developed at a cohort level and often not validated at the individual patient level. Combining integrative computational biology and AI has the potential to improve understanding and treatment of diseases by identifying biomarkers and building explainable models characterizing individual patients. From systematic data analysis to more specific diagnostic, prognostic and predictive biomarkers, drug mechanism of action, and patient selection, such analyses influence multiple steps from prevention to disease characterization, and from prognosis to drug discovery. Data mining, machine learning, graph theory and advanced visualization may help identify diagnostic, prognostic and predictive biomarkers, and create causal models of disease. Intertwining computational prediction and modeling with biological experiments leads to faster, more biologically and clinically relevant discoveries. However, computational analysis results and models are going to be only as accurate and useful as correct and comprehensive are the networks, ontologies and datasets used to build them. High quality, curated data portals provide the necessary foundation for translational research. They help to identify better biomarkers, new drugs, precision treatments, and should lead to improved patient outcomes and their quality of life. Intertwining computational prediction and modeling with biological experiments, efficiently and effectively leads to more useful findings faster.

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来源期刊
CiteScore
9.40
自引率
0.00%
发文量
43
审稿时长
27 days
期刊介绍: Evidence-based updates of best clinical practice across the spectrum of musculoskeletal conditions. Best Practice & Research: Clinical Rheumatology keeps the clinician or trainee informed of the latest developments and current recommended practice in the rapidly advancing fields of musculoskeletal conditions and science. The series provides a continuous update of current clinical practice. It is a topical serial publication that covers the spectrum of musculoskeletal conditions in a 4-year cycle. Each topic-based issue contains around 200 pages of practical, evidence-based review articles, which integrate the results from the latest original research with current clinical practice and thinking to provide a continuous update. Each issue follows a problem-orientated approach that focuses on the key questions to be addressed, clearly defining what is known and not known. The review articles seek to address the clinical issues of diagnosis, treatment and patient management. Management is described in practical terms so that it can be applied to the individual patient. The serial is aimed at the physician in both practice and training.
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