The Application of Knowledge Engineering via the Use of a Biomimetic Digital Twin Ecosystem, Phenotype-Driven Variant Analysis, and Exome Sequencing to Understand the Molecular Mechanisms of Disease

IF 3.4 3区 医学 Q1 PATHOLOGY Journal of Molecular Diagnostics Pub Date : 2024-03-29 DOI:10.1016/j.jmoldx.2024.03.004
William G. Kearns , Georgios Stamoulis , Joseph Glick , Lawrence Baisch , Andrew Benner , Dalton Brough , Luke Du , Bradford Wilson , Laura Kearns , Nicholas Ng , Maya Seshan , Raymond Anchan
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Abstract

Applied artificial intelligence, particularly large language models, in biomedical research is accelerating, but effective discovery and validation requires a toolset without limitations or bias. On January 30, 2023, the National Academies of Sciences, Engineering, and Medicine (NAS) appointed an ad hoc committee to identify the needs and opportunities to advance the mathematical, statistical, and computational foundations of digital twins in applications across science, medicine, engineering, and society. On December 15, 2023, the NAS released a 164-page report, “Foundational Research Gaps and Future Directions for Digital Twins.” This report described the importance of using digital twins in biomedical research. The current study was designed to develop an innovative method that incorporated phenotype-ranking algorithms with knowledge engineering via a biomimetic digital twin ecosystem. This ecosystem applied real-world reasoning principles to nonnormalized, raw data to identify hidden or "dark" data. Clinical exome sequencing study on patients with endometriosis indicated four variants of unknown clinical significance potentially associated with endometriosis-related disorders in nearly all patients analyzed. One variant of unknown clinical significance was identified in all patient samples and could be a biomarker for diagnostics. To the best of our knowledge, this is the first study to incorporate the recommendations of the NAS to biomedical research. This method can be used to understand the mechanisms of any disease, for virtual clinical trials, and to identify effective new therapies.

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通过使用仿生数字双胞胎生态系统、表型驱动变异分析和外显子组测序来应用知识工程,以了解疾病的分子机制。
生物医学研究中的应用人工智能,特别是大型语言模型,正在加速发展,但有效的发现和验证需要一个没有限制或偏见的工具集。2023 年 1 月 30 日,美国国家科学、工程和医学院(NAS)任命了一个特设委员会,以确定在科学、医学、工程和社会应用中推进数字双胞胎的数学、统计和计算基础的需求和机遇。2023 年 12 月 15 日,美国国家科学院发布了一份长达 164 页的报告,题为 "数字孪生的基础研究差距和未来方向"。该报告阐述了在生物医学研究中使用数字双胞胎的重要性。我们开发了一种创新方法,通过仿生数字孪生生态系统将表型排序算法与知识工程相结合。该生态系统将真实世界的推理原则应用于非规范化的原始数据,以识别隐藏或 "暗数据"。我们对子宫内膜异位症患者进行了临床外显子组测序研究,在几乎所有分析的患者中都能识别出与子宫内膜异位症相关疾病潜在相关的四个VUS。其中一个 VUS 在所有患者样本中都得到了鉴定,可作为诊断的生物标记物。据我们所知,这是第一项将美国国家科学院的建议纳入生物医学研究的研究。这种方法可用于了解任何疾病的发病机制,进行虚拟临床试验,以及确定有效的新疗法。
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来源期刊
CiteScore
8.10
自引率
2.40%
发文量
143
审稿时长
43 days
期刊介绍: The Journal of Molecular Diagnostics, the official publication of the Association for Molecular Pathology (AMP), co-owned by the American Society for Investigative Pathology (ASIP), seeks to publish high quality original papers on scientific advances in the translation and validation of molecular discoveries in medicine into the clinical diagnostic setting, and the description and application of technological advances in the field of molecular diagnostic medicine. The editors welcome for review articles that contain: novel discoveries or clinicopathologic correlations including studies in oncology, infectious diseases, inherited diseases, predisposition to disease, clinical informatics, or the description of polymorphisms linked to disease states or normal variations; the application of diagnostic methodologies in clinical trials; or the development of new or improved molecular methods which may be applied to diagnosis or monitoring of disease or disease predisposition.
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