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Defining Disease Diagnosis and Translational Medicine within a Homeostatic Perturbation Paradigm: The National Institutes of Health Undiagnosed Diseases Program Experience

机译:在稳态摄动范式中定义疾病诊断和转化医学:美国国立卫生研究院未诊断疾病计划的经验

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摘要

Traditionally, the use of genomic information for personalized medical decisions relies on prior discovery and validation of genotype–phenotype associations. This approach constrains care for patients presenting with undescribed problems. The National Institutes of Health (NIH) Undiagnosed Diseases Program (UDP) hypothesized that defining disease as maladaptation to an ecological niche allows delineation of a logical framework to diagnose and evaluate such patients. Herein, we present the philosophical bases, methodologies, and processes implemented by the NIH UDP. The NIH UDP incorporated use of the Human Phenotype Ontology, developed a genomic alignment strategy cognizant of parental genotypes, pursued agnostic biochemical analyses, implemented functional validation, and established virtual villages of global experts. This systematic approach provided a foundation for the diagnostic or non-diagnostic answers provided to patients and serves as a paradigm for scalable translational research.
机译:传统上,将基因组信息用于个性化医疗决策取决于对基因型-表型关联的事先发现和验证。这种方法限制了对出现未描述问题的患者的护理。美国国立卫生研究院(NIH)未诊断疾病计划(UDP)假设,将疾病定义为对生态位的适应不良,就可以划定诊断和评估此类患者的逻辑框架。在这里,我们介绍了NIH UDP实现的哲学基础,方法和过程。 NIH UDP结合了人类表型本体论的使用,开发了识别父母基因型的基因组比对策略,进行了不可知论的生化分析,实施了功能验证,并建立了由全球专家组成的虚拟村庄。这种系统的方法为提供给患者的诊断或非诊断答案提供了基础,并成为可扩展翻译研究的范例。

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