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GLIDE2 口腔健康基因组学联盟中的表型协调。

Phenotype Harmonization in the GLIDE2 Oral Health Genomics Consortium.

机构信息

Division of Pediatric and Public Health, Adams School of Dentistry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

出版信息

J Dent Res. 2022 Oct;101(11):1408-1416. doi: 10.1177/00220345221109775. Epub 2022 Aug 24.

Abstract

Genetic risk factors play important roles in the etiology of oral, dental, and craniofacial diseases. Identifying the relevant risk loci and understanding their molecular biology could highlight new prevention and management avenues. Our current understanding of oral health genomics suggests that dental caries and periodontitis are polygenic diseases, and very large sample sizes and informative phenotypic measures are required to discover signals and adequately map associations across the human genome. In this article, we introduce the second wave of the Gene-Lifestyle Interactions and Dental Endpoints consortium (GLIDE2) and discuss relevant data analytics challenges, opportunities, and applications. In this phase, the consortium comprises a diverse, multiethnic sample of over 700,000 participants from 21 studies contributing clinical data on dental caries experience and periodontitis. We outline the methodological challenges of combining data from heterogeneous populations, as well as the data reduction problem in resolving detailed clinical examination records into tractable phenotypes, and describe a strategy that addresses this. Specifically, we propose a 3-tiered phenotyping approach aimed at leveraging both the large sample size in the consortium and the detailed clinical information available in some studies, wherein binary, severity-encompassing, and "precision," data-driven clinical traits are employed. As an illustration of the use of data-driven traits across multiple cohorts, we present an application of dental caries experience data harmonization in 8 participating studies ( = 55,143) using previously developed permanent dentition tooth surface-level dental caries pattern traits. We demonstrate that these clinical patterns are transferable across multiple cohorts, have similar relative contributions within each study, and thus are prime targets for genetic interrogation in the expanded and diverse multiethnic sample of GLIDE2. We anticipate that results from GLIDE2 will decisively advance the knowledge base of mechanisms at play in oral, dental, and craniofacial health and disease and further catalyze international collaboration and data and resource sharing in genomics research.

摘要

遗传风险因素在口腔、牙齿和颅面疾病的病因学中起着重要作用。确定相关的风险基因座并了解其分子生物学可以为新的预防和管理途径提供启示。我们目前对口腔健康基因组学的认识表明,龋齿和牙周炎是多基因疾病,需要非常大的样本量和信息丰富的表型测量来发现信号,并在人类基因组中充分绘制关联。在本文中,我们介绍了基因-生活方式相互作用和口腔终点联盟(GLIDE2)的第二波,并讨论了相关数据分析的挑战、机遇和应用。在这一阶段,该联盟由来自 21 项研究的超过 70 万名参与者组成,这些参与者具有不同的种族和民族背景,为龋齿经历和牙周炎的临床数据做出了贡献。我们概述了从异构人群中组合数据的方法学挑战,以及将详细的临床检查记录简化为可处理的表型的降维问题,并描述了一种解决该问题的策略。具体而言,我们提出了一种 3 级表型分析方法,旨在利用联盟中的大样本量和一些研究中可用的详细临床信息,其中采用了二进制、涵盖严重程度和“精确”的数据驱动临床特征。作为在多个队列中使用数据驱动特征的一个例子,我们展示了使用先前开发的恒牙牙面龋齿模式特征对 8 个参与研究(n=55143)的龋齿经验数据进行协调的应用。我们证明,这些临床模式可以在多个队列之间转移,在每个研究中具有相似的相对贡献,因此是 GLIDE2 中扩展和多样化的多民族样本中进行遗传检测的主要目标。我们预计 GLIDE2 的结果将果断推进口腔、牙齿和颅面健康和疾病中发挥作用的机制知识库,并进一步促进国际合作以及基因组学研究中的数据和资源共享。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a3f/9516631/c6fae2edca09/10.1177_00220345221109775-fig1.jpg

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