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Longitudinal multi-omics of host- microbe dynamics in prediabetes

机译:糖尿病前期宿主微生物动力学的纵向多组学

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摘要

Type 2 diabetes mellitus (T2D) is a growing health problem, but little is known about its early disease stages, its effects on biological processes or the transition to clinical T2D. To understand the earliest stages of T2D better, we obtained samples from 106 healthy individuals and individuals with prediabetes over approximately four years and performed deep profiling of transcriptomes, metabolomes, cytokines, and proteomes, as well as changes in the microbiome. This rich longitudinal data set revealed many insights: first, healthy profiles are distinct among individuals while displaying diverse patterns of intra- and/or inter-personal variability. Second, extensive host and microbial changes occur during respiratory viral infections and immunization, and immunization triggers potentially protective responses that are distinct from responses to respiratory viral infections. Moreover, during respiratory viral infections, insulin-resistant participants respond differently than insulin-sensitive participants. Third, global co-association analyses among the thousands of profiled molecules reveal specific host-microbe interactions that differ between insulin-resistant and insulin-sensitive individuals. Last, we identified early personal molecular signatures in one individual that preceded the onset of T2D, including the inflammation markers interleukin-1 receptor agonist (IL-1RA) and high-sensitivity C-reactive protein (CRP) paired with xenobiotic-induced immune signalling. Our study reveals insights into pathways and responses that differ between glucose-dysregulated and healthy individuals during health and disease and provides an open-access data resource to enable further research into healthy, prediabetic and T2D states.
机译:2型糖尿病(T2D)是一个日益严重的健康问题,但对其早期疾病阶段,其对生物学过程的影响或向临床T2D的转变知之甚少。为了更好地了解T2D的最早阶段,我们从106名健康个体和患有糖尿病的个体中获取了大约四年的样本,并对转录组,代谢组,细胞因子和蛋白质组以及微生物组的变化进行了深度分析。这种丰富的纵向数据集揭示了许多见解:首先,健康的个人资料在个体之间是不同的,同时显示出人际和/或人际变异的各种模式。其次,在呼吸道病毒感染和免疫过程中会发生大量的宿主和微生物变化,而免疫接种会触发潜在的保护性反应,这不同于对呼吸道病毒感染的反应。此外,在呼吸道病毒感染期间,胰岛素抵抗参与者的反应与胰岛素敏感性参与者不同。第三,在数千个分析分子之间进行的全局共缔合分析揭示了在胰岛素抵抗和胰岛素敏感性个体之间特定的宿主微生物相互作用。最后,我们确定了T2D发作之前一个人的早期个人分子特征,包括炎症标志物白细胞介素1受体激动剂(IL-1RA)和高敏感性C反应蛋白(CRP)与异种生物诱导的免疫信号配对。我们的研究揭示了在健康和疾病期间葡萄糖失调和健康个体之间差异途径和反应的见解,并提供了开放获取的数据资源,以使您能够进一步研究健康,糖尿病前期和T2D状态。

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  • 来源
    《Nature》 |2019年第7758期|663-671|共9页
  • 作者单位

    Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA;

    Jackson Lab Genom Med, Farmington, CT 06032 USA|UConn Hlth, Dept Med, Farmington, CT USA;

    Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA;

    Jackson Lab Genom Med, Farmington, CT 06032 USA;

    Stanford Univ, Dept Elect Engn, Stanford, CA 94305 USA;

    Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA;

    Jackson Lab Genom Med, Farmington, CT 06032 USA;

    Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA;

    Jackson Lab Genom Med, Farmington, CT 06032 USA;

    Jackson Lab Genom Med, Farmington, CT 06032 USA;

    Jackson Lab Genom Med, Farmington, CT 06032 USA;

    Jackson Lab Genom Med, Farmington, CT 06032 USA;

    Jackson Lab Genom Med, Farmington, CT 06032 USA;

    Jackson Lab Genom Med, Farmington, CT 06032 USA;

    Jackson Lab Genom Med, Farmington, CT 06032 USA;

    Jackson Lab Genom Med, Farmington, CT 06032 USA;

    Jackson Lab Genom Med, Farmington, CT 06032 USA;

    Jackson Lab Genom Med, Farmington, CT 06032 USA;

    Stanford Ctr Genom & Personalized Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA;

    Jackson Lab Genom Med, Farmington, CT 06032 USA;

    Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA;

    Stanford Univ, Div Endocrinol, Sch Med, Stanford, CA 94305 USA;

    Stanford Univ, Div Endocrinol, Sch Med, Stanford, CA 94305 USA;

    Stanford Univ, Div Endocrinol, Sch Med, Stanford, CA 94305 USA;

    Stanford Univ, Div Endocrinol, Sch Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA|Stanford Ctr Genom & Personalized Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA|Stanford Ctr Genom & Personalized Med, Stanford, CA 94305 USA|Stanford Diabet Res Ctr, Stanford, CA 94305 USA;

    Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA;

    Vet Affairs Palo Alto Hlth Care Syst, Spinal Cord Injury Serv, Palo Alto, CA USA|Stanford Univ, Dept Neurosurg, Sch Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA;

    Providence Canc Ctr, Earle A Chiles Res Inst, Portland, OR USA;

    Univ Toronto, Donnelly Ctr Cellular & Biomol Res, Toronto, ON, Canada;

    Stanford Univ, Dept Elect Engn, Stanford, CA 94305 USA;

    Stanford Univ, Div Endocrinol, Sch Med, Stanford, CA 94305 USA|Stanford Diabet Res Ctr, Stanford, CA 94305 USA;

    Jackson Lab Genom Med, Farmington, CT 06032 USA;

    Jackson Lab Genom Med, Farmington, CT 06032 USA;

    Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA|Stanford Ctr Genom & Personalized Med, Stanford, CA 94305 USA|Stanford Diabet Res Ctr, Stanford, CA 94305 USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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