Influence of the Enteric Microbiome on the Genesis of Bronchopulmonary Dysplasia

肠道微生物组对支气管肺发育不良发生的影响

• 批准号: 8068836
• 负责人: THOMAS W FERKOL
• 金额: $ 47.7万
• 依托单位: WASHINGTON UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-05-01 至 2015-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8068836
• 关键词: 1 year old; Adrenal Cortex Hormones; Alleles; Allergic rhinitis; Bacteria; Biomass; Blood Vessels; Bronchodilator Agents; Bronchopulmonary Dysplasia; Candidate Disease Gene; Cessation of life; Chronic; Clinical Research; DNA; Data; Dependence; Development; Early treatment; Echocardiography; Enteral; Gastrointestinal tract structure; Genes; Human Microbiome; Infant; Instruction; Intervention; Intestines; Life; Link; Lung; Lung Inflammation; Measures; Mediating; Messenger RNA; Metagenomics; Morbidity - disease rate; Mothers; Necrotizing Enterocolitis; Neonatal; Newborn Infant; Organism; Outcome; Pathogenesis; Play; Polysomnography; Pregnancy; Premature Birth; Prevention; Pulmonary Vascular Resistance; Pulmonary function tests; Recurrence; Research; Research Proposals; Risk; Role; Sampling; Severities; Shotgun Sequencing; Specimen; Technology; Testing; Time; Transcript; Universities; Washington; Wheezing; abstracting; adverse outcome; atopy; design; genome sequencing; gut microbiota; lung development; member; microbial; microbial community; microbiome; next generation; postnatal; premature; prevent

DESCRIPTION (provided by applicant): Bronchopulmonary dysplasia (BPD) results from disrupted lung development after premature birth and results in life long pulmonary morbidity. Intrauterine and postnatal lung inflammation contribute to structural airway simplification and increased pulmonary vascular resistance, critical components of BPD. The Human Microbiome Project is designed to understand the interactions between microbial communities that inhabit a host and the host itself. Emerging data suggest that imbalances between components of commensal organisms in the gastrointestinal tract are associated with atopy, allergic rhinitis, or recurrent wheezing. These data prompt consideration of the role for gut microbiota-mediated lung inflammation as a trigger for BPD. In this single center project, limited polysomnography and echocardiography will be used to non- invasively and longitudinally assess airspace and pulmonary vascular development in premature newborns < 30 weeks' gestation who are at risk for developing BPD to test the hypothesis that signatures of the neonatal enteric microbiome are associated with BPD-related adverse pulmonary outcomes, including death, technology dependence, and need for bronchodilators or corticosteroids at 36 weeks and 1 year of age. Ongoing, parallel initiatives at Washington University that are characterizing the enteric microbiome of premature newborns will be leveraged to explore associations between this biomass and the development of BPD-related adverse pulmonary outcomes. The Specific Aims are: 1) utilize existing data to determine differences in the composition of the microbiota between groups of linked mothers and premature newborns with and without BPD, and 2) utilize existing data to determine differences in the metagenomic and/or transcriptional repertoire of the enteric microbiota between linked mothers and premature newborns with and without BPD. The metagenomic and transcriptional differences identified in Specific Aim II that are associated with adverse pulmonary outcomes will permit identification of factors that are amenable to early intervention and prevention of BPD, and furthermore, will inform selection of candidate gene networks that can be interrogated for the multicenter component of this proposal in which next generation sequencing will be used to identify the interactions between and among alleles of the infant and microbiota that are associated with BPD-related adverse pulmonary outcomes. RELEVANCE (See instructions): The proposed studies will evaluate whether bacteria in the intestinal tract of premature newborns play a role in the development of bronchopulmonary dysplasia, the most significant chronic lung problem of prematurity. Identifying the role that these bacteria play will permit early treatment in an effort to prevent the development of these lung problems. (End of Abstract)

描述（由申请人提供）：支气管肺发育不良（BPD）是由早产后肺部发育中断引起的，并导致终生肺部发病率。宫内和产后肺部炎症有助于结构性气道简化和肺血管阻力增加，这是BPD的关键组成部分。人类微生物组计划旨在了解居住在宿主和宿主本身的微生物群落之间的相互作用。新出现的数据表明，胃肠道中共生生物成分之间的不平衡与特应性、变应性鼻炎或复发性喘息有关。这些数据促使人们考虑肠道菌群介导的肺部炎症作为BPD触发因素的作用。在这个单中心项目中，有限的多导睡眠图和超声心动图将用于无创和纵向评估妊娠< 30周、有BPD风险的早产新生儿的空气和肺血管发育，以验证新生儿肠道微生物组特征与BPD相关的不良肺部结局(包括死亡、技术依赖、在36周龄和1岁时需要支气管扩张剂或皮质类固醇。华盛顿大学正在进行的研究早产儿肠道微生物群特征的平行项目将被用来探索这种生物量与bpd相关不良肺部结局发展之间的关系。具体目标是：1)利用现有数据确定关联母亲和患有和不患有BPD的早产儿之间微生物群组成的差异；2)利用现有数据确定关联母亲和患有和不患有BPD的早产儿之间肠道微生物群宏基因组和/或转录库的差异。特异性目标II中确定的与不良肺结局相关的宏基因组和转录差异将允许识别适合早期干预和预防BPD的因素，此外，将为候选基因网络的选择提供信息，这些候选基因网络可用于本提案的多中心组成部分，其中下一代测序将用于确定与bpd相关的不良肺结局相关的婴儿和微生物群等位基因之间的相互作用。