Infant Viral Exposure and Risk of Childhood Asthma
Infant Viral Exposure and Risk of Childhood Asthma
批准号:
7273665
负责人:
PINGSHENG WU
金额:
$4.88万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-08-01 至 2008-07-31
关键词:
AccountingAddressAgeAsthmaBirth CertificatesBlood CirculationBronchiolitisChildChildhoodChildhood AsthmaChronicCohort StudiesComplexConditionDataData SetDevelopmentDoctor of PhilosophyEnrollmentEnvironmental Risk FactorEtiologyExposure toFamily history ofGoalsGrowth and Development functionHigh PrevalenceHospitalizationImmuneImmune responseIncidenceInfantInfectionInfection preventionLifeLinkLower Respiratory Tract InfectionLungMaternal ExposureMedicaidModelingMorbidity - disease rateNumbersOutcomePatternPopulationPredispositionPreventiveRecording of previous eventsRelative (related person)ResearchResearch InfrastructureRiskRisk FactorsSeveritiesSmokeSurrogate MarkersSystemTennesseeTestingThinkingTimeTobaccoTrainingViralViral BronchiolitisVirus DiseasesWheezingadministrative databaseairborne allergenbasecohortexperienceinfancymaternal cigarette smokingpreventprogramsrapid growthrespiratoryrespiratory virus
中文摘要
描述(由申请人提供):本研究申请的目的是探索婴儿期病毒暴露强度对5岁时哮喘发生的影响,并确定婴儿期季节性呼吸道病毒感染增加儿童哮喘易感性的关键时间段。使用与出生证明相关的田纳西州医疗补助索赔数据的既定研究基础设施,我们将使用训练数据集确定与儿童哮喘高风险相关的关键年龄段。病毒暴露强度和婴儿年龄对儿童哮喘发展的关系将在单独的测试数据集中进行检查。此外,婴儿病毒暴露与母亲哮喘(家族性风险因素)和母亲吸烟(环境风险因素)之间的潜在相互作用将被检查。将应用限制性三次样条来确定病毒暴露年龄、强度和儿童哮喘发展之间的平滑关系。这项研究的意义涉及到潜在的识别关键时间段,在此期间,预防感染可以预防或改变易感宿主的哮喘表型表达。
英文摘要
DESCRIPTION (provided by applicant): The objective of this research application is to explore the influence of viral exposure intensity during infancy on the development of asthma by age five years, and to identify critical time periods in infancy during which seasonal respiratory viral infection increases susceptibility to develop childhood asthma. Using the established research infrastructure of the Tennessee Medicaid claims data linked to birth certificates, we will determine the critical age periods associated with high risk of developing childhood asthma using a training dataset. The relationship of viral exposure intensity and infant age on development of childhood asthma will be examined in a separate test dataset. Furthermore, the potential interaction effects between infant viral exposure and maternal asthma (familial risk factor) and maternal smoking (environmental risk factor) will be examined. Restricted cubic splines will be applied to determine the smooth relationship between viral exposure age, intensity and the development of childhood asthma. The implications of this research relate to the potential for identifying critical time periods during which preventing infection could prevent or alter the phenotypic expression of asthma in predisposed hosts.
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海外基金