DETECTION AND DISCOVERY OF VIRUSES IN PEDIATRIC ACUTE LIVER FAILURE
DETECTION AND DISCOVERY OF VIRUSES IN PEDIATRIC ACUTE LIVER FAILURE
批准号:
9089919
负责人:
DAVID WANG
金额:
$19.06万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2015
资助国家:
美国
项目状态:
已结题
起止时间:
2015-07-01 至 2018-06-30
关键词:
Acute Liver FailureBioinformaticsBiological AssayCessation of lifeCharacteristicsChildChildhoodClinicalComplementCountryCritical IllnessDataDetectionDiagnosisDiagnosticDiseaseEtiologyFundingGoalsHealthHepaticInfectionLeadLifeLiverLiver FailureMethodsPathogenesisPatientsPlayPrevalenceRNA SequencesRare DiseasesResourcesReverse Transcriptase Polymerase Chain ReactionRiskRoleSamplingSecondary toSerumSeverity of illnessSiteSpecimenStratificationTestingTissuesUnited States National Institutes of HealthViral GenomeVirusVirus Diseasescase controlclinical biomarkerscohortdisorder subtypeliver transplantationnext generation sequencingnovelnovel virusoutcome forecastpathogenrepositorysuccess
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Pediatric acute liver failure (PALF) is a life threatening disorder in which previously healthy children become critically ill secondary to rapid loss of hepatic function. The ongoing, multi-center, NIH-funded PALF Study Group was started in 1999 with the goal of studying the etiology, pathogenesis, diagnosis, prognosis and treatment of acute liver failure in children. Strikingly, approximately 40% of the subjects in the PALF cohor have no final specific etiologic diagnosis ("indeterminate") for their hepatic failure. It is likel that unrecognized viral infection may play a critical role in the etiology of liver failure in at least ome of these subjects. In this proposal, state-of-the-art methods for pathogen discovery will be used to evaluate liver and serum specimens from PALF patients for the presence of viruses. This patient cohort is unique, and represents the largest repository of specimens from PALF patients in the world. Specifically, ultra-high throughput Next Generation sequencing will be used in conjunction with a customized bioinformatics analysis pipeline to define the spectrum of viruses, both known and novel, present in the indeterminate cases. Any such viruses detected would be potential candidate etiologic agents of PALF. As a first step towards establishing an association with PALF, case-control analyses will be performed to define prevalence of each of these agents in serum of unexplained PALF cases as compared to PALF cases with non-infectious etiologies as well as to healthy controls.
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会议论文
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