Microbial Discovery and Immunity in ME/CFS
Microbial Discovery and Immunity in ME/CFS
批准号:
9102389
负责人:
MADY HORNIG
金额:
$76.62万
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:
2015-08-14 至 2017-07-31
关键词:
AbbreviationsAdvocateAgeAnimal ModelAntibodiesArthralgiaBacteriaBiological AssayBiomedical ResearchBloodBorna disease virusBorrelia burgdorferiCandida albicansChronic Fatigue SyndromeClinicalCognitionCommunitiesCoxiella burnetiiDataDatabasesDevelopmentDiagnosisDiagnosticDiagnostic testsDiseaseEnsureEnterovirusEtiologyFamilyFatigueFecesFoundationsFutureGeographyHeadacheHealthHigh-Throughput Nucleotide SequencingHuman Herpesvirus 4Human Herpesvirus 6ImmuneImmunityInfectionInfectious AgentInfectious Disease EpidemiologyInterventionLaboratoriesLeadLinkLower Gastrointestinal TractLymphatic DiseasesMedicalMedical Care CostsMemoryMethodsMicrobeMulticenter StudiesMyalgiaMycoplasma pneumoniaeNational Institute of Allergy and Infectious DiseaseNight SweatingNucleic AcidsNucleotidesOralOropharyngealPatient advocacyPatientsPeripheral Blood Mononuclear CellPhysical ExaminationPlasmaPopulationPositioning AttributePrevalencePreventionRecording of previous eventsRecruitment ActivityReportingResearchResearch PersonnelResource AllocationRetroviridaeRibosomal RNARiskSamplingSequence AnalysisSerologic testsSerologicalSiteSocioeconomic StatusSore ThroatSurveysSwabSymptomsTestingTherapeutic InterventionTimeTranslational ResearchViralVirusWorkcase controlcostexperiencefollow-upfungusmicrobialpathogenpreventrepositorysample collectionsexvirome
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Myalgic Encephalomyelitis/Chronic Fatigue Syndrome is an idiopathic disabling disorder characterized by persistent, unexplained fatigue in association with impaired memory or cognition, muscle or joint pain, headache, sore throat, tender lymphadenopathy and night sweats. The prevalence in the US is estimated at over 200 cases/100,000 population with annual medical care costs of $24 billion. There is no specific diagnostic test or treatment. Although the majority of cases are sporadic, there are reports of geographic and temporal clusters of CFS and many subjects report a viral prodrome and symptoms consistent with an infection. Efforts to identify causative agents have yielded inconsistent results and in some instances culminated in false leads that polarized the patient advocate and biomedical research communities, led to inappropriate allocation of resources and placed patients at risk for inappropriate therapeutic interventions. This project will test the hypothesis that CFS cases and controls differ with respect to bacterial, fungal or viral microflora
in the oropharynx, lower gastrointestinal tract and blood in a well-powered study, using rigorously characterized cases and controls and state-of-the-art methods for microbial surveillance and discovery. Our proposal builds on the foundation established during the NIAID CFS multicenter study of XMRV/pMLV. It includes the expert clinicians who led work at the original six sites, thereby ensuring credibility within the scientific and CFS patient and advocacy
communities and access to a network within which follow-up studies and translational research can be readily pursued. The laboratory team has extensive experience in infectious disease epidemiology, microbial discovery and de-discovery, as well as in the development of serological assays and animal models needed to test for causal relationships and investigate pathogenetic mechanisms.
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会议论文
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海外基金