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Outcomes of children with juvenile idiopathic arthritis-associated uveitis

Outcomes of children with juvenile idiopathic arthritis-associated uveitis
幼年特发性关节炎相关葡萄膜炎儿童的结局
批准号:
8913977
负责人:
Sheila Therese Angeles-Han
金额:
$14.76万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-09-01 至 2016-11-07
关键词:
AcademyAffectAfricanAfrican AmericanAgeAlgorithmsAllelesAmericanAntinuclear AntibodiesArthritisAutoimmune DiseasesAutoimmune ProcessAwardBlindnessCataractCellsCharacteristicsChildChildhoodChronic Childhood ArthritisChronic DiseaseClinicalCohort StudiesComplementComplicationDataDatabasesDetectionDevelopmentDiagnosisDiseaseEarly DiagnosisEpidemiologyEtiologyEuropeanEvaluationEyeEye diseasesFlareGeneticGenetic PolymorphismGenetic RiskGlaucomaGoalsGuidelinesHLA-B27 AntigenHLA-DR1 AntigenHealthHealthcareImpact evaluationImpairmentInflammatoryInstitutionInterventionLeadMaster of ScienceMeasurementMeasuresMedical RecordsMentorsMonitorOnset of illnessOphthalmologistOphthalmologyOutcomeOutcome MeasureOutcomes ResearchPathogenesisPatient-Focused OutcomesPatientsPediatricsPhysically HandicappedPlayPopulationPredispositionProspective StudiesProteinsPsyche structureQuality of lifeQuestionnairesRaceResearchResourcesRheumatismRheumatologyRiskRisk FactorsRisk MarkerRoleSchemeScientistSecondary toSeveritiesSeverity of illnessSocial FunctioningStandardizationStratificationSymptomsTherapeuticUnited StatesUniversitiesUpdateUveitisVariantVisionVision DisordersVisitVisualVisual AcuityVisual impairmentaggressive therapybasecareerclinical epidemiologyclinical investigationclinical riskcohortdesigndisabilitydisorder riskexperiencegenetic risk factorglobal healthillness lengthimprovedlongitudinal coursepreventprofessorprospectivepsychologicpsychosocialrheumatologistrisk variantscreeningtertiary caretool

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Project Summary Juvenile idiopathic arthritis-associated uveitis (JIA-U) is an inflammatory eye disease that affects 20% of children with JIA and can lead to cataracts, glaucoma, vision loss and blindness. Current screening guidelines are designed to identify children at risk for eye disease in JIA. However, pediatric rheumatologists' and ophthalmologists' ability to provide comprehensive screening for uveitis is limited because the guidelines have not been updated to include all juvenile arthritis subtypes and other known risk factors for vision-limiting complications of JIA. Screening in JIA and other related autoimmune diseases of childhood is crucial because early uveitis detection can prevent visual complications and influence therapeutic management. Likewise, institution of early aggressive therapy when needed may avert serious visual complications. To improve health outcomes and quality of life of children with JIA-U, we need a better understanding of risk factors for uveitis, long-term visual outcomes, and the effects of visual and physical disability on children's lives. Early and accurate identification of JIA-U through the identification of risk factors for susceptibility and severity of uveitis, standardization of outcome measures, and elucidation of the significance of HLA risk alleles would improve the evaluation of the impact of JIA-U and the understanding of disease etiology, pathogenesis and outcome. Likewise, an improved risk stratification scheme could reduce unnecessary ophthalmology visits and help us identify children at greater risk for severe eye disease and complications. The objectives of this study are to 1) Identify differences in the clinical characteristics and course of JIA-U in patients of European and African descent in children with JIA to identify clinical and genetic risk markers for uveitis, 2) Examine the risk factors identified over a 4-year prospective study of a cohort of children diagnosed with early JIA to determine which factors are associated with eventual development of uveitis, and provide data on their longitudinal profile, 3) Determine the impact of having both arthritis and uveitis on physical and visual disability, vision-specific QOL, and overall QOL using subjective and objective measures. Using a comprehensive biologic, genetic and psychosocial approach, we hope to develop more widely applicable risk stratification schemes based on JIA subtype, and to identify new risk factors that will identify the populations of children at greatest risk for severe disability and blindness so that interventions can be developed to improve their overall outcome. The candidate is a pediatric rheumatologist and an assistant professor of pediatrics at Emory University. She has obtained a Masters of Science in Clinical Investigation. She is devoted to a career in clinical outcomes research in children with autoimmune eye diseases. She has assembled an outstanding mentoring team with experience in pediatric rheumatology, pediatric ophthalmology, pediatric epidemiology, outcomes research and measurement, which are relevant to her objectives. This mentored award will help her become a successful independent clinician scientist.
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  • 财政年份:
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