Clinical, Radiologic and Biochemical Factors Related to Diabetes Development after Acute Pancreatitis
Clinical, Radiologic and Biochemical Factors Related to Diabetes Development after Acute Pancreatitis
批准号:
10264897
负责人:
ZHAOLI SUN
金额:
$28.66万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
未结题
起止时间:
2020-09-16 至 2025-07-31
关键词:
AcuteAcute Necrotizing PancreatitisAddressAntibodiesAutoantibodiesAutoantigensAutoimmune DiabetesAutoimmune DiseasesAutoimmune ResponsesAutologous TransplantationBeta CellBiochemicalBiological MarkersBiopsy SpecimenClinicalClinical DataClinical/RadiologicCollectionCommunicable DiseasesDevelopmentDiabetes MellitusDiabetes autoantibodiesDiseaseDisease ProgressionFatty acid glycerol estersFunctional disorderFutureGlucagonGoalsHospitalsHumanHypoglycemiaImageImpairmentIncidenceIndividualInflammatoryInsulinInsulin-Dependent Diabetes MellitusLeadLifeMachine LearningMalignant NeoplasmsMediatingMeta-AnalysisMethodologyModelingMorbidity - disease rateOrganOrgan failurePancreasPancreatic DiseasesPathologyPatientsPrediabetes syndromeProcessProteomeProteomicsPublic HealthRadiology SpecialtyRecording of previous eventsRecoveryRecurrenceResearchResearch DesignResearch PersonnelResolutionResourcesRisk FactorsRoleSerologySerumSystemic Inflammatory Response SyndromeTechniquesTechnologyTextureTimeTotal PancreatectomyVisceralX-Ray Computed Tomographyacute pancreatitisbasebiomarker identificationclinical centerclinical riskexperiencefollow-upimpaired glucose toleranceimprovedisletmacrovascular diseasemodel developmentmortalitynovelnutrient absorptionpredictive modelingradiological imagingradiomicssubcutaneoussystematic review
中文摘要
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英文摘要
Abstract
Nearly 40% of patients develop diabetes after an initial episode of acute pancreatitis (AP). Various studies have
evaluated risk factors for the development of diabetes but they have shown inconsistent findings, suggesting
methodologic shortcomings. The present proposal consists of three specific aims where we will attempt to
determine the biochemical, radiologic and clinical factors related to the development of diabetes after AP. Aim
1: To identify autoantibodies associated with the progression of type 1 diabetes in patients after AP using a large
human proteome array. Aim 2: To study the role of imaging, more specifically quantitative textural analysis to
predict the development of type 1 diabetes after AP. Aim 3 is to build a machine learning model to predict type
1 diabetes after AP using patient-related risk factors, textural analysis on imaging and autoantibodies involved
in disease progression. Our proposal will help us better understand diabetes after AP. Successful completion
of this study has the potential to improve management for AP.
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依托单位:
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