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Chronic Rhinosinusitis Integrative Studies Program (CRISP)

Chronic Rhinosinusitis Integrative Studies Program (CRISP)
慢性鼻窦炎综合研究计划 (CRISP)
批准号:
8551061
负责人:
Robert P Schleimer
金额:
$170.83万
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-08-05 至 2018-07-31
关键词:
AccountingAddressAdrenal Cortex HormonesAffectAllergic rhinitisAmericanAntibioticsArchitectureAreaAsthmaAutoantibodiesAutoimmune ProcessAutoimmune ResponsesAutoimmunityAutomobile DrivingCandidate Disease GeneCell LineageChicagoChronic DiseaseChronic Obstructive Airway DiseaseClinicClinicalClinical ResearchCollaborationsCommon ColdCommunitiesCountyDataDevelopmentDiagnosisDirect CostsDiseaseDisease remissionDrainage procedureElectronic Health RecordElementsEnvironmental ExposureEnvironmental Risk FactorEpidemiologic StudiesEpidemiologyEpigenetic ProcessEpithelial CellsEtiologyFacial PainFacilities and Administrative CostsFailureGeneral PopulationGenesGeneticGenetic PolymorphismGenetic Predisposition to DiseaseGoalsHealth Care CostsHealth systemHeterogeneityHumanImmunologyIncidenceIndividualInflammationInstitutionInstructionInvestmentsKnowledgeLaboratoriesLongitudinal StudiesMeasurementMedicalMolecularMucous MembraneNasal PolypsNasal obstruction present findingNatural HistoryNoseOperative Surgical ProceduresOutcomePathogenesisPathologyPatient Self-ReportPatientsPatternPennsylvaniaPopulationPredispositionPrevalencePrimary Health CareQuality of lifeResearchResourcesRhinovirusRiskRisk FactorsRoleSamplingSeveritiesSinusSiteSmell PerceptionSpontaneous RemissionSymptomsSystemTestingTherapeuticUniversitiesValidationViralbasechronic rhinosinusitiscohortcostdata managementdisease phenotypeepidemiology studygenetic epidemiologyhealth care service utilizationimprovednovelnovel strategiesnovel therapeuticspathogenpopulation basedpressureprogramsresponsetertiary caretooltrait

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中文摘要
翻译
描述(申请人提供):慢性鼻-鼻窦炎(CRS)影响着近3000万美国人,每年的直接成本约为60亿美元,每年负责近50万次手术。对CRS的研究投入不大,我们对CRS的流行病学、遗传学和发病机制的了解也很初级。慢性鼻窦炎综合研究计划(CRISP)的一个主要目标是进行高度协作的研究,以发展与CRS易感性和严重性有关的基因多态的基础知识;状态、特征、环境风险因素和 CRS的成本;以及严重顽固性疾病的恶化机制和免疫学基础。CRISP有五个主要要素。核心A是由该计划的PI罗伯特·施莱默博士领导的行政核心;核心B是由罗伯特·科恩博士领导的临床、实验室和数据管理核心;项目1研究 由Brian Schwartz博士领导;项目2研究CRS的免疫学和 项目3侧重于CRS的遗传学,由Carole Ober博士领导。项目1中的研究确定了盖辛格卫生系统(GHS)大规模(300,000)初级保健人群中CRS的流行病学。芝加哥大学项目3的遗传学研究利用来自项目1的2000名患者和对照的样本来识别CRS疾病基因,并将遗传学与疾病状态、严重程度和环境暴露联系起来。遗传学研究的候选基因将通过一个新的系统遗传学发现平台被发现,该平台基于项目3和项目2的合作。项目1和项目2的合作将评估与CRS恶化相关的病原体以及自身免疫在驱动严重疾病中的作用。项目2还将测试B系细胞和鼻腔自身免疫反应在严重顽固性CRS病因中的重要性。这些合作研究将利用改进的疾病亚表型定义来确定未被识别的遗传易感性以及导致CRS的发展和严重程度的重要分子和细胞机制。 相关性:慢性鼻窦炎综合研究计划(CRISP)统一并整合了三个世界级的研究小组,以了解慢性鼻窦炎的流行病学、遗传学和病理学。CRISP建议利用西北大学、芝加哥大学和盖辛格健康系统的人群队列、专业知识和资源进行高度互动的研究,以促进我们对慢性鼻窦炎的了解,并为新的治疗策略指明方向。 项目1:在基于人群的研究中使用新的验证方法的慢性阻塞性肺病流行病学 项目负责人(PL):施瓦茨,布莱恩·S。 描述(由申请人提供):CRS是一种致残性疾病,与高昂的直接和间接成本相关,但人们对其流行病学、病原学异质性以及个人和社会负担知之甚少。在理解如何确定CRS的研究需求和改善患者结果方面存在着很大的差距。该项目将利用盖辛格诊所的独特数据和人口资产,包括宾夕法尼亚州30多个县的40万名初级保健人口,完成CRS的大规模流行病学研究。我们将把纵向自我报告和电子健康记录数据与新的临床和研究措施结合起来,以解决理解上的差距。虽然对慢性阻塞性肺疾病的自然病史知之甚少,但有一点是清楚的:在普通人群中,许多患者有鼻腔和鼻窦症状;其中一些患者被诊断为过敏性鼻炎或急性呼吸综合征发作(症状持续7天至4周,以消除普通感冒患者);其中一些患者进展到慢性阻塞性肺疾病,症状至少持续12周;许多慢性阻滞性鼻炎患者有发作,症状显著恶化超过基线;许多患者,特别是在三级中心就诊的患者, 顽固性CRS;自然病史必须包括一些治疗性的,可能是自发的 减刑。每个步骤的发病率、患病率、转换率和风险因素 框架并不为人所熟知。由于以人群为基础的样本研究相对较少,很可能大多数研究都集中在治疗失败的患者,即顽固性群体。在拟议的研究中,我们将使用代表CRS全谱的普通人群样本的临床验证标准来估计CRS的患病率、发病率和缓解;描述CRS的恶化和缓解模式以及解释变异性的因素;确定CRS合并鼻息肉病例和不合并鼻息肉病例之间的差异;使用关键环境条件的现有地理空间数据评估CRS的各种社区环境风险因素;以及估计CRS的直接和间接成本。 相关性:慢性鼻-鼻窦炎是一种常见的疾病,可导致患者出现严重症状。它涉及副鼻窦炎症,导致面部疼痛/压力、鼻和鼻窦引流、嗅觉丧失和鼻塞。然而,关于有多少人患有这种疾病,谁感染了这种疾病,他们为什么患有这种疾病,以及治疗这种疾病的最佳方法,人们知之甚少。拟议的研究将解决其中许多问题。
英文摘要
DESCRIPTION (provided by applicant): Chronic rhinosinusitis (CRS) affects nearly 30 million Americans, has direct costs of approximately $6B annually and is responsible for almost 500,000 surgeries per year. Investment in research on CRS has been modest and our knowledge of the epidemiology, genetics and pathogenesis of CRS is rudimentary. A major goal of the Chronic Rhinosinusitis Integrative Studies Program (CRISP) project is to perform highly collaborative studies to develop fundamental knowledge on the genetic polymorphisms responsible for CRS susceptibility and severity; the states, traits, environmental risk factors and costs of CRS; and the mechanisms of exacerbations and immunological basis of severe recalcitrant disease. CRISP has five main elements. Core A is the administrative Core led by Dr. Robert Schleimer, the PI of the program; Core B is the Clinical, Laboratory and Data Management Core led by Dr. Robert Kern; Project 1 studies the Epidemiology of CRS and is led by Dr. Brian Schwartz; Project 2 studies the Immunology of CRS and mechanisms of exacerbation and is led by Dr. Schleimer; and Project 3 focuses on the Genetics of CRS and is led by Dr. Carole Ober. Studies in Project 1 define the epidemiology of CRS in a large (>300,000) primary care population at Geisinger Health Systems (GHS). The Genetics studies in Project 3, based at the University of Chicago, utilize samples from 2000 patients and controls from Project 1 to identify CRS disease genes and to associate genetics with disease states, severity and environmental exposures. Candidate genes for genetic studies will be discovered via a novel systems genetics discovery platform based on collaboration between Project 3 and Project 2. A collaboration between Project 1 and Project 2, based at Northwestern University, will assess the pathogens associated with exacerbations of CRS and the role of autoimmunity in driving severe disease. Project 2 will also test the importance of B lineage cells and nasal autoimmune responses in the etiology of severe recalcitrant CRS. These collaborative studies will leverage an improved definition of sub-phenotypes of disease to identify unrecognized genetic susceptibilities and important molecular and cellular mechanisms responsible for the development and severity of CRS. RELEVANCE: The Chronic Rhinosinusitis Integrative Studies Program (CRISP) unifies and integrates three world-class research groups to understand the epidemiology, genetics and pathology of chronic rhinosinusitis. CRISP proposes highly interactive studies that leverage the population cohorts, expertise and resources of groups at Northwestern University, the University of Chicago and the Geisinger Health Systems in order to advance our understanding of chronic rhinosinusitis and point the way toward new therapeutic strategies. Project 1: CRS Epidemiology Using New Approaches to Validation in Population-based Studies Project Leader (PL): Schwartz, Brian S. DESCRIPTION (provided by applicant): CRS is disabling and is associated with high direct and indirect costs, yet little is known about the epidemiology, etiologic heterogeneity, and individual and societal burden. There is a substantial gap in understanding how to frame research needs for CRS and improve patient outcomes. This project will complete a large-scale epidemiologic study of CRS by leveraging the unique data and population assets of the Geisinger Clinic, including a primary care population of 400,000 patients in over 30 counties in Pennsylvania. We will combine longitudinal self-reported and electronic health record data with new clinical and research measurements to address gaps in understanding. While relatively little is known about the natural history of CRS, it is clear that: many patients in the general population have nasal and sinus symptoms; some of these patients are diagnosed with allergic rhinitis or episodes of ARS (symptoms for 7d to 4wk, to eliminate patients with the common cold); some of these patients progress to CRS with symptoms present for at least 12 weeks; many patients with CRS have episodes of exacerbations, with a prominent worsening of symptoms over the baseline; many patients, especially those seen in tertiary centers, have recalcitrant CRS; and the natural history must include some therapeutic and probably spontaneous remissions. The incidence, prevalence, transition rates, and risk factors for each of the steps in the framework are not well known. Since relatively little research exists in population-based samples, it is likely that most studies have focused on patients who have failed therapy, the recalcitrant group. In the proposed research, we will estimate CRS prevalence, incidence, and remission using clinically validated criteria for general population samples that represent the ful spectrum of CRS; describe patterns of CRS exacerbation and remission and the factors that explain variability; determine how CRS with and without nasal polyps cases differ from each other; evaluate a variety of community environmental risk factors for CRS using existing geospatial data on key environmental conditions; and estimate the direct and indirect costs of CRS. RELEVANCE: Chronic rhinosinusitis is a common condition that can cause severe symptoms in patients. It involves inflammation of the paranasal sinuses that results in facial pain/pressure, nasal and sinus drainage, smell loss, and nasal obstruction. Little is known however about how many people have the condition, who gets it, why they get it, and the best ways to treat it. The proposed research will address many of these issues.
期刊论文(3)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1016/j.jaip.2016.04.008
发表时间: 2016-07
期刊: The journal of allergy and clinical immunology. In practice
影响因子: --
作者: [Bose S, Grammer LC, Peters AT]
通讯作者: Peters AT
DOI: 10.1002/alr.21526
发表时间: 2015-07
期刊: International forum of allergy & rhinology
影响因子: 6.4
作者: [Paz Silva M, Pinto JM, Corey JP, Mhoon EE, Baroody FM, Naclerio RM]
通讯作者: Naclerio RM
Reply to "correspondence to 'association between chronic rhinosinusitis and new onset asthma implications for prevention'".
回复“对应‘慢性鼻窦炎与新发哮喘之间的关联对预防的影响’”。
DOI: 10.1111/all.15984
发表时间: 2024
期刊: Allergy
影响因子: 12.4
作者: [Schwartz,BrianS, Hirsch,AnnemarieG, Bandeen-Roche,Karen, Kato,Atsushi, Schleimer,Robert]
通讯作者: Schleimer,Robert
Mechanisms of barrier dysfunction and tissue hyperplasia in CRS
Administrative Core
Mechanisms of barrier dysfunction and tissue hyperplasia in CRS
Chronic Rhinosinusitis Integrative Studies Program 2 (CRISP2)
  • 批准号:
    10225446
  • 项目类别:
  • 资助金额:
    $185.28万
  • 财政年份:
    2019
  • 负责人:
    Robert P Schleimer
  • 依托单位:
海外基金