University of Miami IBD Genetic Research Center: Understanding the Genetic Architecture of IBD in the LatinX Community
迈阿密大学 IBD 基因研究中心:了解拉丁裔社区 IBD 的遗传结构
基本信息
- 批准号:10543290
- 负责人:
- 金额:$ 53.6万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2022
- 资助国家:美国
- 起止时间:2022-09-30 至 2027-06-30
- 项目状态:未结题
- 来源:
- 关键词:ATAC-seqAdmixtureAffectAfrican AmericanAgeAge of OnsetAllelesAmericanBiologicalBlack PopulationsCaucasiansCellsCharacteristicsChromatinChronicClinicalClinical TrialsCollectionColonCommunitiesCountryCountyCrohn&aposs diseaseDataDatabasesDendritic CellsDevelopmentDietDiseaseEconomicsEnvironmentEnvironmental ExposureEpigenetic ProcessEuropeEuropeanFloridaFunctional disorderGene ExpressionGenerationsGenesGeneticGenetic DiseasesGenetic Predisposition to DiseaseGenetic ResearchGenetic RiskGenetic StructuresGenetic VariationGenetic studyGenomeGenomic approachGenomicsGenotypeGoalsGrantHispanicHispanic AmericansHispanic PopulationsImmigrantImmigrationImmuneImmune System DiseasesImmune responseImmunologicsIncidenceIndividualIndustrializationInflammationInflammatory Bowel DiseasesIntestinesKnowledgeLatin AmericaLatin AmericanLatinxLinkage DisequilibriumLocationMalignant NeoplasmsMapsMeasuresMediatingMedicalMethodsModificationMucosal Immune SystemMucositisMucous MembraneNational Institute of Diabetes and Digestive and Kidney DiseasesNorth AmericaNot Hispanic or LatinoOperative Surgical ProceduresPathogenesisPathogenicityPathway interactionsPatientsPatternPhagocytesPharmaceutical PreparationsPhenotypePopulationPreventionPropertyPublishingResearchResolutionRiskRoleSentinelSeveritiesSusceptibility GeneTexasUlcerative ColitisUniversitiesWorkcohortdisabilitydisease phenotypegene environment interactiongenetic approachgenetic architecturegenome wide association studygenomic locushealth datahispanic communityileumimprovedinterestintergenerationalmacrophagemicrobiomemultiple omicsneutrophilnovelrecruitresponserisk variantsample collectionsocialsocial health determinantstranscriptome sequencingtranscriptomics
项目摘要
PROJECT SUMMARY
Inflammatory bowel disease (IBD) is a common and devastating immune-mediated disease in which the
mucosal immune system abnormally recognizes the intestinal bacterial flora leading to chronic inflammation.
Approximately, 1% of the US population is affected. The causes of Crohn's disease (CD) and ulcerative colitis
(UC) lie in the interplay between host response genes and a microbiome with pathogenic properties. IBD
incidence has leveled off in the developed world and rising in the newly industrialized world. In the US, we are
witnessing a rising incidence in immigrants from low-risk parts of the world, particularly Hispanics. This provides
an opportunity for discovery of disease pathogenesis towards a goal of prevention and improved therapies.
Unfortunately, most genetic studies of IBD, including from the IBDGC, have focused on individuals of European
ancestry from North America and Europe. Moreover, most clinical trials of IBD medications include too few
Hispanics or Blacks and thus do not represent the totality of the affected population.
Our group has a dedicated research interest on IBD in Latin-American immigrants and American-born
Hispanic patients. We have published highly-cited studies of the genotype and phenotype of IBD in the Hispanic
population of South Florida. We have also described disparities in medication usage and surgical rates. Important
for the notion that IBD is caused by a gene-environment interaction, we have found that IBD is occurring faster
in the last 20 years in immigrants from Latin-America. We have been very successful in our collection efforts
because of our location and our commitment and engagement in the Hispanic community. We have a unique
opportunity and obligation to study this disease within the Hispanic population. Miami-Dade County is over 50%
Hispanic. The state of Florida has the 3rd largest Hispanic population and the most diverse in terms of countries
of origin. We are poised with the support of an IBDGC grant to expand our collection efforts to the broader state
of Florida. Genome-wide association studies (GWAS) have facilitated the discovery of previously unrecognized
genes and pathways in IBD and provided the opportunity for unbiased exploration of the genomes of patients
with IBD. We will explore genetic variation in a large set of US-born and foreign-born Hispanic IBD cases by
focusing on targeted genomic, transcriptomic, and epigenetic differences between immigrant and first-generation
Hispanic-Americans with IBD. We will edify how genes and environment interact to result in diverse phenotypic
manifestations of IBD. Our group has particular expertise and interest in methods to fine-map previously
identified risk loci and access the impact of local genetic ancestry on genotype-ancestry interactions in relation
to phenotypic characteristics, with the goal of identifying genetic variation of functional significance. Our
proposed studies will expand knowledge of disease phenotype and genetic underpinnings in IBD in this growing
Hispanic cohort in the hopes of developing prevention and improved treatment approaches.
We will use the complementary strengths of the two PIs to catapult discoveries and meet the goals of the
NIDDK IBD Genetics Consortium (IBDGC) to expand the collection of Hispanic IBD patients in the US.
项目概要
炎症性肠病(IBD)是一种常见且具有破坏性的免疫介导疾病,其中
粘膜免疫系统异常识别肠道菌群,导致慢性炎症。
大约 1% 的美国人口受到影响。克罗恩病 (CD) 和溃疡性结肠炎的病因
(UC)在于宿主反应基因和具有致病特性的微生物组之间的相互作用。炎症性肠病
发达国家的发病率已趋于平稳,而新兴工业化国家的发病率则呈上升趋势。在美国,我们是
来自世界低风险地区的移民,尤其是西班牙裔移民的发病率不断上升。这提供了
为实现预防和改进治疗目标而发现疾病发病机制的机会。
不幸的是,大多数 IBD 基因研究,包括来自 IBDGC 的研究,都集中在欧洲人身上。
血统来自北美和欧洲。此外,大多数 IBD 药物的临床试验涉及的数据太少。
因此,西班牙裔或黑人并不代表受影响人口的全部。
我们小组对拉丁美洲移民和美国出生的 IBD 有专门的研究兴趣
西班牙裔患者。我们发表了关于西班牙裔 IBD 基因型和表型的高被引研究
南佛罗里达州的人口。我们还描述了药物使用和手术率的差异。重要的
对于 IBD 是由基因与环境相互作用引起的观点,我们发现 IBD 发生得更快
过去 20 年来自拉丁美洲的移民。我们的收集工作非常成功
因为我们的地理位置以及我们对西班牙裔社区的承诺和参与。我们有独特的
在西班牙裔人群中研究这种疾病的机会和义务。迈阿密戴德县超过 50%
西班牙裔。佛罗里达州拥有第三大西班牙裔人口,也是最多元化的国家
原产地。我们准备在 IBDGC 拨款的支持下将我们的收集工作扩大到更广泛的州
佛罗里达州。全基因组关联研究(GWAS)促进了以前未被识别的发现
IBD 的基因和通路,并为公正地探索患者基因组提供了机会
患有炎症性肠病。我们将通过以下方式探索大量美国出生和外国出生的西班牙裔 IBD 病例的遗传变异:
重点关注移民和第一代之间的目标基因组、转录组和表观遗传差异
患有 IBD 的西班牙裔美国人。我们将阐明基因和环境如何相互作用以产生不同的表型
IBD 的表现。我们的团队对先前精细绘制地图的方法具有特殊的专业知识和兴趣
确定风险位点并了解当地遗传血统对基因型-血统相互作用的影响
表型特征,目的是识别具有功能意义的遗传变异。我们的
拟议的研究将扩大对 IBD 疾病表型和遗传基础的了解
西班牙裔队列希望制定预防措施和改进治疗方法。
我们将利用两个 PI 的互补优势来推动发现并实现
NIDDK IBD 遗传学联盟 (IBDGC) 将扩大美国西班牙裔 IBD 患者的收集范围。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Maria Teresa Abreu其他文献
Maria Teresa Abreu的其他文献
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{{ truncateString('Maria Teresa Abreu', 18)}}的其他基金
University of Miami IBD Genetic Research Center: Understanding the Genetic Architecture of IBD in the LatinX Community
迈阿密大学 IBD 基因研究中心:了解拉丁裔社区 IBD 的遗传结构
- 批准号:
10707450 - 财政年份:2022
- 资助金额:
$ 53.6万 - 项目类别:
Translational Research Training in Gastroenterology and Hepatology
胃肠病学和肝病学转化研究培训
- 批准号:
9906212 - 财政年份:2018
- 资助金额:
$ 53.6万 - 项目类别:
Translational Research Training in Gastroenterology and Hepatology
胃肠病学和肝病学转化研究培训
- 批准号:
10396477 - 财政年份:2018
- 资助金额:
$ 53.6万 - 项目类别:
Nanocarrier-targeted mesenchymal stem cells to treat inflammatory bowel disease
纳米载体靶向间充质干细胞治疗炎症性肠病
- 批准号:
9093326 - 财政年份:2016
- 资助金额:
$ 53.6万 - 项目类别:
INNATE IMMUNE PATHWAYS AND THE MICROBIOME IN HISPANICS WITH INFLAMMATORY BOWEL DISEASE
西班牙裔炎症性肠病患者的先天免疫途径和微生物组
- 批准号:
9106760 - 财政年份:2016
- 资助金额:
$ 53.6万 - 项目类别:
Role of TLR4 in Colitis Associated Neoplasia
TLR4 在结肠炎相关肿瘤中的作用
- 批准号:
8761283 - 财政年份:2014
- 资助金额:
$ 53.6万 - 项目类别:
Role of TLR4 and the microbiome in colitis associated neoplasia
TLR4 和微生物组在结肠炎相关肿瘤中的作用
- 批准号:
9906898 - 财政年份:2014
- 资助金额:
$ 53.6万 - 项目类别:
Role of TLR4 in Colitis Associated Neoplasia
TLR4 在结肠炎相关肿瘤中的作用
- 批准号:
9102094 - 财政年份:2014
- 资助金额:
$ 53.6万 - 项目类别:
Role of innate immunity and the microbiome in colitis-associated dysplasia
先天免疫和微生物组在结肠炎相关发育不良中的作用
- 批准号:
10659444 - 财政年份:2014
- 资助金额:
$ 53.6万 - 项目类别:
Role of TLR4 and the microbiome in colitis associated neoplasia
TLR4 和微生物组在结肠炎相关肿瘤中的作用
- 批准号:
10361471 - 财政年份:2014
- 资助金额:
$ 53.6万 - 项目类别:
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