GENE TARGETS FOR IVH
IVH 的基因靶标
基本信息
- 批准号:8166700
- 负责人:
- 金额:$ 2.52万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2009
- 资助国家:美国
- 起止时间:2009-12-01 至 2010-11-30
- 项目状态:已结题
- 来源:
- 关键词:AllelesBlood VesselsBrainCaringCensusesCenters for Disease Control and Prevention (U.S.)CephalicCerebral PalsyCerebrovascular CirculationChildCoagulation ProcessComputer Retrieval of Information on Scientific Projects DatabaseDNADataEnrollmentEnvironmentEnvironmental Risk FactorFundingGene TargetingGenesGeneticGenomeGrantHaplotypesHemorrhageHypotensionHypoxemiaIncidenceInfantInfarctionInflammationInflammatoryInstitutionLow Birth Weight InfantMedicineMental RetardationMultivariate AnalysisNational Institute of Child Health and Human DevelopmentNeonatalPathogenesisPathway interactionsPlayPredispositionPremature BirthPremature InfantProteinsRandomizedRelative (related person)ResearchResearch PersonnelResourcesRoleSecondary toSeizuresSiteSourceThrombophiliaTissuesTwin Multiple BirthUltrasonographyUnited States National Institutes of HealthVenousadverse outcomebasecollegecostexperiencegenetic analysisgenome wide association studyintraventricular hemorrhageneonate
项目摘要
This subproject is one of many research subprojects utilizing the
resources provided by a Center grant funded by NIH/NCRR. The subproject and
investigator (PI) may have received primary funding from another NIH source,
and thus could be represented in other CRISP entries. The institution listed is
for the Center, which is not necessarily the institution for the investigator.
Numerous studies have identified Grades 3-4 intraventricular hemorrhage (IVH) as a significant cause of adverse outcome for very low birthweight (VLBW) neonates. IVH, or hemorrhage into the germinal matrix tissues of the developing brain, is believed to be secondary to changes in cerebral blood flow to the immature germinal matrix microvasculature and secondary periventricular venous infarction. Over 12% of all VLBW infants experience Gr. 3-4 IVH, and three quarters of these develop mental retardation, cerebral palsy and/or seizures.
Based on data from the U.S. Census Bureau, the NICHD Neonatal Network and the CDC, there are over 3600 new cases of mental retardation attributable to Gr. 3-4 IVH in the U.S. each year, and the lifetime care costs for these children exceed 3.6 billion dollars. Preterm birth represents a unique environment for the developing brain; many factors such as inflammation, hypotension
and hypoxemia that contribute to IVH have been identified. The incidence of Gr. 3-4 IVH has not changed, however, over the past ten years. Until recently, there has been limited information on whether genetic factors play a role in the pathogenesis of Gr. 3-4 IVH. New data, however, strongly suggest familial susceptibility for IVH in VLBW twins, and several studies have
investigated the role of thrombophilia, inflammatory and vascular genes in the genesis of Gr. 3-4 IVH. We hypothesize that for VLBW infants, Gr. 3-4 IVH is attributable to both environmental and genetic factors. The genetic factors are alleles and haplotypes of as yet unidentified genes that render VLBW infants susceptible to Gr. 3-4 IVH. It is likely that many are part of
inflammatory, vascular, oxidative and/or coagulation pathways. To accomplish these aims, this randomized, multi-center study, in aggregate, will collect DNA from 1000 neonates of 500-1250g birthweight with Gr. 3-4 IVH and 1000 matched control preterm infants with normal
cranial ultrasounds and no evidence for IVH. The genetic analyses will include a whole genome association study of 500,000 markers distributed throughout the genome and candidate pathway gene studies targeting genes that encode proteins known to subserve vascular, inflammatory, oxidative and/or coagulation pathways. In order to determine the contribution of environmental factors to Gr. 3-4 IVH, pre-, peri- and neo-natal data will be collected; using
multivariate analyses, the relative contribution of genetic and environmental factors to the susceptibility to IVH will be assessed.
This is an NIH funded, randomized multi-center trial, of which Baylor College of Medicine is one of 14 participating institutions. The total number of study infants will be 1000 with Grade 3 or 4 IVH and 1000 matched controls. Enrollment will take place over the first four years of the study. Our site plans to enroll at total of 248 infants (124 with Gr 3 or 4 IVH and 124 matched controls) over the four year grant period.
1. For preterm neonates, IVH is attributable to a combination of environmental and genetic factors.
2. The genetic factors are alleles and haplotypes of as yet unidentified genes that render VLBW infants susceptible to IVH when born at 500 ¿¿?? 1250 g.
3. Many of these as yet unidentified genes are part of vascular, inflammatory, oxidative and/or coagulation pathways.
这个子项目是众多研究子项目之一
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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HEIDI Eigenrauch KARPEN其他文献
HEIDI Eigenrauch KARPEN的其他文献
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{{ truncateString('HEIDI Eigenrauch KARPEN', 18)}}的其他基金
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Hedgehog受体运输和功能的调控
- 批准号:
6613777 - 财政年份:2002
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$ 2.52万 - 项目类别:
Regulation of Hedgehog Receptor Trafficking and Function
Hedgehog受体运输和功能的调控
- 批准号:
7079414 - 财政年份:2002
- 资助金额:
$ 2.52万 - 项目类别:
Regulation of Hedgehog Receptor Trafficking and Function
Hedgehog受体运输和功能的调控
- 批准号:
6901835 - 财政年份:2002
- 资助金额:
$ 2.52万 - 项目类别:
Regulation of Hedgehog Receptor Trafficking and Function
Hedgehog受体运输和功能的调控
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6752501 - 财政年份:2002
- 资助金额:
$ 2.52万 - 项目类别:
Regulation of Hedgehog Receptor Trafficking and Function
Hedgehog受体运输和功能的调控
- 批准号:
6460054 - 财政年份:2002
- 资助金额:
$ 2.52万 - 项目类别:
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