IRPG (NOVEL PHENOTYPES)

本子项目是利用由NIH/NCRR资助的中心赠款提供的资源的众多研究子项目之一。子项目和研究者（PI）可能已经从另一个NIH来源获得了主要资金，因此可以在其他CRISP条目中表示。列出的机构是中心的，不一定是研究者的机构。酗酒影响非裔美国人的社会、环境和医疗结果，并造成毁灭性的经济后果。胡互动研究计划（Howard-IRPG）提出的这项研究的总体目标是增加对非裔美国人酒精中毒遗传易感性和酒精中毒风险的理解。这项研究基于这样一个概念模型：遗传影响在酗酒的三个必要条件中都表现出来：行为去抑制、大量饮酒的能力和身体依赖的发展。行为去抑制可能与酗酒风险增加有关，而神经去抑制可能是这种行为的基础。Howard-IRPG是八个被提出的IRPG位点之一，其长期目标是阐明导致酒精中毒易感性和严重程度的新型遗传表型。使用IRPG确定标准，我们计划对50个受影响严重的城市非裔美国家庭和20个对照家庭进行确定、筛选、招募和确定和评估研究。这些研究将通过特定的诊断标准来量化酒精滥用和依赖高风险的表型，估计特定表型性状的遗传力，并确定它们与候选基因和数量性状位点（qtl）的关联和联系。这些评估将包括定量表型和神经去抑制的遗传性，以及与易感和/或共病I轴和II轴疾病的临床诊断的相关性。BrAC夹紧程序将用于定义酒精急性反应的新表型和酒精消除率。Howard将提供一个重要的非裔美国人队列，用于全基因组调查分析、候选基因关联研究和测试这些假设所需的基因多态性的确定，因为非裔美国人可能在乙醇代谢方面具有显著的、基因决定的差异。此外，Howard0IRPG结合了许多招聘网站的可用性和现有的科学和行政团队，以应对招聘大量信息丰富的非裔美国家庭的挑战；提供管理类似测试仪器和程序（如SSAGA和BrAC夹紧技术）方面的大量现有培训/经验；美国国立卫生研究院资助的一个新的GCRC的可用性，该GCRC具有支持BrAC夹紧共享资源的能力，以及NIAAA少数民族酒精合作研究中心现有的行政和科学基础设施。这些研究将通过与所有拟议的IRPG成员网站的重要互动来完成。

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. Alcoholism affects social, environmental and medical outcomes in African Americans with devastating economic consequences. The overall goal of the research proposed by the HU Interactive Research Program (Howard-IRPG) is to increase the understanding of the genetic susceptibility to alcoholism and alcoholism risk among African Americans. The research is based on the conceptual model that genetic influence is manifest in each of three conditions necessary for alcoholism: behavioral disinhibition, the capacity to consume large quantities of alcohol, and the development of physical dependence. Behavioral disinhibition may be associated with increased risk of alcoholism and neural disinhibition may underlie the behavior. The Howard-IRPG is one of eight proposed IRPG sites whose long-term goal is the elucidation of novel heritable phenotypes that contribute to alcoholism susceptibility and severity. Using the IRPG ascertainment criteria, we plan to identify, screen, recruit and perform ascertainment and assessment studies on a cohort of 50 densely affected urban African American families and 20 control families. These studies will quantify phenotypes of high risk of alcohol abuse and dependence as defined by specific diagnostic criteria, estimate the heritability of specific phenotypic traits and determine their association and linkage to candidate genes and quantitative trait loci (QTLs). These assessment will include heritability of quantitative phenotypes and neural disinhibition and the correlation with clinical diagnoses of predisposing and/or co-morbid Axis I and II disorders. The BrAC clamping procedure will be used to define novel phenotypes of the acute response to alcohol and the alcohol elimination rate. Howard will contribute a significant cohort of African Americans for a genome-wide survey analysis, candidate gene association studies and the determination of genetic polymorphism required to test these hypotheses since African Americans may have significant, genetically-determined differences in ethanol metabolism. In addition, the Howard0IRPG combines the availability of many recruitment sites and an existing scietific and administrative team to meet the challenge of recruiting large numbers of informative African American families; offers substantial existing training/experiences in the administration of similar tests instruments and procedures such as the SSAGA and the BrAC clamping technique; availability of a new, NIH-funded GCRC with the ability to support the BrAC clamping Shared Resource, and the existing administrative and scientific infrastructure of a NIAAA Collaborative Minority Alcohol Research Center. These studies will be accomplished through significant interaction with all of the proposed IRPG member sites.