Family Blood Pressure Program (GenNet Network)

家庭血压计划（GenNet 网络）

• 批准号: 7123491
• 负责人: ALAN B WEDER
• 金额: $ 130.1万
• 依托单位: UNIVERSITY OF MICHIGAN AT ANN ARBOR
• 依托单位国家: 美国
• 财政年份: 1995
• 资助国家: 美国
• 起止时间: 1995-09-05 至 2008-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7123491
• 关键词: albuminuria; bioinformatics; blood pressure; cardiovascular disorder risk; clinical research; cooperative study; familial hypertension; family genetics; genetic markers; genetic registry /resource /referral center; genetic screening; genetic susceptibility; human data; human genetic material tag; human tissue; kidney disorder; linkage mapping; medical complication; molecular biology information system; single nucleotide polymorphism; statistics /biometry; ventricular hypertrophy

DESCRIPTION (provided by applicant): The Family Blood Pressure Program [FBPP] is an unprecedented collaboration to identify genes influencing blood pressure levels, hypertension and its cardiovascular complications (hereafter referred to as "hypertension genes"). To date, the Program has carried out 21,600 physical examinations, assembled a shared database of 294 hypertension-relevant variables, measured quantitative echocardiograms on 7,321 individuals, carried-out genome-wide linkage analyses for hypertension status and 13 related phenotypes, published (or in press) 128 manuscripts and identified 5 hypertension susceptibility genes by following-up 4 linkage peaks. In the proposed next phase of the FBPP, a major emphasis is placed on making the Program a shared resource for hypertension researchers in the United States and throughout the world. In Aim 1, we will build, maintain and update a publicly available knowledge-base to facilitate research by non-FBPP investigators on the genetics of hypertension, its risk factors and its complications. In Aim 2, we will use state-of-the-art genetic linkage analysis methods to identify additional linkage regions using subgroups of pedigrees and physiologically relevant combinations of phenotypes that will aid in localizing hypertension genes. In Aim 3, we will use a combination of bioinformatics, a dense array of SNPs, and state-of-the-art data analysis to follow-up regions of interest and identify the underlying hypertension genes. The regions to be followed-up include those identified during the current phase of the FBPP and Aim 2 of this renewal phase. In Aim 4, we will evaluate the hypertension genes identified in Aim 3 for their association with multiple measures reflecting the cardiovascular and renal complications of hypertension, including left ventricular mass and microalbuminuria. It is the long-term goal of the FBPP to have the hypertension genetics community develop a comprehensive picture of the genetic architecture of human hypertension, including its risk factors, complications, and response to treatment. (End of Abstract)

描述（由申请人提供）： 家庭血压计划[FBPP]是一项前所未有的合作，以确定影响血压水平，高血压及其心血管并发症的基因（以下简称为“高血压基因”）。迄今为止，该计划已进行了21，600次体检，建立了294个高血压相关变量的共享数据库，对7，321名个体进行了定量超声心动图测量，对高血压状况和13种相关表型进行了全基因组连锁分析，发表（或出版）128篇论文，并通过跟踪4个连锁峰确定了5个高血压易感基因。在FBPP的下一阶段，重点是使该计划成为美国和世界各地高血压研究人员的共享资源。在目标1中，我们将建立、维护和更新一个公开的知识库，以促进非FBPP研究者对高血压遗传学、其危险因素及其并发症的研究。在目标2中，我们将使用最先进的遗传连锁分析方法，以确定额外的连锁区域，使用亚组的谱系和生理相关的组合的表型，这将有助于定位高血压基因。在目标3中，我们将结合生物信息学、密集的SNP阵列和最先进的 数据分析，以跟踪感兴趣的区域，并确定潜在的高血压基因。需要采取后续行动的地区包括在FBPP当前阶段和更新阶段目标2中确定的地区。在目标4中，我们将评估目标3中鉴定的高血压基因与反映高血压心血管和肾脏并发症（包括左心室质量和微量白蛋白尿）的多项指标的相关性。FBPP的长期目标是让高血压遗传学界全面了解人类高血压的遗传结构，包括其危险因素，并发症和对治疗的反应。 (End摘要）