Genetics of Renal End Organ Damage in Hypertension

高血压肾终末器官损伤的遗传学

• 批准号: 8289584
• 负责人: MICHAEL R GARRETT
• 金额: $ 37万
• 依托单位: UNIVERSITY OF MISSISSIPPI MED CTR
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-08-01 至 2014-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8289584
• 关键词: 1q21; Accounting; Albumins; Alleles; Animals; Biological Assay; Blood Glucose; Blood Pressure; Breeding; Candidate Disease Gene; Cardiovascular system; Cell Line; Cells; Chromosomes, Human, Pair 2; Code; Complex; Complex Genetic Trait; Congenic Strain; Development; Diabetes Mellitus; Dialysis procedure; Diploidy; Disease; Disease Progression; Disease model; End stage renal failure; Epithelial; Evaluation; Event; Exhibits; Expenditure; Fibrosis; Filtration; Focal Segmental Glomerulosclerosis; Functional disorder; Gene Expression; Gene Expression Profile; Genes; Genetic; Genetic Techniques; Genetic Variation; Genome; Genome Scan; Genomics; Glomerular Capillary; Goals; Haplotypes; Health; Human; Human Chromosomes; Human Genetics; Human Genome; Hypertension; In Vitro; Inbred SHR Rats; Inbred Strains Rats; Inbreeding; Incidence; Inflammation; Injury; Insurance; Kidney; Kidney Diseases; Kidney Failure; Knowledge; Link; Measurement; Measures; Mediating; Medicare; Mesenchymal; Modeling; Mutation; Nephrotic Syndrome; Organ; Pathway interactions; Patients; Permeability; Phase; Physiological; Play; Population; Preparation; Primary Cell Cultures; Production; Proteins; Proteinuria; Quantitative Trait Loci; Rattus; Recombinants; Renal Blood Flow; Renal function; Research; Resistance; Rodent Model; Role; Sequence Analysis; Signal Transduction; Staging; Structure; Subfamily lentivirinae; Susceptibility Gene; System; Testing; Time; Transcript; Transplantation; Tubular formation; United States; Validation; Variant; Western Blotting; Work; abstracting; arteriole; base; blood pressure regulation; comparative; congenic; cost; design; economic impact; effective therapy; genetic analysis; genetic linkage analysis; genetic variant; glomerular filtration; glomerular function; hemodynamics; human disease; in vitro testing; in vivo; interest; interstitial; kidney cell; lentiviral-mediated; overexpression; podocyte; population based; pressure; prevent; protein expression; research study; response; salt sensitive; success; trait; transmission process; uptake

DESCRIPTION (provided by applicant): Abstract There is an alarming increase in the incidence of end-stage renal disease in the Unites States, with hypertension and diabetes being the major cause. Currently, 25.6 million people are in the early phase of kidney disease (stage 1 to 3) and while strict control of blood pressure and glucose levels may slow, it will not prevent the progressive decline of renal function in these patients. Therefore, understanding the genetic basis of hypertension-induced renal disease is of considerable interest. Significant progress has been made to identify the genetic causes of familial forms of renal disease (nephrotic syndrome). However, no genetic variants have been found to be causally linked to common forms of renal disease. It is our goal to develop a better understanding of the genetic basis of hypertension-induced renal disease observed in the Dahl salt- sensitive (S) rat, which exhibits significant proteinuria and focal segmental glomerulosclerosis (FSGS). An initial genetic analysis for proteinuria and renal injury was performed using a population derived from the S. The study identified ten genomic regions linked to renal damage (measured by proteinuria) and/or function. A congenic strain developed on chromosome 2 exhibited significantly less proteinuria and FSGS. This proposal will evaluate the hypothesis that genetic variant(s) located to a small region on rat chromosome 2 play a significant role in the progressive FSGS and proteinuria observed in the S rat. Based on congenic strain analysis, the causative locus has been narrowed to <1.2 Mbs containing 27 genes. However, cross-species comparative, inbred-based SNP analysis, comprehensive coding sequence and gene expression analysis has convincingly identified 4 genes for further study. The aims of the proposed study are: (1) to perform temporal studies of blood pressure and renal hemodynamics, including renal blood flow, glomerular capillary pressure, and glomerular permeability in the S and small congenic strain; (2) to perform comprehensive gene expression, western blot analysis, sequencing, and haplotype analysis for genes narrowed to the small region on rat chromosome 2; and (3) to evaluate the functional significance of identified allelic variants using cell- based and whole-animal approaches. In summary, this proposal will identify and prioritize gene(s) linked to proteinuria and FSGS in the Dahl S model of hypertension-induced renal disease and provide a basis for functional studies, gene validation, and eventually study in human-based populations. PUBLIC HEALTH RELEVANCE: Project Narrative High blood pressure is major contributor to end-stage renal disease (ESRD). The number of ESRD patients treated by either dialysis or transplantation has more than doubled in the period from 1991 to 2004 from 209,000 to 472,000. In the next 20 years, the numbers of ESRD patients are expected to increase to over 2 million. Additionally, the economic impact is substantial, burdening the Medicare system (costing $20.1 billion or 7% percent of total Medicare expenditures), and the private insurance sector (estimated at $12.1 billion). The unfortunate reality is that treatment options are limited and only slow the progression of the disease. The focus of the proposed work is to identify genes that predispose the Dahl salt-sensitive (S) rat to develop hypertension-induced kidney disease. Previous genetic analysis using the S rat identified several chromosomal regions linked to kidney disease. In particular, a region on rat chromosome 2 was found to play a significant role in the kidney injury observed in the S rat. The homologous region on human chromosome 1q21 has also been linked to kidney disease in multiple studies. This underlies the importance in identifying the gene in the rat because the findings may be readily applied to human kidney disease. In summary, it is the goal of this proposal to utilize a rodent model of human disease and advanced genetic techniques to expedite the identification of a gene involved in kidney disease. The application of knowledge gained from this research will contribute to a better understanding of the how and why of the disease and ultimately provide earlier and more effective treatments of the disease before kidney failure is reached.

描述(申请人提供)：摘要在美国，终末期肾病的发病率有惊人的增长，高血压和糖尿病是主要原因。目前，有2560万人处于肾脏疾病的早期(1至3期)，虽然严格控制血压和血糖水平可能会放缓，但这不能阻止这些患者肾功能的进行性下降。因此，了解高血压引起的肾脏疾病的遗传基础是相当有意义的。在确定家族性肾脏疾病(肾病综合征)的遗传原因方面取得了重大进展。然而，还没有发现基因变异与常见形式的肾脏疾病有因果关系。我们的目标是更好地了解在Dahl盐敏感(S)大鼠中观察到的高血压肾病的遗传基础，该大鼠表现出显著的蛋白尿和局灶性节段性肾小球硬化(FSGS)。对蛋白尿和肾损伤的初步遗传分析是使用来自S的人群进行的。这项研究确定了与肾损伤(通过蛋白尿衡量)和/或功能相关的10个基因组区域。在2号染色体上培育的同源菌株的蛋白尿和FSGS显著减少。这项建议将评估位于大鼠2号染色体上一个小区域的遗传变异(S)在S大鼠的进行性FSGS和蛋白尿中起重要作用的假设。根据同源菌株分析，致病基因已缩小到包含27个基因的&lt；1.2 MBS。然而，跨物种比较、基于近交系的SNP分析、全面的编码序列和基因表达分析已经令人信服地确定了4个基因，用于进一步研究。拟议研究的目的是：(1)对S和小基因系大鼠的血压和肾脏血流动力学，包括肾脏血流量、肾小球毛细血管压和肾小球通透性进行时序研究；(2)对缩小到大鼠2号染色体上较小区域的基因进行全面的基因表达、蛋白质印迹分析、测序和单倍型分析；以及(3)使用基于细胞和全动物的方法评估已识别的等位基因变异的功能意义。综上所述，这项建议将在Dahl S高血压肾病模型中识别并优先选择与蛋白尿和FSGS相关的基因(S)，并为功能研究、基因验证以及最终在以人为基础的人群中的研究提供基础。公共卫生相关性：项目简介高血压是终末期肾病(ESRD)的主要贡献者。在1991年至2004年期间，接受透析或移植治疗的终末期肾病患者的数量增加了一倍多，从20.9万人增加到472,000人。在未来20年内，终末期肾病患者预计将增加到200多万人。此外，经济影响是巨大的，给医疗保险系统(成本为201亿美元，占医疗保险总支出的7%)和私人保险部门(估计为121亿美元)带来了负担。不幸的现实是，治疗选择有限，而且只能减缓疾病的发展。这项拟议工作的重点是确定使达尔盐敏感(S)大鼠患高血压肾病的易感基因。之前使用S大鼠进行的遗传分析发现了几个与肾脏疾病有关的染色体区域。特别是，大鼠染色体2上的一个区域被发现在S大鼠的肾脏损伤中起着重要作用。在多项研究中，人类染色体1q21上的同源区域也与肾脏疾病有关。这突显了在老鼠身上识别该基因的重要性，因为这一发现可能很容易应用于人类肾脏疾病。总而言之，这项建议的目标是利用人类疾病的啮齿动物模型和先进的基因技术来加快识别与肾脏疾病有关的基因。从这项研究中获得的知识的应用将有助于更好地了解这种疾病的方式和原因，并最终在肾衰竭发生之前提供更早和更有效的疾病治疗。