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NAPS2 Continuation - Genome-Wide Association Study of Pancreatitis

NAPS2 Continuation - Genome-Wide Association Study of Pancreatitis
NAPS2 延续 - 胰腺炎全基因组关联研究
批准号:
7929157
负责人:
DAVID Clement WHITCOMB
金额:
$9.89万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-30 至 2011-08-31

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项目成果

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中文摘要
翻译
描述(由申请人提供):NAPS 2-续:胰腺炎的全基因组关联研究北美胰腺炎研究2(NAPS 2)是一项20个地点的前瞻性急性和慢性胰腺炎复发的分子遗传学研究。超额完成了1000名受试者的入组目标,同时也确定了近700名对照受试者。该研究的主要目的是研究6-10个候选基因的作用,以及主要环境因素(如吸烟和饮酒)的影响。现在,技术的快速进步允许以合理的成本进行全基因组关联研究(GWAS)。本次更新的目标是对胰腺炎性疾病受试者进行GWAS。通过获得500例原始受试者的5年随访数据,加上招募另外500例慢性胰腺炎患者作为确证性人群,将进一步提高研究的效力。具体目标是:目标1。对来自NAPS 2研究的1000例复发性急性胰腺炎和慢性胰腺炎受试者以及600例对照者进行全基因组关联研究。目标2.招募另外500例慢性胰腺炎受试者进行确证性研究。目标3。重新确定来自原始中心的500例RAP和CP受试者,随访时间> 5年,以确定与疾病进展率相关的因素。我们相信,这种全面、公正的方法将揭示多个重要的基因和治疗靶点,以预防复发性急性胰腺炎、慢性胰腺炎和常见并发症。这种方法在与具有强遗传基础的其他慢性炎症性疾病比较途径和关键机制方面也很重要。因此,我们希望这个项目能为我们对胰腺疾病的理解提供重大进展。 公共卫生相关性:NAPS 2 GWAS:概述和意义。复发性急性和慢性胰腺炎都是胰腺炎性疾病,目前尚无有效的治疗方法。在过去,大多数病例都归因于酗酒,这降低了患者治疗和研究工作的热情。我们发现突变型胰蛋白酶原是一种易感基因,这使许多人重新评估胰腺炎症的原因。我们组织了一项20个地点的研究(NAPS 2),招募了1000多例复发性急性和慢性胰腺炎病例,加上近700例对照,发现过量饮酒仅见于少数患者。这意味着其他罪魁祸首(包括基因变化)是重要的,但仍然是虚幻的。本研究的目的是使用NAPS 2研究的DNA样本进行全基因组关联研究(GWAS),以发现主要的遗传原因。了解胰腺炎的遗传基础将导致新的治疗方法,并有助于消除慢性胰腺炎只是醉酒者的疾病的耻辱。
英文摘要
DESCRIPTION (provided by applicant): NAPS2-Continuation: Genome-wide association study for pancreatitis The North American Pancreatitis Study 2 (NAPS2) was a 20-site, prospective molecular genetics study of recurrent acute and chronic pancreatitis. The enrollment target of 1000 subjects was exceeded, and nearly 700 control subjects were also ascertained. The primary purpose of the study was to investigate the role of 6-10 candidate genes, plus the influence of major environmental factors (e.g. tobacco smoking and alcohol consumption). Now, the rapid advances in technology allow for genome-wide association studies (GWAS) to be conducted at a reasonable cost. The goal of this renewal is to conduct a GWAS of subjects with inflammatory diseases of the pancreas. The power of the study will be further advanced by obtaining 5 year follow-up data on 500 of the original subjects, plus the recruitment of an additional 500 patients with chronic pancreatitis as a confirmatory population. The specific aims will be: Aim 1. To conduct a genome-wide association studies on 1000 subjects with recurrent acute pancreatitis and chronic pancreatitis plus 600 controls from the NAPS2 study. Aim 2. To recruit an additional 500 subjects with chronic pancreatitis for confirmatory studies. Aim 3. To re-ascertain 500 subjects with RAP and CP from the original centers with > 5 years of follow-up to determine factors associated with rates of diseases progression. We believe that this comprehensive, unbiased approach will uncover multiple important genes and therapeutic targets to prevent recurrent acute pancreatitis, chronic pancreatitis and common complications. This approach will also be important in comparing pathways and key mechanism with other chronic inflammatory disorders with strong genetic basis. Thus, we expect this project to provide major advances in our understanding of pancreatic diseases. PUBLIC HEALTH RELEVANCE: NAPS2 GWAS: Overview and significance. Both recurrent acute and chronic pancreatitis are inflammatory diseases of the pancreas for which there is no effective treatment. In the past, the majority of cases were attributed to alcoholism, which lowered enthusiasm for patient treatment and for research efforts. Our discovery of mutant trypsinogen as a susceptibility gene caused many to reassess the causes of pancreatic inflammation. We organized a 20 site study (NAPS2) to enroll over 1000 cases of recurrent acute and chronic pancreatitis, plus nearly 700 controls and discovered that excessive alcohol drinking is only found in a minority of patients. This means that other culprits (including genetic changes) are important, but remain illusive. The purpose of this study is to use DNA samples from the NAPS2 study to conduct a genome-wide association study (GWAS) to discover the major genetic causes. Knowledge of the genetic basis of pancreatitis will lead to new treatments, and help remove the stigma that chronic pancreatitis is only a disease of drunkards.
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