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Pharmacogenetics of antenatal corticosteroids to improve neonatal outcomes

Pharmacogenetics of antenatal corticosteroids to improve neonatal outcomes
产前皮质类固醇改善新生儿结局的药物遗传学
批准号:
8115763
负责人:
DAVID M. HAAS
金额:
$13.48万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-08-11 至 2012-07-31

项目摘要

项目成果

DAVID M. HAAS的其他基金

相关文献

中文摘要
翻译
描述(由申请人提供):早产呈上升趋势,并导致显著的新生儿死亡率和发病率。不断扩大的药物遗传学领域有望提高医生照顾这些患者的能力。在这个提案中,Dr. David M. Haas提出了一个全面的为期五年的以患者为导向的临床研究指导培训,旨在通过药物遗传学改善早产儿的新生儿结局。候选人:Dr. Haas是一名普通妇产科医生,拥有基本的研究技能,并在该研究领域发表了两篇背景文章。他的长期目标是成为一名独立的妇产科研究者,研究重点是早产和通过药物遗传学改善产科结果。在这个临床领域需要新的、合格的研究人员。环境:在国际公认的研究者David Flockhart博士和一组优秀的共同导师和顾问的指导下,Haas博士将继续专注于临床研究,并将在临床研究的各个方面接受正式和实用的指导。印第安纳大学医学院(usm)丰富的学术环境致力于哈斯博士作为独立内科科学家的发展,并在指导年轻研究人员方面有着悠久的历史。作为他的K23计划的一部分,Haas博士将完成usm临床研究者培训增强计划,这将导致临床研究理学硕士学位。这将伴随着药物遗传学和实验室培训、发展研讨会和研究伦理培训。研究:本应用程序的目的是评估药物遗传变异,可能导致新生儿结局改变,以应对早产的产前皮质类固醇。中心假设是糖皮质激素受体和代谢途径的药理学差异与结果差异相关,并可能有助于确定最佳的产前皮质类固醇剂量方案。两阶段的研究计划将验证这一假设,并将测试1)细胞色素P450和硫转移酶基因序列变化与新生儿结局之间的关联,以及2)糖皮质激素途径基因序列变化与产前皮质类固醇药效学反应变化之间的关联。这项研究的重要意义在于,提高对早产和新生儿呼吸功能中糖皮质激素代谢和功能的药理学理解,可能有助于改善结局和更好的治疗方案。这些研究将为未来的研究奠定基础,这些研究旨在将药物基因组学发现转化为改善早产妇女的治疗方案。与公共卫生的相关性:早产的后果对家庭和社会产生重大影响。改善早产儿的新生儿结局可以减少这种影响。K23奖的最终目标是让哈斯博士成为一名独立的临床研究人员,专注于改善早产和其他情况下的母婴健康结果。
英文摘要
DESCRIPTION (provided by applicant): Preterm birth is on the rise and leads to significant neonatal mortality and morbidity. The expanding field of pharmacogenetics promises to improve physicians' ability to care for these patients. In this proposal, Dr. David M. Haas proposes a comprehensive five-year period of mentored training in patient-oriented clinical research aimed at improving neonatal outcomes stemming from preterm birth through pharmacogenetics. Candidate: Dr. Haas is a general OB/GYN physician who possesses basic research skills and has already published two background articles in this research area. His long-term objective is to become an independent investigator in obstetrics and gynecology with a research focus on preterm labor and improving obstetric outcomes through pharmacogenetics. There is a need for new, wellqualified researchers in this clinical field. Environment: Under the mentorship of Dr. David Flockhart, an internationally recognized investigator, and a panel of excellent co-mentors and advisors, Dr. Haas will pursue focused clinical research and will receive formal and practical instruction in all aspects of clinical investigation. The rich academic environment of the Indiana University School of Medicine (IUSM) is committed to Dr. Haas's development as an independent physician scientist and has a strong history of mentoring young investigators. As part of his K23 plan, Dr. Haas will complete the IUSM Clinical Investigator Training Enhancement program which will lead to a Masters of Science in Clinical Research degree. This will be accompanied by pharmacogenetics and laboratory training, developmental seminars, and training in research ethics. Research: The objective of this application is to evaluate pharmacogenetic variations that may lead to altered neonatal outcomes in response to antenatal corticosteroids in preterm labor. The central hypothesis is that pharmacogenetic differences in the glucocorticoid receptors and metabolic pathway correlate with outcome disparities and may help determine optimal antenatal corticosteroid dosing regimens. The two-phased research plan tests that hypothesis and will 1) Test for associations between gene sequence variations in the cytochrome P450 and sulfotransferase enzymes and neonatal outcomes, and 2) Test for associations between gene sequence variations in the glucocorticoid pathway and variation in pharmacodynamic response to antenatal corticosteroids. The research is significant in that improved pharmacogenetic understanding of glucocorticoid metabolism and function in preterm labor and neonatal respiratory function may help lead to improved outcomes and better treatment regimens. These studies will lay the foundation for future research designed to translate pharmacogenomic findings into improved treatment regimens for women with preterm labor. Relevance to public health: Consequences of preterm birth significantly impact families and society. Improving neonatal outcomes from preterm birth can reduce this impact. The ultimate goal of this K23 award is for Dr. Haas to become an independent clinical researcher focused on improvements in maternal and infant health outcomes from preterm labor and other conditions.
期刊论文(7)
专著(0)
科研奖励(0)
会议论文
Pharmacogenetics and other reasons why drugs can fail in pregnancy: higher dose or different drug?
药物遗传学和药物在怀孕期间失败的其他原因:更高剂量或不同药物?
DOI: 10.1097/aog.0b013e3182698538
发表时间: 2012
期刊: Obstetrics and gynecology
影响因子: 7.2
作者: [Haas,DavidM, DʼAlton,Mary]
通讯作者: DʼAlton,Mary
DOI: 10.3109/14767058.2011.650249
发表时间: 2012
期刊: The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians
影响因子: --
作者: [Haas,DavidM, Kirkpatrick,Page, McIntosh,JenniferJ, Caldwell,DeborahM]
通讯作者: Caldwell,DeborahM
DOI: --
发表时间: 2011
期刊: The Journal of reproductive medicine
影响因子: --
作者: [Haas,DavidM, Weida,Jennifer, Smith,Ronda, Abernathy,MaryPell]
通讯作者: Abernathy,MaryPell
Machine learning approaches towards risk assessment and prediction of adverse pregnancy outcomes
Machine learning approaches towards risk assessment and prediction of adverse pregnancy outcomes
Machine learning approaches towards risk assessment and prediction of adverse pregnancy outcomes
Pharmacokinetics and modeling of betamethasone therapy in threatened preterm birth