Cortisol Regulation in PCOS

多囊卵巢综合征中的皮质醇调节

基本信息

项目摘要

DESCRIPTION (provided by applicant): Project Summary Candidate: Bethany Klopfenstein, MD, is completing her fellowship in Endocrinology at Oregon Health & Science University (OHSU). This proposal will promote her scientific development and laboratory skills as she transitions into an independent academic, patient-oriented, clinical investigator. Her immediate career goals are to solidify her training in clinical research and develop new laboratory techniques for the study of cortisol metabolism. Her long-term goal is to develop an independent research career in the field of cortisol metabolism in insulin resistance. To accomplish these objectives, she will participate in a comprehensive didactic curriculum and perform the studies described in the research plan. Environment: OHSU has strong interdisciplinary training programs in both clinical and basic science research, including the Human Investigations Program funded by a K30 award. The 12,500 square foot OHSU General Clinical Research Center (GCRC) includes state-of-the-art outpatient and inpatient units, as well as a Core Laboratory, Bionutrition Unit, Bioinformatics Core and biostatistics support. Research Project: The overall goal of this research project is to investigate the relationships between cortisol metabolism, fat patterning, glucose metabolism, and adrenal androgens using the model of polycystic ovary syndrome (PCOS). Specific Aim 1 is a cross-sectional study designed to examine relationships between insulin sensitivity, central (visceral) obesity, androgen levels, and cortisol regulation (both at the systemic level of the hypothalamic-pituitary-adrenal (HPA) axis and locally in adipose tissue by the enzyme 11 betahydroxysteroid dehydrogenase type 1 (HSD 1) in women with PCOS and controls. Specific Aim 2 will prospectively test the novel hypothesis that insulin sensitizing agents improve body fat distribution and androgen levels in women with PCOS in part through reductions in HPA axis and adipocyte HSD 1 activity. Relevance: Individuals with central obesity, such as women with PCOS, are at high risk for developing infertility, diabetes, and heart disease. Abnormalities in cortisol metabolism may contribute to these comorbidities. Studies proposed here will improve our understanding of the regulation of cortisol metabolism, central obesity and insulin resistance. These findings may lead to new tools for managing PCOS.
描述(由申请人提供): 项目概要候选人:Bethany Klopfenstein,医学博士,正在俄勒冈州健康与科学大学(OHSU)完成她的内分泌学奖学金。这项建议将促进她的科学发展和实验室技能,因为她过渡到一个独立的学术,以病人为导向,临床研究者。她的近期职业目标是巩固她在临床研究方面的培训,并为皮质醇代谢的研究开发新的实验室技术。她的长期目标是在胰岛素抵抗的皮质醇代谢领域发展独立的研究事业。为了实现这些目标,她将参加一个全面的教学课程,并执行研究计划中描述的研究。工作环境:OHSU在临床和基础科学研究方面都有强大的跨学科培训计划,包括由K30奖资助的人类调查计划。12,500平方英尺的OHSU综合临床研究中心(GCRC)包括最先进的门诊和住院单位,以及核心实验室,生物营养单位,生物信息学核心和生物统计学支持。研究项目:本研究项目的总体目标是使用多囊卵巢综合征(PCOS)模型研究皮质醇代谢、脂肪模式、葡萄糖代谢和肾上腺雄激素之间的关系。具体目标1是一项横断面研究,旨在检查PCOS女性和对照组中胰岛素敏感性、中心性(内脏)肥胖、雄激素水平和皮质醇调节(下丘脑-垂体-肾上腺(HPA)轴的全身水平和脂肪组织中11 β羟类固醇脱氢酶1型(HSD 1)的局部水平)之间的关系。具体目标2将前瞻性地检验新的假设,即胰岛素增敏剂部分通过降低HPA轴和脂肪细胞HSD 1活性来改善PCOS女性的体脂分布和雄激素水平。相关性:中心性肥胖的个体,如PCOS女性,患不孕症、糖尿病和心脏病的风险很高。皮质醇代谢异常可能导致这些合并症。本文提出的研究将提高我们对皮质醇代谢、向心性肥胖和胰岛素抵抗的调节的理解。这些发现可能会导致管理PCOS的新工具。

项目成果

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BETHANY J KLOPFENSTEIN其他文献

BETHANY J KLOPFENSTEIN的其他文献

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{{ truncateString('BETHANY J KLOPFENSTEIN', 18)}}的其他基金

Cortisol Regulation in PCOS
多囊卵巢综合征中的皮质醇调节
  • 批准号:
    7876629
  • 财政年份:
    2006
  • 资助金额:
    $ 13.18万
  • 项目类别:
Cortisol Regulation in PCOS
多囊卵巢综合征中的皮质醇调节
  • 批准号:
    7681273
  • 财政年份:
    2006
  • 资助金额:
    $ 13.18万
  • 项目类别:
Cortisol Regulation in PCOS
多囊卵巢综合征中的皮质醇调节
  • 批准号:
    7480975
  • 财政年份:
    2006
  • 资助金额:
    $ 13.18万
  • 项目类别:
Cortisol Regulation in PCOS
多囊卵巢综合征中的皮质醇调节
  • 批准号:
    7035108
  • 财政年份:
    2006
  • 资助金额:
    $ 13.18万
  • 项目类别:

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