STRESS BIOMARKERS IN SLEEP APNEA

睡眠呼吸暂停中的压力生物标志物

• 批准号: 7607455
• 负责人: Alan R. Schwartz
• 金额: $ 0.06万
• 依托单位: JOHNS HOPKINS UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-12-01 至 2007-09-16
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7607455
• 关键词: Biological Markers; Cardiovascular Diseases; Cardiovascular system; Computer Retrieval of Information on Scientific Projects Database; Event; Funding; Glucose Intolerance; Grant; Heart failure; Hypoxemia; Inflammatory; Inflammatory Response; Institution; Link; Metabolic; Patients; Protocols documentation; Reactive Oxygen Species; Research; Research Personnel; Resistance; Resources; Sleep Apnea Syndromes; Source; Stress; United States National Institutes of Health; cardiovascular disorder risk; cardiovascular risk factor

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Patients with sleep apnea are at increased risk for cardiovascular disease. Notably, apneic and hypoxemic events associated with sleep apnea have been linked to alterations in metabolic activity (i.e., glucose intolerance adn isulin resistance), increases in the systemic inflammatory response and an increase in reactive oxygen species, all of which could potentially increase the risk of cardiovascular illness. However, the relationship between nocturnal apneic episodes and cardiovascular disease in patients with sleep apnea has not been elucidated. The primary objective of this protocol is to determine whether sleep apnea is associated with an increase in metabolic, inflammatory and cardiovascular stress in patients with and without heart failure.

这个子项目是许多研究子项目中的一个 由NIH/NCRR资助的中心赠款提供的资源。子项目和 研究者（PI）可能从另一个NIH来源获得了主要资金， 因此可以在其他CRISP条目中表示。所列机构为 研究中心，而研究中心不一定是研究者所在的机构。 睡眠呼吸暂停患者患心血管疾病的风险增加。值得注意的是，与睡眠呼吸暂停相关的呼吸暂停和低氧血症事件与代谢活动的改变有关（即，葡萄糖耐受不良和胰岛素抵抗）、全身炎症反应增加和活性氧增加，所有这些都可能增加心血管疾病的风险。然而，睡眠呼吸暂停患者夜间呼吸暂停发作与心血管疾病之间的关系尚未阐明。本方案的主要目的是确定睡眠呼吸暂停是否与伴有和不伴有心力衰竭的患者的代谢、炎症和心血管应激增加相关。