Phenotypic and Molecular Signatures for Sleep Apnea and Related Morbidities

睡眠呼吸暂停及相关疾病的表型和分子特征

• 批准号: 9244394
• 负责人: Susan S. Redline
• 金额: $ 105.75万
• 依托单位: BRIGHAM AND WOMEN'S HOSPITAL
• 依托单位国家: 美国
• 财政年份: 2017
• 资助国家: 美国
• 起止时间: 2017-01-01 至 2023-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9244394
• 关键词: Address; Adult; Affect; African American; Age; Anatomy; Apnea; Asian Americans; Big Data; Biological; Candidate Disease Gene; Cardiovascular system; Child; Clinical Data; Clinical Trials; Cognitive; Cohort Studies; Collaborations; Continuous Positive Airway Pressure; Data; Development; Diabetes Mellitus; Disease; Disease Outcome; Disease susceptibility; Environment; Environmental Risk Factor; Ethnic Origin; Family; Functional disorder; Genetic; Genomics; Health; Healthcare; Heart failure; Heritability; Hypertension; Individual; Individual Differences; Intervention; Laboratories; Leadership; Link; Measures; Medicine; Metabolic; Modernization; Molecular; Molecular Profiling; Morbidity - disease rate; Multicenter Studies; Outcome; Pathway interactions; Patients; Pattern; Phenotype; Physiological; Play; Polysomnography; Problem behavior; Race; Research Personnel; Resources; Risk; Risk Factors; Role; Severities; Severity of illness; Sleep; Sleep Apnea Syndromes; Sleep Disorders; Sleep Stages; Statistical Methods; Stents; Stream; Stroke; Subgroup; Technology; Translating; base; biobank; clinical care; disorder subtype; epidemiology study; experience; functional genomics; gene function; genetic association; genetic epidemiology; genetic variant; genome-wide; genomic data; improved; indexing; insight; multidisciplinary; novel; personalized medicine; precision medicine; prediction algorithm; programs; respiratory; sex; social; trait

I have over 25 years of experience in sleep medicine epidemiological research and have played a leading role in studies that address the contributions of genetic, social and environmental risk factors to sleep disorders, the influences of sleep on health outcomes in children and adults, and the role of sleep interventions in improving health outcomes. My collaborators, mentees and I have identified that sleep apnea (SA) is highly prevalent, disproportionately affects Asians and African American children, and is associated with significantly increased risks for developing hypertension, stroke, heart failure, diabetes, and behavioral problems. We also have identified variability in these outcomes by sex, race/ethnicity, age, and genetic background. We have characterized the patterns of heritability for several SDB traits and through use of family-based and cohort studies (>20,000 individuals) have identified genome-wide significant associations for genetic variants in biological candidate genes, and sex- and sleep stage-specific analyses have provided insight into mechanisms that may explain the known sex and REM/NREM differences in SA severity. Despite this progress, however, the underlying molecular and physiological mechanisms for SA are not well understood, limiting both our ability to predict which patients with SA are most vulnerable to adverse health outcomes and our ability to develop treatments that reflect individual differences in SDB pathophysiology. Our emerging data suggest that these gaps may be overcome through systematic analysis of larger sets of polysomnography data, deriving more precise SDB phenotypes that reflect specific sleep and respiratory patterns, and linking these phenotypes to genomic and clinical data. Through leadership in multiple national consortia and multi-center studies we are poised to make transformative advances in understanding the phenotypic variability and genetics of sleep apnea and related traits. We plan to harness a critical mass of data, including those in the National Sleep Research Resource and genetic, genomic and clinical data available through several consortia, including the Trans- Omics in Precision Medicine and Partners HealthCare Biobank. We will expand our genetics/epidemiology team with leaders in sophisticated respiratory phenotyping, developing a multi-disciplinary program that will systematically extract quantitative metrics of SA phenotypes and link these to genetics, genomics, specific treatment responsiveness, and cardiovascular, metabolic and cognitive outcomes. Through collaborations with functional genomics laboratories, we will help identify functional genetic variants and clarify the function of genes and pathways associated with SA. We will use sophisticated statistical methods to derive and validate personalized medicine prediction algorithms based on these data streams. This enhanced biological understanding of SA will be translated into improved clinical care through better-informed clinical trials. Finally, we will create an environment that nurtures the development of new investigators equipped to use modern technologies and “big data” to identify signatures of disease susceptibility and outcomes.

我在睡眠医学流行病学研究方面有超过25年的经验，并发挥了主导作用 在解决遗传、社会和环境风险因素对睡眠障碍的影响的研究中， 睡眠对儿童和成人健康结局的影响，以及睡眠干预在改善健康方面的作用 健康结果。我的合作者、被辅导者和我已经确认睡眠呼吸暂停(SA)非常普遍， 对亚裔和非裔美国儿童的影响不成比例，并与显著增加的 患高血压、中风、心力衰竭、糖尿病和行为问题的风险。我们还有 确定了性别、种族/民族、年龄和遗传背景在这些结果中的变异性。我们有 描述了几个SDB性状的遗传力模式，并通过使用基于家庭和队列的方法 研究(&gt；20,000人)已经确定了全基因组范围内与 生物候选基因，以及特定性别和睡眠阶段的分析提供了对机制的洞察 这可能解释了已知的性别和REM/NREM在SA严重性上的差异。然而，尽管取得了这些进展， SA的潜在分子和生理机制尚不清楚，限制了我们的能力 预测哪些SA患者最容易受到不良健康后果的影响，以及我们的发展能力 反映SDB病理生理学个体差异的治疗方法。我们不断涌现的数据表明，这些 差距可以通过对更大的多导睡眠图数据进行系统分析来克服，得出更多 准确的SDB表型，反映特定的睡眠和呼吸模式，并将这些表型与 基因组和临床数据。通过在多个国家财团和多中心研究中的领导，我们 准备在理解睡眠呼吸暂停的表型变异性和遗传学方面取得革命性进展 以及相关的特征。我们计划利用大量数据，包括国家睡眠研究中的数据 资源和遗传、基因组和临床数据可通过几个财团获得，包括Trans- 精准医学与合作伙伴保健生物库中的组学。我们将扩大我们的遗传学/流行病学 与先进的呼吸系统表型鉴定领域的领导者合作，开发一个多学科计划，将 系统地提取SA表型的定量指标，并将其与遗传学、基因组学、特异性 治疗反应性以及心血管、代谢和认知结果。通过与 功能基因组学实验室，我们将帮助识别功能遗传变异并阐明 与SA相关的基因和途径。我们将使用复杂的统计方法来推导和验证 基于这些数据流的个性化药物预测算法。这一增强的生物 对SA的了解将通过更知情的临床试验转化为更好的临床护理。最后， 我们将创造一个环境，促进新的调查员的发展，使他们具备使用现代技术的能力 技术和“大数据”，以确定疾病易感性和结果的特征。