Whole Genome Association Study of Migraine in Women

女性偏头痛的全基因组关联研究

• 批准号: 7940906
• 负责人: Tobias Kurth
• 金额: $ 24.56万
• 依托单位: BRIGHAM AND WOMEN'S HOSPITAL
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-09-28 至 2012-02-29
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7940906
• 关键词: 11q24; 17p13; 19p13; 1q31; 4q21; 9q21; 9q22; Accident and Emergency department; Accounting; Affect; Age; Age-Years; American; Applications Grants; Aspirin; Auras; Autonomic nervous system; Benefits and Risks; Biological Markers; Blood specimen; Candidate Disease Gene; Cardiovascular Diseases; Chromosomes; Chromosomes, Human, Pair 4; Chronic; Classic Migraine; Clinic; Coagulation Process; Common Migraine; Complex; Contraceptive Usage; DNA; Data; Disease; Dose; Environmental Risk Factor; Enzyme Gene; Enzymes; Epidemiology; Evaluation; Exogenous Factors; Facilities and Administrative Costs; Failure; Familial Hemiplegic Migraine; Family; Finland; Frequencies; Functional disorder; Funding; Gene Mutation; Genes; Genetic; Genetic Heterogeneity; Genetic Markers; Genetic Polymorphism; Genetic Variation; Genome; Genomics; Headache; Headache Disorders; Health; Health Professional; Heritability; High Prevalence; Homocysteine; Homocystine; Hormonal; Hormone replacement therapy; Hypertension; Iceland; Individual; Inflammation; International; Life; Link; Location; Longevity; Malignant Neoplasms; Medical; Menopausal Status; Methylenetetrahydrofolate reductase (NADPH); Migraine; NIH Program Announcements; Nausea; Nausea and Vomiting; Neurologic Symptoms; Oral Contraceptives; Overlapping Genes; Pain; Participant; Patients; Peptidyl-Dipeptidase A; Phenotype; Phonophobias; Photophobia; Physical activity; Plasma; Population; Primary Prevention; Principal Investigator; Recording of previous events; Reporting; Request for Applications; Research; Resources; Sample Size; Sampling; Serotonin; Severities; Smoking; Societies; Symptoms; System; Testing; Time; Triglycerides; Twin Studies; U-Series Cooperative Agreements; Visit; Vitamin E; Vomiting; Weight; Woman; Women' s Health; Xq24; base; cardiovascular risk factor; cohort; cost; dopamine system; endophenotype; experience; follow-up; gastrointestinal; gene environment interaction; genetic analysis; genetic linkage analysis; genetic variant; genome wide association study; men; novel; prospective; public health relevance; response; trait

DESCRIPTION (provided by principal investigator): This is a resubmission of grant application 1 R01 NS061836-01, now entitled "Whole Genome Association Study of Migraine in Women," which is a response to program announcement PA-07-305. In this application, we request funding to conduct a genome-wide association study of migraine and migraine traits within a large prospective cohort of more than 27,000 women, of whom more than 5,000 reported migraine. DNA from blood samples of all participants is presently undergoing a whole genome scan using the Illumina platform. In addition, extensive plasma-based phenotyping has been performed. Approximately 20 percent of the population suffers from migraine headaches; however, at any age, women are affected 3 to 4 times more often than men. Migraines account for most pain-related emergency room visits, and may persist as a chronic condition throughout the lifespan. Despite the high prevalence of migraine and a long history of relevant research, many questions remain regarding the pathophysiology and the multitude of endogenous and exogenous factors that influence this complex disorder. Gene mutations for rare forms of migraine have been recently identified. While linkage analyses have identified chromosomal loci in common forms of migraine, the underlying genes are unknown. In addition, candidate gene approaches in common forms of migraine have been disappointing, mainly due to lack of replication and small samples sizes. Thus, the genetic causes for common forms of migraine remain elusive. We propose 1) to identify novel candidate genetic variants/genes of migraine using (i) a conventional genome-wide association approach and (ii) a novel weighted genome-wide association approach that utilizes information from previously proposed chromosomal loci and 2) to explore interactions between identified candidate genetic variants/genes of migraine with biomarkers and environmental factors. We further propose two secondary aims in which we extend the evaluation of our primary aims to migraine traits, in particular migraine aura status. To achieve these aims, we propose to utilize information from the Women's Health Study (WHS), a large, well-characterized cohort of women 45 years of age and older in 1993. DNA has been extracted from collected blood samples from 27,939 women, and a whole genome scan of all available DNA samples is underway and expected to be completed by December 2008. At baseline and during follow-up, over 5,000 women reported migraine. In contrast to other large cohorts of US women, the WHS is an extraordinary resource that not only has extensive data on many traditional epidemiologic exposures, but also detailed information about migraine. Furthermore, plasma-based phenotyping is available on an exceptionally large number of samples. Thus, the WHS is particularly suited to study the genomics of migraine as well as gene-gene, gene-biomarker, and gene-environment interactions in a very cost-effective way. PUBLIC HEALTH RELEVANCE Migraine is a very common headache disorder that particularly affects women. Despite a large body of research, little is know about the pathophysiology and the multitude of endogenous and exogenous factors that influence this complex disorder. Although recently gene mutations for rare forms and candidate genes for more common forms of migraine have been identified, the mode of inheritance has only been established a very rare migraine form. Thus, we request funding to study the genomic of migraine using a whole genome approach and to evaluate gene-environment interactions.

描述（由主要研究者提供）：这是重新提交的资助申请1 R 01 NS 061836 -01，现在题为“妇女偏头痛的全基因组关联研究”，这是对项目公告PA-07-305的回应。在这项申请中，我们要求资助在一个超过27，000名女性的大型前瞻性队列中进行偏头痛和偏头痛特征的全基因组关联研究，其中超过5，000人报告偏头痛。所有参与者血液样本的DNA目前正在使用Illumina平台进行全基因组扫描。此外，还进行了广泛的基于血浆的表型分析。大约20%的人口患有偏头痛;然而，在任何年龄，女性受影响的频率都是男性的3至4倍。偏头痛占大多数与疼痛相关的急诊室就诊，并可能在整个生命周期中作为慢性疾病持续存在。尽管偏头痛的高患病率和相关研究的悠久历史，许多问题仍然存在的病理生理学和众多的内源性和外源性因素，影响这种复杂的疾病。最近已经确定了罕见形式的偏头痛的基因突变。虽然连锁分析已经确定了常见形式的偏头痛的染色体位点，潜在的基因是未知的。此外，在常见形式的偏头痛的候选基因的方法一直令人失望，主要是由于缺乏复制和小样本量。因此，常见形式的偏头痛的遗传原因仍然难以捉摸。我们提出1）使用（i）常规的全基因组关联方法和（ii）利用来自先前提出的染色体基因座的信息的新的加权全基因组关联方法来鉴定偏头痛的新的候选遗传变体/基因，和2）探索鉴定的偏头痛的候选遗传变体/基因与生物标志物和环境因素之间的相互作用。我们进一步提出了两个次要目标，其中我们将主要目标的评估扩展到偏头痛特征，特别是偏头痛先兆状态。为了实现这些目标，我们建议利用妇女健康研究（WHS），一个大的，特点鲜明的队列妇女45岁及以上的1993年的信息。从27 939名妇女的血样中提取了DNA，目前正在对所有现有DNA样本进行全基因组扫描，预计将于2008年12月完成。在基线和随访期间，超过5,000名女性报告了偏头痛。与其他大型美国女性队列相比，WHS是一个非凡的资源，不仅有许多传统流行病学暴露的广泛数据，而且还有关于偏头痛的详细信息。此外，基于血浆的表型分析可用于大量样本。因此，WHS特别适合于以非常具有成本效益的方式研究偏头痛的基因组学以及基因-基因、基因-生物标志物和基因-环境相互作用。偏头痛是一种非常常见的头痛疾病，尤其影响女性。尽管有大量的研究，很少有人知道的病理生理学和众多的内源性和外源性因素，影响这种复杂的疾病。虽然最近已经确定了罕见形式的基因突变和更常见形式的偏头痛的候选基因，但遗传模式仅建立在非常罕见的偏头痛形式上。因此，我们要求资助使用全基因组方法研究偏头痛的基因组，并评估基因-环境相互作用。