Genetics of Reproductive Life Period and Health Outcomes
Genetics of Reproductive Life Period and Health Outcomes
批准号:
7673745
负责人:
JOANNE M MURABITO
金额:
$24.19万
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:
2008-08-15 至 2011-07-31
关键词:
AchievementAffectAgeAge at MenarcheAge-Related Bone LossAgingBioinformaticsBiologicalBiotechnologyCardiovascular DiseasesClinical TrialsCommunitiesComplexComputer SimulationDataDiagnosticDisciplineDiseaseElderlyFamily history ofFemaleFramingham Heart StudyFunctional disorderGenesGeneticGenetic DatabasesGenome ScanGenotypeHandHealthHealth behaviorHeritabilityKnowledgeLeadLifeLongitudinal StudiesMeasurementMediatingMenarcheMenopauseMethodsOsteoporosisOutcomeOutcome MeasurePathway interactionsPhasePhenotypePostmenopauseReproductionReproductive HistoryResearchResearch PersonnelResourcesRiskRisk FactorsSamplingScanningSiteTherapeutic InterventionTimeVariantWomanWomen&aposs HealthWorkbasebone lossbone masscohortgene discoverygenetic epidemiologygenetic variantgenome wide association studyimprovedinnovationinsightmalignant breast neoplasmmennovelphenomepublic health relevancereproductivesexstatisticstrait
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The onset and conclusion of the reproductive life period are central factors influencing women's health later in life. Age at menarche and menopausal age affect risk for adverse health outcomes including osteoporosis, cardiovascular disease, and breast cancer. Further scientific study is needed to elucidate the contribution of menopause and reproductive factors versus aging per se to health conditions common in women in later life. More than half the variation in age at menarche and menopause is attributable to genetic factors yet the genes regulating these traits remain largely unknown. Data from longitudinal studies, such as the Framingham Heart Study (FHS), provide a wealth of data across adulthood including reproductive factors, disease occurrence, and health behaviors in both women and men. The FHS is multigenerational and includes an extensive genetics database with extant genotyping from a 550K genome-wide scan obtained through the NHLBI's SNP Health Association Resource (SHARe) project. We postulate that novel genetic variants influencing the age of menarche and natural menopause can be identified using a dense genome-wide association study (GWAS). This proposal has the following specific aims: Aim 1. To identify genetic variants that influence age at menarche and age at natural menopause through a GWAS using extant 550K genotyping data. To perform in silico replication of significant associations in independent samples. Aim 2. To examine the associations between genetic variants identified in aim 1 and osteoporosis-related traits obtained using dual x-ray absorptiometry (DXA) and hand radiogrammetry, in women as well as in men. Aim 3. To perform a phenome scan using the genotypes associated with reproductive aging to identify other associated phenotypes that may provide additional insights into underlying biological mechanisms mediating the associations in women. The phenome scan will also be performed in men to explore sex-specific associations. The use of the 550K genotyping will be resource effective and our work will be publicly available through the FHS SHARe Project located at the NCBI permitting investigators around the world to embark on this research. Insights from this project may lead to the discovery of genes related to female reproductive aging and associated health outcomes and in turn lead to innovative diagnostic and therapeutic interventions to improve the overall health of women and possibly of men. PUBLIC HEALTH RELEVANCE: This project may lead to the discovery of genes related to female reproductive aging (menarche and menopause) and in turn provide insights into the pathophysiologic mechanisms leading to important health conditions later in life in women. Knowledge gained may lead to innovative diagnostic and therapeutic interventions to improve the overall health of women and possibly of men.
期刊论文(1)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1038/ncomms8756
发表时间:
2015-08-04
期刊:
Nature communications
影响因子:
16.6
作者:
[Lunetta KL, Day FR, Sulem P, Ruth KS, Tung JY, Hinds DA, Esko T, Elks CE, Altmaier E, He C, Huffman JE, Mihailov E, Porcu E, Robino A, Rose LM, Schick UM, Stolk L, Teumer A, Thompson DJ, Traglia M, Wang CA, Yerges-Armstrong LM, Antoniou AC, Barbieri C, Coviello AD, Cucca F, Demerath EW, Dunning AM, Gandin I, Grove ML, Gudbjartsson DF, Hocking LJ, Hofman A, Huang J, Jackson RD, Karasik D, Kriebel J, Lange EM, Lange LA, Langenberg C, Li X, Luan J, Mägi R, Morrison AC, Padmanabhan S, Pirie A, Polasek O, Porteous D, Reiner AP, Rivadeneira F, Rudan I, Sala CF, Schlessinger D, Scott RA, Stöckl D, Visser JA, Völker U, Vozzi D, Wilson JG, Zygmunt M, EPIC-InterAct Consortium, Generation Scotland, Boerwinkle E, Buring JE, Crisponi L, Easton DF, Hayward C, Hu FB, Liu S, Metspalu A, Pennell CE, Ridker PM, Strauch K, Streeten EA, Toniolo D, Uitterlinden AG, Ulivi S, Völzke H, Wareham NJ, Wellons M, Franceschini N, Chasman DI, Thorsteinsdottir U, Murray A, Stefansson K, Murabito JM, Ong KK, Perry JR]
通讯作者:
Perry JR
Monitoring Health in Older Adults Using mHealth Technology: Framingham Offspring Study
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批准号:10627872
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项目类别:
-
资助金额:$62.58万
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财政年份:2022
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负责人:JOANNE M MURABITO
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依托单位:
Exceptional Aging Across the Life Span: Framingham Study
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批准号:8068869
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项目类别:
-
资助金额:$32.79万
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财政年份:2008
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负责人:JOANNE M MURABITO
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依托单位:
Genetics of Reproductive Life Period and Health Outcomes
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批准号:7509705
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项目类别:
-
资助金额:$21.69万
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财政年份:2008
-
负责人:JOANNE M MURABITO
-
依托单位:
Exceptional Aging Across the Life Span: Framingham Study
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批准号:7803575
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项目类别:
-
资助金额:$37.9万
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财政年份:2008
-
负责人:JOANNE M MURABITO
-
依托单位:
Exceptional Aging Across the Life Span: Framingham Study
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批准号:7615476
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项目类别:
-
资助金额:$32.0万
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财政年份:2008
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负责人:JOANNE M MURABITO
-
依托单位:
Exceptional Aging Across the Life Span: Framingham Study
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批准号:7458465
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项目类别:
-
资助金额:$31.38万
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财政年份:2008
-
负责人:JOANNE M MURABITO
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依托单位:
海外基金