Biomarker and Phenotypic Risk Factors for Breast Cancer Lymphedema
Biomarker and Phenotypic Risk Factors for Breast Cancer Lymphedema
批准号:
9750639
负责人:
CHRISTINE A. MIASKOWSKI
金额:
$77.48万
依托单位国家:
美国
项目类别:
财政年份:
2015
资助国家:
美国
项目状态:
已结题
起止时间:
2015-07-01 至 2021-06-30
关键词:
AffectApplications GrantsBiological MarkersBreast Cancer PatientBreast Cancer Risk FactorBreast Cancer TreatmentBreast Cancer survivorCandidate Disease GeneCellulitisCharacteristicsClinicalClinical TrialsCorrelation StudiesCyclophosphamideDNA MethylationDevelopmentDiagnosisEpigenetic ProcessFoundationsFundingGene ExpressionGenesGenotypeHigh Risk WomanIndustrializationIntervention StudiesLeadLiquid substanceLymphLymphangitisLymphatic SystemLymphedemaMalignant NeoplasmsMeasuresMolecularMoodsOperative Surgical ProceduresOutcomePathway interactionsPatientsPhenotypePhysiological ProcessesPrevalenceProspective StudiesProteinsPublishingQuality of lifeRadiation therapyRiskRisk FactorsRisk stratificationSamplingSeveritiesSubgroupSymptomsTestingTimeUnited StatesUnited States National Institutes of HealthVariantWomanWorkarmcancer surgerychemotherapycohortdisabilityexperiencefunctional disabilityfunctional statusgenetic predictorshigh riskinter-individual variationinterstitialmalignant breast neoplasmnovel strategiespatient subsetspreemptive interventionpreventpublic health relevancerecruit
中文摘要
描述(由申请人提供):乳腺癌治疗后的淋巴水肿(LE)是工业化世界中最常见的继发性LE形式。它发生在20%至87%的乳腺癌治疗后的患者中,并导致严重残疾。在
目前,确定性的表型、基因型和表观基因型预测因子尚不清楚,这些预测因子使患者处于发生LE的最高风险中。因此,在乳腺癌治疗后的患者样本中,本研究的具体目的是:使用候选基因方法确定LE的遗传预测因子,并评估与LE诊断相关的候选基因中的表观遗传变化,如通过DNA甲基化和随后的基因表达所测量的。本研究的次要目的是:评估具有不同LE表型预测因子的潜在女性类别;并评估患有LE和未患有LE的女性之间以及患有LE的潜在类别之间在症状、功能状态和QOL结局方面的差异。这项研究的结果将为LE的潜在机制提供新的信息,并允许开发和测试新的方法来预防或减少LE的负面影响。
英文摘要
DESCRIPTION (provided by applicant): Lymphedema (LE) following treatment for breast cancer is the most common form of secondary LE in the industrialized world. It occurs in 20% to 87% of patients following treatment for breast cancer and results in significant disability. At the
present time, the definitive phenotypic, genotypic and epigenotypic predictors that place patients at highest risk for the development of LE are not known. Therefore, the specific aims of this study, in a sample of patients following treatment for breast cancer, are to: determine genetic predictors of LE using a candidate gene approach and evaluate for epigenetic changes, as measured by DNA methylation and subsequent gene expression, in candidate genes associated with the diagnosis of LE. The secondary aims of this study are to: evaluate for latent classes of women with distinct phenotypic predictors of LE; and evaluate for differences in symptoms, functional status, and QOL outcomes between women with and without LE and among the latent classes with LE. The results of this study will provide new information on the underlying mechanisms for LE and allow for the development and testing of novel approaches to prevent or reduce the negative effects of LE.
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