Identification of Genetic Markers Associated With Attentional Fatigue

与注意力疲劳相关的遗传标记的鉴定

基本信息

项目摘要

DESCRIPTION (provided by applicant): The direction of attention (i.e., purposeful concentration) during demanding situations, like the diagnosis and treatment of breast cancer, results in attentional fatigue. This symptom is experienced as a decreased ability to concentrate and to maintain purposeful activity at a time when attentional demands are high. Approximately 22% of women with breast cancer report high levels of attentional fatigue before treatment. However, very little longitudinal data are available on this symptom before, during, and after breast cancer treatment. No studies have attempted to link genetic markers with the severity or trajectories of self-reported attentional fatigue. Cognitive changes, including attentional fatigue, may occur when the production of proinflammatory cytokines is disregulated. Therefore, it is possible that SNPs in the genes that code for proinflammatory cytokines influence inter-individual differences in the severity of attentional fatigue in women with breast cancer. Therefore, the specific aims of this study, in a sample of women who were recruited prior to surgery for breast cancer and were followed at monthly intervals for six months, are to: (1) determine how self-ratings of attentional fatigue change over time; (2) determine which personal, health and illness, and environmental variables predict inter-individual differences in initial levels of attentional fatigue and/or the trajectories of attentional fatigue; and (3) determine whether specific candidate genes associated with proinflammatory cytokine regulation contribute to inter-individual differences in initial levels of attentional fatigue and/or the trajectories of attentional fatigue. Four hundred ten women who underwent surgery for breast cancer completed a number of instruments that included the Attentional Function Index (AFI) before surgery and each month after surgery for six months, and 318 of these women provided blood samples. Candidate genes for three proinflammatory cytokines (IL-1beta, IL-6, TNFA) will be screened using a custom SNP genotyping array (Illumina Inc., San Diego, CA). Attentional fatigue ratings and genotypes will be evaluated using G2 analyses, analysis of variance, and hierarchical linear modeling (HLM) to answer the specific aims of this study. An investigation of changes in attentional fatigue, as well as the associations between attentional fatigue and genomic markers, may provide information about potential mechanisms that underlie the development of the symptom, lead to the identification of women at greatest risk, and identify new therapeutic targets to decrease attentional fatigue. PUBLIC HEALTH RELEVANCE: The American Cancer Society estimates that 254,650 women were diagnosed with breast cancer in 2009. For women with breast cancer, attentional fatigue may be experienced as difficulty concentrating and completing tasks when there are many competing demands. This study, which examines patient characteristics and genetic (inherited) factors that contribute to attentional fatigue, may provide information about the causes of this symptom, which women are at greatest risk, and identify new treatment approaches to be used to decrease attentional fatigue.
描述(由申请人提供):注意方向(即,有目的的集中)在苛刻的情况下,如乳腺癌的诊断和治疗,导致注意力疲劳。这种症状表现为在注意力需求很高的时候,注意力集中和保持有目的活动的能力下降。大约22%的乳腺癌患者在治疗前报告了高度的注意力疲劳。然而,很少有纵向数据可用于此症状之前,期间和之后的乳腺癌治疗。没有研究试图将遗传标记与自我报告的注意力疲劳的严重程度或轨迹联系起来。当促炎细胞因子的产生失调时,可能会发生认知变化,包括注意力疲劳。因此,编码促炎细胞因子的基因中的SNP可能影响乳腺癌女性注意力疲劳严重程度的个体间差异。因此,本研究的具体目标是:(1)确定注意力疲劳的自我评定如何随时间变化;(2)确定哪些人,健康和疾病,和环境变量预测注意疲劳的初始水平和/或注意疲劳的轨迹的个体间差异;以及(3)确定与促炎细胞因子调节相关的特定候选基因是否有助于注意力疲劳的初始水平和/或注意力疲劳的轨迹的个体间差异。410名接受乳腺癌手术的女性在手术前和手术后每个月(持续六个月)完成了许多仪器,包括注意力功能指数(AFI),其中318名女性提供了血液样本。使用定制的SNP基因分型阵列(Illumina Inc.,San Diego,CA)。将使用G2分析、方差分析和分层线性模型(HLM)评估注意力疲劳评级和基因型,以回答本研究的特定目的。对注意力疲劳变化的研究,以及注意力疲劳与基因组标记之间的关联,可能会提供有关症状发展的潜在机制的信息,导致识别风险最大的女性,并确定新的治疗靶点以减少注意力疲劳。 公共卫生相关性:美国癌症协会估计,2009年有254,650名妇女被诊断患有乳腺癌。对于患有乳腺癌的女性来说,注意力疲劳可能会表现为当有许多竞争需求时难以集中注意力和完成任务。这项研究检查了导致注意力疲劳的患者特征和遗传(遗传)因素,可能会提供有关这种症状的原因的信息,这些症状是女性风险最大的,并确定了用于减少注意力疲劳的新治疗方法。

项目成果

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John D. Merriman其他文献

John D. Merriman的其他文献

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{{ truncateString('John D. Merriman', 18)}}的其他基金

Mindfulness-Based Stress Reduction to Improve Cognitive Function During Aromatase Inhibitor Therapy
在芳香酶抑制剂治疗期间,基于正念的减压可改善认知功能
  • 批准号:
    9499504
  • 财政年份:
    2017
  • 资助金额:
    $ 3.43万
  • 项目类别:
Brain Biomarkers of Cognitive and Mood Changes Related to Aromatase Inhibitor Use
与芳香酶抑制剂使用相关的认知和情绪变化的大脑生物标志物
  • 批准号:
    9032606
  • 财政年份:
    2015
  • 资助金额:
    $ 3.43万
  • 项目类别:
Brain Biomarkers of Cognitive and Mood Changes Related to Aromatase Inhibitor Use
与芳香酶抑制剂使用相关的认知和情绪变化的大脑生物标志物
  • 批准号:
    9149033
  • 财政年份:
    2015
  • 资助金额:
    $ 3.43万
  • 项目类别:
Identification of Genetic Markers Associated With Attentional Fatigue
与注意力疲劳相关的遗传标记的鉴定
  • 批准号:
    8267247
  • 财政年份:
    2011
  • 资助金额:
    $ 3.43万
  • 项目类别:
Identification of Genetic Markers Associated With Attentional Fatigue
与注意力疲劳相关的遗传标记的鉴定
  • 批准号:
    8402801
  • 财政年份:
    2011
  • 资助金额:
    $ 3.43万
  • 项目类别:

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Identification of Genetic Markers Associated With Attentional Fatigue
与注意力疲劳相关的遗传标记的鉴定
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    8267247
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    2011
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    $ 3.43万
  • 项目类别:
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