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This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Tuberculosis (TB) is a growing global public health problem. Several studies suggest a role for host genetics in disease susceptibility, but studies to date have been inconsistent and a comprehensive genetic model has not emerged. A limitation of previous genetic studies is that they only analyzed the binary trait TB, which does not reflect disease heterogeneity. Furthermore, these studies have not accounted for the influence of shared environment within households on TB risk, which may spuriously inflate estimates of heritability. We conducted a household contact study in a TB-endemic community in Uganda. Previously, we estimated the heritability of three cytokines as endophenotypes for TB: interferon-gamma, tumor necrosis factor-alpha, and transforming growth factor-beta. In that analysis, tumor necrosis factor-alpha demonstrated high (68%) heritability, and we followed it up with path and segregation analysis. Path analysis, conducted to assess the effect of shared environment, suggested that TNFalpha is heritable (narrow sense heritability = 34-66%); the effect of shared environment is minimal (1-14%), but gene-environment interaction may be involved. Segregation analysis of TNFalpha suggested a major gene model that explained one-third of the phenotypic variance, and provided putative evidence of natural selection acting on this phenotype. Linkage and association analyses demonstrated an association between TNF alpha, TB, and the genes coding for interferon-gamma receptor 1, TNF receptor 1, and interleukin 10. Our data further support TNFalpha as an endophenotype for TB, as it may increase power to detect disease-predisposing loci. A microsatellite genome scan is ongoing.
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Systems Biology, Bioinformatics, & Data Integration
  • 批准号:
    10459538
  • 项目类别:
  • 资助金额:
    $63.71万
  • 财政年份:
    2021
  • 负责人:
    Catherine Marie Stein
  • 依托单位:
Systems Biology, Bioinformatics, & Data Integration
  • 批准号:
    10653908
  • 项目类别:
  • 资助金额:
    $41.52万
  • 财政年份:
    2021
  • 负责人:
    Catherine Marie Stein
  • 依托单位:
Systems Biology, Bioinformatics, & Data Integration
  • 批准号:
    10271171
  • 项目类别:
  • 资助金额:
    $25.48万
  • 财政年份:
    2021
  • 负责人:
    Catherine Marie Stein
  • 依托单位:
Genetics of TB resistance in HIV positive subjects
  • 批准号:
    9511030
  • 项目类别:
  • 资助金额:
    $58.77万
  • 财政年份:
    2017
  • 负责人:
    Catherine Marie Stein
  • 依托单位:
国内基金
海外基金
基于Big Code深度背景增强的Android应用代码反混淆研究
  • 批准号:
    61972290
  • 项目类别:
    面上项目
  • 资助金额:
    60.0万元
  • 批准年份:
    2019
  • 负责人:
    刘进
  • 依托单位:
基于强自旋轨道耦合纳米线自旋量子比特的Surface code量子计算实验研究
  • 批准号:
    11574379
  • 项目类别:
    面上项目
  • 资助金额:
    73.0万元
  • 批准年份:
    2015
  • 负责人:
    姬忠庆
  • 依托单位:
提高网络存储可靠性- P2P文件Erasure Code机制研究
  • 批准号:
    60303002
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    24.0万元
  • 批准年份:
    2003
  • 负责人:
    韩华
  • 依托单位:
新一代乘积编码(Product Code)及解码方法的研究
  • 批准号:
    60372070
  • 项目类别:
    面上项目
  • 资助金额:
    22.0万元
  • 批准年份:
    2003
  • 负责人:
    余轮
  • 依托单位: