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Issues of selection bias and limitations of the use of family history in the study of disease familial aggregation.

机译:在疾病家族聚集的研究中,选择偏见的问题和家族史的使用限制。

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摘要

Familial aggregation of disease is an important issue in genetic epidemiology. It refers to the increased disease occurrence among relatives of a case compared to that among relatives of a control. This dissertation focuses on the question of selection bias and the limitation of the use of family history in epidemiologic studies of familial aggregation.; Selection bias in studies of familial aggregation occurs when study subjects are selected through affected or unaffected family members. In some published studies, family members are counted only once as exposed or unexposed even multiple cases or controls have been identified from that family. In other studies, the way of selecting family members through cases or controls were not specified. This study illustrates the potential bias of the selection method that was used in some published studies by using a reconstructed cohort study design. It is shown that the method in the published studies can cause severe bias under some conditions and in order to get an unbiased estimate of effect measure, a family should be counted once each time a case or a control is selected from the family.; Family history has been used as an exposure variable to indicate one's genetic susceptibility in epidemiology literatures. Family history is affected by several factors such as one's family structure and disease occurrence in the general population. Hypothetical sibship data was used to study the dependency of family history on age and time in a follow-up study. It is shown that family history depends on the age of the study subject and the age of his/her relatives when the proportional hazard model is assumed for the effect of the susceptible genotype. Also it is shown that family history depends on disease occurrence and mortality from competing risks. The implication of this study is that recurrence risk ratio, which measures disease familial aggregation, should be interpreted as an age-specific measure and analysis of family data should reflect this dependency.
机译:疾病的家族聚集是遗传流行病学中的重要问题。它是指与对照的亲属相比,病例的亲属中疾病的发生增加。本文主要针对家庭聚集流行病学研究中的选择偏向问题和家族史的使用限制。通过受影响或未受影响的家庭成员选择研究对象时,会发生家族聚集研究中的选择偏见。在一些已发表的研究中,即使已从该家​​族中鉴定出多个病例或对照,该家族成员也只算一次暴露或未暴露的成员。在其他研究中,未指定通过病例或​​对照来选择家庭成员的方式。这项研究说明了使用一些重建的队列研究设计在某些已发表的研究中使用的选择方法的潜在偏见。结果表明,已发表的研究中的方法在某些情况下会引起严重的偏见,并且为了获得公正的效果量度估计值,每次从病例或对照中选择一个病例时,应对一个家庭进行计数。在流行病学文献中,家族史已被用作暴露变量,以表明一个人的遗传易感性。家族史受几个因素的影响,例如一个人的家庭结构和普通人群中的疾病发生率。在后续研究中,使用假想的同居关系数据来研究家族史对年龄和时间的依赖性。结果表明,当对易感基因型的影响采用比例风险模型时,家族史取决于研究对象的年龄及其亲属的年龄。还表明,家族史取决于疾病的发生和竞争风险引起的死亡率。这项研究的意义在于,衡量疾病家族聚集的复发风险比应被解释为针对特定年龄的衡量指标,对家庭数据的分析应反映这种依赖性。

著录项

  • 作者

    Bai, Yan.;

  • 作者单位

    Emory University.;

  • 授予单位 Emory University.;
  • 学科 Health Sciences Public Health.; Biology Genetics.
  • 学位 Ph.D.
  • 年度 1999
  • 页码 115 p.
  • 总页数 115
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 预防医学、卫生学;遗传学;
  • 关键词

  • 入库时间 2022-08-17 11:48:02

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