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首页> 外文期刊>Genetic epidemiology. >A review of statistical methods for testing genetic anticipation: looking for an answer in Lynch syndrome.
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A review of statistical methods for testing genetic anticipation: looking for an answer in Lynch syndrome.

机译:检验基因预期的统计方法的综述:寻找林奇综合征的答案。

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Anticipation, manifested through decreasing age of onset or increased severity in successive generations, has been noted in several genetic diseases. Statistical methods for genetic anticipation range from a simple use of the paired t-test for age of onset restricted to affected parent-child pairs to a recently proposed random effects model which includes extended pedigree data and unaffected family members [Larsen et al., 2009]. A naive use of the paired t-test is biased for the simple reason that age of onset has to be less than the age at ascertainment (interview) for both affected parent and child, and this right truncation effect is more pronounced in children than in parents. In this study, we first review different statistical methods for testing genetic anticipation in affected parent-child pairs that address the issue of bias due to right truncation. Using affected parent-child pair data, we compare the paired t-test with the parametric conditional maximum likelihood approach of Huang and Vieland [1997] and the nonparametric approach of Rabinowitz and Yang [1999] in terms of Type I error and power under various simulation settings and departures from the modeling assumptions. We especially investigate the issue of multiplex ascertainment and its effect on the different methods. We then focus on exploring genetic anticipation in Lynch syndrome and analyze new data on the age of onset in affected parent-child pairs from families seen at the University of Michigan Cancer Genetics clinic with a mutation in one of the three main mismatch repair (MMR) genes. In contrast to the clinic-based population, we re-analyze data on a population-based Lynch syndrome cohort, derived from the Danish HNPCC-register. Both datasets indicate evidence of genetic anticipation in Lynch syndrome. We then expand our review to incorporate recently proposed statistical methods that consider family instead of affected pairs as the sampling unit. These prospective censored regression models offer additional flexibility to incorporate unaffected family members, familial correlation and other covariates into the analysis. An expanded dataset from the Danish HNPCC-register is analyzed by this alternative set of methods.
机译:在几种遗传性疾病中,人们已经注意到了预期的发生,即通过发病年龄的降低或连续几代人的严重性增加。遗传预期的统计方法范围很广,从简单地使用成对t检验(仅限于受影响的亲子对的发病年龄)到最近提出的随机效应模型,其中包括扩展的系谱数据和未受影响的家庭成员[Larsen等,2009 ]。配对t检验的天真使用是有偏见的,原因很简单,患病的父母和孩子的发病年龄都必须小于确定(访谈)的年龄,并且这种正确的截断作用在儿童中比在儿童中更明显。父母。在这项研究中,我们首先回顾了不同的统计方法来测试受影响的亲子对中的遗传预期,以解决由于右截断而引起的偏倚问题。使用受影响的亲子对数据,我们将配对t检验与Huang和Vieland [1997]的参数条件最大似然方法以及Rabinowitz和Yang [1999]的非参数方法在不同条件下的I型误差和功效进行了比较。模拟设置以及与建模假设的背离。我们特别研究多重确定的问题及其对不同方法的影响。然后,我们重点研究Lynch综合征的遗传预期,并分析来自密歇根大学癌症遗传学诊所所见家庭中三个主要错配修复(MMR)之一发生突变的受影响亲子对发病年龄的新数据。基因。与基于诊所的人群相反,我们重新分析了基于人群的Lynch综合征队列的数据,该队列源自丹麦HNPCC登记册。这两个数据集都表明林奇综合征的遗传预期证据。然后,我们将审查范围扩大到纳入最近提出的统计方法,该方法将家庭而不是受影响的对视为抽样单位。这些前瞻性审查的回归模型提供了额外的灵活性,可以将未受影响的家庭成员,家族相关性和其他协变量纳入分析。通过此备选方法集分析了来自丹麦HNPCC寄存器的扩展数据集。

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