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家庭中风险函数的建模。

Modeling hazard functions in families.

作者信息

Siegmund K, McKnight B

机构信息

Division of Biostatistics, Washington University School of Medicine, St. Louis, Missouri 63110, USA.

出版信息

Genet Epidemiol. 1998;15(2):147-71. doi: 10.1002/(SICI)1098-2272(1998)15:2<147::AID-GEPI4>3.0.CO;2-3.

Abstract

A genetic frailty model is presented for censored age of onset data in nuclear families where individuals carrying a genetic susceptibility gene have an increased risk of becoming affected. We use maximum likelihood via the EM algorithm to estimate the genetic relative risk and the allele frequency under a dominant susceptibility type and a proportional hazards model. When sampling is from a disease registry, likelihood corrections are necessary for reducing bias in the parameter estimates. In these biased samples, the full conditional likelihood is approximated by a likelihood conditional on the proband's age of onset. For unbiased samples, simulations show the distributions of the estimates are similar under both a semiparametric and the correctly specified parametric likelihoods. For biased samples, simulations under the approximate conditional likelihood show the median estimates of the allele frequency and genetic relative risk tend to under- and overestimate, respectively, the true values; however, the approximation is better for rarer allele frequencies (0.0033 vs. 0.01). In practice, large samples or more complex ascertainment corrections are recommended. Using the approximate conditional likelihood on familial breast cancer onset data collected as part of a case-control study at the Fred Hutchinson Cancer Research Center in Seattle, Washington, we estimate an allele frequency of 0.0009 (approximate 95% CI 0.0006-0.002) and a genetic relative risk of 104 (approximate 95% CI 55-181).

摘要

针对核心家庭中发病年龄数据存在删失的情况,提出了一种遗传脆弱性模型,其中携带遗传易感性基因的个体发病风险增加。我们通过期望最大化(EM)算法使用最大似然法来估计显性易感性类型和比例风险模型下的遗传相对风险和等位基因频率。当从疾病登记处进行抽样时,需要进行似然校正以减少参数估计中的偏差。在这些有偏样本中,完全条件似然通过先证者发病年龄的条件似然来近似。对于无偏样本,模拟表明在半参数似然和正确设定的参数似然下估计值的分布相似。对于有偏样本,在近似条件似然下的模拟表明等位基因频率和遗传相对风险的中位数估计值往往分别低估和高估真实值;然而,对于较罕见的等位基因频率(0.0033对0.01),近似效果更好。在实际中,建议使用大样本或更复杂的确定校正方法。利用作为华盛顿州西雅图市弗雷德·哈钦森癌症研究中心一项病例对照研究一部分收集的家族性乳腺癌发病数据的近似条件似然,我们估计等位基因频率为0.0009(近似95%置信区间0.0006 - 0.002),遗传相对风险为104(近似95%置信区间55 - 181)。

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