METHODS FOR ANALYZING REPEATED CATEGORICAL DATA
METHODS FOR ANALYZING REPEATED CATEGORICAL DATA
批准号:
2007984
负责人:
Stuart R. Lipsitz
金额:
$12.13万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1992
资助国家:
美国
项目状态:
已结题
起止时间:
1992-05-06 至 2000-04-30
中文摘要
描述:(改编自研究者摘要)重复测量
在公共卫生的所有领域都进行了研究。 在重复的措施
研究,基本抽样单位是一组或一组受试者;
对集群内的每个对象进行测量。 缺失的回答
和协变量在重复测量研究中很常见,
大多数提案涉及重复数据缺失问题,
措施研究。 首先,我们将评估和扩展现有的方法,
有缺失的纵向研究中关联测度的估计
应答 第二,似然方法可以计算
因此,我们提出了一种伪卡尔曼滤波方法来估计参数
非单调非线性纵向研究的边际模型
缺失的结果。 第三,条件Logistic回归常用于
消除滋扰'固定'集群效应,我们提出了一个修改后的
条件logistic回归适合用于缺失
协变量 第四,由于目前的基因测定技术,
突变,研究人员现在有兴趣估计比值比
基因状态(突变,无突变)和治疗成功之间的关系是,
否)。 不幸的是,并不总是能够进行完整的遗传学检查。
评估以确定基因是否发生突变,从而导致“缺失数据”。
我们将应用缺失数据方法来分析突变状态,
基因 我们最后提出的项目不涉及缺失数据,尽管它
确实评估了一种方法,该方法可能会在聚类数据中给出有偏差的结果
问题研究 我们将确定聚类是否影响通常的检验统计量
在随机临床试验中没有治疗效果。
英文摘要
DESCRIPTION: (Adapted from investigator's abstract) Repeated measures
studies are undertaken in all areas of Public Health. In repeated measures
studies, the basic sampling unit is a group or cluster of subjects; a
measurement is made on each subject within the cluster. Missing 'responses
and covariates are common occurrences in repeated measures studies, and the
majority of the proposal relates to missing data problems in repeated
measures studies. First, we will evaluate and extend existing methods for
estimating measures of association in longitudinal studies with missing
responses. Secondly, the likelihood methods can be computationally
intensive, so we propose a pseudolikelihood methods to estimate parameters
of marginal models for longitudinal studies with nonignorable nonmonotone
missing outcomes. Thirdly, conditional logistic regression is often used to
eliminate nuisance 'fixed' cluster effects, and we propose a modified
conditional logistic regression which is appropriate to use with missing
covariates. Fourthly, because of current techniques of determining gene
mutation, investigators are now interested in estimating the odds ratio
between genetic status (mutation, no mutation) and treatment success yes,
no). Unfortunately, it is not always possible to perform a complete genetic
evaluation to determine if a gene has mutated, resulting in 'missing data'.
We will apply missing data methods to analyze the mutation status of the
gene. Our final proposed project does not concern missing data, although it
does evaluate a method that can give biased results in clustered data
studies. We will determine if clustering affects the usual test statistics
of no treatment effect in a randomized clinical trial.
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海外基金