Instrumental variable model average with applications in Mendelian randomization

被引:2
|
作者
Seng, Loraine Liping [1 ,2 ]
Liu, Ching-Ti [3 ,4 ]
Wang, Jingli [5 ]
Li, Jialiang [1 ,2 ]
机构
[1] Natl Univ Singapore, Dept Stat & Data Sci, Singapore, Singapore
[2] Natl Univ Singapore, Duke NUS Grad Med Sch, Singapore, Singapore
[3] Boston Univ, Dept Biostat, Sch Publ Hlth, Boston, MA USA
[4] Natl Cheng Kung Univ, Dept Stat, Tainan, Taiwan
[5] Nankai Univ, Sch Stat & Data Sci, Tianjin, Peoples R China
基金
美国国家卫生研究院;
关键词
causal inference; genetics; genome-wide association study; instrument variable; model average; penalty function; single nucleotide polymorphism; CORONARY-HEART-DISEASE; CONFIDENCE-INTERVALS; LOGISTIC-REGRESSION; CLASS ESTIMATORS; PULSE PRESSURE; BLOOD-PRESSURE; INFERENCE; DISTRIBUTIONS; SELECTION; HEIGHT;
D O I
10.1002/sim.9819
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mendelian randomization is a technique used to examine the causal effect of a modifiable exposure on a trait using an observational study by utilizing genetic variants. The use of many instruments can help to improve the estimation precision but may suffer bias when the instruments are weakly associated with the exposure. To overcome the difficulty of high-dimensionality, we propose a model average estimator which involves using different subsets of instruments (single nucleotide polymorphisms, SNPs) to predict the exposure in the first stage, followed by weighting the submodels' predictions using penalization by common penalty functions such as least absolute shrinkage and selection operator (LASSO), smoothly clipped absolute deviation (SCAD) and minimax concave penalty (MCP). The model averaged predictions are then used as a genetically predicted exposure to obtain the estimation of the causal effect on the response in the second stage. The novelty of our model average estimator also lies in that it allows the number of submodels and the submodels' sizes to grow with the sample size. The practical performance of the estimator is examined in a series of numerical studies. We apply the proposed method on a real genetic dataset investigating the relationship between stature and blood pressure.
引用
收藏
页码:3547 / 3567
页数:21
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