TY - JOUR
T1 - Adaptive testing for multiple traits in a proportional odds model with applications to detect SNP-brain network associations
AU - for the Alzheimer's Disease Neuroimaging Initiative
AU - Kim, Junghi
AU - Pan, Wei
N1 - Publisher Copyright:
© 2017 WILEY PERIODICALS, INC.
PY - 2017/4/1
Y1 - 2017/4/1
N2 - There has been increasing interest in developing more powerful and flexible statistical tests to detect genetic associations with multiple traits, as arising from neuroimaging genetic studies. Most of existing methods treat a single trait or multiple traits as response while treating an SNP as a predictor coded under an additive inheritance mode. In this paper, we follow an earlier approach in treating an SNP as an ordinal response while treating traits as predictors in a proportional odds model (POM). In this way, it is not only easier to handle mixed types of traits, e.g., some quantitative and some binary, but it is also potentially more robust to the commonly adopted additive inheritance mode. More importantly, we develop an adaptive test in a POM so that it can maintain high power across many possible situations. Compared to the existing methods treating multiple traits as responses, e.g., in a generalized estimating equation (GEE) approach, the proposed method can be applied to a high dimensional setting where the number of phenotypes (p) can be larger than the sample size (n), in addition to a usual small P setting. The promising performance of the proposed method was demonstrated with applications to the Alzheimer's Disease Neuroimaging Initiative (ADNI) data, in which either structural MRI driven phenotypes or resting-state functional MRI (rs-fMRI) derived brain functional connectivity measures were used as phenotypes. The applications led to the identification of several top SNPs of biological interest. Furthermore, simulation studies showed competitive performance of the new method, especially for p > n.
AB - There has been increasing interest in developing more powerful and flexible statistical tests to detect genetic associations with multiple traits, as arising from neuroimaging genetic studies. Most of existing methods treat a single trait or multiple traits as response while treating an SNP as a predictor coded under an additive inheritance mode. In this paper, we follow an earlier approach in treating an SNP as an ordinal response while treating traits as predictors in a proportional odds model (POM). In this way, it is not only easier to handle mixed types of traits, e.g., some quantitative and some binary, but it is also potentially more robust to the commonly adopted additive inheritance mode. More importantly, we develop an adaptive test in a POM so that it can maintain high power across many possible situations. Compared to the existing methods treating multiple traits as responses, e.g., in a generalized estimating equation (GEE) approach, the proposed method can be applied to a high dimensional setting where the number of phenotypes (p) can be larger than the sample size (n), in addition to a usual small P setting. The promising performance of the proposed method was demonstrated with applications to the Alzheimer's Disease Neuroimaging Initiative (ADNI) data, in which either structural MRI driven phenotypes or resting-state functional MRI (rs-fMRI) derived brain functional connectivity measures were used as phenotypes. The applications led to the identification of several top SNPs of biological interest. Furthermore, simulation studies showed competitive performance of the new method, especially for p > n.
KW - ADNI
KW - GWAS
KW - MRI
KW - aSPU
KW - default mode network (DMN)
KW - functional connectivity
KW - high dimensional phenotypes
KW - rs-fMRI
UR - http://www.scopus.com/inward/record.url?scp=85012996301&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85012996301&partnerID=8YFLogxK
U2 - 10.1002/gepi.22033
DO - 10.1002/gepi.22033
M3 - Article
C2 - 28191669
AN - SCOPUS:85012996301
SN - 0741-0395
VL - 41
SP - 259
EP - 277
JO - Genetic epidemiology
JF - Genetic epidemiology
IS - 3
ER -