TY - JOUR
T1 - A Structured Approach to Evaluating Life-Course Hypotheses
T2 - Moving beyond Analyses of Exposed Versus Unexposed in the -Omics Context
AU - Zhu, Yiwen
AU - Simpkin, Andrew J.
AU - Suderman, Matthew J.
AU - Lussier, Alexandre A.
AU - Walton, Esther
AU - Dunn, Erin C.
AU - Smith, Andrew D.A.C.
N1 - Publisher Copyright:
© 2021 The Author(s) 2020.
PY - 2021/6/1
Y1 - 2021/6/1
N2 - The structured life-course modeling approach (SLCMA) is a theory-driven analytical method that empirically compares multiple prespecified life-course hypotheses characterizing time-dependent exposure-outcome relationships to determine which theory best fits the observed data. In this study, we performed simulations and empirical analyses to evaluate the performance of the SLCMA when applied to genomewide DNA methylation (DNAm). Using simulations (n = 700), we compared 5 statistical inference tests used with SLCMA, assessing the familywise error rate, statistical power, and confidence interval coverage to determine whether inference based on these tests was valid in the presence of substantial multiple testing and small effects - 2 hallmark challenges of inference from -omics data. In the empirical analyses (n = 703), we evaluated the time-dependent relationship between childhood abuse and genomewide DNAm. In simulations, selective inference and the max-|t|-test performed best: Both controlled the familywise error rate and yielded moderate statistical power. Empirical analyses using SLCMA revealed time-dependent effects of childhood abuse on DNAm. Our findings show that SLCMA, applied and interpreted appropriately, can be used in high-throughput settings to examine time-dependent effects underlying exposure-outcome relationships over the life course. We provide recommendations for applying the SLCMA in -omics settings and encourage researchers to move beyond analyses of exposed versus unexposed individuals.
AB - The structured life-course modeling approach (SLCMA) is a theory-driven analytical method that empirically compares multiple prespecified life-course hypotheses characterizing time-dependent exposure-outcome relationships to determine which theory best fits the observed data. In this study, we performed simulations and empirical analyses to evaluate the performance of the SLCMA when applied to genomewide DNA methylation (DNAm). Using simulations (n = 700), we compared 5 statistical inference tests used with SLCMA, assessing the familywise error rate, statistical power, and confidence interval coverage to determine whether inference based on these tests was valid in the presence of substantial multiple testing and small effects - 2 hallmark challenges of inference from -omics data. In the empirical analyses (n = 703), we evaluated the time-dependent relationship between childhood abuse and genomewide DNAm. In simulations, selective inference and the max-|t|-test performed best: Both controlled the familywise error rate and yielded moderate statistical power. Empirical analyses using SLCMA revealed time-dependent effects of childhood abuse on DNAm. Our findings show that SLCMA, applied and interpreted appropriately, can be used in high-throughput settings to examine time-dependent effects underlying exposure-outcome relationships over the life course. We provide recommendations for applying the SLCMA in -omics settings and encourage researchers to move beyond analyses of exposed versus unexposed individuals.
KW - -omics
KW - Avon Longitudinal Study of Parents and Children
KW - DNA methylation
KW - life course
KW - postselection inference
KW - structured approach
UR - http://www.scopus.com/inward/record.url?scp=85107390400&partnerID=8YFLogxK
U2 - 10.1093/aje/kwaa246
DO - 10.1093/aje/kwaa246
M3 - Article
SN - 0002-9262
VL - 190
SP - 1101
EP - 1112
JO - American Journal of Epidemiology
JF - American Journal of Epidemiology
IS - 6
ER -