1. Metabolomic data presents challenges for epidemiological meta-analysis: a case study of childhood body mass index from the ECHO consortium
- Author
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Prince, Nicole, Liang, Donghai, Tan, Youran, Alshawabkeh, Akram, Angel, Elizabeth Esther, Busgang, Stefanie A, Chu, Su H, Cordero, José F, Curtin, Paul, Dunlop, Anne L, Gilbert-Diamond, Diane, Giulivi, Cecilia, Hoen, Anne G, Karagas, Margaret R, Kirchner, David, Litonjua, Augusto A, Manjourides, Justin, McRitchie, Susan, Meeker, John D, Pathmasiri, Wimal, Perng, Wei, Schmidt, Rebecca J, Watkins, Deborah J, Weiss, Scott T, Zens, Michael S, Zhu, Yeyi, Lasky-Su, Jessica A, and Kelly, Rachel S
- Subjects
Medical Biochemistry and Metabolomics ,Reproductive Medicine ,Biomedical and Clinical Sciences ,Women's Health ,Clinical Research ,Pediatric ,Reproductive health and childbirth ,Child ,Female ,Pregnancy ,Humans ,Child ,Preschool ,Body Mass Index ,Reproducibility of Results ,Metabolomics ,Linear Models ,Lysine ,Metabolomic meta-analysis ,Metabolomic epidemiology ,Maternal metabolites ,Childhood obesity ,Analytical Chemistry ,Biochemistry and Cell Biology ,Clinical Sciences ,Biochemistry and cell biology ,Medical biochemistry and metabolomics ,Analytical chemistry - Abstract
IntroductionMeta-analyses across diverse independent studies provide improved confidence in results. However, within the context of metabolomic epidemiology, meta-analysis investigations are complicated by differences in study design, data acquisition, and other factors that may impact reproducibility.ObjectiveThe objective of this study was to identify maternal blood metabolites during pregnancy (> 24 gestational weeks) related to offspring body mass index (BMI) at age two years through a meta-analysis framework.MethodsWe used adjusted linear regression summary statistics from three cohorts (total N = 1012 mother-child pairs) participating in the NIH Environmental influences on Child Health Outcomes (ECHO) Program. We applied a random-effects meta-analysis framework to regression results and adjusted by false discovery rate (FDR) using the Benjamini-Hochberg procedure.ResultsOnly 20 metabolites were detected in all three cohorts, with an additional 127 metabolites detected in two of three cohorts. Of these 147, 6 maternal metabolites were nominally associated (P 100), we failed to identify significant metabolite associations after FDR correction. Our investigation demonstrates difficulties in applying epidemiological meta-analysis to clinical metabolomics, emphasizes challenges to reproducibility, and highlights the need for standardized best practices in metabolomic epidemiology.
- Published
- 2024