Dataset Information

Meta-analysis of epigenome-wide association studies of cognitive abilities.

ABSTRACT: Cognitive functions are important correlates of health outcomes across the life-course. Individual differences in cognitive functions are partly heritable. Epigenetic modifications, such as DNA methylation, are susceptible to both genetic and environmental factors and may provide insights into individual differences in cognitive functions. Epigenome-wide meta-analyses for blood-based DNA methylation levels at ~420,000 CpG sites were performed for seven measures of cognitive functioning using data from 11 cohorts. CpGs that passed a Bonferroni correction, adjusting for the number of CpGs and cognitive tests, were assessed for: longitudinal change; being under genetic control (methylation QTLs); and associations with brain health (structural MRI), brain methylation and Alzheimer's disease pathology. Across the seven measures of cognitive functioning (meta-analysis n range: 2557-6809), there were epigenome-wide significant (P < 1.7 × 10^-8) associations for global cognitive function (cg21450381, P = 1.6 × 10^-8), and phonemic verbal fluency (cg12507869, P = 2.5 × 10^-9). The CpGs are located in an intergenic region on chromosome 12 and the INPP5A gene on chromosome 10, respectively. Both probes have moderate correlations (~0.4) with brain methylation in Brodmann area 20 (ventral temporal cortex). Neither probe showed evidence of longitudinal change in late-life or associations with white matter brain MRI measures in one cohort with these data. A methylation QTL analysis suggested that rs113565688 was a cis methylation QTL for cg12507869 (P = 5 × 10^-5 and 4 × 10^-13 in two lookup cohorts). We demonstrate a link between blood-based DNA methylation and measures of phonemic verbal fluency and global cognitive ability. Further research is warranted to understand the mechanisms linking genomic regulatory changes with cognitive function to health and disease.

SUBMITTER: Marioni RE

PROVIDER: S-EPMC6035894 | biostudies-literature | 2018 Nov

REPOSITORIES: biostudies-literature

ACCESS DATA

Publications

Meta-analysis of epigenome-wide association studies of cognitive abilities.

Marioni Riccardo E RE McRae Allan F AF Bressler Jan J Colicino Elena E Hannon Eilis E Li Shuo S Prada Diddier D Smith Jennifer A JA Trevisi Letizia L Tsai Pei-Chien PC Vojinovic Dina D Simino Jeannette J Levy Daniel D Liu Chunyu C Mendelson Michael M Satizabal Claudia L CL Yang Qiong Q Jhun Min A MA Kardia Sharon L R SLR Zhao Wei W Bandinelli Stefania S Ferrucci Luigi L Hernandez Dena G DG Singleton Andrew B AB Harris Sarah E SE Starr John M JM Kiel Douglas P DP McLean Robert R RR Just Allan C AC Schwartz Joel J Spiro Avron A Vokonas Pantel P Amin Najaf N Ikram M Arfan MA Uitterlinden Andre G AG van Meurs Joyce B J JBJ Spector Tim D TD Steves Claire C Baccarelli Andrea A AA Bell Jordana T JT van Duijn Cornelia M CM Fornage Myriam M Hsu Yi-Hsiang YH Mill Jonathan J Mosley Thomas H TH Seshadri Sudha S Deary Ian J IJ

Molecular psychiatry 20180108 11

Cognitive functions are important correlates of health outcomes across the life-course. Individual differences in cognitive functions are partly heritable. Epigenetic modifications, such as DNA methylation, are susceptible to both genetic and environmental factors and may provide insights into individual differences in cognitive functions. Epigenome-wide meta-analyses for blood-based DNA methylation levels at ~420,000 CpG sites were performed for seven measures of cognitive functioning using dat ...[more]

PMID: 29311653

Similar Datasets

Project description:BackgroundIn DNA methylation analyses like epigenome-wide association studies, effects in differentially methylated CpG sites are assessed. Two kinds of outcomes can be used for statistical analysis: Beta-values and M-values. M-values follow a normal distribution and help to detect differentially methylated CpG sites. As biological effect measures, differences of M-values are more or less meaningless. Beta-values are of more interest since they can be interpreted directly as differences in percentage of DNA methylation at a given CpG site, but they have poor statistical properties. Different frameworks are proposed for reporting estimands in DNA methylation analysis, relying on Beta-values, M-values, or both.ResultsWe present and discuss four possible approaches of achieving estimands in DNA methylation analysis. In addition, we present the usage of M-values or Beta-values in the context of bioinformatical pipelines, which often demand a predefined outcome. We show the dependencies between the differences in M-values to differences in Beta-values in two data simulations: a analysis with and without confounder effect. Without present confounder effects, M-values can be used for the statistical analysis and Beta-values statistics for the reporting. If confounder effects exist, we demonstrate the deviations and correct the effects by the intercept method. Finally, we demonstrate the theoretical problem on two large human genome-wide DNA methylation datasets to verify the results.ConclusionsThe usage of M-values in the analysis of DNA methylation data will produce effect estimates, which cannot be biologically interpreted. The parallel usage of Beta-value statistics ignores possible confounder effects and can therefore not be recommended. Hence, if the differences in Beta-values are the focus of the study, the intercept method is recommendable. Hyper- or hypomethylated CpG sites must then be carefully evaluated. If an exploratory analysis of possible CpG sites is the aim of the study, M-values can be used for inference.

Dataset Information

Meta-analysis of epigenome-wide association studies of cognitive abilities.

Publications

Meta-analysis of epigenome-wide association studies of cognitive abilities.

Similar Datasets

OmicsDI is part of the ELIXIR infrastructure

Tweets