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Updated: Mar 8, 2026

Methodology for Accurate Detection of Mitochondrial DNA Methylation
Published on: May 20, 2018
DNA Methylation Patterns in Cord Blood of Neonates Across Gestational Age: Association With Cell-Type Proportions
Susan M Braid1, Kwame Okrah, Amol Shetty
1Susan M. Braid, DrPH, MSN, NNP-BC, is Assistant Professor, College of Health Sciences, Old Dominion University, Norfolk, Virginia. Kwame Okrah, PhD, is Biostatistician, Genentech, Inc., South San Francisco, California. Amol Shetty, MS, is Senior Bioinformatics Software Engineer, School of Medicine, Institute for Genome Sciences, University of Maryland, Baltimore. Hector Corrada Bravo, PhD, is Associate Professor, Institute for Advanced Computer Studies, Center for Bioinformatics and Computational Biology, and Department of Computer Science, University of Maryland, College Park.
Background:
A statistical methodology is available to estimate the proportion of cell types (cellular heterogeneity) in adult whole blood specimens used in epigenome-wide association studies (EWAS). However, there is no methodology to estimate the proportion of cell types in umbilical cord blood (also a heterogeneous tissue) used in EWAS.
Objectives:
The objectives of this study were to determine whether differences in DNA methylation (DNAm) patterns in umbilical cord blood are the result of blood cell type proportion changes that typically occur across gestational age and to demonstrate the effect of cell type proportion confounding by comparing preterm infants exposed and not exposed to antenatal steroids.
Methods:
We obtained DNAm profiles of cord blood using the Illumina HumanMethylation27k BeadChip array for 385 neonates from the Boston Birth Cohort. We estimated cell type proportions for six cell types using the deconvolution method developed by .
Results:
The cell type proportion estimates segregated into two groups that were significantly different by gestational age, indicating that gestational age was associated with cell type proportion. Among infants exposed to antenatal steroids, the number of differentially methylated CpGs dropped from 127 to 1 after controlling for cell type proportion.
Discussion:
EWAS utilizing cord blood are confounded by cell type proportion. Careful study design including correction for cell type proportion and interpretation of results of EWAS using cord blood are critical.
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