4.6 Article

Maternal blood contamination of collected cord blood can be identified using DNA methylation at three CpGs

Journal

CLINICAL EPIGENETICS
Volume 9, Issue -, Pages -

Publisher

BMC
DOI: 10.1186/s13148-017-0370-2

Keywords

Cord blood; Contamination; DNA methylation; 450K; Genotyping; Maternal blood; Blood banking

Funding

  1. National Institutes of Health [R21HD085849]
  2. AllerGen Network of Centers of Excellence [GE-2]
  3. Bill and Melinda Gates Foundation [OPP 1017641]
  4. National Research Foundation
  5. South African Medical Research Council
  6. Canadian Institute of Health Research

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Background: Cord blood is a commonly used tissue in environmental, genetic, and epigenetic population studies due to its ready availability and potential to inform on a sensitive period of human development. However, the introduction of maternal blood during labor or cross-contamination during sample collection may complicate downstream analyses. After discovering maternal contamination of cord blood in a cohort study of 150 neonates using Illumina 450K DNA methylation (DNAm) data, we used a combination of linear regression and random forest machine learning to create a DNAm-based screening method. We identified a panel of DNAm sites that could discriminate between contaminated and non-contaminated samples, then designed pyrosequencing assays to pre-screen DNA prior to being assayed on an array. Results: Maternal contamination of cord blood was initially identified by unusual X chromosome DNA methylation patterns in 17 males. We utilized our DNAm panel to detect contaminated male samples and a proportional amount of female samples in the same cohort. We validated our DNAm screening method on an additional 189 sample cohort using both pyrosequencing and DNAm arrays, as well as 9 publically available cord blood 450K data sets. The rate of contamination varied from 0 to 10% within these studies, likely related to collection specific methods. Conclusions: Maternal blood can contaminate cord blood during sample collection at appreciable levels across multiple studies. We have identified a panel of markers that can be used to identify this contamination, either post hoc after DNAm arrays have been completed, or in advance using a targeted technique like pyrosequencing.

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