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

Journal: Clinical epigenetics

Volume: 9

Issue: 

Year of Publication: 2018

Affiliated Institutions:  Centre for Molecular Medicine and Therapeutics, BC Children's Hospital, Department of Medical Genetics, University of British Columbia, W th Ave, Vancouver, BC VZ H Canada. Department of Psychiatry and Mental Health, South African Medical Research Council (SAMRC) Unit on Anxiety and Stress Disorders, University of Cape Town, Groote Schuur Hospital, J, Anzio Road, Observatory, Cape Town, South Africa. Max Planck Institute of Psychiatry, Department of Translational Research in Psychiatry, Kraepelinstraße -, Munich, Germany. Department of Psychology and Logopedics, Faculty of Medicine, University of Helsinki, P.O.Box , Helsinki, Finland. Department of Paediatrics, MRC Unit on Child and Adolescent Health, University of Cape Town, Room ICH Building Red Cross Children's Hospital Klipfontein Road, Cape Town, South Africa. Department of Epidemiology, Harvard T. H. Chan School of Public Health, Huntington Avenue, Kresge Building, , Boston, MA USA.

Abstract summary 

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.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.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.

Authors & Co-authors:  Morin Alexander M AM Gatev Evan E McEwen Lisa M LM MacIsaac Julia L JL Lin David T S DTS Koen Nastassja N Czamara Darina D Räikkönen Katri K Zar Heather J HJ Koenen Karestan K Stein Dan J DJ Kobor Michael S MS Jones Meaghan J MJ

Study Outcome 

Source Link: Visit source

Statistics
Citations :  Hodyl NA, Roberts CT, Bianco-Miotto T. Cord blood DNA methylation biomarkers for predicting neurodevelopmental outcomes. Genes (Basel). 2016;7.
Authors :  13
Identifiers
Doi : 75
SSN : 1868-7083
Study Population
Male,Female
Mesh Terms
Cohort Studies
Other Terms
450K;Blood banking;Contamination;Cord blood;DNA methylation;Genotyping;Maternal blood
Study Design
Cohort Study,Cross Sectional Study
Study Approach
Country of Study
Publication Country
Germany