DNA Methylation Signatures in Paired Placenta and Umbilical Cord Samples: Relationship with Maternal Pregestational Body Mass Index and Offspring Metabolic Outcomes

• Published in: Biomedicines Vol. 12; no. 2; p. 301
• Main Authors: Gómez-Vilarrubla, Ariadna, Mas-Parés, Berta, Carreras-Badosa, Gemma, Bonmatí-Santané, Alexandra, Martínez-Calcerrada, Jose-Maria, Niubó-Pallàs, Maria, de Zegher, Francis, Ibáñez, Lourdes, López-Bermejo, Abel, Bassols, Judit
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.01.2024
• Subjects: Birth weight; Body mass index; Diabetes mellitus (non-insulin dependent); Disease susceptibility; DNA; DNA methylation; Epigenetic inheritance; Epigenetics; Genes; Genomes; Genotype & phenotype; Gestational age; Glucose; Insulin resistance; Laboratories; Metabolic disorders; Metabolic pathways; Metabolism; Methylation; Newborn babies; Obesity; Offspring; Phenotypes; Physiology; Placenta; pregestational obesity; Pregnancy; Type 2 diabetes; Ultrasonic imaging; Umbilical cord; Spain; United States > US; DNA methylation; pregestational obesity; placenta; umbilical cord
• ISSN: 2227-9059; 2227-9059
• DOI: 10.3390/biomedicines12020301

An epigenomic approach was used to study the impact of maternal pregestational body mass index (BMI) on the placenta and umbilical cord methylomes and their potential effect on the offspring’s metabolic phenotype. DNA methylome was assessed in 24 paired placenta and umbilical cord samples. The differentially methylated CpGs associated with maternal pregestational BMI were identified and the metabolic pathways and the potentially related diseases affected by their annotated genes were determined. Two top differentially methylated CpGs were studied in 90 additional samples and the relationship with the offspring’s metabolic phenotype was determined. The results showed that maternal pregestational BMI is associated with the methylation of genes involved in endocrine and developmental pathways with potential effects on type 2 diabetes and obesity. The methylation and expression of HADHA and SLC2A8 genes in placenta and umbilical cord were related to several metabolic parameters in the offspring at 6 years (weight SDS, height SDS, BMI SDS, Δ BW-BMI SDS, FM SDS, waist, SBP, TG, HOMA-IR, perirenal fat; all p < 0.05). Our data suggest that epigenetic analysis in placenta and umbilical cord may be useful for identifying individual vulnerability to later metabolic diseases.