Altered DNA methylation in human placenta after (suspected) preterm labor

Author:

Schoorlemmer Jon123ORCID,Macías-Redondo Sofía1,Strunk Mark4,Ramos-Ruíz Ricardo5ORCID,Calvo Pilar26,Benito Rafael7,Paules Cristina26,Oros Daniel268

Affiliation:

1. Instituto Aragonés de Ciencias de la Salud (IACS) & Aragon Institute for Health Research (IIS Aragón), Zaragoza, Spain

2. Placental pathophysiology & fetal programming research group, B05 DGA & GIIS-028 del IISA

3. ARAID Foundation, Zaragoza, Spain

4. Instituto Aragonés de Ciencias de la Salud (IACS), Sequencing & Functional Genomics, Aragon Biomedical Research Center (CIBA), Zaragoza, Spain

5. Unidad de Genómica, Fundación Parque Científico de Madrid, Madrid, Spain

6. Aragon Institute for Health Research (IIS Aragón), Obstetrics Department, Hospital Clínico Universitario Zaragoza, Spain

7. Aragon Institute for Health Research (IIS Aragón), Microbiology Department, Hospital Clínico Universitario Zaragoza, Spain

8. Red de Salud Materno Infantil y del Desarrollo (SAMID), RETICS, Instituto de Salud Carlos III (ISCIII), Subdirección General de Evaluación y Fomento de la Investigación, Fondo Europeo de Desarrollo Regional (FEDER), Spain

Abstract

Aim: The aim of this study was to determine if alterations in DNA methylation in the human placenta would support suspected preterm labor as a pathologic insult associated with diminished placental health. Methods: We evaluated placental DNA methylation at seven loci differentially methylated in placental pathologies using targeted bisulfite sequencing, in placentas associated with preterm labor (term birth after suspected preterm labor [n = 15] and preterm birth [n = 15]), and controls (n = 15). Results: DNA methylation levels at the NCAM1 and PLAGL1 loci in placentas associated with preterm labor did differ significantly (p < 0.05) from controls. Discussion: Specific alterations in methylation patterns indicative of an unfavourable placental environment are associated with preterm labor per se and not restricted to preterm birth.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Genetics

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