Genome-wide DNA methylation and gene expression in human placentas derived from assisted reproductive technology

Decreased expressions of TRIM28, NOTCH3, and DLK1 bring forth potential mechanisms for several phenotypic features associated with ART. Our results support previous procedure specific findings: the changes associated with growth and metabolism link more prominently to the fresh embryo transfer with smaller placentas and newborns, than to the frozen embryo transfer with larger placentas and newborns. Furthermore, since the observed changes associate also with subfertility, they offer a precious insight to the molecular background of infertility.

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Publication Details

Journal
Communications Medicine
Published
2024-12-19
DOI
https://doi.org/10.1038/s43856-024-00694-6
Citations
6
Primary Topic
Genetic Syndromes and Imprinting
Type
article
Field-Weighted Citation Impact
3.30

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article

Genome-wide DNA methylation and gene expression in human placentas derived from assisted reproductive technology

E. Wallén, Christel Hydén‐Granskog, Aila Tiitinen, K. Rämö et al.
6 citations
Communications Medicine
Genetic Syndromes and Imprinting
3.30
article

Genome-wide DNA methylation and gene expression in human placentas derived from assisted reproductive technology

E. Wallén, Christel Hydén‐Granskog, Aila Tiitinen, K. Rämö, Heidi Marjonen, Juho Vehviläinen, Viveca Söderström‐Anttila, Timo Tuuri, Hanna Kahila, Nina Kaminen‐Ahola, Pauliina Auvinen, Ida Laukkanen
article en
6 citations

Abstract

Decreased expressions of TRIM28, NOTCH3, and DLK1 bring forth potential mechanisms for several phenotypic features associated with ART. Our results support previous procedure specific findings: the changes associated with growth and metabolism link more prominently to the fresh embryo transfer with smaller placentas and newborns, than to the frozen embryo transfer with larger placentas and newborns. Furthermore, since the observed changes associate also with subfertility, they offer a precious insight to the molecular background of infertility.

Communications MedicineVol. 4(1)
University of Helsinki (FI), Helsinki University Hospital (FI), Väestöliitto (FI)
Helsingin Yliopisto, Suomen Kulttuurirahasto
Openalex Percentile: Top 7%
Genetic Syndromes and Imprinting
3.30
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