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A prospective study of non-invasive preimplantation genetic testing for Rh status, sex prediction and mtDNA copy number analysis using ddPCR on spent culture media

dc.contributor.authorGumusoglu-Acar, Ece
dc.contributor.authorSubasi, Sude
dc.contributor.authorCebeci, Merve
dc.contributor.authorSisman, Zehranur
dc.contributor.authorKaradisogullari, Ecenur
dc.contributor.authorKaramustafaoglu-Balci, Burcin
dc.contributor.authorGoksever-Celik, Hale
dc.contributor.authorBastu, Ercan
dc.contributor.authorBuyru, Faruk
dc.contributor.authorGunel, Tuba
dc.date.accessioned2026-11-05T11:00:52Z
dc.date.issued2026
dc.description.abstractPresence of embryo-derived cell-free DNA (cfDNA) in spent culture medium (SCM) represents a promising non-invasive alternative to the conventional preimplantation genetic testing (PGT). The present study evaluated the feasibility of using cfDNA isolated from SCM to determine Rhesus (Rh) status through Rh blood group D antigen (RHD) gene analysis, predicting sex-linked disorders using sex determining region Y (SRY) gene detection and assessing the association between mitochondrial cfDNA (cf-mtDNA) levels and maternal age using mitochondrially encoded cytochrome b (MT-CYB) gene quantification. SCM samples collected during the IVF process were subjected to cfDNA isolation and target regions including RHD exon 7 and exon 10, SRY and MT-CYB were analyzed using droplet digital PCR. RHD gene amplification was detected in 6 of 15 samples for exon 7 and in 11 samples for exon 10, with partial concordance between exons. SRY amplification was observed in 16 of 31 samples and was largely consistent with clinical sex data. MT-CYB was detected in 19 of 31 samples, with higher cf-mtDNA/nuclear cfDNA ratios observed in women >40 years of age. A moderate positive correlation trend was noted between maternal age and MT-CYB levels (r=0.46; P=0.354). These findings demonstrate the potential applicability of SCM-derived cfDNA for non-invasive Rh and sex determination without compromising embryo integrity, while mtDNA quantification may provide additional insights into embryo quality. Overall, SCM-based cfDNA analysis exhibited promise as a complementary tool for embryo selection in IVF workflows.
dc.description.issue3
dc.description.pages251
dc.description.sponsorshipThe present study was funded by the Istanbul University Scientific Research Projects Department (grant nos. 41128 and 41083) and TUBITAK 2209-A (grant nos. 1919B012433914 and 1919B012447586).
dc.description.volume32
dc.identifier.doi10.3892/etm.2026.13245
dc.identifier.issn1792-0981
dc.identifier.issn1792-1015
dc.identifier.urihttps://doi.org/10.3892/etm.2026.13245
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/10578
dc.identifier.wosWOS:001837342900001
dc.language.isoen
dc.publisherSPANDIDOS PUBL LTD
dc.relation.fundingIstanbul University Scientific Research Projects Department(Istanbul University)
dc.relation.fundingTUBITAK 2209-A(Turkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK))
dc.relation.fundingIstanbul University Scientific Research Projects Department [41128, 41083]
dc.relation.fundingTUBITAK 2209-A [1919B012433914, 1919B012447586]
dc.relation.hasversion10.3892/etm.2026.13245
dc.relation.ispartofEXPERIMENTAL AND THERAPEUTIC MEDICINE
dc.subjectspent culture media
dc.subjectRh blood group D antigen
dc.subjectsex determining region Y
dc.subjectmitochondrially encoded cytochrome b
dc.subjectnon-invasive preimplantation genetic testing
dc.subjectin vitro fertilization
dc.subjectCELL-FREE DNA
dc.subjectFETAL DNA
dc.subjectMATERNAL PLASMA
dc.subjectEMBRYO CULTURE
dc.subjectMUTATION
dc.subjectMITOCHONDRIA
dc.subjectDEFICIENCY
dc.subjectMedicine, Research & Experimental
dc.subjectResearch & Experimental Medicine
dc.titleA prospective study of non-invasive preimplantation genetic testing for Rh status, sex prediction and mtDNA copy number analysis using ddPCR on spent culture media
dc.typeArticle
oaire.citation.editionScience Citation Index Expanded (SCI-EXPANDED)
oaire.citation.issue3
oaire.citation.volume32
person.identifier.orcid0009-0007-7559-5378
person.identifier.ridQTU-5335-2026
person.identifier.ridA-8941-2018
person.identifier.ridAAD-3095-2020
person.identifier.ridA-8982-2018

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