The Utility of Sperm DNA Fragmentation as a Diagnostic Tool for Male Infertility and Its Predictive Value for Assisted Reproductive Technology Outcomes

Standard semen parameters remain the cornerstone of male infertility evaluation, though they often poorly reflect the likelihood of success in assisted reproductive technology (ART). This study evaluates sperm DNA fragmentation (SDF) as a diagnostic tool for male infertility and predictive biomarker...

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Detalles Bibliográficos
Autores: Zurera Egea, Coral|||0000-0003-1712-5216, Mateo, Sílvia, Novo Bruña, Sergio, Asensio, Marta, Boada i Palà, Montserrat|||0000-0003-0389-0638, Antich, Marta, Rovira, Sergi, Sarrate Navas, Zaida|||0000-0001-9677-1376, Blanco, Joan|||0000-0003-0647-3856, Anton, Ester|||0000-0002-8914-2667
Tipo de recurso: artículo
Fecha de publicación:2025
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:318769
Acceso en línea:https://ddd.uab.cat/record/318769
https://dx.doi.org/urn:doi:10.3390/ijms26136314
Access Level:acceso abierto
Palabra clave:SDF
Infertility
Seminal alterations
Fertilization
Blastocyst formation
Embryoquality
Implantation
Descripción
Sumario:Standard semen parameters remain the cornerstone of male infertility evaluation, though they often poorly reflect the likelihood of success in assisted reproductive technology (ART). This study evaluates sperm DNA fragmentation (SDF) as a diagnostic tool for male infertility and predictive biomarker for ART success. Semen samples were collected from 20 fertile donors and 40 infertile patients with abnormal semen parameters. A fraction of each sample was used for SDF assessment via TUNEL assay and flow cytometry, while the remaining portion was processed for conventional semen analysis and ART. Infertile patients exhibited higher SDF levels (32.77 ± 13.61%) compared to donors (22.19 ± 8.37%; p < 0.01), a difference that remained statistically significant across all subgroups stratified by semen parameters. Additionally, significant correlations were obtained between the percentage of SDF and sperm count (r = -0.4036), motility (r = -0.6377), and morphology (r = -0.2783). Regarding ART outcomes, patients with low-quality embryos exhibited higher SDF levels compared to those with high-quality embryos (30.02 ± 12.52% vs. 23.16 ± 8.41%; p = 0.0036). Receiver operating characteristic (ROC) curve analysis revealed an area under the curve (AUC) above 0.7 for the classification of male infertility as well as the assessment of embryo quality. Overall, our results support the utility of SDF as both a diagnostic biomarker for male infertility and a predictive indicator of embryo quality in ART, particularly in the presence of an oocyte-related female factor.