Human semen cryopreservation

Sperm cryopreservation is widely used for both research and reproduction purposes, but its effect on sperm DNA damage remains controversial. Sperm DNA fragmentation (SDF) has become an important biomarker to assess male infertility. In particular, the differentiation between single- and double-stran...

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Detalles Bibliográficos
Autores: Ribas-Maynou, Jordi|||0000-0002-9101-2044, Fernandez Encinas, Alba|||0000-0003-2701-4739, García-Peiró, Agustí, Prada, E., Abad, Carlos|||0000-0002-2703-4062, Amengual Guedan, Maria Jose|||0000-0002-5385-3061, Navarro, J., Benet i Català, Jordi|||0000-0001-6185-2555
Tipo de recurso: artículo
Fecha de publicación:2014
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:307189
Acceso en línea:https://ddd.uab.cat/record/307189
https://dx.doi.org/urn:doi:10.1111/j.2047-2927.2013.00158.x
Access Level:acceso abierto
Palabra clave:Comet assay
Cryopreservation
Miscarriage
Oxidative stress
Sperm DNA fragmentation
Descripción
Sumario:Sperm cryopreservation is widely used for both research and reproduction purposes, but its effect on sperm DNA damage remains controversial. Sperm DNA fragmentation (SDF) has become an important biomarker to assess male infertility. In particular, the differentiation between single- and double-stranded DNA fragmentation (ssSDF and dsSDF) has clinical implications for male infertility where ssSDF is associated with reduced fertility, whereas dsSDF is associated with increased risk of miscarriage. In this study, semen samples from 30 human males have been analysed in both fresh and cryopreserved using the alkaline and neutral Comet assays. Results show an increase of about 10% of ssSDF, assessed by the alkaline Comet assay, regardless of the male fertility status. Neutral Comet analysis of dsSDF does not show any statistical increase when comparing fresh and cryopreserved samples in any of the patient groups. Results support previous reports that oxidative stress is the major effector in DNA damage during sample cryopreservation, as, on one hand, ssSDF has previously been related to oxidative damage and, on the other hand, we have not found any effect on dsSDF. Therefore, there might be a slight risk of decreased fertility after using a freezed sample, but no evidence for increased miscarriage risk from cryopreserved spermatozoa should be expected.