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Does centrifugation and semen processing with swim up at 37°C yield sperm with better DNA integrity compared to centrifugation and processing at room temperature?

AIM: To evaluate whether semen processing at 37°C yield sperm with better DNA integrity compared to centrifugation and processing at room temperature (RT) by swim-up method. SETTINGS: This study was done at tertiary care center attached to Reproductive Medicine Unit and Medical College. DESIGN: Pros...

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Detalles Bibliográficos
Autores principales: Repalle, Deepthi, Chittawar, Priya Bhave, Bhandari, Shilpa, Joshi, Geetanjali, Paranjape, Mansi, Joshi, Charudutta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3713571/
https://www.ncbi.nlm.nih.gov/pubmed/23869146
http://dx.doi.org/10.4103/0974-1208.112375
Descripción
Sumario:AIM: To evaluate whether semen processing at 37°C yield sperm with better DNA integrity compared to centrifugation and processing at room temperature (RT) by swim-up method. SETTINGS: This study was done at tertiary care center attached to Reproductive Medicine Unit and Medical College. DESIGN: Prospective pilot study. PATIENTS: Normozoospermic men (n = 50) undergoing diagnostic semen analysis. MATERIALS AND METHODS: Normozoospermic samples (World Health Organization, 2010 criteria) after analysis was divided into two aliquots (0.5 mL each); one was processed at 37°C and the other at RT by swim-up method. DNA fragmentation of both samples post wash was calculated by acridine orange method. STATISTICAL ANALYSIS USED: The values of sperm DNA fragmentation were represented as mean and standard error (mean ± SEM) of the mean. Paired t-test was used for calculating the sperm DNA integrity difference between post wash at RT and 37°C. RESULTS: Statistically significant difference was not observed in post wash sperm DNA fragmentation values at 37°C compared to RT. CONCLUSION: Our data represents that there was no significant difference in sperm DNA fragmentation values of samples processed at 37°C and at RT. Hence, sperm processing at 37°C does not yield sperm with better DNA integrity compared to centrifugation and processing at RT.