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. 2017 Dec 1;21(4):343-350.
doi: 10.5935/1518-0557.20170061.

Effect of sperm DNA fragmentation on embryo development: clinical and biological aspects

Cristian Alvarez Sedó  1 , Melina Bilinski  1 , Daniela Lorenzi  1 , Heydy Uriondo  1 , Felicitas Noblía  1 , Valeria Longobucco  1 , Estefanía Ventimiglia Lagar  1 , Florencia Nodar  1
Affiliations

Effect of sperm DNA fragmentation on embryo development: clinical and biological aspects

Cristian Alvarez Sedó et al. JBRA Assist Reprod. .

Abstract

Objective: The aim of this study was to investigate the effect of sperm DNA fragmentation on fertilization rate, embryo development (blastulation rate), and pregnancy outcomes for ICSI cycles performed in a cohort of couples using donor eggs and to assess the remaining embryos that were not transferred or frozen for apoptotic markers.

Methods: Eighty-two women (egg recipients) were included in the study (2016) were included in the study. The recipients' mean age was 41.8±5.1 y/o (36-49), while the egg donors' mean age was 30.8±2.1 y/o (27-33). Even though donor egg cycles with frozen sperm samples are performed regularly in our center, 35 cycles were done using fresh sperm samples. The mean age of the males involved in the procedure was 40.1±5.2 y/o. Fertilization, blastulation, and pregnancy rates were assessed. The patients were divided into two groups, TUNEL <15% and ≥15%. In arrested embryos, ICC was performed to detect cleaved caspase-3, survivin, TUNEL, and DNA. The Student's t-test was used in between-group comparisons. The Mann-Whitney U-test was used to assess homogeneity. Pearson's correlation coefficient was also calculated. p<0.05 was considered statistically significant.

Results: This study showed that there is a negative correlation (R=-0.5) between DNA fragmentation and blastulation rate. High levels of DNA fragmentation were associated with low blastulation and pregnancy rates (per transfer); however, fertilization rate was not affected. Samples with higher levels of DNA fragmentation were associated with higher levels of DNA fragmentation in blastomeres without activating the apoptotic pathway (9.1% vs. 15.9%) (p<0.05). Blastomeres from samples with high DNA fragmentation activated the apoptotic pathway in higher levels than samples with TUNEL <15% (16.4% vs. 21.9%) (p<0.05).

Conclusion: Sperm DNA fragmentation was negatively correlated with blastulation and pregnancy rates even in good quality oocytes. High levels of DNA damage promote embryo arrest and induce the activation of the apoptotic pathway.

Keywords: DNA fragmentation; blastocyst; blastulation rate.

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Figures

Figure 1
Figure 1
In A, ICC for TUNEL and DNA staining fragmented DNA (1 and 2), non-fragmented DNA (3), and some blastomeres without DNA (arrows). In B, Blastomeres without DNA damage and Surv (+) (*) or DNA fragmentation and Surv (-) (**).
Figure 2
Figure 2
Embryos with condensed DNA (arrowhead) and TUNEL (+) (arrow). Surv and CC3 show different positive staining.
Figure 3
Figure 3
TUNEL assay to assess sperm DNA fragmentation. Positive cells (*), negative cells (**).
Figure 4
Figure 4
Correlation analysis between DNA fragmentation and Blastulation rate (R=-0.5).
See this image and copyright information in PMC

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