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Impact of sperm DNA fragmentation on clinical in vitro fertilization outcomes

OBJECTIVE: We studied the association between sperm DNA fragmentation (SDF) and several clinical in vitro fertilization outcomes. METHODS: We retrospectively analyzed 169 consecutive fresh IVF cycles. Semen was collected on the day of oocyte retrieval, and we assessed standard semen parameters and t...

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Autores principales: Choi, Hwa Young, Kim, Seul Ki, Kim, Seok Hyun, Choi, Young Min, Jee, Byung Chul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Reproductive Medicine 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5783920/
https://www.ncbi.nlm.nih.gov/pubmed/29376020
http://dx.doi.org/10.5653/cerm.2017.44.4.224
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author Choi, Hwa Young
Kim, Seul Ki
Kim, Seok Hyun
Choi, Young Min
Jee, Byung Chul
author_facet Choi, Hwa Young
Kim, Seul Ki
Kim, Seok Hyun
Choi, Young Min
Jee, Byung Chul
author_sort Choi, Hwa Young
collection PubMed
description OBJECTIVE: We studied the association between sperm DNA fragmentation (SDF) and several clinical in vitro fertilization outcomes. METHODS: We retrospectively analyzed 169 consecutive fresh IVF cycles. Semen was collected on the day of oocyte retrieval, and we assessed standard semen parameters and the SDF level (by terminal deoxynucleotidyl transferase dUTP nick-end labeling). Poor ovarian response (POR) was defined as the collection of three or fewer mature oocytes. Oocytes were inseminated by the conventional method or intracytoplasmic sperm injection. RESULTS: SDF did not affect the fertilization or pregnancy rate, but did have a significant effect on the miscarriage rate. In the miscarriage group (n=10), the SDF level was significantly higher (23.9% vs. 14.1%) and number of mature oocytes was significantly lower (4.3 vs. 7.6) than in the live birth group (n=45). Multiple regression analysis showed that SDF was an independent predictor of miscarriage (odds ratio, 1.051; 95% confidence interval, 1.001–1.104). The cutoffs for the SDF level and number of mature oocytes that could predict miscarriage were >13% and ≤3, respectively. In the low-SDF group (≤13%), the miscarriage rate was similar in POR patients and those with a normal ovarian response (NOR; 14.2% vs. 4.3%). In the high-SDF group (>13%), the miscarriage rate was significantly higher in the POR group than in the NOR group (60.0% vs. 13.3%, p=0.045). CONCLUSION: Our study demonstrated that a high SDF level (>13%) was associated with a high miscarriage rate, and that it mainly contributed to miscarriage in the POR group. The results suggest that SDF measurements should be considered in couples with POR in order to predict the prognosis of the pregnancy.
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spelling pubmed-57839202018-01-26 Impact of sperm DNA fragmentation on clinical in vitro fertilization outcomes Choi, Hwa Young Kim, Seul Ki Kim, Seok Hyun Choi, Young Min Jee, Byung Chul Clin Exp Reprod Med Original Article OBJECTIVE: We studied the association between sperm DNA fragmentation (SDF) and several clinical in vitro fertilization outcomes. METHODS: We retrospectively analyzed 169 consecutive fresh IVF cycles. Semen was collected on the day of oocyte retrieval, and we assessed standard semen parameters and the SDF level (by terminal deoxynucleotidyl transferase dUTP nick-end labeling). Poor ovarian response (POR) was defined as the collection of three or fewer mature oocytes. Oocytes were inseminated by the conventional method or intracytoplasmic sperm injection. RESULTS: SDF did not affect the fertilization or pregnancy rate, but did have a significant effect on the miscarriage rate. In the miscarriage group (n=10), the SDF level was significantly higher (23.9% vs. 14.1%) and number of mature oocytes was significantly lower (4.3 vs. 7.6) than in the live birth group (n=45). Multiple regression analysis showed that SDF was an independent predictor of miscarriage (odds ratio, 1.051; 95% confidence interval, 1.001–1.104). The cutoffs for the SDF level and number of mature oocytes that could predict miscarriage were >13% and ≤3, respectively. In the low-SDF group (≤13%), the miscarriage rate was similar in POR patients and those with a normal ovarian response (NOR; 14.2% vs. 4.3%). In the high-SDF group (>13%), the miscarriage rate was significantly higher in the POR group than in the NOR group (60.0% vs. 13.3%, p=0.045). CONCLUSION: Our study demonstrated that a high SDF level (>13%) was associated with a high miscarriage rate, and that it mainly contributed to miscarriage in the POR group. The results suggest that SDF measurements should be considered in couples with POR in order to predict the prognosis of the pregnancy. The Korean Society for Reproductive Medicine 2017-12 2017-12-31 /pmc/articles/PMC5783920/ /pubmed/29376020 http://dx.doi.org/10.5653/cerm.2017.44.4.224 Text en Copyright © 2017. The Korean Society for Reproductive Medicine http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Choi, Hwa Young
Kim, Seul Ki
Kim, Seok Hyun
Choi, Young Min
Jee, Byung Chul
Impact of sperm DNA fragmentation on clinical in vitro fertilization outcomes
title Impact of sperm DNA fragmentation on clinical in vitro fertilization outcomes
title_full Impact of sperm DNA fragmentation on clinical in vitro fertilization outcomes
title_fullStr Impact of sperm DNA fragmentation on clinical in vitro fertilization outcomes
title_full_unstemmed Impact of sperm DNA fragmentation on clinical in vitro fertilization outcomes
title_short Impact of sperm DNA fragmentation on clinical in vitro fertilization outcomes
title_sort impact of sperm dna fragmentation on clinical in vitro fertilization outcomes
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5783920/
https://www.ncbi.nlm.nih.gov/pubmed/29376020
http://dx.doi.org/10.5653/cerm.2017.44.4.224
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