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Effects of abnormal structure of sperm chromatin on the outcome of in vitro fertilization and embryo transfer / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 156-159, 2011.
Article in Chinese | WPRIM | ID: wpr-326973
ABSTRACT
<p><b>OBJECTIVE</b>To explore the effects of sperm chromatin structure abnormalities on the outcome of in vitro fertilization and embryo transfer (IVF-ET).</p><p><b>METHODS</b>Sperm DNA fragmentation and chromatin packaging defects were assessed in 136 couples undergoing IVF-ET because of infertility. The relationship between sperm DNA fragmentation, chromatin packaging defects and fertilization rate and clinical pregnancy was evaluated.</p><p><b>RESULTS</b>Both sperm DNA fragmentation and chromatin packaging defect had a negative correlation with fertilization rate (r=-0.198, P<0.05, and r=-0.389, P<0.01, respectively). Both parameters were higher in couples who failed to achieve pregnancy than those who achieved clinical pregnancy (10.74% vs. 5.40%, P<0.01 and 23.58% vs. 11.83%, P<0.01, respectively).</p><p><b>CONCLUSION</b>Abnormality of sperm chromatin structure is one of the reasons for IVF-ET failure. Examination of sperm chromatin structure is helpful in predicting the risk of IVF-ET failure and optimizing treatment of infertility.</p>
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Physiology / Spermatozoa / Therapeutics / Chromatin / Fertilization in Vitro / Treatment Outcome / Embryo Transfer / DNA Fragmentation / Genetics / Infertility Type of study: Prognostic study Limits: Adult / Female / Humans / Male / Pregnancy Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2011 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Physiology / Spermatozoa / Therapeutics / Chromatin / Fertilization in Vitro / Treatment Outcome / Embryo Transfer / DNA Fragmentation / Genetics / Infertility Type of study: Prognostic study Limits: Adult / Female / Humans / Male / Pregnancy Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2011 Type: Article