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首页> 外文期刊>Protein and peptide letters >Sperm Mitochondrial DNA Copy Number Is Not a Predictor of Intracytoplasmic Sperm Injection (ICSI) Cycle Outcomes
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Sperm Mitochondrial DNA Copy Number Is Not a Predictor of Intracytoplasmic Sperm Injection (ICSI) Cycle Outcomes

机译:精子线粒体DNA拷贝数不是Intracytoplasmic精子注射的预测因子(ICSI)循环结果

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摘要

This study is to determine if sperm mitochondrial DNA copy number (mtDNA CN) is associated with fertilization, blastulation, blastocyst euploidy, and live birth rates in in vitro fertilization (IVF) with ICSI cycles. This is a cohort study conducted on stored sperm samples which were collected prospectively and used to create blastocysts transferred in a couple's first ICSI transfer cycle between 2007 and 2013 at a single large infertility center. Samples from ICSI cycles utilizing surgical or cryopreserved sperm or day 3 embryo biopsy were excluded. The primary outcome was live birth rate. Secondary outcomes included fertilization, usable blastocyst development, and blastocyst euploidy rates. Unique sperm samples used to create transferred embryos were identified. Mitochondrial DNA CN was evaluated using TaqMan (R) quantitative real-time polymerase chain reaction (qPCR) assays normalized to a nuclear control for relative quantitation. Linear regression and mixed effects logistic regression used were appropriate. A total of 2062 unique sperm samples used to create transferred embryos were included. Lower relative sperm mtDNA content was associated with increased pre-wash sperm motility (p < 0.001). No significant association was identified between sperm mtDNA CN and fertilization (p = 0.40), usable blastocyst development (p = 0.36), blastocyst euploid (p = 0.10), and live birth rates (p = 0.42) while adjusting for sperm pre-wash motility and maternal age. Sperm mtDNA CN is not prognostic of fertilization, usable blastocyst development, euploidy and live birth rates in an infertile population undergoing IVF with ICSI.
机译:该研究是确定精子线粒体DNA拷贝数(MTDNA CN)是否与具有ICSI循环的体外施肥(IVF)中的施肥,脱节,胚泡欧洲倍性和活率相关。这是在储存的精子样品上进行的队列研究,其预期收集并用于在夫妇在2007年至2013年在一个大型不孕症中产生在夫妇的第一个ICSI转移周期中转移的胚泡。排除了来自ICSI循环的样品,利用外科手术或冷冻保存的精子或第3天胚胎活检。主要结果是出生率。二次结果包括施肥,可用的胚泡发展和胚泡欧洲倍性率。鉴定了用于产生转移胚胎的独特精子样品。使用Taqman定量实时聚合酶链反应(QPCR)测定来评估线粒体DNA CN,其标准化为相对定量的核对控制。使用的线性回归和混合效应使用的逻辑回归是合适的。包括用于产生转移胚胎的2062个独特的精子样品。较低的相对精子MTDNA含量与增加的预洗涤精子活性有关(P <0.001)。在精子MTDNA CN和施肥之间没有鉴定明显关联(P = 0.40),可用的囊胚发育(P = 0.36),胚泡欧倍体(P = 0.10),并在调节精子预洗的同时(P = 0.42)动力和产妇年龄。 Sperm MTDNA CN不是施肥,可用的胚泡发育,欧洲稀释性和患者患者的不孕群体和活产率的预后。

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