assisted reproductive technology (art)

辅助生殖技术 ( ART )
  • 文章类型: Journal Article
    BACKGROUND: Hepatitis B virus (HBV) is one of the most widespread viruses worldwide and a major cause of hepatitis, cirrhosis, and hepatocellular carcinoma. Previous studies have revealed the impacts of HBV infection on fertility. An increasing number of infertile couples with chronic hepatitis B (CHB) virus infection choose assisted reproductive technology (ART) to meet their fertility needs. Despite the high prevalence of HBV, the effects of HBV infection on assisted reproduction treatment remain limited and contradictory. OBJECTIVE: The aim of this study was to provide a comprehensive overview of the effect of HBV infection on fertility and discuss its effects on pregnancy outcomes, vertical transmission, pregnancy complications, and viral activity during ART treatment. METHODS: We conducted a literature search in PubMed for studies on HBV infection and ART published from 1996 to 2022. RESULTS: HBV infection negatively affected fertility in both males and females. Existing research shows that HBV infection may increase the risk of pregnancy complications in couples undergoing assisted reproduction treatment. The impact of HBV infection on the pregnancy outcomes of ART is still controversial. Current evidence does not support that ART increases the risk of vertical transmission of HBV, while relevant studies are limited. With the development of ART, the risk of HBV reactivation (HBVr) is increasing, especially due to the wide application of immunosuppressive therapy. CONCLUSIONS: Regular HBV infection screening and HBVr risk stratification and management are essential to prevent HBVr during ART. The determination of optimal strategy and timing of prophylactic anti-HBV therapy during ART still needs further investigation.
    乙型肝炎病毒(HBV)是世界范围内传播最广泛的病毒之一,也是肝炎、肝硬化和肝细胞癌的主要病因。既往研究已经揭示了HBV感染对生育能力的影响。近年来越来越多患有乙肝的不孕夫妇选择通过辅助生殖技术(ART)来满足他们的生育需求。尽管HBV感染率很高,但目前其感染对辅助生殖治疗影响的研究仍较为有限且存在矛盾。本研究旨在全面概述HBV感染对生育能力的影响,并讨论其对妊娠结局、垂直传播、妊娠并发症和ART治疗期间病毒活性的影响。我们通过在PubMed上检索1996年至2022年间发表的关于HBV和ART的研究,发现HBV感染对男性和女性的生育能力均存在负面的影响。现有研究表明,在接受ART治疗的夫妇中,HBV感染可能会增加妊娠并发症的风险。HBV感染对ART妊娠结局的影响目前仍然存在争议,且现有的证据不支持ART增加HBV垂直传播风险的观点,同时相关研究较为有限。随着ART的发展,特别是免疫抑制疗法的广泛应用,HBV再激活(HBVr)的风险正在增加。综上所述,定期进行HBV感染筛查和HBVr风险分层及管理对预防ART期间的HBVr至关重要,但ART期间预防性抗HBV治疗的最佳策略和时机的确定仍需进一步研究。.
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  • 文章类型: Journal Article
    卵巢纤维化,以卵巢成纤维细胞的过度增殖和细胞外基质(ECM)的积累为特征,是卵巢功能障碍的主要原因之一。尽管卵巢纤维化在维持哺乳动物卵巢的正常生理功能方面具有关键作用,对这种情况的研究被大大低估了,这导致临床上对纤维化引起的卵巢功能障碍缺乏治疗选择。本文综述了卵巢纤维化分子机制的研究进展,包括TGF-β,细胞外基质,炎症,和其他促纤维化因素导致卵巢异常纤维化。此外,我们总结了目前针对卵巢纤维化的卵巢功能障碍的治疗方法,包括抗纤维化药物,干细胞移植,和外泌体疗法。本文就卵巢纤维化的研究进展作一综述,提出针对卵巢纤维化治疗卵巢功能障碍的潜在治疗策略。
    Ovarian fibrosis, characterized by the excessive proliferation of ovarian fibroblasts and the accumulation of extracellular matrix (ECM), serves as one of the primary causes of ovarian dysfunction. Despite the critical role of ovarian fibrosis in maintaining the normal physiological function of the mammalian ovaries, research on this condition has been greatly underestimated, which leads to a lack of clinical treatment options for ovarian dysfunction caused by fibrosis. This review synthesizes recent research on the molecular mechanisms of ovarian fibrosis, encompassing TGF-β, extracellular matrix, inflammation, and other profibrotic factors contributing to abnormal ovarian fibrosis. Additionally, we summarize current treatment approaches for ovarian dysfunction targeting ovarian fibrosis, including antifibrotic drugs, stem cell transplantation, and exosomal therapies. The purpose of this review is to summarize the research progress on ovarian fibrosis and to propose potential therapeutic strategies targeting ovarian fibrosis for the treatment of ovarian dysfunction.
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  • 文章类型: Journal Article
    这篇全面的综述探讨了辅助生殖技术(ART)领域内精子选择技术的发展。我们的分析深入研究了一系列方法,从传统方法如密度梯度离心到先进技术,如磁激活细胞分选(MACS)和胞浆内形态选择精子注射(IMSI)。我们严格评估这些方法在精子运动性方面的功效,形态学,DNA完整性,和其他功能属性,提供了他们的临床结果的详细比较。我们强调了从传统精子选择方法的转变,主要关注物理特征,更复杂的技术,提供精子分子特性的全面评估。这种转变不仅有望增强对受精成功的预测,而且对提高胚胎质量和增加活产的机会具有重要意义。通过综合各种研究和研究论文,我们对ART中不同精子选择程序的可预测性进行了深入分析.该综述还讨论了这些方法的临床适用性,强调他们在塑造辅助生殖未来方面的潜力。我们的研究结果表明,在ART中整合先进的精子选择策略可以导致更具成本效益的治疗,缩短持续时间和更高的成功率。这篇综述旨在为生殖医学的临床医生和研究人员提供有关ART中精子选择技术的现状和未来前景的全面见解。
    This comprehensive review explores the evolving landscape of sperm selection techniques within the realm of Assisted Reproductive Technology (ART). Our analysis delves into a range of methods from traditional approaches like density gradient centrifugation to advanced techniques such as Magnetic-Activated Cell Sorting (MACS) and Intracytoplasmic Morphologically Selected Sperm Injection (IMSI). We critically assess the efficacy of these methods in terms of sperm motility, morphology, DNA integrity, and other functional attributes, providing a detailed comparison of their clinical outcomes. We highlight the transition from conventional sperm selection methods, which primarily focus on physical characteristics, to more sophisticated techniques that offer a comprehensive evaluation of sperm molecular properties. This shift not only promises enhanced prediction of fertilization success but also has significant implications for improving embryo quality and increasing the chances of live birth. By synthesizing various studies and research papers, we present an in-depth analysis of the predictability of different sperm selection procedures in ART. The review also discusses the clinical applicability of these methods, emphasizing their potential in shaping the future of assisted reproduction. Our findings suggest that the integration of advanced sperm selection strategies in ART could lead to more cost-effective treatments with reduced duration and higher success rates. This review aims to provide clinicians and researchers in reproductive medicine with comprehensive insights into the current state and future prospects of sperm selection technologies in ART.
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  • 文章类型: Journal Article
    Klinefelter综合征(KS)是男性中最常见的染色体疾病。它由额外的X染色体定义,47,XXY,由于亲本配子发生过程中染色体分离的错误。主要表型是生殖功能受损,低睾酮和不孕症的形式。这篇综述全面考察了导致KS不孕的遗传和生理因素。除了紧急辅助生殖技术,以及KS患者在寻求不孕症治疗时面临的独特伦理挑战。KS的病理基础是精子发生过程中减数分裂错误的易感性增加,导致非整倍体甚至多倍体配子。增强这种易感性的特定遗传元件包括调节染色体突触和分离的检查点基因中的多态性。生理学上,额外的性染色体也通过调节间质和支持细胞功能而改变睾丸内分泌和代谢,共同损害正常的精子发育。此外,表观遗传修饰如异常DNA甲基化越来越多地参与这些破坏。我们还讨论了KS患者不孕症管理中的辅助生殖方法。辅助生殖方法的应用,随着对多余X染色体导致的减数分裂和内分泌紊乱的深刻理解,在为KS个体提供亲生父母方面显示出希望。这将需要具有遗传学背景的专家之间继续进行多学科合作,生理学,伦理与临床生殖医学。
    Klinefelter syndrome (KS) is the most prevalent chromosomal disorder occurring in males. It is defined by an additional X chromosome, 47,XXY, resulting from errors in chromosomal segregation during parental gametogenesis. A major phenotype is impaired reproductive function, in the form of low testosterone and infertility. This review comprehensively examines the genetic and physiological factors contributing to infertility in KS, in addition to emergent assisted reproductive technologies, and the unique ethical challenges KS patients face when seeking infertility treatment. The pathology underlying KS is increased susceptibility for meiotic errors during spermatogenesis, resulting in aneuploid or even polyploid gametes. Specific genetic elements potentiating this susceptibility include polymorphisms in checkpoint genes regulating chromosomal synapsis and segregation. Physiologically, the additional sex chromosome also alters testicular endocrinology and metabolism by dysregulating interstitial and Sertoli cell function, collectively impairing normal sperm development. Additionally, epigenetic modifications like aberrant DNA methylation are being increasingly implicated in these disruptions. We also discuss assisted reproductive approaches leveraged in infertility management for KS patients. Application of assisted reproductive approaches, along with deep comprehension of the meiotic and endocrine disturbances precipitated by supernumerary X chromosomes, shows promise in enabling biological parenthood for KS individuals. This will require continued multidisciplinary collaboration between experts with background of genetics, physiology, ethics and clinical reproductive medicine.
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  • 文章类型: Journal Article
    目的:探讨不同年龄女性进行冻融优质单囊胚移植的可行性。
    方法:将1,279名妇女分为四组:38-40岁组(n=147),35-37岁组(n=164),30-34岁组(n=483),<30岁组(n=485)。进行基线特征和妊娠及新生儿结局的组间比较。
    结果:临床妊娠率(47.6%),38-40岁组的活产率(34.0%)显着低于30-34岁组(64.4%,50.9%,分别;所有P<0.001)和<30岁组(62.9%,50.7%,分别;所有P<0.001)。然而,35~37岁组与其他三组在这两个维度上差异均无统计学意义(均P>0.05)。此外,生化妊娠率没有差异,流产,或产科或新生儿并发症四组(均P>0.05)。根据多元逻辑回归分析,35-37岁组与非活产结局无关,不良妊娠结局,或产科或新生儿并发症。然而,38-40岁是非活产(OR=2.121,95%CI:1.233-3.647)和不良妊娠结局(OR=1.630,95%CI:1.010-2.633)的危险因素。事后功效分析表明,该研究具有足够的功效来检测有意义的差异。
    结论:冻融的高质量单囊胚移植对35-37岁女性的妊娠结局与年轻患者相同。未来需要更大人群的前瞻性随机对照研究来验证该方法的可行性和安全性。
    OBJECTIVE: To investigate the feasibility of performing frozen-thawed high-quality single blastocyst transfer in women of different ages.
    METHODS: A total of 1,279 women were divided into four groups: a 38-40-year-old group (n = 147), 35-37-year-old group (n = 164), 30-34-year-old group (n = 483), and < 30-year-old group (n = 485). Intergroup comparisons of baseline characteristics and pregnancy and neonatal outcomes were made.
    RESULTS: The clinical pregnancy rate (47.6%), and live birth rate (34.0%) in the 38-40-year-old group were significantly lower than those in the 30-34-year-old group (64.4%, 50.9%, respectively; all P < 0.001) and < 30-year-old group (62.9%, 50.7%, respectively; all P < 0.001). However, the 35-37-year-old group did not differ from the other three groups in these two dimensions (all P > 0.05). Moreover, there were no differences in the rates of biochemical pregnancy, miscarriage, or obstetric or neonatal complications among the four groups (all P > 0.05). According to the multivariate logistic regression analysis, the 35-37-year-old group was not associated with non-live birth outcomes, adverse pregnancy outcomes, or obstetric or neonatal complications. However, being 38-40 years of age was a risk factor for non-live birth (OR = 2.121, 95% CI: 1.233-3.647) and adverse pregnancy outcomes (OR = 1.630, 95% CI: 1.010-2.633). Post hoc power analysis showed that the study was sufficiently powered to detect meaningful differences.
    CONCLUSIONS: Frozen-thawed high-quality single blastocyst transfer produces the same satisfactory pregnancy outcomes for women aged 35-37 years as younger patients. Future prospective randomized controlled studies with larger populations are needed to verify the feasibility and safety of this method.
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  • 文章类型: Journal Article
    探索在非侵入性植入前染色体筛查(NICS)中,胚泡形成前不同数量的胚胎洗涤对NICS结果准确性的影响。
    在这项研究中,在我们的机构收集了来自植入前遗传测试(PGT)辅助妊娠的68个胚泡。胚胎培养的第四天,将胚胎转移到新的囊胚培养培养基中,洗涤3次(NICS1组)或10次(NICS2组).对胚泡进行滋养外胚层(TE)活检,收集相应的胚胎培养基进行全基因组扩增(WGA)和高通量测序。
    WGA的成功率为100%(TE活检),76.7%(NICS1组),和89.5%(NICS2组)。在培养的第5天和第6天,胚胎培养基中WGA的成功率分别为75.0%(33/44)和100%(24/24),分别。使用TE作为黄金标准,NICS1和NICS2组胚胎培养基样本与TE结果的核型一致率为43.5%(10/23)和73.5%(25/34),分别。使用TE时,NICS2组检测染色体异常的敏感性和特异性高于NICS1组(83.3%vs60.0%;62.5%vs30.8%,分别)。假阳性率和假阴性率(即误诊率和漏诊率,NICS2组分别低于NICS1组(37.5%vs69.2%;16.7%vs40.0%,分别)。
    NICS在胚胎洗涤十次后产生了良好的结果。这些发现提供了一种新颖的方法,可以降低用于胚胎发育的培养基中非胚胎来源的无细胞DNA污染量。优化采样程序,提高NICS测试的准确性。
    UNASSIGNED: To explore the effect of varying numbers of embryo washings prior to blastocyst formation in non-invasive preimplantation chromosome screening (NICS) on the accuracy of NICS results.
    UNASSIGNED: In this study, 68 blastocysts from preimplantation genetic testing (PGT)-assisted pregnancy were collected at our institution. On the fourth day of embryo culture, the embryos were transferred to a new medium for blastocyst culture and were washed either three times (NICS1 group) or ten times (NICS2 group). A trophectoderm (TE) biopsy was performed on the blastocysts, and the corresponding embryo culture media were collected for whole genome amplification (WGA) and high-throughput sequencing.
    UNASSIGNED: The success rate of WGA was 100% (TE biopsy), 76.7% (NICS1 group), and 89.5% (NICS2 group). The success rate of WGA in embryo medium on days 5 and 6 of culture was 75.0% (33/44) and 100% (24/24), respectively. Using TE as the gold standard, the karyotype concordance rate between the results of the NICS1 and NICS2 groups\' embryo culture medium samples and TE results was 43.5% (10/23) and 73.5% (25/34), respectively. The sensitivity and specificity of detecting chromosomal abnormalities were higher in the NICS2 group than in the NICS1 group when TE was used (83.3% vs 60.0%; 62.5% vs 30.8%, respectively). The false-positive rate and false-negative rate (i.e., misdiagnosis rate and missed diagnosis rate, respectively) were lower in the NICS2 group than in the NICS1 group (37.5% vs 69.2%; 16.7% vs 40.0%, respectively).
    UNASSIGNED: The NICS yielded favorable results after ten washings of the embryos. These findings provide a novel method for lowering the amount of cell-free DNA contamination from non-embryonic sources in the medium used for embryo development, optimizing the sampling procedure and improving the accuracy of the NICS test.
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  • 文章类型: Journal Article
    最近,辅助生殖技术(ART)的使用迅速增加。因此,越来越多的人担心通过ART产生的后代的安全性。此外,新出现的证据表明,使用ART受孕的后代患心血管疾病(CVD)的风险增加。在这次审查中,我们讨论了DNA甲基化改变的表观遗传机制,组蛋白修饰,和microRNA表达,以及印记障碍。我们还总结了心血管变化和其他心血管疾病危险因素的研究,如不良的宫内环境,围产期并发症,辅助生殖技术(ART)后代谢改变。最后,我们强调了通过ART受孕的后代心血管疾病风险增加的表观遗传机制,这可能有助于ART人群中CVD的早期诊断和预防。
    Recently, the use of assisted reproductive technology (ART) has rapidly increased. As a result, an increasing number of people are concerned about the safety of offspring produced through ART. Moreover, emerging evidence suggests an increased risk of cardiovascular disease (CVD) in offspring conceived using ART. In this review, we discuss the epigenetic mechanisms involved in altered DNA methylation, histone modification, and microRNA expression, as well as imprinting disorders. We also summarize studies on cardiovascular changes and other risk factors for cardiovascular disease, such as adverse intrauterine environments, perinatal complications, and altered metabolism following assisted reproductive technology (ART). Finally, we emphasize the epigenetic mechanisms underlying the increased risk of CVD in offspring conceived through ART, which could contribute to the early diagnosis and prevention of CVD in the ART population.
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  • 文章类型: Journal Article
    背景:囊性纤维化(CF)是一种在亚洲人群中很少发现的常染色体隐性遗传疾病。大多数患有CF的男性由于先天性双侧输精管缺失(CBAVD)引起的阻塞性无精子症(OA)而不育。囊性纤维化跨膜传导调节因子(CFTR)的复合杂合突变是CBAVD中最常见的致病因素之一。然而,很少进行系谱分析。
    方法:在本研究中,在一个涉及两个CBAVD兄弟姐妹的中国家系中进行了全外显子组测序和共分离分析.此外,体外基因表达用于分析新的CFTR突变的致病性。
    结果:我们鉴定了CFTR的复合杂合突变,包括已知的致病变体c.1210-11T>G(也称为IVS9-5T)和c.2144delA;p。q715fs在两个兄弟姐妹与CBAVD。为了验证其体外效果,我们将表达野生型和突变CFTR的载体转染到293T细胞中。结果表明,含有移码突变(c.2144delA)的CFTR蛋白小60kD。睾丸精子抽吸/胞浆内精子注射-胚胎移植(TESA/ICSI-ET),两名CBAVD患者都是健康后代的父亲。
    结论:我们的研究表明CFTR的复合杂合突变与CBAVD有关,扩大了CBAVD患者已知的CFTR基因突变谱,为复合杂合突变可引起家族性CBAVD提供了更多证据。
    BACKGROUND: Cystic fibrosis (CF) is an autosomal recessive disorder rarely found in Asian populations. Most males with CF are infertile because of obstructive azoospermia (OA) caused by congenital bilateral absence of the vas deferens (CBAVD). Compound heterozygous mutations of cystic fibrosis transmembrane conductance regulator (CFTR) are among the most common pathogenic factors in CBAVD. However, few genealogical analyses have been performed.
    METHODS: In this study, whole-exome sequencing and cosegregation analysis were performed in a Chinese pedigree involving two siblings with CBAVD. Moreover, in vitro gene expressions were used to analyze the pathogenicity of a novel CFTR mutation.
    RESULTS: We identified compound heterozygous mutations of CFTR comprising the known disease-causing variant c.1210-11T>G (also known as IVS9-5 T) and c.2144delA;p.q715fs in two siblings with CBAVD. To verify the effects in vitro, we transfected vectors expressing wild-type and mutated CFTR into 293T cells. The results showed that the CFTR protein containing the frameshift mutation (c.2144delA) was 60 kD smaller. With testicular sperm aspiration/intracytoplasmic sperm injection-embryo transfer (TESA/ICSI-ET), both CBAVD patients fathered healthy offspring.
    CONCLUSIONS: Our study revealed that compound heterozygous mutations of CFTR are involved in CBAVD, expanding the known CFTR gene mutation spectrum of CBAVD patients and providing more evidence that compound heterozygous mutations can cause familial CBAVD.
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  • 文章类型: Journal Article
    睡眠障碍影响身心健康。接受辅助生殖技术(ART)治疗的不孕妇女容易出现睡眠障碍。睡眠条件,其影响因素,在样本量较大的人群中,尚未研究治疗前睡眠状况与ART治疗结果之间的关系.因此,我们调查了1002名中国不孕妇女诱导排卵前的睡眠特征,并调查了影响因素(消极和积极的心理因素,人口统计,和生育特征)。我们还检查了治疗前的睡眠状况是否可以预测生殖结果。我们发现,24.1%的参与者报告睡眠质量差。原发性不孕症妇女报告睡眠比继发性不孕症妇女差。消极的心理因素,包括抑郁症,焦虑,感觉到的压力与睡眠不足有关,而积极的影响与良好的睡眠有关。不良睡眠特征,包括主观睡眠质量差,睡眠障碍,睡眠效率差,降低了回收卵母细胞的数量和质量,受精率,和临床妊娠率。这项研究表明,在ART治疗之前,大量不孕症女性患有睡眠问题,受心理因素和不孕类型的影响,不健康的睡眠特征可能会损害治疗结果。我们的发现强调了在不孕妇女接受ART治疗之前筛查和治疗睡眠障碍的重要性。
    Sleep disorders affect mental and physical health. Infertile women undergoing assisted reproductive technology (ART) treatment are prone to sleep disorders. Sleep condition, its influencing factors, and the association between sleep condition and ART treatment outcomes before treatment have not been explored within a population with a large sample size. Therefore, we investigated the sleep characteristics of 1002 Chinese infertile women before ovulation induction and investigated the influencing factors (negative and positive psychological factors, demographics, and fertility characteristics). We also examined whether sleep conditions before treatment predicted reproductive outcomes. We found that 24.1% of participants reported poor sleep quality. Women with primary infertility reported poorer sleep than women with secondary infertility. Negative psychological factors, including depression, anxiety, and perceived stress were associated with poor sleep, whereas positive affect was linked with good sleep. Adverse sleep characteristics, including poor subjective sleep quality, sleep disturbances, and poor sleep efficiency, decreased the quantity and quality of oocytes retrieved, fertilization rates, and clinical pregnancy rates. This study indicates that before ART treatment, a large number of females with infertility suffer from sleep problems, which are affected by psychological factors and infertility type, and unhealthy sleep characteristics may impair treatment outcomes. Our findings highlight the importance of screening and treatment for sleep disorders before the enrollment of ART treatment in infertile women.
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  • 文章类型: Journal Article
    激光技术在辅助生殖技术(ART)领域的应用在过去几十年中经历了快速增长,这是由于诸如卵胞浆内单精子注射(ICSI)等革命性技术。植入前基因检测(PGT),以及配子和胚胎的体外操作。对于雄配子,体外操作技术包括精子选择,排序,固定化,和质量评估。已经进行了许多研究以研究不同激光技术在人类精子操纵中的应用。然而,对激光在精子体外操作中的应用和ART中的安全性考虑缺乏统一的认识,随后,无法对这些激光技术的临床价值做出明确和准确的决定。本文综述了激光技术在人类精子操纵中的进步和改进。如光生物调节疗法,激光捕获系统,用于精子分析和分选,在ICSI之前,激光辅助选择不运动精子和激光辅助固定精子。还讨论了ART中使用的这些技术的安全性。这篇综述将为激光技术在人类精子操纵中的应用提供有益和全面的见解。
    The application of laser technology in the field of assisted reproductive technology (ART) has experienced rapid growth over the past decades owing to revolutionary techniques such as intracytoplasmic sperm injection (ICSI), preimplantation genetic testing (PGT), and in vitro manipulation of gametes and embryos. For male gametes, in vitro manipulation techniques include spermatozoa selection, sorting, immobilization, and quality assessment. A number of studies have been conducted to investigate the application of different laser technologies in the manipulation of human spermatozoa. However, there is a lack of a unified understanding of laser application in the in vitro manipulation of sperm and safety considerations in ART and, subsequently, the inability to make clear and accurate decisions on the clinical value of these laser technologies. This review summarizes the advancements and improvements of laser technologies in the manipulation of human spermatozoa, such as photobiomodulation therapy, laser trap systems for sperm analysis and sorting, laser-assisted selection of immotile sperm and laser-assisted immobilization of sperm prior to ICSI. The safety of those technologies used in ART is also discussed. This review will provide helpful and comprehensive insight into the applications of laser technology in the manipulation of human spermatozoa.
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