Urinary follicle-stimulating hormone is not different than recombinant follicle-stimulating hormone on embryo quality and karyotype makeup during induction of ovulation in women with recurrent pregnancy failure

IF 0.7 Q4 PHARMACOLOGY & PHARMACY
Nada Mohamed, Amr E Ahmed, O. Azmy, S. Kamel, K. Hashem
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Abstract

Background and objectives Follicle-stimulating hormone (FSH) is critical for the onset and duration of follicular development. This can be promoted medically by drugs such as follitropin beta and recombinant follicle-stimulating hormone (rFSH) technology. The former is purified from CHO cell culture supernatant (111 amino acid) and has a high biochemical purity (>99%), with specific biological activity (about 10 000 IU/mg protein), and no luteinizing hormone activity. The drugs used for ovulation induction during in vitro fertilization may affect the number and quality of follicles produced. This in turn may affect the quality and the integrity of the embryos generated. Bad-quality embryos may cause recurrent pregnancy failure. We aimed to assess the relationship of urinary follicle-stimulating hormone (uFSH) versus recombinant follicle-stimulating hormone (rFSH) drugs in producing embryos with chromosomal abnormalities. Patients and methods Seven women were enrolled for the intracytoplasmic sperm injection trial: Three had highly purified uFSH and four had rFSH. All embryos had blastomere extraction on day 3 after injection but the preimplantation genetic screening was carried out 6 weeks after embryo transfer. Only one embryo was transferred to each woman. Results and conclusion The results revealed that there was no difference between the two drugs in terms of number and quality of embryos fertilized or abnormal karyotype assessed. Overall, 71% of the women included had some form of chromosomal abnormality (4/7). However, two of them miscarried between 2 and 3 weeks later. Either of uFSH or rFSH did not improve the quality or integrity of the embryos. However, preimplantation genetic screening is a valuable tool in the selection of embryos in assisted conception cycles to increase the take-home baby rate.
在复发性妊娠失败妇女促排卵过程中,尿促卵泡激素与重组促卵泡激素在胚胎质量和核型组成方面没有差异
背景和目的卵泡刺激素(FSH)对卵泡发育的开始和持续时间至关重要。这可以通过药物如促卵泡素和重组促卵泡激素(rFSH)技术来促进。前者从CHO细胞培养上清(111个氨基酸)中纯化,生化纯度高(约99%),具有特定生物活性(约10000 IU/mg蛋白),无促黄体激素活性。体外受精过程中用于促排卵的药物可能会影响卵泡的数量和质量。这反过来可能会影响胚胎的质量和完整性。质量差的胚胎可能导致反复妊娠失败。我们的目的是评估促卵泡激素(uFSH)与重组促卵泡激素(rFSH)药物在产生染色体异常胚胎中的关系。患者和方法7名妇女参加卵胞浆内单精子注射试验:3名高纯度uFSH, 4名低纯度rFSH。所有胚胎在注射后第3天提取卵裂球,胚胎移植后6周进行着床前遗传学筛查。每位女性只移植了一个胚胎。结果与结论两种药物在受精卵数量和质量及核型异常评定方面均无差异。总体而言,71%的女性有某种形式的染色体异常(4/7)。然而,其中两人在2至3周后流产。无论是uFSH还是rFSH都没有改善胚胎的质量或完整性。然而,植入前遗传学筛查是在辅助受孕周期中选择胚胎以增加带回家婴儿率的有价值的工具。
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来源期刊
Egyptian Pharmaceutical Journal
Egyptian Pharmaceutical Journal PHARMACOLOGY & PHARMACY-
CiteScore
1.10
自引率
0.00%
发文量
37
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