2019
DOI: 10.1038/s41598-019-41846-2
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Comparison of recombinant and urinary follicle-stimulating hormones over 2000 gonadotropin-releasing hormone antagonist cycles: a retrospective study

Abstract: The objective of this paper was to compare the effect of recombinant follicle-stimulating hormone (rFSH) and urinary follicle-stimulating hormone (uFSH) on pregnancy rates and live birth rates with the gonadotropin-releasing hormone ( GnRH) antagonist protocol in China. This retrospective study was conducted from January 2014 through August 2017. Patients treated with uFSH had significantly higher levels of luteinizing hormone (3.79 mIU/ml vs. 3.09 mIU/ml) and progesterone (0.93 ng/ml vs… Show more

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Cited by 10 publications
(5 citation statements)
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“…A logistic regression model was used to assess the relationship between FSH regimens and CLBR after adjusting for age, BMI, baseline FSH, and AFC. We selected confounders based on the associations reported with the outcomes of interest [ 6 , 14 16 ]. A 1:2 propensity score matching (PSM) was also used to balance factors, including age, BMI, basic FSH, and AFC.…”
Section: Methodsmentioning
confidence: 99%
“…A logistic regression model was used to assess the relationship between FSH regimens and CLBR after adjusting for age, BMI, baseline FSH, and AFC. We selected confounders based on the associations reported with the outcomes of interest [ 6 , 14 16 ]. A 1:2 propensity score matching (PSM) was also used to balance factors, including age, BMI, basic FSH, and AFC.…”
Section: Methodsmentioning
confidence: 99%
“…Ovarian stimulation protocols, including the long agonist protocol, short agonist protocol, and prolonged agonist protocol, were carried out as previously described [ 11 , 12 ],Ai et al [1] . The long agonist protocol (GnRH agonist protocol) was as follows: 0.1 mg/d Triptorelin (Diphereline, IPSEN, Paris, France) was subcutaneously injected from the midluteal phase of the last menstrual cycle.…”
Section: Methodsmentioning
confidence: 99%
“…The study was approved by the ethics committees at the Reproductive Medicine Center of Tongji Hospital, and informed consent was signed before patient participation. According to the IRB of Tongji Hospital, our study did not require an ethics review because all women participating in the study received routine IVF treatment in the hospital and no additional intervention or sampling was performed [ 11 , 12 ].…”
Section: Methodsmentioning
confidence: 99%
“…In the last decades, numerous studies have compared recombinant FSH (r-FSH) and urinary FSH (HMG or uFSH) preparations for ovarian stimulation and clinical efficacy [4][5] .These gonadotropins vary according to the amount of LH activity.While human menopausal gonadotropin (HMG) contains both hCG and LH in addition to FSH and 1:1 ratio of FSH and LH bioactivities (e.g, 75 IU each), and uFSH, with less than 1 IU of LH per 75 IU FSH, recombinant follicle stimulation hormone (rFSH) was produced using recombinant DNA technology and has no LH activity [6] .…”
Section: Introductionmentioning
confidence: 99%