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1.
Artículo en Chino | WPRIM (Pacífico Occidental) | ID: wpr-1020099

RESUMEN

Objective:To analyse the clinical significance of selective single embryo transfer by time-lapse mo-nitoring(TLM)or conventional morphology assessment(CMA)in vitro fertilization/intracytoplasmic sperm in-jection and embryo transfer(IVF/ICSI-ET),and to initially explore the predictive value of Raman spectral analy-sis of embryo culture medium for clinical pregnancy rate.Methods:The study is a prospective randomized con-trolled clinical trial.We assigned 139 patients treated with IVF/ICSI-ET in Reproductive and Genetics Center of Suzhou Municipal Hospital from April 2019 to July 2020,which were randomly assigned to either the CMA or the TLM group.We performed selective single-embryo transfer(fresh cycle and FET)after selecting the optimal em-bryos with TLM or CMA respectively.If the patient's first embryo transfer was unsuccessful,a second one would be performed to compare the differences in the cumulative live birth rate of embryo transfer and other pregnancy outcomes between the two groups.Meanwhile,we collected 15 μl of embryo culture medium at day 3 after IVF/ISCI fertilization for Raman spectroscopy analysis.Results:There were no differences in cumulative live birth,cu-mulative clinical pregnancy,cumulative premature birth,cumulative early spontaneous abortion,cumulative ectopic pregnancy and LGA or SGA between TLM and CMA groups(P>0.05).The Neonatal sex ratio in the TLM group was lower than that in the CMA group,but the difference was not significant(P>0.05).Raman spectros-copy analysis of embryo culture medium predicted the clinical pregnancy rate with 67.21%accuracy.Conclu-sions:In young women with a good ovarian reserve,the advantage of using TLM to evaluate embryos is not obvi-ous,so we should remain vigilant that embryo selection based on morphokinetic parameters may affect the sex ratio.Raman spectroscopic analysis of embryo culture medium is not yet able to effectively predict the planting ability of embryos.

2.
Reprod Biol Endocrinol ; 20(1): 168, 2022 Dec 12.
Artículo en Inglés | MEDLINE | ID: mdl-36510317

RESUMEN

BACKGROUND: Preimplantation embryonic lethality is a driver of female infertility. Certain microRNAs (miRNAs) have previously been demonstrated to play important roles in the regulation of embryogenesis. METHODS: Normally developing blastocysts and arrested embryos were collected from patients undergoing intracytoplasmic sperm injection (ICSI), and the expression of specific miRNAs therein was evaluated by qPCR. The overexpression of target molecule miR-145 in early mice embryos was achieved via oocyte microinjection, enabling the subsequent monitoring of how such overexpression impacted embryonic development. Bioinformatics approaches were utilized to identify putative miR-145 target mRNAs, and luciferase reporter assessments were implemented to confirm the ability of miR-145 to regulate Abca1 in HEK293T cells. The functional relationship between miR-145 and Abca1 in the mice's embryonic development was then confirmed through rescue assays. RESULTS: Abnormally increased miR-145 expression was observed in patients' arrested embryos, and the exogenous overexpression of this miRNA significantly suppressed mural blastocyst formation. Mechanistically, miR-145 was found to bind to the 3'-untranslated area of the Abca1 mRNA in HK293T cells, thus suppressing its expression and increasing embryonic cholesterol levels. In line with the importance of these cholesterol levels to embryogenesis, the upregulation of Abca1 was sufficient to rescue the observed change in cholesterol levels and the associated retardation of mice embryonic development that occurred in response to the overexpression of miR-145. CONCLUSION: The regulatory dynamics of the miR-145/Abca1 axis play an important role in shaping normal embryonic development.


Asunto(s)
Transportador 1 de Casete de Unión a ATP , Colesterol , Embrión de Mamíferos , MicroARNs , Animales , Femenino , Humanos , Masculino , Ratones , Transportador 1 de Casete de Unión a ATP/metabolismo , Blastocisto/metabolismo , Colesterol/metabolismo , Células HEK293 , MicroARNs/metabolismo , ARN Mensajero , Embrión de Mamíferos/metabolismo
3.
Sleep Breath ; 26(4): 2059-2068, 2022 12.
Artículo en Inglés | MEDLINE | ID: mdl-35018557

RESUMEN

BACKGROUND: Sleep disorders are thought to be common in women with in vitro fertilization and embryo transfer (IVF-ET) conception. Although a few studies have investigated the association between maternal sleep quality and infant birth weight, it is unclear to what extent birth weight is associated with sleep quality during pregnancy among these women. Therefore, we conducted a cohort study to assess sleep quality among women receiving IVF-ET during the subsequent pregnancy and investigated the association of self-report sleep quality on infant birth weight. METHODS: This study was a prospective cohort study recruiting women who were to receive assisted reproductive technology (ART). Sleep quality was measured by the Pittsburgh Sleep Quality Index (PSQI) before oocyte retrieval and in the first trimester, second trimester, and third trimester during pregnancy. A generalized estimating equation (GEE) model was applied to evaluate the associations between sleep quality at specific times and infant birth weight. A general linear model was conducted to explore which component of the PSQI questionnaire was most associated with infant birth weight. RESULTS: Between August 2016 and August 2020, a total of 1344 women who had singleton births with IVF conception were included in the analysis. PSQI scores in the first trimester were highest (4.59 ± 2.47) but had no significant relationship with birth weight. After accounting for potential influencing factors, we found that poor maternal sleep quality in the second trimester was significantly associated with small for gestational age (SGA) among female infants (OR = 3.03, 95% CI = 1.04 to 9.71, P = 0.044), while no association was observed between sleep quality and birth weight in male infants (OR = 1.64, 95% CI = 0.68 to 3.99, P = 0.271). CONCLUSIONS: These findings suggest that the sleep quality of women with IVF pregnancies may influence fetal weight in a trimester- and sex-specific manner.


Asunto(s)
Calidad del Sueño , Inyecciones de Esperma Intracitoplasmáticas , Embarazo , Masculino , Femenino , Humanos , Peso al Nacer , Estudios de Cohortes , Estudios Prospectivos , Semen , Fertilización In Vitro , Técnicas Reproductivas Asistidas , Estudios Retrospectivos , Espermatozoides
4.
The Journal of Practical Medicine ; (24): 3585-3589, 2017.
Artículo en Chino | WPRIM (Pacífico Occidental) | ID: wpr-663704

RESUMEN

Objective To estimate the effect of blastocysts morphological score on pregnancy outcomes and neonate′s condition in vitrified-warmed single-blastocyst transfer cycles. Methods A retrospective analysis of 586 cycles of vitrified-warmed single-blastocyst transfer from Mar. 2010 to Feb.2016 was performed and the influ-ence of day of vitrification,inner cell mass(ICM)and trophectoderm(TE)scores on pregnancy outcomes and neo-nate′s condition were observed. Results There were no significant differences in clinical pregnancy rate,birth weight and sex ration of newborn between different vitrification day,ICM score and TE score.The day of vitrifica-tion and ICM score can significantly influence pregnancy loss rate,and were the two primary predictors of pregnan-cy loss rate. Vitrification day,ICM score and TE score exerted significant influence on live birth rate(P < 0.05) and TE score was the primary factor of live birth rate. Conclusions Day 5 vitrified blastocysts with higher quality of ICM and TE can provide high live birth rate and low pregnancy loss rate,but it could not predict the weight and gender of the newborn.

5.
Artículo en Chino | WPRIM (Pacífico Occidental) | ID: wpr-328079

RESUMEN

<p><b>OBJECTIVE</b>The spectral imaging method was used to quickly identify the Cortex Dictamni pieces and its counterfeit alangium Chinese, which is a potential method would be applied to control the quality of the Cortex Dictamni pieces.</p><p><b>METHOD</b>Standard sample, 5 cortex dictamni samples and its counterfeit alangium Chinese of different sources were tested by the liquid crystal imaging instrument. The spectrum resolution was 5 nm, the spectral range was from 405 nm to 680 nm, and the spatial resolution was 50 lp x mm(-1). The characteristic spectrum curves were picked up from spectral cube and principal analysis method was used to analyze the results.</p><p><b>RESULT</b>The identification results by the spectral imaging method accorded well with the results by the traditional biology and chemistry analysis method.</p><p><b>CONCLUSION</b>The spectral imaging analysis method can be used to identify the cortex dictamni pieces and its counterfeit alangium Chinense. The testing course is convenient, quick and noninvasive.</p>


Asunto(s)
Alangiaceae , Química , Control de Calidad , Rutaceae , Química , Análisis Espectral , Métodos
6.
Artículo en Chino | WPRIM (Pacífico Occidental) | ID: wpr-573892

RESUMEN

Objective To study the effect of controlled ovarian Hyperstimulation(COH)on expression of AQP3 mRNA in mouse oocytes at metaphase Ⅱ. Methods Twenty female mice(6-7 weeks) were randomly allocated into 2 groups, mice in COH group were superovulated by intraperitoneal injection of 7.5 IU pregnant mare's serum gonadotropin(PMSG) followed by 5 IU human chorionic gonadotropin(HCG) after 46-48?h. Nothing was given to mice in control group and the estrus cycle was observed at 9?am everyday. 12-16?h following hCG injection (COH group) or at 8?am next day after the estrus (control group), mice were killed by cervical dislocation. The oviducts were excised.Cumulus masses were recovered from the dilated ampullae under a dissecting microscope,digested granulosa cells using hyaluronidase. Semi-quantitative real-time PCR of AQP3 mRNA in mouse MⅡoocytes was investigated with ?-actin as the internal control. Results Oocytes swelling assay showed that AQP3 mRNA expressed in mouse MⅡ oocytes. Using semi-quantitative real-time PCR, the expression of AQP3 mRNA was significantly decreased(P

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