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1.
J Assist Reprod Genet ; 40(2): 389-398, 2023 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-36586007

RESUMEN

PURPOSE: Limited research has been published comparing PIEZO-ICSI with conventional ICSI. While positive effects have been documented in improving fertilization and degeneration, the outcomes in patients with previous poor results from conventional ICSI remain unclear. It is hypothesized that these patients may benefit the most from this form of insemination. METHODS: This retrospective paired within-patient cohort study investigated patients (n=72) undertaking PIEZO-ICSI after a previous conventional ICSI cycle resulted in poor outcomes (including low fertilization (<50%), high degeneration (>15%), and/or poor embryo development and utilization). Patients required at least five oocytes collected in both cycles and a period of less than 2 years between the cycles. The outcomes of both cycles were compared in respect to fertilization, degeneration, embryo utilization, and pregnancy rates. Further analyses were applied to patients <38 and ≥38 years of age, with <50% or ≥50% fertilization with conventional ICSI and with <20% or ≥20% utilization with conventional ICSI. RESULTS: PIEZO-ICSI resulted in significantly higher fertilization (61.9% vs 45.3%, P<0.0001) and lower degeneration (7.7% vs 18.2%, P=0.0001) when compared to the conventional ICSI cycles. The greatest benefit was seen in patients who had less than 50% fertilization or <20% utilization in their conventional ICSI cycle, with improvements in fertilization and degeneration rates resulting in a significantly higher number of embryos utilized (frozen or transferred) per cycle. CONCLUSIONS: PIEZO-ICSI improved fertilization, degeneration, and utilization rates in patients with previous poor outcomes from conventional ICSI. The number of embryos available for use per cycle was also increased. Further significant improvements were achieved in patients who exhibited poor fertilization (<50%) or low utilization (<20%) from conventional ICSI.


Asunto(s)
Fertilización In Vitro , Inyecciones de Esperma Intracitoplasmáticas , Embarazo , Femenino , Humanos , Fertilización In Vitro/métodos , Inyecciones de Esperma Intracitoplasmáticas/métodos , Estudios Retrospectivos , Índice de Embarazo , Fertilización , Pronóstico
2.
J Assist Reprod Genet ; 39(5): 1055-1064, 2022 May.
Artículo en Inglés | MEDLINE | ID: mdl-35262809

RESUMEN

PURPOSE: To determine if 5mM calcium chloride dihydrate supplementation of the Polyvinylpyrrolidone (PVP) media at the time of ICSI (ICSI-Ca) improves fertilization, utilization, and clinical pregnancy rates compared to ICSI alone, particularly in patients with a history of low fertilization (< 50%). METHODS: Retrospective study between 2016 and 2021 at Monash IVF Victoria on a paired cohort of patients (n = 178 patients) where an ICSI cycle was analyzed coupled with the subsequent ICSI-Ca cycle. The paired cohort was further subdivided into a low-fertilization cohort (< 50% fertilization on previous cycles: n = 66 patients) compared to the remaining patients with fertilization ≥ 50% (n = 122). Exclusion criteria included donor cycles, PGT patients, surgical sperm retrieval, women ≥ 45 years old, patients with > 6 cycles, and patients with ≤ 5 inseminated oocytes. RESULTS: Calcium supplementation significantly increased both fertilization (28.8% ICSI vs 49.7% ICSI-Ca, P < 0.0001) and clinical pregnancy rate (4.9% ICSI vs 25.0% ICSI-Ca: P < 0.05) in the low-fertilization cohort but not in the normal-fertilization cohort. Interestingly, utilization rate significantly increased in the normal-fertilization cohort (32.6% ICSI vs ICSI-Ca: 44.9%, P < 0.01) but not in the low-fertilization cohort, although the number of embryos utilized per patient after ICSI-Ca increased in both groups. CONCLUSION: Calcium supplementation does not appear to be a detrimental addition to ICSI and may improve IVF outcomes, particularly for patients with a history of low fertilization. Further investigations including prospective case-matched studies or a RCT are required to confirm these findings.


Asunto(s)
Fertilización In Vitro , Inyecciones de Esperma Intracitoplasmáticas , Calcio , Cloruro de Calcio , Suplementos Dietéticos , Femenino , Fertilización , Humanos , Oocitos , Embarazo , Índice de Embarazo , Estudios Retrospectivos
3.
J Clin Invest ; 123(12): 5351-60, 2013 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-24231354

RESUMEN

Ionizing radiation (IR) and germline mutations in the retinoblastoma tumor suppressor gene (RB1) are the strongest risk factors for developing osteosarcoma. Recapitulating the human predisposition, we found that Rb1+/- mice exhibited accelerated development of IR-induced osteosarcoma, with a latency of 39 weeks. Initial exposure of osteoblasts to carcinogenic doses of IR in vitro and in vivo induced RB1-dependent senescence and the expression of a panel of proteins known as senescence-associated secretory phenotype (SASP), dominated by IL-6. RB1 expression closely correlated with that of the SASP cassette in human osteosarcomas, and low expression of both RB1 and the SASP genes was associated with poor prognosis. In vivo, IL-6 was required for IR-induced senescence, which elicited NKT cell infiltration and a host inflammatory response. Mice lacking IL-6 or NKT cells had accelerated development of IR-induced osteosarcomas. These data elucidate an important link between senescence, which is a cell-autonomous tumor suppressor response, and the activation of host-dependent cancer immunosurveillance. Our findings indicate that overcoming the immune response to senescence is a rate-limiting step in the formation of IR-induced osteosarcoma.


Asunto(s)
Neoplasias Óseas/inmunología , Senescencia Celular/fisiología , Células T Asesinas Naturales/inmunología , Neoplasias Inducidas por Radiación/inmunología , Osteosarcoma/inmunología , Proteína de Retinoblastoma/fisiología , Animales , Neoplasias Óseas/etiología , Neoplasias Óseas/genética , Neoplasias Óseas/patología , Radioisótopos de Calcio/toxicidad , Citocinas/fisiología , Genes de Retinoblastoma , Humanos , Vigilancia Inmunológica , Péptidos y Proteínas de Señalización Intercelular/fisiología , Interleucina-6/deficiencia , Interleucina-6/fisiología , Ratones , Ratones Endogámicos C57BL , Proteínas de Neoplasias/antagonistas & inhibidores , Proteínas de Neoplasias/fisiología , Trasplante de Neoplasias/inmunología , Neoplasias Inducidas por Radiación/etiología , Neoplasias Inducidas por Radiación/genética , Neoplasias Inducidas por Radiación/patología , Osteoblastos/patología , Osteosarcoma/etiología , Osteosarcoma/genética , Osteosarcoma/patología , Fenotipo , Pronóstico , Interferencia de ARN , Proteína de Retinoblastoma/antagonistas & inhibidores
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