Enhancing oocyte activation in women with ovarian failure: clinical outcomes of the Stem Cell Regenera study using G-CSF mobilization of peripheral blood stem cells and intraovarian injection of stem cell factor-enriched platelet rich plasma in real-world-practice.

IF 3.9 3区 医学 Q2 CELL BIOLOGY
Aging-Us Pub Date : 2025-06-27 DOI:10.18632/aging.206274
Amparo Santamaria, Ana Ballester, Manuel Muñoz
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Abstract

The study assesses the effectiveness and safety of the Stem Cell Regenera Treatment for oocyte activation in women with ovarian failure, including conditions such as Poor Ovarian Response (POR), Diminished Ovarian Reserve (DOR), and Premature Ovarian Insufficiency (POI). This retrospective observational study was conducted from January 2023 to December 2024 at the IVIRMA Alicante Clinics in Spain. Women diagnosed with ovarian failure participated in the study, which involved mobilizing Hematopoietic Stem Cells from bone marrow into peripheral blood using granulocyte colony- stimulating factor (G-CSF). This was followed by an intraovarian injection of Stem Cell Factor- enriched Platelet Rich Plasma (SCFE-PRP). The primary outcome measures were the rate of oocyte activation, leukocytes and stem cell count, and pregnancy rates. Oocyte activation was defined as an increase in total Antral Follicle Count of three or more follicles after treatment and/or at least a 20% rise in Anti-Müllerian Hormone levels. Safety was assessed based on adverse effects. Pregnancy rates were evaluated for both spontaneous gestation and following in vitro fertilization (IVF) treatment. A total of 145 women participated: the overall activation rate was 68.28%, with 7.07% achieving spontaneous gestation and 14.14% achieving pregnancy following IVF. Mobilization of CD34+ cells was successful in all participants, with an average collection of 32.96 CD34+ cells/μl. No severe adverse effects were observed. The study concluded that the Stem Cell Regenera Treatment is effective and safe for oocyte activation in women with ovarian failure in real-world practice.

增强卵巢功能衰竭女性的卵母细胞活化:在现实世界中使用G-CSF动员外周血干细胞和卵巢内注射富含干细胞因子的富血小板血浆的干细胞再生研究的临床结果。
该研究评估了干细胞再生治疗卵巢功能衰竭女性卵母细胞激活的有效性和安全性,包括卵巢反应差(POR)、卵巢储备减少(DOR)和卵巢功能不全(POI)等情况。这项回顾性观察性研究于2023年1月至2024年12月在西班牙IVIRMA阿利坎特诊所进行。诊断为卵巢功能衰竭的妇女参加了这项研究,其中包括使用粒细胞集落刺激因子(G-CSF)从骨髓中动员造血干细胞进入外周血。随后卵巢内注射干细胞因子富集血小板富血浆(SCFE-PRP)。主要结局指标为卵母细胞活化率、白细胞和干细胞计数以及妊娠率。卵母细胞活化被定义为治疗后三个或三个以上卵泡总卵泡计数增加和/或抗勒氏激素水平至少上升20%。安全性是根据不良反应来评估的。评估自然妊娠和体外受精(IVF)治疗后的妊娠率。共有145名妇女参与,总激活率为68.28%,其中7.07%实现自然妊娠,14.14%实现体外受精后妊娠。所有参与者都成功动员了CD34+细胞,平均收集了32.96个CD34+细胞/μl。未观察到严重的不良反应。该研究得出结论,在现实世界中,干细胞再生治疗对卵巢功能衰竭妇女的卵母细胞激活是有效和安全的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Aging-Us
Aging-Us CELL BIOLOGY-
CiteScore
10.00
自引率
0.00%
发文量
595
审稿时长
6-12 weeks
期刊介绍: Information not localized
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