4.7 Article

Autologous stem cell ovarian transplantation to increase reproductive potential in patients who are poor responders

Journal

FERTILITY AND STERILITY
Volume 110, Issue 3, Pages 496-+

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.fertnstert.2018.04.025

Keywords

Poor responder; bone marrow-derived stem cell transplant; ovarian reserve; AMH; antral follicular count

Funding

  1. Regional Valencian Ministry of Education [PROMETEOII/2014/045]
  2. Spanish Ministry of Economy and Competitiveness [FIS PI15/00312, PTQ-16-08222]

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Objective: To evaluate effects of autologous stem cell ovarian transplant (ASCOT) on ovarian reserve and IVF outcomes of women who arc poor responders with very poor prognosis. Design: Prospective observational pilot study. Setting: University hospital. Patient(s): Seventeen women who are poor responders. Intervention(s): Ovarian infusion of bone marrow-derived stem cells. Main Outcome Measure(s): Serum antimullerian hormone levels and antral follicular count (AFC), punctured follicles, and oocytes retrieved after stimulation (controlled ovarian stimulation) were measred. Apheresis was analyzed for growth factor concentrations. Result(s): The ASCOT resulted in a significant improvement in AFC 2 weeks after treatment. With an increase in AFC of three or more follicles and/or two consecutive increases in antimullerian hormone levels as success criteria, ovarian function improved in 81.3% of women. These positive effects were associated with the presence of fibroblast growth factor-2 and thrombospondin. During controlled ovarian stimulation, ASCOT increased the number of stimulable antral follicles and oocytes, but the embryo euploidy rate was low (16.1%). Five pregnancies were achieved: two after ET, three by natural conception. Conclusion(s): Our results suggest that ASCOT optimized the mobilization and growth of existing follicles, possibly related to fibroblast growth factor-2 and thrombospondin-1 within apheresis. The ASCOT improved follicle and oocyte quantity enabling pregnancy in women who are poor responders previously limited to oocyte donation. (C) 2018 by American Society for Reproductive Medicine.

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