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Autologous stem cell transplantation in refractory Asherman's syndrome: A novel cell based therapy
BACKGROUND: There is substantial evidence that adult stem cell populations exist in human endometrium, and hence it is suggested that either endogenous endometrial stem/progenitor cells can be activated or bone marrow derived stem cells can be transplanted in the uterine cavity for endometrial regen...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4150149/ https://www.ncbi.nlm.nih.gov/pubmed/25191021 http://dx.doi.org/10.4103/0974-1208.138864 |
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author | Singh, Neeta Mohanty, Sujata Seth, Tulika Shankar, Meenakshi Bhaskaran, Sruthi Dharmendra, Sona |
author_facet | Singh, Neeta Mohanty, Sujata Seth, Tulika Shankar, Meenakshi Bhaskaran, Sruthi Dharmendra, Sona |
author_sort | Singh, Neeta |
collection | PubMed |
description | BACKGROUND: There is substantial evidence that adult stem cell populations exist in human endometrium, and hence it is suggested that either endogenous endometrial stem/progenitor cells can be activated or bone marrow derived stem cells can be transplanted in the uterine cavity for endometrial regeneration in Asherman's syndrome (AS). AIMS AND OBJECTIVES: The objective was to evaluate the role of sub-endometrial autologous stem cell implantation in women with refractory AS in attaining menstruation and fertility. SETTING: Tertiary care referral center. DESIGN: Prospective case series. MATERIALS AND METHODS: Six cases of refractory AS with failed standard treatment option of hysteroscopic adhesiolysis in the past were included. Mononuclear stem cells (MNCs) were implanted in sub-endometrial zone followed by exogenous oral estrogen therapy. Endometrial thickness (ET) was assessed at 3, 6, and 9 months. RESULTS: Descriptive statistics and statistical analysis of study variables was carried out using STATA version 9.0. The mean MNC count was 103.3 × 106 (±20.45) with mean CD34+ count being 203,642 (±269,274). Mean of ET (mm) at 3 months (4.05 ± 1.40), 6 months (5.46 ± 1.36) and 9 months (5.48 ± 1.14) were significantly (P < 0.05) increased from pretreatment level (1.38 ± 0.39). Five out of six patients resumed menstruation. CONCLUSION: The autologous stem cell implantation leads to endometrial regeneration reflected by restoration of menstruation in five out of six cases. Autologous stem cell implantation is a promising novel cell based therapy for refractory AS. |
format | Online Article Text |
id | pubmed-4150149 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-41501492014-09-04 Autologous stem cell transplantation in refractory Asherman's syndrome: A novel cell based therapy Singh, Neeta Mohanty, Sujata Seth, Tulika Shankar, Meenakshi Bhaskaran, Sruthi Dharmendra, Sona J Hum Reprod Sci Original Article BACKGROUND: There is substantial evidence that adult stem cell populations exist in human endometrium, and hence it is suggested that either endogenous endometrial stem/progenitor cells can be activated or bone marrow derived stem cells can be transplanted in the uterine cavity for endometrial regeneration in Asherman's syndrome (AS). AIMS AND OBJECTIVES: The objective was to evaluate the role of sub-endometrial autologous stem cell implantation in women with refractory AS in attaining menstruation and fertility. SETTING: Tertiary care referral center. DESIGN: Prospective case series. MATERIALS AND METHODS: Six cases of refractory AS with failed standard treatment option of hysteroscopic adhesiolysis in the past were included. Mononuclear stem cells (MNCs) were implanted in sub-endometrial zone followed by exogenous oral estrogen therapy. Endometrial thickness (ET) was assessed at 3, 6, and 9 months. RESULTS: Descriptive statistics and statistical analysis of study variables was carried out using STATA version 9.0. The mean MNC count was 103.3 × 106 (±20.45) with mean CD34+ count being 203,642 (±269,274). Mean of ET (mm) at 3 months (4.05 ± 1.40), 6 months (5.46 ± 1.36) and 9 months (5.48 ± 1.14) were significantly (P < 0.05) increased from pretreatment level (1.38 ± 0.39). Five out of six patients resumed menstruation. CONCLUSION: The autologous stem cell implantation leads to endometrial regeneration reflected by restoration of menstruation in five out of six cases. Autologous stem cell implantation is a promising novel cell based therapy for refractory AS. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4150149/ /pubmed/25191021 http://dx.doi.org/10.4103/0974-1208.138864 Text en Copyright: © Journal of Human Reproductive Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Singh, Neeta Mohanty, Sujata Seth, Tulika Shankar, Meenakshi Bhaskaran, Sruthi Dharmendra, Sona Autologous stem cell transplantation in refractory Asherman's syndrome: A novel cell based therapy |
title | Autologous stem cell transplantation in refractory Asherman's syndrome: A novel cell based therapy |
title_full | Autologous stem cell transplantation in refractory Asherman's syndrome: A novel cell based therapy |
title_fullStr | Autologous stem cell transplantation in refractory Asherman's syndrome: A novel cell based therapy |
title_full_unstemmed | Autologous stem cell transplantation in refractory Asherman's syndrome: A novel cell based therapy |
title_short | Autologous stem cell transplantation in refractory Asherman's syndrome: A novel cell based therapy |
title_sort | autologous stem cell transplantation in refractory asherman's syndrome: a novel cell based therapy |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4150149/ https://www.ncbi.nlm.nih.gov/pubmed/25191021 http://dx.doi.org/10.4103/0974-1208.138864 |
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