Cargando…

Autologous Bone Marrow-Derived Stem Cell Therapy for Asherman's Syndrome and Endometrial Atrophy: A 5-Year Follow-up Study

BACKGROUND: Based on the role of bone marrow (BM) stem cells in regeneration of endometrium, refractory cases of Asherman's syndrome (AS) and endometrial atrophy (EA) may benefit with BM-derived intrauterine stem cell instillation. Aims and Objectives: To evaluate the role of BM-derived autolog...

Descripción completa

Detalles Bibliográficos
Autores principales: Singh, Neeta, Shekhar, Bhawani, Mohanty, Sujata, Kumar, Sunesh, Seth, Tulika, Girish, Bhavana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7295252/
https://www.ncbi.nlm.nih.gov/pubmed/32577066
http://dx.doi.org/10.4103/jhrs.JHRS_64_19
_version_ 1783546618772979712
author Singh, Neeta
Shekhar, Bhawani
Mohanty, Sujata
Kumar, Sunesh
Seth, Tulika
Girish, Bhavana
author_facet Singh, Neeta
Shekhar, Bhawani
Mohanty, Sujata
Kumar, Sunesh
Seth, Tulika
Girish, Bhavana
author_sort Singh, Neeta
collection PubMed
description BACKGROUND: Based on the role of bone marrow (BM) stem cells in regeneration of endometrium, refractory cases of Asherman's syndrome (AS) and endometrial atrophy (EA) may benefit with BM-derived intrauterine stem cell instillation. Aims and Objectives: To evaluate the role of BM-derived autologous stem cell therapy in endometrial regeneration and restoration of menstruation and fertility in refractory cases of AS and EA. SETTING: This study was conducted at a tertiary care center. DESIGN: This was a prospective, single-arm longitudinal study. MATERIALS AND METHODS: Twenty-five cases with refractory AS or EA were included. BM-derived mononuclear stem cells were instilled into the subendometrial zone followed by oral estrogen therapy for 3 months. Menstrual flow and endometrial thickness (ET) were assessed at 3, 6, and 9 months and 5 years. RESULTS: Statistical analysis was carried out using statistical software STATA version 12.0. Mean prestem cell transfer ET (mm) was 3.3 ± 1.0. At the end of 3 months, there was a significant increase in ET (mm) to 5.1 ± 1.9 (P = 0.001), but there was no significant change at 6 months (5.6 ± 1.5; P = 0.164), at 9 months (6.1 ± 1.7; P = 0.135), or at the end of 5 years. Six of the seven amenorrheic patients resumed menses. Three patients had a successful pregnancy outcome. CONCLUSION: Intrauterine stem cell treatment is a promising novel approach for refractory cases of AS and EA.
format Online
Article
Text
id pubmed-7295252
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Wolters Kluwer - Medknow
record_format MEDLINE/PubMed
spelling pubmed-72952522020-06-22 Autologous Bone Marrow-Derived Stem Cell Therapy for Asherman's Syndrome and Endometrial Atrophy: A 5-Year Follow-up Study Singh, Neeta Shekhar, Bhawani Mohanty, Sujata Kumar, Sunesh Seth, Tulika Girish, Bhavana J Hum Reprod Sci Original Article BACKGROUND: Based on the role of bone marrow (BM) stem cells in regeneration of endometrium, refractory cases of Asherman's syndrome (AS) and endometrial atrophy (EA) may benefit with BM-derived intrauterine stem cell instillation. Aims and Objectives: To evaluate the role of BM-derived autologous stem cell therapy in endometrial regeneration and restoration of menstruation and fertility in refractory cases of AS and EA. SETTING: This study was conducted at a tertiary care center. DESIGN: This was a prospective, single-arm longitudinal study. MATERIALS AND METHODS: Twenty-five cases with refractory AS or EA were included. BM-derived mononuclear stem cells were instilled into the subendometrial zone followed by oral estrogen therapy for 3 months. Menstrual flow and endometrial thickness (ET) were assessed at 3, 6, and 9 months and 5 years. RESULTS: Statistical analysis was carried out using statistical software STATA version 12.0. Mean prestem cell transfer ET (mm) was 3.3 ± 1.0. At the end of 3 months, there was a significant increase in ET (mm) to 5.1 ± 1.9 (P = 0.001), but there was no significant change at 6 months (5.6 ± 1.5; P = 0.164), at 9 months (6.1 ± 1.7; P = 0.135), or at the end of 5 years. Six of the seven amenorrheic patients resumed menses. Three patients had a successful pregnancy outcome. CONCLUSION: Intrauterine stem cell treatment is a promising novel approach for refractory cases of AS and EA. Wolters Kluwer - Medknow 2020 2020-04-07 /pmc/articles/PMC7295252/ /pubmed/32577066 http://dx.doi.org/10.4103/jhrs.JHRS_64_19 Text en Copyright: © 2020 Journal of Human Reproductive Sciences http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Singh, Neeta
Shekhar, Bhawani
Mohanty, Sujata
Kumar, Sunesh
Seth, Tulika
Girish, Bhavana
Autologous Bone Marrow-Derived Stem Cell Therapy for Asherman's Syndrome and Endometrial Atrophy: A 5-Year Follow-up Study
title Autologous Bone Marrow-Derived Stem Cell Therapy for Asherman's Syndrome and Endometrial Atrophy: A 5-Year Follow-up Study
title_full Autologous Bone Marrow-Derived Stem Cell Therapy for Asherman's Syndrome and Endometrial Atrophy: A 5-Year Follow-up Study
title_fullStr Autologous Bone Marrow-Derived Stem Cell Therapy for Asherman's Syndrome and Endometrial Atrophy: A 5-Year Follow-up Study
title_full_unstemmed Autologous Bone Marrow-Derived Stem Cell Therapy for Asherman's Syndrome and Endometrial Atrophy: A 5-Year Follow-up Study
title_short Autologous Bone Marrow-Derived Stem Cell Therapy for Asherman's Syndrome and Endometrial Atrophy: A 5-Year Follow-up Study
title_sort autologous bone marrow-derived stem cell therapy for asherman's syndrome and endometrial atrophy: a 5-year follow-up study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7295252/
https://www.ncbi.nlm.nih.gov/pubmed/32577066
http://dx.doi.org/10.4103/jhrs.JHRS_64_19
work_keys_str_mv AT singhneeta autologousbonemarrowderivedstemcelltherapyforashermanssyndromeandendometrialatrophya5yearfollowupstudy
AT shekharbhawani autologousbonemarrowderivedstemcelltherapyforashermanssyndromeandendometrialatrophya5yearfollowupstudy
AT mohantysujata autologousbonemarrowderivedstemcelltherapyforashermanssyndromeandendometrialatrophya5yearfollowupstudy
AT kumarsunesh autologousbonemarrowderivedstemcelltherapyforashermanssyndromeandendometrialatrophya5yearfollowupstudy
AT sethtulika autologousbonemarrowderivedstemcelltherapyforashermanssyndromeandendometrialatrophya5yearfollowupstudy
AT girishbhavana autologousbonemarrowderivedstemcelltherapyforashermanssyndromeandendometrialatrophya5yearfollowupstudy