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Comprehensive analysis of early pregnancy loss based on cytogenetic findings from a tertiary referral center

BACKGROUND: Pregnancy loss is one of the most common complications during pregnancy. Clinical consultation based on etiology analysis are critical for reducing anxiety and distress. This study aimed to perform a comprehensive analysis for products of conception (POC) in miscarriage based on genetic...

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Autores principales: Wu, Xiaoqing, Su, Linjuan, Xie, Xiaorui, He, Deqin, Chen, Xuemei, Wang, Meiying, Wang, Linshuo, Zheng, Lin, Xu, Liangpu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8645092/
https://www.ncbi.nlm.nih.gov/pubmed/34863241
http://dx.doi.org/10.1186/s13039-021-00577-8
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author Wu, Xiaoqing
Su, Linjuan
Xie, Xiaorui
He, Deqin
Chen, Xuemei
Wang, Meiying
Wang, Linshuo
Zheng, Lin
Xu, Liangpu
author_facet Wu, Xiaoqing
Su, Linjuan
Xie, Xiaorui
He, Deqin
Chen, Xuemei
Wang, Meiying
Wang, Linshuo
Zheng, Lin
Xu, Liangpu
author_sort Wu, Xiaoqing
collection PubMed
description BACKGROUND: Pregnancy loss is one of the most common complications during pregnancy. Clinical consultation based on etiology analysis are critical for reducing anxiety and distress. This study aimed to perform a comprehensive analysis for products of conception (POC) in miscarriage based on genetic etiology and clinical information. METHODS: A retrospective study was conducted according to cytogenetic findings of 1252 POC from spontaneous pregnancy loss over 11 years. The frequencies and profiles of chromosomal abnormalities were discussed according to the classification of women with different maternal ages, previous miscarriage history, normal live birth history, and different modes of conception. RESULTS: A total of 667 (53.2%) chromosomal abnormalities were observed, including 592 (47.3%) cases of numerical abnormalities, 38 (3.0%) cases of structural abnormalities, and 37 (3.0%) cases of mosaic aberrations. In women above 40 years of age, the rates of chromosomal abnormalities and viable autosomal trisomy were significantly higher than those in women with ≤ 29, 30–34, and 35–39 years of age (p < 0.05). The frequency of abnormal karyotype in women with normal live birth history was 61.1%, significantly higher than 52.5% in women without normal live birth history (p < 0.05). There was no significant differences among women without, with 1–2, and ≥ 3 previous miscarriages regarding the rate of abnormal karyotype (p > 0.05); viable autosomal trisomy was less common in women with ≥ 3 previous miscarriages than women with < 3 miscarriages. The frequency of chromosomal abnormalities was 49.0% and 55.0% in women with assisted conception and natural conception (p > 0.05), respectively; monosomy X was more frequently detected in women with natural conception than assisted conception. CONCLUSION: The frequencies and profiles of chromosomal abnormalities in early miscarriages are strongly associated with clinical information including maternal age, previous miscarriage, live birth history, and mode of conception. Cytogenetic analysis of POC should be recommended to women with a first miscarriage and women with normal live birth history.
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spelling pubmed-86450922021-12-06 Comprehensive analysis of early pregnancy loss based on cytogenetic findings from a tertiary referral center Wu, Xiaoqing Su, Linjuan Xie, Xiaorui He, Deqin Chen, Xuemei Wang, Meiying Wang, Linshuo Zheng, Lin Xu, Liangpu Mol Cytogenet Research BACKGROUND: Pregnancy loss is one of the most common complications during pregnancy. Clinical consultation based on etiology analysis are critical for reducing anxiety and distress. This study aimed to perform a comprehensive analysis for products of conception (POC) in miscarriage based on genetic etiology and clinical information. METHODS: A retrospective study was conducted according to cytogenetic findings of 1252 POC from spontaneous pregnancy loss over 11 years. The frequencies and profiles of chromosomal abnormalities were discussed according to the classification of women with different maternal ages, previous miscarriage history, normal live birth history, and different modes of conception. RESULTS: A total of 667 (53.2%) chromosomal abnormalities were observed, including 592 (47.3%) cases of numerical abnormalities, 38 (3.0%) cases of structural abnormalities, and 37 (3.0%) cases of mosaic aberrations. In women above 40 years of age, the rates of chromosomal abnormalities and viable autosomal trisomy were significantly higher than those in women with ≤ 29, 30–34, and 35–39 years of age (p < 0.05). The frequency of abnormal karyotype in women with normal live birth history was 61.1%, significantly higher than 52.5% in women without normal live birth history (p < 0.05). There was no significant differences among women without, with 1–2, and ≥ 3 previous miscarriages regarding the rate of abnormal karyotype (p > 0.05); viable autosomal trisomy was less common in women with ≥ 3 previous miscarriages than women with < 3 miscarriages. The frequency of chromosomal abnormalities was 49.0% and 55.0% in women with assisted conception and natural conception (p > 0.05), respectively; monosomy X was more frequently detected in women with natural conception than assisted conception. CONCLUSION: The frequencies and profiles of chromosomal abnormalities in early miscarriages are strongly associated with clinical information including maternal age, previous miscarriage, live birth history, and mode of conception. Cytogenetic analysis of POC should be recommended to women with a first miscarriage and women with normal live birth history. BioMed Central 2021-12-04 /pmc/articles/PMC8645092/ /pubmed/34863241 http://dx.doi.org/10.1186/s13039-021-00577-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Wu, Xiaoqing
Su, Linjuan
Xie, Xiaorui
He, Deqin
Chen, Xuemei
Wang, Meiying
Wang, Linshuo
Zheng, Lin
Xu, Liangpu
Comprehensive analysis of early pregnancy loss based on cytogenetic findings from a tertiary referral center
title Comprehensive analysis of early pregnancy loss based on cytogenetic findings from a tertiary referral center
title_full Comprehensive analysis of early pregnancy loss based on cytogenetic findings from a tertiary referral center
title_fullStr Comprehensive analysis of early pregnancy loss based on cytogenetic findings from a tertiary referral center
title_full_unstemmed Comprehensive analysis of early pregnancy loss based on cytogenetic findings from a tertiary referral center
title_short Comprehensive analysis of early pregnancy loss based on cytogenetic findings from a tertiary referral center
title_sort comprehensive analysis of early pregnancy loss based on cytogenetic findings from a tertiary referral center
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8645092/
https://www.ncbi.nlm.nih.gov/pubmed/34863241
http://dx.doi.org/10.1186/s13039-021-00577-8
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