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Autoimmune-associated Congenital Heart Block: A New Insight in Fetal Life
OBJECTIVE: Congenital heart block (CHB) is a rare but life-threatening disorder. More than half of CHB cases are associated with maternal autoimmune, which are termed as autoimmune-associated CHB. This review summarized the recent research findings in understanding autoimmune-associated CHB, discuss...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5717867/ https://www.ncbi.nlm.nih.gov/pubmed/29176145 http://dx.doi.org/10.4103/0366-6999.219160 |
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author | Zhou, Kai-Yu Hua, Yi-Min |
author_facet | Zhou, Kai-Yu Hua, Yi-Min |
author_sort | Zhou, Kai-Yu |
collection | PubMed |
description | OBJECTIVE: Congenital heart block (CHB) is a rare but life-threatening disorder. More than half of CHB cases are associated with maternal autoimmune, which are termed as autoimmune-associated CHB. This review summarized the recent research findings in understanding autoimmune-associated CHB, discussed the current diagnostic approaches and management strategies, and summarized the problems and future directions for this disorder. DATA SOURCES: We retrieved the articles published in English from the PubMed database up to January 2017, using the keywords including “Autoimmune-associated”, “Autoimmune-mediated”, and “Congenital heart block”. STUDY SELECTION: Articles about autoimmune-associated CHB were obtained and reviewed. RESULTS: Observational studies consistently reported that transplacental maternal antibodies might recognize fetal or neonatal antigens in various tissues and result in immunological damages, but the molecular mechanisms underlying CHB pathogenesis still need illuminated. Multiple factors were involved in the process of atrioventricular block development and progression. While several susceptibility genes had been successfully defined, how these genes and their protein interact and impact each other remains to be explored. With currently available diagnostic tools, fetal ultrasound cardiography, and fetal magnetocardiography, most of CHB could be successfully diagnosed and comprehensively evaluated prenatally. The efficacy of current approaches for preventing the progression and recurrence of CHB and other autoimmune-mediated damages was still controversial. CONCLUSIONS: This review highlighted the relationships between autoimmune injuries and CHB and strengthened the importance of perinatal management and therapy for autoimmune-associated CHB. |
format | Online Article Text |
id | pubmed-5717867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-57178672017-12-20 Autoimmune-associated Congenital Heart Block: A New Insight in Fetal Life Zhou, Kai-Yu Hua, Yi-Min Chin Med J (Engl) Review Article OBJECTIVE: Congenital heart block (CHB) is a rare but life-threatening disorder. More than half of CHB cases are associated with maternal autoimmune, which are termed as autoimmune-associated CHB. This review summarized the recent research findings in understanding autoimmune-associated CHB, discussed the current diagnostic approaches and management strategies, and summarized the problems and future directions for this disorder. DATA SOURCES: We retrieved the articles published in English from the PubMed database up to January 2017, using the keywords including “Autoimmune-associated”, “Autoimmune-mediated”, and “Congenital heart block”. STUDY SELECTION: Articles about autoimmune-associated CHB were obtained and reviewed. RESULTS: Observational studies consistently reported that transplacental maternal antibodies might recognize fetal or neonatal antigens in various tissues and result in immunological damages, but the molecular mechanisms underlying CHB pathogenesis still need illuminated. Multiple factors were involved in the process of atrioventricular block development and progression. While several susceptibility genes had been successfully defined, how these genes and their protein interact and impact each other remains to be explored. With currently available diagnostic tools, fetal ultrasound cardiography, and fetal magnetocardiography, most of CHB could be successfully diagnosed and comprehensively evaluated prenatally. The efficacy of current approaches for preventing the progression and recurrence of CHB and other autoimmune-mediated damages was still controversial. CONCLUSIONS: This review highlighted the relationships between autoimmune injuries and CHB and strengthened the importance of perinatal management and therapy for autoimmune-associated CHB. Medknow Publications & Media Pvt Ltd 2017-12-05 /pmc/articles/PMC5717867/ /pubmed/29176145 http://dx.doi.org/10.4103/0366-6999.219160 Text en Copyright: © 2017 Chinese Medical Journal 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-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Review Article Zhou, Kai-Yu Hua, Yi-Min Autoimmune-associated Congenital Heart Block: A New Insight in Fetal Life |
title | Autoimmune-associated Congenital Heart Block: A New Insight in Fetal Life |
title_full | Autoimmune-associated Congenital Heart Block: A New Insight in Fetal Life |
title_fullStr | Autoimmune-associated Congenital Heart Block: A New Insight in Fetal Life |
title_full_unstemmed | Autoimmune-associated Congenital Heart Block: A New Insight in Fetal Life |
title_short | Autoimmune-associated Congenital Heart Block: A New Insight in Fetal Life |
title_sort | autoimmune-associated congenital heart block: a new insight in fetal life |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5717867/ https://www.ncbi.nlm.nih.gov/pubmed/29176145 http://dx.doi.org/10.4103/0366-6999.219160 |
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