Orphan Heritable Thoracic Aortic Diseases and Pregnancy. Modern Outlooks and Guidance

Pregnancy is a period of high risk for all patients with aortic pathology. Heritable thoracic aortic diseases (HTAD) refer to aortopathies with a high risk of formation and dissection of thoracic aortic aneurysm (TAA). HTAD are caused by a mutation of a certain gene. This paper reviews current perce...

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Main Author: S. O. Siromakha
Format: Article
Language:English
Published: Professional Edition Eastern Europe 2020-05-01
Series:Український журнал серцево-судинної хірургії
Subjects:
Online Access:http://cvs.org.ua/index.php/ujcvs/article/view/356
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spelling doaj-36123933cb23441ab99794a328ebbd812020-11-25T04:01:10ZengProfessional Edition Eastern EuropeУкраїнський журнал серцево-судинної хірургії 2664-59632664-59712020-05-012 (39)697410.30702/ujcvs/20.3905/028069-074356Orphan Heritable Thoracic Aortic Diseases and Pregnancy. Modern Outlooks and GuidanceS. O. Siromakha0https://orcid.org/0000-0002-7031-5732National Amosov Institute of Cardiovascular Surgery of the National Academy of Medical Sciences of Ukraine, Kyiv, Ukraine Bogomolets National Medical University, Kyiv, UkrainePregnancy is a period of high risk for all patients with aortic pathology. Heritable thoracic aortic diseases (HTAD) refer to aortopathies with a high risk of formation and dissection of thoracic aortic aneurysm (TAA). HTAD are caused by a mutation of a certain gene. This paper reviews current perceptions of manifestations of rare hereditary diseases of the thoracic aorta during pregnancy and general recommendations for the medical care of these patients. To date, 16 genes (or loci of unidentified genes) are known to be associated with the development of thoracic aortic aneurysm, and since many families with a history of TAA (about 70%) have no pathogenic changes in any of these 16 genes, additional genes associated with HTAD have not yet been identified. In this paper, HTAD are considered which occur (or are identified) quite rare but provide a significant risk for patients, which is significantly increased during pregnancy (multisystemic smooth muscle dysfunction syndrome, Meester Lois syndrome, LOX and PRKG1 genes mutations, vascular Ehlers-Danlos syndrome, mutations in TGFB2, TGFBR1, TGFBR2, SMAD3 loci, Loeys-Dietz syndrome). The article analyzes the frequency of occurrence of the most threatening complication of HTAD – acute aortic dissection – in various syndromes, defines general recommendations for the examination of patients with HTAD, recommendations for conservative treatment of these patients. Recommendations for the patients (especially fertility women) concerning the preventive cardiac surgery are also summarized in the paper. These principles of pregravidary preparation and multidisciplinary medical support during pregnancy are the most effective prophylactic measures for major cardiac events and maternal death. Pregnancy heart team that has been working in Ukraine since 2013 does all its best to organize medical support for every pregnant woman with suspected HTAD. In this context, it is very important to collaborate with general practitioners and genetics to “catch” such patients before they become pregnant or in very early terms. Individualized plan of pregravidary preparation and medical care during pregnancy and delivery should be developed by a multidisciplinary team.http://cvs.org.ua/index.php/ujcvs/article/view/356heritable thoracic aortic diseasepregnancycardiac surgery
collection DOAJ
language English
format Article
sources DOAJ
author S. O. Siromakha
spellingShingle S. O. Siromakha
Orphan Heritable Thoracic Aortic Diseases and Pregnancy. Modern Outlooks and Guidance
Український журнал серцево-судинної хірургії
heritable thoracic aortic disease
pregnancy
cardiac surgery
author_facet S. O. Siromakha
author_sort S. O. Siromakha
title Orphan Heritable Thoracic Aortic Diseases and Pregnancy. Modern Outlooks and Guidance
title_short Orphan Heritable Thoracic Aortic Diseases and Pregnancy. Modern Outlooks and Guidance
title_full Orphan Heritable Thoracic Aortic Diseases and Pregnancy. Modern Outlooks and Guidance
title_fullStr Orphan Heritable Thoracic Aortic Diseases and Pregnancy. Modern Outlooks and Guidance
title_full_unstemmed Orphan Heritable Thoracic Aortic Diseases and Pregnancy. Modern Outlooks and Guidance
title_sort orphan heritable thoracic aortic diseases and pregnancy. modern outlooks and guidance
publisher Professional Edition Eastern Europe
series Український журнал серцево-судинної хірургії
issn 2664-5963
2664-5971
publishDate 2020-05-01
description Pregnancy is a period of high risk for all patients with aortic pathology. Heritable thoracic aortic diseases (HTAD) refer to aortopathies with a high risk of formation and dissection of thoracic aortic aneurysm (TAA). HTAD are caused by a mutation of a certain gene. This paper reviews current perceptions of manifestations of rare hereditary diseases of the thoracic aorta during pregnancy and general recommendations for the medical care of these patients. To date, 16 genes (or loci of unidentified genes) are known to be associated with the development of thoracic aortic aneurysm, and since many families with a history of TAA (about 70%) have no pathogenic changes in any of these 16 genes, additional genes associated with HTAD have not yet been identified. In this paper, HTAD are considered which occur (or are identified) quite rare but provide a significant risk for patients, which is significantly increased during pregnancy (multisystemic smooth muscle dysfunction syndrome, Meester Lois syndrome, LOX and PRKG1 genes mutations, vascular Ehlers-Danlos syndrome, mutations in TGFB2, TGFBR1, TGFBR2, SMAD3 loci, Loeys-Dietz syndrome). The article analyzes the frequency of occurrence of the most threatening complication of HTAD – acute aortic dissection – in various syndromes, defines general recommendations for the examination of patients with HTAD, recommendations for conservative treatment of these patients. Recommendations for the patients (especially fertility women) concerning the preventive cardiac surgery are also summarized in the paper. These principles of pregravidary preparation and multidisciplinary medical support during pregnancy are the most effective prophylactic measures for major cardiac events and maternal death. Pregnancy heart team that has been working in Ukraine since 2013 does all its best to organize medical support for every pregnant woman with suspected HTAD. In this context, it is very important to collaborate with general practitioners and genetics to “catch” such patients before they become pregnant or in very early terms. Individualized plan of pregravidary preparation and medical care during pregnancy and delivery should be developed by a multidisciplinary team.
topic heritable thoracic aortic disease
pregnancy
cardiac surgery
url http://cvs.org.ua/index.php/ujcvs/article/view/356
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