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SARS-CoV-2 Infection in Hereditary Hemorrhagic Telangiectasia Patients Suggests Less Clinical Impact Than in the General Population.

Authors :
Marcos, Sol
Albiñana, Virginia
Recio-Poveda, Lucia
Tarazona, Belisa
Verde-González, María Patrocinio
Ojeda-Fernández, Luisa
Botella, Luisa-María
Cuesta, Angel M.
Ergün, Süleyman
Source :
Journal of Clinical Medicine; May2021, Vol. 10 Issue 9, p1884-1884, 1p
Publication Year :
2021

Abstract

At the moment of writing this communication, the health crisis derived from the COVID-19 pandemic has affected more than 120 million cases, with 40 million corresponding to Europe. In total, the number of deaths is almost 3 million, but continuously rising. Although COVID-19 is primarily a respiratory disease, SARS-CoV-2 infects also endothelial cells in the pulmonary capillaries. This affects the integrity of the endothelium and increases vascular permeability. In addition, there are serious indirect consequences, like disruption of endothelial cells' junctions leading to micro-bleeds and uncontrolled blood clotting. The impact of COVID-19 in people with rare chronic cardiovascular diseases is unknown so far, and interesting to assess, because the virus may cause additional complications in these patients. The aim of the present work was to study the COVID-19 infection among the patients with Hereditary Hemorrhagic Telangiectasia (HHT). A retrospective study was carried out in a 138 HHT patients' sample attending an Ear Nose and Throat (ENT) reference consult. The evaluation of the COVID-19 infection in them reveals milder symptoms; among the 25 HHT patients who were infected, only 3 cases were hospitalized, and none of them required ICU or ventilation assistance. The results are discussed in the light of macrophage immune response. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20770383
Volume :
10
Issue :
9
Database :
Complementary Index
Journal :
Journal of Clinical Medicine
Publication Type :
Academic Journal
Accession number :
150375509
Full Text :
https://doi.org/10.3390/jcm10091884