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ACE1 polymorphism and progression of SARS
We have hypothesized that genetic predisposition influences the progression of SARS. Angiotensin converting enzyme (ACE1) insertion/deletion (I/D) polymorphism was previously reported to show association with the adult respiratory distress syndrome, which is also thought to play a key role in damagi...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2004
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7092806/ https://www.ncbi.nlm.nih.gov/pubmed/15381116 http://dx.doi.org/10.1016/j.bbrc.2004.08.208 |
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author | Itoyama, Satoru Keicho, Naoto Quy, Tran Phi, Nguyen Chi Long, Hoang Thuy Ha, Le Dang Ban, Vo Van Ohashi, Jun Hijikata, Minako Matsushita, Ikumi Kawana, Akihiko Yanai, Hideki Kirikae, Teruo Kuratsuji, Tadatoshi Sasazuki, Takehiko |
author_facet | Itoyama, Satoru Keicho, Naoto Quy, Tran Phi, Nguyen Chi Long, Hoang Thuy Ha, Le Dang Ban, Vo Van Ohashi, Jun Hijikata, Minako Matsushita, Ikumi Kawana, Akihiko Yanai, Hideki Kirikae, Teruo Kuratsuji, Tadatoshi Sasazuki, Takehiko |
author_sort | Itoyama, Satoru |
collection | PubMed |
description | We have hypothesized that genetic predisposition influences the progression of SARS. Angiotensin converting enzyme (ACE1) insertion/deletion (I/D) polymorphism was previously reported to show association with the adult respiratory distress syndrome, which is also thought to play a key role in damaging the lung tissues in SARS cases. This time, the polymorphism was genotyped in 44 Vietnamese SARS cases, with 103 healthy controls who had had a contact with the SARS patients and 50 controls without any contact history. SARS cases were divided into either non-hypoxemic or hypoxemic groups. Despite the small sample size, the frequency of the D allele was significantly higher in the hypoxemic group than in the non-hypoxemic group (p = 0.013), whereas there was no significant difference between the SARS cases and controls, irrespective of a contact history. ACE1 might be one of the candidate genes that influence the progression of pneumonia in SARS. |
format | Online Article Text |
id | pubmed-7092806 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70928062020-03-25 ACE1 polymorphism and progression of SARS Itoyama, Satoru Keicho, Naoto Quy, Tran Phi, Nguyen Chi Long, Hoang Thuy Ha, Le Dang Ban, Vo Van Ohashi, Jun Hijikata, Minako Matsushita, Ikumi Kawana, Akihiko Yanai, Hideki Kirikae, Teruo Kuratsuji, Tadatoshi Sasazuki, Takehiko Biochem Biophys Res Commun Article We have hypothesized that genetic predisposition influences the progression of SARS. Angiotensin converting enzyme (ACE1) insertion/deletion (I/D) polymorphism was previously reported to show association with the adult respiratory distress syndrome, which is also thought to play a key role in damaging the lung tissues in SARS cases. This time, the polymorphism was genotyped in 44 Vietnamese SARS cases, with 103 healthy controls who had had a contact with the SARS patients and 50 controls without any contact history. SARS cases were divided into either non-hypoxemic or hypoxemic groups. Despite the small sample size, the frequency of the D allele was significantly higher in the hypoxemic group than in the non-hypoxemic group (p = 0.013), whereas there was no significant difference between the SARS cases and controls, irrespective of a contact history. ACE1 might be one of the candidate genes that influence the progression of pneumonia in SARS. Elsevier Inc. 2004-10-22 2004-09-17 /pmc/articles/PMC7092806/ /pubmed/15381116 http://dx.doi.org/10.1016/j.bbrc.2004.08.208 Text en Copyright © 2004 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Itoyama, Satoru Keicho, Naoto Quy, Tran Phi, Nguyen Chi Long, Hoang Thuy Ha, Le Dang Ban, Vo Van Ohashi, Jun Hijikata, Minako Matsushita, Ikumi Kawana, Akihiko Yanai, Hideki Kirikae, Teruo Kuratsuji, Tadatoshi Sasazuki, Takehiko ACE1 polymorphism and progression of SARS |
title | ACE1 polymorphism and progression of SARS |
title_full | ACE1 polymorphism and progression of SARS |
title_fullStr | ACE1 polymorphism and progression of SARS |
title_full_unstemmed | ACE1 polymorphism and progression of SARS |
title_short | ACE1 polymorphism and progression of SARS |
title_sort | ace1 polymorphism and progression of sars |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7092806/ https://www.ncbi.nlm.nih.gov/pubmed/15381116 http://dx.doi.org/10.1016/j.bbrc.2004.08.208 |
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