Angiotensin converting enzyme insertion/deletion polymorphism is associated with susceptibility and outcome in acute respiratory distress syndrome
- PMID: 12204859
- DOI: 10.1164/rccm.2108086
Angiotensin converting enzyme insertion/deletion polymorphism is associated with susceptibility and outcome in acute respiratory distress syndrome
Abstract
Acute respiratory distress syndrome (ARDS) is an often fatal condition for which a genetic predisposition is postulated, although no specific genes have been identified to date. Angiotensin converting enzyme (ACE) has a potential role in the pathogenesis of ARDS via effects on pulmonary vascular tone/permeability, epithelial cell survival, and fibroblast activation. Forty-seven percent of the variance in plasma ACE activity is accounted for by the ACE insertion/deletion (I/D) polymorphism, the D allele being associated with higher activity. We therefore hypothesized that the presence of the D allele would be associated with the development of ARDS. Ninety-six white patients fulfilling American/European Consensus Committee criteria for ARDS were genotyped for the ACE polymorphism together with individuals from three comparison groups: 88 white patients with non-ARDS respiratory failure ventilated in the intensive care unit (ICU), 174 ICU patients undergoing coronary artery bypass grafting, and 1,906 individuals from a general population group. DD genotype frequency was increased in the patients with ARDS compared with the ICU (p = 0.00008), coronary artery bypass grafting (p = 0.0009), and general population group (p = 0.00004) control groups and was significantly associated with mortality in the ARDS group (p < 0.02). These data suggest a potential role for renin-angiotensin systems in the pathogenesis of ARDS and for the first time implicate genetic factors in the development and progression of this syndrome.
Comment in
-
Genomics and acute respiratory distress syndrome.Am J Respir Crit Care Med. 2002 Sep 1;166(5):633-4. doi: 10.1164/rccm.2206004. Am J Respir Crit Care Med. 2002. PMID: 12204853 No abstract available.
Similar articles
-
Polymorphism of the angiotensin-converting enzyme gene affects the outcome of acute respiratory distress syndrome.Crit Care Med. 2006 Apr;34(4):1001-6. doi: 10.1097/01.CCM.0000206107.92476.39. Crit Care Med. 2006. PMID: 16484896
-
ACE I/D but not AGT (-6)A/G polymorphism is a risk factor for mortality in ARDS.Eur Respir J. 2007 Mar;29(3):482-8. doi: 10.1183/09031936.00046106. Epub 2006 Nov 15. Eur Respir J. 2007. PMID: 17107992
-
Absence of association between angiotensin converting enzyme polymorphism and development of adult respiratory distress syndrome in patients with severe acute respiratory syndrome: a case control study.BMC Infect Dis. 2005 Apr 9;5:26. doi: 10.1186/1471-2334-5-26. BMC Infect Dis. 2005. PMID: 15819995 Free PMC article.
-
Genetic heterogeneity and risk of acute respiratory distress syndrome.Semin Respir Crit Care Med. 2013 Aug;34(4):459-74. doi: 10.1055/s-0033-1351121. Epub 2013 Aug 11. Semin Respir Crit Care Med. 2013. PMID: 23934715 Review.
-
Early Evaluation and Monitoring of Critical Patients with Acute Respiratory Distress Syndrome (ARDS) Using Specific Genetic Polymorphisms.Biochem Genet. 2017 Jun;55(3):204-211. doi: 10.1007/s10528-016-9787-0. Epub 2017 Jan 9. Biochem Genet. 2017. PMID: 28070694 Review.
Cited by
-
Role of vitamin D in COVID-19 and other viral infections.World J Virol. 2024 Sep 25;13(3):95349. doi: 10.5501/wjv.v13.i3.95349. World J Virol. 2024. PMID: 39323448 Free PMC article. Review.
-
The Association Between Genetic Variants in ACE1and ACE2 Genes with Susceptibility to COVID-19 Infection.Biochem Genet. 2024 Feb 13. doi: 10.1007/s10528-024-10722-8. Online ahead of print. Biochem Genet. 2024. PMID: 38349438
-
Association of IL-10-592 C > A /-1082 A > G and the TNFα -308 G > A with susceptibility to COVID-19 and clinical outcomes.BMC Med Genomics. 2024 Jan 29;17(1):40. doi: 10.1186/s12920-023-01793-4. BMC Med Genomics. 2024. PMID: 38287362 Free PMC article.
-
The Effect of Angiotensin-Converting Enzyme Insertion/Deletion Polymorphism on the Severity and Death Rate of COVID-19 in Iranian Patients.Biochem Genet. 2024 Oct;62(5):3568-3585. doi: 10.1007/s10528-023-10614-3. Epub 2023 Dec 25. Biochem Genet. 2024. PMID: 38145438
-
Relationship between Angiotensin-Converting Enzyme Insertion/Deletion Polymorphism and the Risk of COVID-19: A Meta-Analysis.J Renin Angiotensin Aldosterone Syst. 2023 Nov 28;2023:3431612. doi: 10.1155/2023/3431612. eCollection 2023. J Renin Angiotensin Aldosterone Syst. 2023. PMID: 38058963 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous