Why the study?
Increasing evidence suggested angiotensin II plays an important role in acute lung injury pathogenesis and evolution. This study investigated whether polymorphisms of the angiotensin-converting enzyme gene affect the risk and outcome of acute respiratory distress syndrome (ARDS).
Does the insertion/deletion (I/D) polymorphism of the angiotensin-converting enzyme (ACE) gene affect the risk of developing ARDS and 28-day/in-hospital mortality outcomes in medical ICU patients?
Cohort (n=449)
No
Does the insertion/deletion (I/D) polymorphism of the angiotensin-converting enzyme (ACE) gene affect the risk of developing ARDS and 28-day/in-hospital mortality outcomes in medical ICU patients?
Answers are grounded in this paper and cite their sources.
In Chinese patients, the ACE gene I/D polymorphism does not increase the risk of developing ARDS, but serves as a significant prognostic factor where the II genotype confers substantially better 28-day and in-hospital survival.
Objective There has been increasing evidence that angiotensin II may play an important role in the pathogenesis and in the evolution of acute lung injury. It was therefore hypothesized that polymorphisms of the angiotensin-converting enzyme gene affects the risk and outcome of acute respiratory distress syndrome (ARDS). Design Prospective, observational study. Patients and settings The ARDS group consisted of 101 patients treated at the medical intensive care unit; the control groups consisted of 138 "at-risk" patients treated at the medical intensive care unit due to acute respiratory failure but did not meet the ARDS criteria throughout the hospital course, and 210 non-at-risk subjects. Intervention None. Measurements and main results The ARDS patients and control subjects were genotyped for the insertion/deletion (I/D) polymorphism of the angiotensin-converting enzyme gene. Association of the polymorphism and the risk and the outcome of ARDS was analyzed. There was no significant difference in the frequencies of the genotypes between the ARDS, at-risk, and non-at-risk groups. The 28-day mortality rates were significantly different between the three angiotensin-converting enzyme genotypes (42%, 65%, and 75% for II, ID, and DD, respectively; p = .036). Survival analysis showed that the II genotype favorably affected 28-day survival (hazard ratio, 0.46; 95% confidence interval, 0.26-0.81; p = .007), whereas ARDS caused by hospital-acquired pneumonia had a negative effect (hazard ratio, 2.34; 95% confidence interval, 1.25-4.40; p = .008). The II genotype (hazard ratio, 0.53; 95% confidence interval, 0.32-0.87; p = .012) and ARDS caused by hospital-acquired pneumonia (hazard ratio, 2.13; 95% confidence interval, 1.24-3.68; p = .006) were also significant prognostic factors for the in-hospital mortality. Conclusions The angiotensin-converting enzyme I/D polymorphism is a significant prognostic factor for the outcome of ARDS. Patients with the II genotype have a significantly better chance of survival. This study did not show an increased risk for ARDS in Chinese patients with the D allele.
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Jerng et al. (2006) conducted a cohort in Acute respiratory distress syndrome (ARDS) (n=449). Angiotensin-converting enzyme (ACE) gene II genotype vs. ACE ID and DD genotypes was evaluated on 28-day mortality in ARDS patients (HR 0.46, 95% CI 0.26-0.81, p=0.007).
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