Key result
ACE I/D polymorphism shows no link to community-acquired pneumonia or adverse outcomes in pediatric patients.
Why the study?
The role of ACE I/D polymorphism in the risk and outcome of community-acquired pneumonia in pediatric populations has yielded inconsistent results across ethnicities.
Is the ACE I/D polymorphism associated with the risk and clinical outcomes of community-acquired pneumonia in children?
Case-Control (n=150)
Is the ACE I/D polymorphism associated with the risk and clinical outcomes of community-acquired pneumonia in children?
p-value: p=0.773
The ACE I/D polymorphism does not appear to influence the risk or clinical outcomes of community-acquired pneumonia in Egyptian children.
No association in Egyptian children; leaves open ACE I/D role in pediatric pneumonia across populations.
Objective Pneumonia is one of the leading causes of death for the Pediatric age group under five years worldwide. The role of the angiotensin-converting enzyme (ACE) insertion/deletion (I/D) polymorphism in the risk and outcome of community-acquired pneumonia (CAP) has been studied in different ethnic populations and yielded inconsistent results. Therefore, the present study aimed to investigate whether this polymorphism is associated with the risk and outcome of CAP in the Egyptian pediatric population. Methods The prospective observational case-control study was performed on 77 children aged 2 months to 12yrs hospitalized with CAP and 73 matched healthy controls. Candidates were subjected to clinical and radiological evaluation in addition to complete blood count, c-reactive protein and genotyping for the ACE I/D polymorphism using PCR technique. Follow up of the outcome in the form of need for oxygen, ICU admission, need for mechanical ventilation, duration of hospital stay and death was done for all patients. Results No statistically significant differences was observed between pneumonia patients and controls regarding the different genotypes of the ACE polymorphism II, ID and DD genotypes (p = 0.773). No association was detected between the different genotypes of the ACE polymorphism II, ID and DD genotypes and the need for oxygen, ICU admission, need for mechanical ventilation, duration of hospital stay and death (P = 0.143, 0.527, 0.716, 0.288, 0.544). Conclusion The ACE I/D polymorphism is not associated with the risk nor the outcome of pneumonia in our pediatric population.
No takes yet. Share an insight, caveat, or question.
Rifai et al. (2018) conducted a case-control in Community-acquired pneumonia (n=150). Angiotensin-converting enzyme (ACE) insertion/deletion (I/D) polymorphism vs. Matched healthy controls was evaluated on Risk of community-acquired pneumonia based on ACE polymorphism genotypes (p=0.773). The ACE I/D polymorphism was not associated with the risk of community-acquired pneumonia (P=0.773) or adverse clinical outcomes in pediatric patients.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: