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Published on: September 1, 2015
Angiotensin-converting enzyme insertion/deletion gene polymorphism in Egyptian children with CAP: A case-control
Heba Abouzeid1, Usama M Alkholy1, Mohammed A Abdou1
1Faculty of Medicine, Department of Pediatrics, Zagazig University, Zagazig, Egypt.
The angiotensin-converting enzyme (ACE) I/D polymorphism (rs4340) is linked to increased community-acquired pneumonia (CAP) risk in Egyptian children. The ACE D allele and DD genotype correlate with higher serum ACE levels in CAP patients.
Area of Science:
- Genetics and Molecular Biology
- Pediatric Infectious Diseases
- Biochemistry
Background:
- Community-acquired pneumonia (CAP) is a significant global health concern in children.
- The angiotensin-converting enzyme (ACE) gene is investigated for its potential role in CAP susceptibility.
Purpose of the Study:
- To determine if the ACE insertion/deletion (I/D) polymorphism (rs4340) serves as a genetic marker for CAP susceptibility in Egyptian children.
- To examine the relationship between serum ACE levels and the ACE I/D polymorphism in this population.
Main Methods:
- A prospective case-control study involving 300 Egyptian children with CAP and 300 matched healthy controls.
- Genotyping of the ACE I/D polymorphism (rs4340) using PCR-RFLP.
- Measurement of serum ACE levels via ELISA.
Main Results:
- The ACE DD genotype and D allele were significantly more frequent in children with CAP compared to controls (OR=3.05 for DD, OR=1.8 for D allele).
- Patients with the DD genotype exhibited substantially higher mean serum ACE levels (45.6 U/L) than those with ID (36.5 U/L) or II (21.6 U/L) genotypes.
- The ACE D allele and DD genotype were associated with elevated serum ACE levels in CAP patients.
Conclusions:
- The ACE I/D polymorphism (rs4340) may play a role in the genetic predisposition to CAP in Egyptian children.
- Higher serum ACE levels are linked to the ACE D allele and DD genotype in children with CAP.
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