Association of vitamin D receptor gene FokI polymorphism and susceptibility to CAP in Egyptian children: a multicenter study
Background Community-acquired pneumonia (CAP) is the leading cause of child deaths around the world. Recently, the vitamin D receptor (VDR) gene has emerged as a susceptibility gene for CAP. Objectives To evaluate the association of the VDR gene Fok I polymorphism with susceptibility to CAP in Egypt...
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Veröffentlicht in: | Pediatric research 2018-11, Vol.84 (5), p.639-644 |
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Hauptverfasser: | , , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Background
Community-acquired pneumonia (CAP) is the leading cause of child deaths around the world. Recently, the vitamin D receptor (VDR) gene has emerged as a susceptibility gene for CAP.
Objectives
To evaluate the association of the VDR gene Fok I polymorphism with susceptibility to CAP in Egyptian children.
Methods
This was a multicenter case-control study of 300 patients diagnosed with CAP, and 300 well-matched healthy control children. The VDR Fok I (rs2228570) polymorphism was genotyped by
PCR
-restriction fragment length polymorphism (
RFLP
), meanwhile serum 25-hydroxy vitamin D (25D) level was assessed using
ELISA
method.
Results
The frequencies of the VDR
FF
genotype and
F
allele were more common in patients with CAP than in our control group (OR = 3.6; (95% CI: 1.9–6.7) for the
FF
genotype;
P
= 0.001) and (OR: 1.8; (95% CI: 1.4–2.3) for the
F
allele;
P
= 0.01). Patients carrying the VDR
FF
genotype had lower serum (25D) level (mean; 14.8 ± 3.6 ng/ml) than
Ff
genotype (20.6 ± 4.5 ng/ml) and the
ff
genotype (24.5 ± 3.7 ng/ml);
P
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ISSN: | 0031-3998 1530-0447 |
DOI: | 10.1038/s41390-018-0149-y |