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Interleukin 1 receptor antagonist (IL1RN) genetic variations condition post-orthodontic external root resorption in endodontically-treated teeth.

Authors :
Iglesias-Linares A
Yañez-Vico RM
Ballesta-Mudarra S
Ortiz-Ariza E
Mendoza-Mendoza A
Perea-Pérez E
Moreno-Fernández AM
Solano-Reina E
Source :
Histology and histopathology [Histol Histopathol] 2013 Jun; Vol. 28 (6), pp. 767-73. Date of Electronic Publication: 2012 Dec 05.
Publication Year :
2013

Abstract

External apical root resorption (EARR) is a frequent iatrogenic problem following orthodontic treatment in endodontically-treated teeth, about which the literature reports substantial variability in post-orthodontic treatment EARR responses. The main focus of the present study is to clarify whether variants in the interleukin-1 receptor antagonist gene coding for the IL-1ra protein have a positive/negative influence on EARR of endodontically-treated teeth. Ninety-three orthodontic patients were genetically screened for a single nucleotide polymorphism (SNP:rs419598) in the IL1 cluster. The sample was classified into 2 groups: group 1 (affected-group) showed radiographic EARR of more than 2mm; group 2 (control-group), had no EARR or EARR ≤ to 2mm following orthodontic treatment on root-filled teeth. Logistic regression analysis was performed to obtain an adjusted estimate between the SNPs studied and EARR. Genotype distributions, allelic frequencies, adjusted odds ratios (OR) and 95% confidence intervals were also calculated. We found that subjects homozygous [1/1(TT)] for the IL1RN gene [OR:10.85; p=0.001;CI:95%] were at risk of EARR in root-filled teeth. Genetic variants in the antagonist axis balance of the IL1RN (rs419598) have a direct repercussion on the predisposition to post-orthodontic EARR in root-filled teeth. Variants in allele 1 of the interleukin-1 receptor antagonist gene(rs419598) are associated(p=0.001**) with an increased risk of suffering post-orthodontic EARR in root-filled teeth.

Details

Language :
English
ISSN :
1699-5848
Volume :
28
Issue :
6
Database :
MEDLINE
Journal :
Histology and histopathology
Publication Type :
Academic Journal
Accession number :
23212299
Full Text :
https://doi.org/10.14670/HH-28.767