4.7 Article

The Role of Polymorphisms at the Interleukin-1, Interleukin-4, GATA-3 and Cyclooxygenase-2 Genes in Non-Surgical Periodontal Therapy

Journal

Publisher

MDPI
DOI: 10.3390/ijms23137266

Keywords

periodontitis; polymorphisms; risk factor; periodontal therapy; antibiotics; GATA-3; Interleukin-1; Interleukin-4; Cyclooxygenase-2

Funding

  1. German Research Foundation (Deutsche Forschungsgemeinschaft (DFG)) [EH365 1-1]
  2. DeutscheGesellschaft fur Zahn-, Mundund Kieferheilkunde Research Grant [62880362]

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This study investigated the role of Interleukin-(IL)-1, IL-4, GATA-3, and Cyclooxygenase-(COX)-2 polymorphisms in periodontitis progression after non-surgical therapy with adjunctive systemic antibiotics in a Caucasian population. The study found a slight association between GATA-3 gene locus and clinical attachment levels (CAL).
Periodontitis is a multifactorial disease. The aim of this explorative study was to investigate the role of Interleukin-(IL)-1, IL-4, GATA-3 and Cyclooxygenase-(COX)-2 polymorphisms after non-surgical periodontal therapy with adjunctive systemic antibiotics (amoxicillin/metronidazole) and subsequent maintenance in a Caucasian population. Analyses were performed using blood samples from periodontitis patients of a multi-center trial (ClinicalTrials.gov NCT00707369=ABPARO-study). Polymorphisms were analyzed using quantitative real-time PCR. Clinical attachment levels (CAL), percentage of sites showing further attachment loss (PSAL) >= 1.3 mm, bleeding on probing (BOP) and plaque score were assessed. Exploratory statistical analysis was performed. A total of 209 samples were genotyped. Patients carrying heterozygous genotypes and single-nucleotide-polymorphisms (SNP) on the GATA-3-IVS4 +1468 gene locus showed less CAL loss than patients carrying wild type. Heterozygous genotypes and SNPs on the IL-1A-889, IL-1B +3954, IL-4-34, IL-4-590, GATA-3-IVS4 +1468 and COX-2-1195 gene loci did not influence CAL. In multivariate analysis, CAL was lower in patients carrying GATA-3 heterozygous genotypes and SNPs than those carrying wild-types. For the first time, effects of different genotypes were analyzed in periodontitis progression after periodontal therapy and during supportive treatment using systemic antibiotics demonstrating a slight association of GATA-3 gene locus with CAL. This result suggests that GATA-3 genotypes are a contributory but non-essential risk factor for periodontal disease progression.

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