AI Article Synopsis

  • The study investigated the link between specific genetic haplotypes in the IL8 and IL4 genes and the presence of Aggregatibacter actinomycetemcomitans (A.a.) in patients with and without chronic periodontitis (CP).
  • The research involved analyzing subgingival biofilm from various sites (596 samples from 104 patients) before and after periodontal treatment to quantify A.a. levels and examine clinical and immunological factors.
  • Results indicated that IL4 haplotypes were significantly associated with A.a. levels, with patients carrying the IL4- haplotype experiencing more severe periodontal issues and higher A.a. levels post-treatment compared to others.

Article Abstract

This study aimed to evaluate the association between haplotypes in the interleukin 8 (IL8) and IL4 genes previously associated to chronic periodontitis (CP) and the levels of Aggregatibacter actinomycetemcomitans (A.a.) in subgingival sites of patients with and without CP. Moreover, multifaceted evaluations were made to search associations among patients' genetic background with the A.a. levels and previous clinical/immunological/microbiological findings. Subgingival sites (n = 596) of 104 patients were divided into susceptible to CP by the IL8 haplotype ATC/TTC (IL8+); non-susceptible to CP by the IL8 AGT/TTC (IL8-); susceptible to CP by the IL4 TCI/CCI (IL4+); protection against CP by the IL4 TTD/CTI (IL4-). Subgingival biofilm samples from diseased and healthy sites of CP patients and from control sites of health patients were obtained for absolute quantification of A.a. by quantitative real-time polymerase chain reaction. For diseased sites, samples were collected before and 45 days after periodontal treatment. The IL4 but not the IL8 haplotypes were associated with levels of A.a. (in both periods). After periodontal treatment, higher levels of A.a. were found in subgingival sites of (IL4-) patients, and higher levels of IL-4 were associated with deeper probing pockets in these same patients. Significant correlations were found among genetic (patients carrying IL8 or IL4 haplotypes), microbiological and immunological data showing the interrelationship of different factors in the CP.

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Source
http://dx.doi.org/10.1093/femspd/ftx092DOI Listing

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