2016
Interleukin-8 receptor 2 (CXCR2) gene variability in patients with chronic periodontitis alone or in combination with type 2 diabetes mellitus in the Czech population
BOŘILOVÁ LINHARTOVÁ, Petra; Denisa KAVŘÍKOVÁ; Světlana LUČANOVÁ; Hana POSKEROVÁ; Jan VOKURKA et al.Základní údaje
Originální název
Interleukin-8 receptor 2 (CXCR2) gene variability in patients with chronic periodontitis alone or in combination with type 2 diabetes mellitus in the Czech population
Autoři
BOŘILOVÁ LINHARTOVÁ, Petra; Denisa KAVŘÍKOVÁ; Světlana LUČANOVÁ; Hana POSKEROVÁ; Jan VOKURKA; Antonín FASSMANN a Lydie IZAKOVIČOVÁ HOLLÁ
Vydání
International Congress of Immunology 2016, Melbourne, 2016
Další údaje
Jazyk
angličtina
Typ výsledku
Konferenční abstrakt
Obor
Genetika a molekulární biologie
Stát vydavatele
Austrálie
Utajení
není předmětem státního či obchodního tajemství
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14110/16:00088129
Organizační jednotka
Lékařská fakulta
ISSN
Klíčová slova anglicky
chemokine receptor; polymorphism; periodontitis; type 2 diabetes mellitus
Štítky
Změněno: 20. 12. 2016 13:22, Ing. Mgr. Věra Pospíšilíková
Anotace
V originále
Background: Periodontitis is a chronic inflammatory disease triggered by specific subgingival bacteria. Evidence suggests that diabetes mellitus (DM) may modulate periodontal tissue destruction, e.g. by reducing the polymorphonuclear leukocyte functions, including chemotaxis, adherence and phagocytosis. CXCR2 is a specific receptor for the interleukin-8 (IL-8) that is chemoattractant for neutrophils with an important role in the regulation of inflammatory response. Material and Methods: We analyzed CXCR2 +785C/T (rs2230054), +1208C/T (rs1126579) and +1440A/G (rs1126580) polymorphisms in patients with chronic periodontitis (CP) or CP with type 2 DM (T2DM+CP) and healthy controls and determined their associations with risk of diseases and occurrence of periodontal pathogens. Totally, 575 subjects (170 controls, 325 patients with CP and 80 subjects with T2DM+CP) were genotyped using methods based on polymerase chain reaction (PCR). Bacterial colonization (A. actinomycetemcomitans, P. gingivalis, P. intermedia, T. forsythia, T. denticola, P. micros, F. nucleatum) was investigated by a DNA-microarray kit. Results: Although no differences in the allele/genotype frequencies between controls and patients with CP or T2DM+CP were found, TCA haplotype significantly increased the risk of T2DM+CP (P<0.05, OR=2.21, 95%CI:1.11-4.40 vs. controls and P<0.05, OR=1.52, 95%CI:1.08-2.16 vs. CP alone). A. actinomycetemcomitans occurred significantly more frequently in men patients with CP positive for T allele of CXCR2 +1208C/T variant (61.8% vs. 38.6%, P<0.05; OR=2.57, 95%CI=1.14-5.79) or positive for C allele of CXCR2 +785C/T polymorphism (61.8% vs. 40.9%, P<0.05; OR=2.33, 95%CI=1.04-5.25). Conclusion: Our findings demonstrated that CXCR2 gene variability may be one of the risk factors for T2DM+CP.
Návaznosti
| GB14-37368G, projekt VaV |
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| MUNI/A/1258/2015, interní kód MU |
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