NLRP3-Inflammasome Gene Variations in the Risk of Type 2 Diabetes


Özbayer C., Kurt H., Yağcı E., Kebapçı M. N., Gunes H. V., Değirmenci İ.

JOURNAL OF ENVIRONMENTAL PATHOLOGY TOXICOLOGY AND ONCOLOGY, cilt.41, sa.2, ss.1-13, 2022 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 41 Sayı: 2
  • Basım Tarihi: 2022
  • Doi Numarası: 10.1615/jenvironpatholtoxicoloncol.2021040001
  • Dergi Adı: JOURNAL OF ENVIRONMENTAL PATHOLOGY TOXICOLOGY AND ONCOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Aquatic Science & Fisheries Abstracts (ASFA), BIOSIS, EMBASE, Environment Index, Greenfile, MEDLINE, Pollution Abstracts
  • Sayfa Sayıları: ss.1-13
  • Anahtar Kelimeler: inflammasome, NLRP3, type 2 diabetes, genetic variation, NLRP3 INFLAMMASOME ACTIVATION, INSULIN-RESISTANCE, ASSOCIATION, OBESITY, SUSCEPTIBILITY, VARIANTS, MELLITUS, POLYMORPHISMS, POPULATION, MECHANISMS
  • Eskişehir Osmangazi Üniversitesi Adresli: Evet

Özet

Inflammation is the natural immunological response of an organism against any harmful, foreign or destructive effect to heal and repair damaged tissue. The nod-like receptor pyrin domain-containing-3 (NLRP3) inflammasome is one of the main components of the inflammatory mechanism and is associated with many inflammatory diseases, but it is also closely related to metabolic abnormalities, such as type 2 diabetes mellitus (T2DM), insulin resistance and obesity. NLRP3 activates inflammation and causes interleukin-1 beta release, exogenous and endogenous danger signals, as well as insulin resistance. In this direction, we focus on the gene structure of NLRP3 in diabetes and accordingly, we aim to determine the relationship between eight gene variations in the NLRP3 gene and T2DM. We investigated the rs10802501, rs10733113, rs10754558, rs10925026, rs10925027, rs35829419, rs4612666 and rs4925659 single-nucleotide polymorphisms of NLRP3 gene using the Sequenom MassARRAY system in 100 T2DM patients and 100 control individuals. There were no significant differences between T2DM risk and the genotype frequencies of rs10802501, rs10733113, rs35829419 and rs10925026 variants (p > 0.05). However, significant genotype frequencies were determined for rs10925027 (p = 0.0013) and rs4925659 (p < 0.001). For the risk allele G of the rs10754558 variant, significant differences were found in the heterozygous and dominant model (p = 0.036, p = 0.033). The genotype distribution of the rs4612666 variant was significant only in the heterozygous model (p = 0.047). In this hospital-based case-control study, rs10925027, rs4925659 and rs10754558 variants were found to be closely related to T2DM risk. The rs10925027 CC genotype, rs4925659 GG genotype, rs10754558 GG and GC+GG genotypes of the NLRP3 were deter-mined as important risk factors for the T2DM.