Tongtawee Taweesak, Bartpho Theeraya, Wattanawongdon Wareeporn, Dechsukhum Chavaboon, Leeanansaksiri Wilairat, Matrakool Likit, Panpimanmas Sukij
Department of Surgery, Suranaree University of Technology, Institute of Medicine, Nakhon Ratchasima, Thailand.
Turk J Gastroenterol. 2017 Jul;28(4):243-247. doi: 10.5152/tjg.2017.16673.
BACKGROUND/AIMS: Helicobacter pylori stimulates the host's toll-like receptors (TLRs). Single-nucleotide polymorphism (SNP) of TLRs is related to the manipulation of regulatory cytokines and also implicated in the varied outcomes of the inflammatory response, including the development of precancerous lesions of gastric mucosa and disease progression. We hypothesized that TLR10 rs10004195 polymorphism is associated with gastric mucosal patterns.
TLR10 rs10004195 polymorphisms were identified in a total of 400 gastritis patients using the TagMan SNP genotyping assay. Gastric mucosal patterns were classified by Conventional Narrow Band Imaging gastroscopy (C-NBI gastroscopy). Logistic regression was used to analyze the association.
The gastritis patients was Type 1, 37.5% of Thai patients. The T/T homozygous genotype was exhibited by the highest percentage (46.5%) of patients, and the A/A homozygous and A/T heterozygous genotypes were exhibited by 20.25% and 33.25%, respectively, of patients. TLR10 rs10004195 was significantly associated with gastric mucosal patterns. After adjusting for confounding factors, patients with the A/A homozygous genotype showed a significantly increased risk of severe inflammation (OR=1.35, 95% CI=0.97-2.13, p=0.028). Patients with the A/T heterozygous and T/T homozygous genotypes showed a significantly increased risk of mild inflammation (OR=1.24, 95% CI=0.78-2.07, p=0.042 and OR=1.78, 95% CI=0.51-3.35, p=0.001, respectively).
Our results indicate that the presence of TLR10 rs10004195, A/T heterozygous, and T/T homozygous genotypes is associated with type 1, 2, and 3 whereas that of the A/A homozygous genotype is associated with type 4 and 5 of gastric mucosal patterns. This suggests that the A/A homozygous genotype contributes to severe inflammation in H. pylori-associated gastritis in Thai patients.
背景/目的:幽门螺杆菌刺激宿主的 Toll 样受体(TLRs)。TLRs 的单核苷酸多态性(SNP)与调节性细胞因子的调控有关,也与炎症反应的不同结果有关,包括胃黏膜癌前病变的发展和疾病进展。我们假设 TLR10 rs10004195 多态性与胃黏膜形态有关。
使用 TaqMan SNP 基因分型检测法在总共 400 例胃炎患者中鉴定 TLR10 rs10004195 多态性。通过传统窄带成像胃镜检查(C-NBI 胃镜检查)对胃黏膜形态进行分类。采用逻辑回归分析相关性。
胃炎患者为 1 型,占泰国患者的 37.5%。T/T 纯合基因型患者的比例最高(46.5%),A/A 纯合基因型和 A/T 杂合基因型患者的比例分别为 20.25%和 33.25%。TLR10 rs10004195 与胃黏膜形态显著相关。在调整混杂因素后,A/A 纯合基因型患者出现严重炎症的风险显著增加(OR = 1.35,95%CI = 0.97 - 2.13,p = 0.028)。A/T 杂合基因型和 T/T 纯合基因型患者出现轻度炎症的风险显著增加(分别为 OR = 1.24,95%CI = 0.78 - 2.07,p = 0.042 和 OR = 1.78,95%CI = 0.51 - 3.35,p = 0.001)。
我们的结果表明,TLR10 rs10004195 的 A/T 杂合基因型和 T/T 纯合基因型与胃黏膜形态的 1 型、2 型和 3 型相关,而 A/A 纯合基因型与 4 型和 5 型相关。这表明 A/A 纯合基因型导致泰国患者幽门螺杆菌相关性胃炎中的严重炎症。