华西口腔医学杂志

• 基础研究 • 上一篇    下一篇

转化生长因子-β1和白细胞介素-10单核苷酸多态性与复发性口腔溃疡易感性的研究

张敬1  沙晶晶2  龚娟1   

  1. 1.宁夏医科大学总医院口腔医院牙体牙髓病科;2.宁夏医科大学研究生院,银川 750004
  • 出版日期:2016-02-01 发布日期:2016-02-01
  • 通讯作者: 张敬,主任医师,硕士,E-mail:zhj20045@163.com
  • 作者简介:张敬,主任医师,硕士,E-mail:zhj20045@163.com
  • 基金资助:

    宁夏自然科学基金(NZ201322)

Relationship between transforming growth factor-β1 and interleukin-10 single nucleotide polymorphism and susceptibility of recurrent aphthous ulcer

Zhang Jing1, Sha Jingjing2, Gong Juan1   

  1. 1. Dept. of Endodontic Disease, Stomatological Hospital of Ningxia Medical University General Hospital, Yinchuan 750004, China; 2. Graduate School of Ningxia Medical University, Yinchuan 750004, China
  • Online:2016-02-01 Published:2016-02-01

摘要:

目的  研究转化生长因子-β1(TGF-β1)-509T/C位点与白细胞介素-10(IL-10)-1082A/G位点的单核苷酸多态性与复发性口腔溃疡(RAU)易感性的相关性。方法  采用限制性片段长度多态性-聚合酶链式反应(RFLPPCR)RFLPPCR)法和序列特异性引物-聚合酶链式反应(SSP-PCR)法对138例RAU患者和124例健康对照者进行TGF-β1-509位点与IL-10-1082位点的单核苷酸多态性的检测分析,用比值比(OR)和95%可信区间(95%CI)估计相对危险度。结果  TGF-β1-509位点与IL-10-1082位点在基因型频率与等位基因频率的分布上,病例组与正常对照组之间均存在明显差异(P<0.05)。TGF-β1-509位点基因型CT(OR=1.231,95%CI=0.702~2.160)与TT(OR=2.482,95%CI= 1.250~4.927)为高风险基因型,T等位基因为高风险等位基因(OR=1.465,95%CI=1.036~2.074)。IL-10-1082位点基因型AG(OR=1.391,95%CI=0.808~2.396)与GG(OR=4.165,95%CI=1.944~8.924)为高风险基因型,G等位基因为高风险等位基因(OR=2.134,95%CI=1.474~3.089)。结论  TGF-β1-509位点与IL-10-1082位点是RAU患者的易感基因位点。TGF-β1-509位点携带T等位基因患RAU的风险性是携带C等位基因者的1.465倍。IL-10-1082位点携带G等位基因患RAU的风险性是携带A等位基因者的2.134倍。

关键词: 转化生长因子-&beta, 1, 白细胞介素-10, 单核苷酸多态性, 复发性口腔溃疡

Abstract:

Objective  To explore the possible relationship between recurrent aphthous ulcer (RAU) and single nucleotide polymorphism (SNP) of transforming growth factor-β1 (TGF-β1)-509T/C and interleukin-10 (IL-10)-1082A/G sites. Methods  A total of 138 RAU patients were recruited for this study. The control group consisted of 124 subjects. TGF-β1-509T/C and IL-10-1082A/G sites were detected by restriction fragment length polymorphism-polymerase chain reaction (RFLP-PCR) and sequence specific primer-polymerase chain reaction (SSP-PCR). Relative risk ratios were estimated by odds ratios (OR) and 95% confidence interval (95%CI). Results  Significant differences were found in the genotype frequencies or allele frequencies of TGF-β1-509T/C and IL-10-1082A/G sites between the RAU patients and controls (P<0.05). CT genotype (OR=1.231, 95%CI=0.702–2.160), TT genotype (OR=2.482, 95%CI=1.250–4.927), and T allele (OR=1.465, 95%CI=1.036–2.074) at the TGF-β1-509 site exhibited high risks. AG genotype (OR=1.391, 95%CI=0.808–2.396), GG genotype (OR=4.165, 95%CI=1.944–8.924), and G allele (OR=2.134, 95%CI=1.474–3.089) at the IL-10-1082A/G site also showed high risks. Conclusion  TGF-β1-509T/C and IL-10-1082A/G sites are associated with the risk of RAU. The TGF-β1 gene-509T allele and IL-10 gene-1082G allele may serve as genetic determinants for RAU.

Key words: transforming growth factor-β1, interleukin-10, single nucleotide polymorphism, recurrent aphthous ulcer