机构地区:[1]扬州大学医学院消化病研究室,江苏省扬州市225001 [2]扬州市疾病预防控制中心检验科,江苏省扬州市225001
出 处:《世界华人消化杂志》2014年第24期3580-3586,共7页World Chinese Journal of Digestology
基 金:国家自然科学基金资助项目;No.81173392~~
摘 要:目的:探讨腹泻型肠易激综合征(diarrheairritable bowel syndrome,D-IBS)重叠功能性消化不良(functional dyspepsia,FD)患者白介素-10(interleukin-10,IL-10)基因启动子区域多态性及其血浆水平与疾病易感性的关系.方法:对164例D-IBS重叠FD患者和200例健康对照者抽血提取其白细胞DNA,应用聚合酶反应-限制性片段多态性(polymerasechain reaction-restriction fragment lengthpolymorphism,PCR-RFLP)分析方法以及扩增受阻突变系统-聚合酶链反应(amplificationrefractory mutation system-polymerase chainreactions,ARMS-PCR)结合DNA测序法,对IL-10基因启动子区-592与-1082位点进行多态性分析,并使用酶联免疫吸附法测定血浆IL-10水平.结果:D-IBS重叠FD病例组与正常对照组相比,IL-10启动子区域592位点基因型分布与等位基因频率无显著差异,592CC基因频率显著下降,基因型频率风险相关分析表示,AA基因型是CC基因型患病风险的1.989倍;A等位基因携带型(AA+AC基因型)为CC型纯合子的1.808倍;-1082位点基因型分布与等位基因频率均无显著差异;-592位点与-1082位点组合基因型分布与等位基因频率也无显著差异;不同IL-10分泌水平基因型分布无显著差异.D-IBS重叠FD病例组血浆IL-10平均水平为14.60 pg/mL±7.14 pg/mL,对照组为22.86 pg/mL±10.62 pg/mL,两组比较,病例组显著低于正常对照组(P<0.001).D-IBS重叠FD病例组592位点AA、AC、CC、AA+AC基因型血浆IL-10水平分别为14.50 pg/mL±6.37 pg/mL、14.85 pg/mL±7.75 pg/mL、13.92 pg/mL±7.63 pg/mL,14.68 pg/mL±7.10 pg/mL,病例组各基因型之间血浆IL-10水平无显著差异,592位点AA+AC与CC基因型血浆IL-10水平也无显著差异.结论:IL-10-592位点A和IL-10血浆水平降低可能与罹患D-IBS重叠FD的相关,但这二者之间并无关联.AIM: To investigate the relationship betweeninterleukin-10(IL-10) promoter gene polymor-phisms and plasma levels and susceptibility tooverlap syndrome of diarrhea irritable bowelsyndrome(D-IBS) and functional dyspepsia(FD).METHODS: Blood samples were collected from164 patients and 200 healthy controls and ge-nomic DNA was extracted. Polymerase chain reaction-restriction fragment length polymor-phism(PCR-RFLP) was used to determine the genotypes in the-592A/C site, and amplification refractory mutation system polymerase chain re-actions(ARMS-PCR) and DNA sequencing were performed to detect the polymorphism of the-1082G/A site. IL-10 plasma levels were deter-mined by enzyme-linked immunosorbent assay(ELISA). RESULTS: The-592A/C site in the IL-10 gene showed no significant differences in genotypes or allele frequency between the D-IBS-FD over-lap syndrome group and control group, but the frequency of-592 CC genotype was significant-ly decreased in the D-IBS-FD overlap syndrome group. Compared with the CC genotype, the AA genotype and the AA+AC genotypes in-creased the risk of D-IBS-FD overlap syndrome 1.989 and 1.808 times, respectively. There were no significant differences in the distribution or the allele frequency of-1082 genotypes, the genotypes of the combination of-592 and-1082, and the distribution of the genotypes of differ-ent IL-10 levels between the D-IBS-FD overlap syndrome and healthy control groups. The average plasma IL-10 levels were significantly lower in patients with D-IBS-FD overlap syn-drome than in healthy controls(14.60 pg/mL ± 7.14 pg/mL vs 22.86 pg/mL ± 10.62 pg/mL, P 0.001). Among patients with D-IBS-FD overlap syndrome, the average plasma IL-10 levels in patients with-592 AA,-592 AC,-592 CC, and-592 AA+AC genotypes were 14.50 pg/mL ± 6.37 pg/mL, 14.85 pg/mL ± 7.75 pg/mL, 13.92 pg/mL ± 7.63 pg/mL, 14.68 pg/mL ± 7.10 pg/mL, respectively, which showed no significant differences. Plasma IL-10 levels showed no significant difference between the carri
关 键 词:腹泻型肠易激综合征重叠功能性消化不良 白介素-10 基因多态性 启动子区域
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