期刊文献+

不同亚型食管癌反流病患者胃组织白细胞介素-1β表达差异及临床意义

The expression of interleukin 1β in the patients with typical symptoms and atypical symptoms of NERD
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摘要 目的对比研究典型症状与非典型症状的非糜烂反流病(NERD)患者胃组织白细胞介素-1β(IL-1β)的差异及临床意义。方法 NERD患者70例,按照有无典型反流症状,分为2个亚型:典型症状组43例、非典型症状组27例;采用化学发光法评估不同亚型NERD患者胃组织中IL-1β的表达差异。结果与非典型症状组比较,典型症状组IL-1β水平明显降低,差异有统计学意义[(75.26±7.20)pg/mLvs.(107.22±13.13)pg/mL,P=0.039]。结论典型症状和非典型症状的NERD患者胃组织IL-1β有明显差异,提示IL-1β可能参与了不同亚型的NERD发生的机制。 Objective To study the differences and its clinical significance of the expression of interleukin 1-beta (interleukin 1 beta ,IL-1 beta) between the patients with typical symptoms and atypical symptoms of non-erosive reflux diseases(NERD) in the stomach tissue .Methods 70 cases of patients with NERD were divided into two subtypes according to the presence or absence of typical reflux symptoms ,the typical group (43 cases) ,and the atypical symptoms group (27 cases);The interleukin-1 assay kit (chemiluminescence) was applied to assess the differences of IL-1βin stomach tissue of NERD patients with different subtypes .Re-sults Compared with the atypical symptoms group ,the concentration of IL-1 beta in typical symptoms group was obviously lower and the difference was statistically significant [(75 .26 ± 7 .20) pg/mL vs .(107 .22 ± 13 .13) pg/mL ,P=0 .039] .Conclusion Significant differences of the expression of IL-1βin the stomach tissue were found between the typical symptoms group and the a-typical symptoms group ,suggesting that IL-1βmay be involved in the occurrence of different subtypes of NERD .
出处 《重庆医学》 CAS CSCD 北大核心 2014年第29期3864-3865,3869,共3页 Chongqing medicine
基金 重庆市自然科学基金重点资助项目(cstc2013jjB0143)
关键词 胃食管反流 白细胞介素-1Β 烧心 反酸 食管外症状 gastroesophageal reflux interleukin-1β heart burn acid reflux extra-esophageal symptoms
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  • 1Hom C, Vaezi MF. Extra esophageal manifestations of gastroesophageal reflux disease: diagnosis and treatment [J]. Drugs, 2013,73(12) : 1281-1295.
  • 2Powitzky ES, Khaitan L, Garrett CG, et al. Symptoms, quality of Life, videolaryngoscopy, and twenty-four-hour triple-probe pH monitoring in patients with typical and extraesophageal reflux[J]. Ann Otol Rhinol Laryngol, 2003,112(10) :859-865.
  • 3Souza RF, H uo X, Mittal V, et al. Gastroesophageal reflux might cause esophagitis through a cytokine-mediated mechanism rather than caustic acid injury[J]. Gastroen- terology, 2009,137 (5) : 1776-1784.
  • 4Rieder F, Biancani P, Harnett K, et al. Inflammatory media- tors in gastroesophageal reflux disease: impact on esophageal motility, fibrosis, and carcinogenesis [J]. Am J Physiol Gas- trointest Liver Physiol, 2010,98 (5) :G571-581.
  • 5Hamaguchi M, Fujiwara Y,Takashima T, et al. Increased expression of cytokines and adhesion molecules in rat chronic esophagitis[J]. Digestion, 2003,68(4) : 189-197.
  • 6Monkemuller K, Wex T, Kuester D, et al. Interleukin- lbeta and interleukin-8 expression correlate with the his- tomorphological changes in esophageal mucosa of patients with erosive and non-erosive reflux disease[J]. Digestion, 2009,79(3):186-195.
  • 7Izakovicova Holla L, Borilova Linhartova P, Hrdlickova B,et al. Haplotypes of the IL-1 gene cluster are associat- ed with gastroesophageal reflux disease and BarrettPs e- sophagus[J]. Hum Immunol,2013,74(9):1161-1169.
  • 8Chourasia D,Achyut BR, Tripathi S, et al. Genotypic and functional roles of IL-1B and IL-1RN on the risk of gas- troesophageal reflux disease: the presence of IL-1B-511 T/IL-1RN * 1 (T1) haplotype may protect against the disease[J]. Am J Gastroenterol, 2009,104(11):2704- 2713.
  • 9Ando T,El-Omar EM,Goto Y,et al. Interleukin 1B proin- flammatory genotypes protect against gastro-oesophageal reflux disease through induction of corpus atrophy[J]. Gut,2006,55(2) :158-164.
  • 10Kim J J, Kim N, Hwang S, et al. Relationship of interleukin-lb levels and gastroesophageal reflux dis- ease in Korea[J]. J Gastroenterol Hepatol, 2013,28 (1) : 90-98.

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