The Role of Host NOD1 and IL-8 Polymorphism in Helicobacter pylori-induced Peptic Ulcer Disease in Taiwan

碩士 === 中山醫學大學 === 生化暨生物科技研究所 === 97 === Background: H. pylori - induced inflammation is central to the pathogenesis of all H. pylori - associated diseases. The type IV secretion system of H. pylori delivers peptidoglycan into the host cells, which can then be sensed by the intracellular receptor NOD...

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Main Authors: Hsiang-Yi, 曾湘怡
Other Authors: Fen-Pi Chou
Format: Others
Language:zh-TW
Published: 2009
Online Access:http://ndltd.ncl.edu.tw/handle/42534949551352590639
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spelling ndltd-TW-097CSMU51070112015-10-28T04:07:06Z http://ndltd.ncl.edu.tw/handle/42534949551352590639 The Role of Host NOD1 and IL-8 Polymorphism in Helicobacter pylori-induced Peptic Ulcer Disease in Taiwan 台灣地區幽門螺旋桿菌引起之消化性潰瘍與宿主NOD1及IL-8基因多型性的相關性探討 Hsiang-Yi 曾湘怡 碩士 中山醫學大學 生化暨生物科技研究所 97 Background: H. pylori - induced inflammation is central to the pathogenesis of all H. pylori - associated diseases. The type IV secretion system of H. pylori delivers peptidoglycan into the host cells, which can then be sensed by the intracellular receptor NOD1 (nucleotide-biding oligomerization domain-containing protein 1), leading to NF-κB activation and consequent IL-8 (interleukin 8) production. It had been reported NOD1 G796A and IL-8 -251 A/T polymorphism were important in H. pylori - induced peptic ulcer. However, the results were inconclusive. The aim of this study was to evaluate the role of NOD1 G796A and IL-8 -251 A/T genetic polymorphism in the development of H. pylori -induced peptic ulcer diseases in Taiwan. Materials and Methods: 146 patients with endoscope and CLO test (Campylobacter like organism test) were enrolled in the study. NOD1 G796A and IL-8 -251 A/T polymorphism were typed by PCR restriction fragment length polymorphism, TaqMan® SNP genotyping assays (real-time PCR) and multilocus sequence typing. Results: Old age was significantly associated with gastric ulcer in our study population. Duodenal ulcer was associated with H. pylori infection and gender. The prevalence of duodenal ulcer was higher in male. The H. pylori infection rate was similar in male and in female. Male NOD1 796A carriers and male IL-8 -251A carriers significantly had higher risk of H. pylori-induced duodenal ulcer. Since the genotype distribution was similar in H. pylori-infected male and female, polymorphism and gender may be independent factors of H. pylori-induced duodenal ulcer. There was no association between the polymorphism and H. pylori-induced gastric ulcer. Conclusion: NOD1 796A carriers and IL-8 -251A carriers significantly had higher risk of H. pylori-induced duodenal ulcer in male. However, it still needs further studies to clarify whether genotype or gender-related- factor plays a major role of H. pylori-induced duodenal ulcer in advance. Fen-Pi Chou 周芬碧教授 2009 學位論文 ; thesis 73 zh-TW
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description 碩士 === 中山醫學大學 === 生化暨生物科技研究所 === 97 === Background: H. pylori - induced inflammation is central to the pathogenesis of all H. pylori - associated diseases. The type IV secretion system of H. pylori delivers peptidoglycan into the host cells, which can then be sensed by the intracellular receptor NOD1 (nucleotide-biding oligomerization domain-containing protein 1), leading to NF-κB activation and consequent IL-8 (interleukin 8) production. It had been reported NOD1 G796A and IL-8 -251 A/T polymorphism were important in H. pylori - induced peptic ulcer. However, the results were inconclusive. The aim of this study was to evaluate the role of NOD1 G796A and IL-8 -251 A/T genetic polymorphism in the development of H. pylori -induced peptic ulcer diseases in Taiwan. Materials and Methods: 146 patients with endoscope and CLO test (Campylobacter like organism test) were enrolled in the study. NOD1 G796A and IL-8 -251 A/T polymorphism were typed by PCR restriction fragment length polymorphism, TaqMan® SNP genotyping assays (real-time PCR) and multilocus sequence typing. Results: Old age was significantly associated with gastric ulcer in our study population. Duodenal ulcer was associated with H. pylori infection and gender. The prevalence of duodenal ulcer was higher in male. The H. pylori infection rate was similar in male and in female. Male NOD1 796A carriers and male IL-8 -251A carriers significantly had higher risk of H. pylori-induced duodenal ulcer. Since the genotype distribution was similar in H. pylori-infected male and female, polymorphism and gender may be independent factors of H. pylori-induced duodenal ulcer. There was no association between the polymorphism and H. pylori-induced gastric ulcer. Conclusion: NOD1 796A carriers and IL-8 -251A carriers significantly had higher risk of H. pylori-induced duodenal ulcer in male. However, it still needs further studies to clarify whether genotype or gender-related- factor plays a major role of H. pylori-induced duodenal ulcer in advance.
author2 Fen-Pi Chou
author_facet Fen-Pi Chou
Hsiang-Yi
曾湘怡
author Hsiang-Yi
曾湘怡
spellingShingle Hsiang-Yi
曾湘怡
The Role of Host NOD1 and IL-8 Polymorphism in Helicobacter pylori-induced Peptic Ulcer Disease in Taiwan
author_sort Hsiang-Yi
title The Role of Host NOD1 and IL-8 Polymorphism in Helicobacter pylori-induced Peptic Ulcer Disease in Taiwan
title_short The Role of Host NOD1 and IL-8 Polymorphism in Helicobacter pylori-induced Peptic Ulcer Disease in Taiwan
title_full The Role of Host NOD1 and IL-8 Polymorphism in Helicobacter pylori-induced Peptic Ulcer Disease in Taiwan
title_fullStr The Role of Host NOD1 and IL-8 Polymorphism in Helicobacter pylori-induced Peptic Ulcer Disease in Taiwan
title_full_unstemmed The Role of Host NOD1 and IL-8 Polymorphism in Helicobacter pylori-induced Peptic Ulcer Disease in Taiwan
title_sort role of host nod1 and il-8 polymorphism in helicobacter pylori-induced peptic ulcer disease in taiwan
publishDate 2009
url http://ndltd.ncl.edu.tw/handle/42534949551352590639
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