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Interleukin-1 and TNF-α polymorphisms and Helicobacter pylori in a Brazilian Amazon population 被引量:17
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作者 Hivana Patricia Melo Barbosa Luisa Caricio Martins +4 位作者 Sidney Emanuel Batista dos Santos Samia Demachki Mnica Baraúna Assumpo charliana damasceno arago Tereza Cristina de oliveira Corvelo 《World Journal of Gastroenterology》 SCIE CAS CSCD 2009年第12期1465-1471,共7页
AIM:To study the association between Interleukin-1(IL-1)and tumor necrosis factor(TNF)-αpolymorphisms,infection by Helicobacter pylori(H pylori)and the development of gastrointestinal diseases.METHODS:Genomic DNA was... AIM:To study the association between Interleukin-1(IL-1)and tumor necrosis factor(TNF)-αpolymorphisms,infection by Helicobacter pylori(H pylori)and the development of gastrointestinal diseases.METHODS:Genomic DNA was extracted from the peripheral blood of 177 patients with various gastrointestinal diseases and from 100 healthy volunteers.The polymorphisms in IL-1βand TNF-αgenes were analyzed using the polymerase chain reactionrestriction fragment length polymorphism method(PCRRFLP)and those from IL-1RN with PCR.The presence of infection due to H pylori and the presence of the CagA toxin were detected by serology.The histopathological parameters in the gastric biopsies of the patients were according to the Sydney classification.RESULTS:A comparison of the frequencies of the different polymorphisms studied among the patients and the control group demonstrated that the allele IL1RN*2 was more frequent among patients with gastric ulcers and adenocarcinoma.Carriers of the allele ILRN*2 and those with reactive serology for anti-CagA IgG had a greater risk of developing peptic ulcer and gastric adenocarcinoma,as well as a higher degree of inflammation and neutrophilic activity in the gastric mucosa.CONCLUSION:Our results indicate a positive association between IL-1RN gene polymorphism and infection by positive H pylori CagA strains and the development of gastric ulcers and adenocarcinoma. 展开更多
关键词 白细胞介素1 多态性分析法 肿瘤坏死因子 幽门螺杆菌 PCRRFLP 幽门螺旋杆菌 组织病理学参数 RN基因多态性
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