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Associations of Helicobacter pylori infection and chronic atrophic gastritis with accelerated epigenetic ageing in older adults

机译:老年人幽门螺杆菌感染和慢性萎缩性胃炎与表观遗传加速老化的关系

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Background: Helicobacter pylori (HP) infection and chronic atrophic gastritis (CAG) have shown strong associations with the development of gastric cancer. This study aimed to examine whether both risk factors are associated with accelerated epigenetic ageing, as determined by the ‘DNA methylation age’, in a population-based study of older adults ( n =1477). Methods: Serological measurements of HP antibodies and pepsinogen I and II for CAG definition were obtained by ELISA kits. Whole blood DNA methylation profiles were measured by Illumina Human Methylation450K Beadchip. DNA methylation ages were calculated by two algorithms proposed by Horvath and Hannum et al. Results: After adjusting for potential covariates in linear regression models, we found that HP infection, infection with virulent HP strains (CagA+) and severe CAG were significantly associated with an increase in DNA methylation age by ~0.4, 0.6 and 1 year (all P -values <0.05), respectively. Conclusions: Our study indicates that both CagA+ HP infection and CAG go along with accelerated epigenetic ageing.
机译:背景:幽门螺杆菌(HP)感染和慢性萎缩性胃炎(CAG)与胃癌的发展密切相关。这项研究的目的是在以人群为基础的老年人研究中(n = 1477)检查这两种危险因素是否都与表观遗传加速老化有关,如“ DNA甲基化年龄”所确定的。方法:通过ELISA试剂盒获得HP抗体和胃蛋白酶原I和II的血清学测定,以测定CAG。全血DNA甲基化谱通过Illumina Human Methylation450K Beadchip测量。 DNA甲基化年龄由Horvath和Hannum等提出的两种算法计算。结果:在线性回归模型中校正了潜在的协变量后,我们发现HP感染,强毒HP菌株(CagA +)和严重的CAG感染与DNA甲基化年龄的增加显着相关,分别为〜0.4、0.6和1年(所有P -值<0.05)。结论:我们的研究表明,CagA + HP感染和CAG都伴随着表观遗传加速老化。

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