Department of Gastroenterology, Manisa Celal Bayar University Faculty of Medicine, Manisa, Turkey.
Department of Medical Biology, Manisa Celal Bayar University Faculty of Medicine, Manisa, Turkey; Department of Nephrology, Manisa Celal Bayar University Faculty of Medicine, Manisa, Turkey.
Turk J Gastroenterol. 2023 May;34(5):533-541. doi: 10.5152/tjg.2023.21282.
Gastroesophageal reflux disease is a common condition worldwide. There is no curative treatment for gastroesophageal reflux disease. Endoplasmic reticulum stress leads to the activation of the unfolded protein response and has an important role in inflammation. The aim is to determine the role of endoplasmic reticulum stress in the follow-up of individuals with gastroesophageal reflux disease and the temporal changes of endoplasmic reticulum stress markers with treatment.
Twenty-four subjects in total were recruited prospectively, of whom 15 had nonerosive reflux disease. Two biopsies from 2 cm above the esophagogastric junction, 2 biopsies from gastric antrum mucosa, and 2 biopsies from gastric corpus mucosa were taken. Simultaneously, 2 tubes of venous blood samples were drawn from each individual (1 tube for studying the genetic markers and 1 tube for analyzing the CYP2C19 polymorphism).
The mean age was 42.3 ± 17.6 for women and 34.66 ± 11.2 for men. Pantoprazole, esomeprazole, rabeprazole, and lansoprazole preparations were used for treatment. There was no significant difference between tissue and blood samples for panel genes ATF-6, XBP-1, DDIT-3, DNAJC-10, and EIF-2-AK before treatment. There was a significant decrease in the level of ATF-6, XBP-1, DNAJC-9, EIF2-AK, and NF-2L-2 genes in blood after treatment. In the comparison of proton pump inhibitors, significant decreases in the expression of the ATF-6, XBP-1, and DNAJC-9 mRNAs were detected in blood from individuals after treatment.
Endoplasmic reticulum stress can be for evaluating the clinical improvement and the effectiveness of treatment in gastroesophageal reflux disease.
胃食管反流病是一种全球范围内常见的疾病。目前尚无针对胃食管反流病的根治性治疗方法。内质网应激导致未折叠蛋白反应的激活,并在炎症中起重要作用。本研究旨在确定内质网应激在胃食管反流病患者随访中的作用,以及内质网应激标志物在治疗过程中的时间变化。
共前瞻性招募 24 名受试者,其中 15 名患有非糜烂性反流病。从食管胃交界处上方 2cm 处取 2 块活检组织、胃窦黏膜取 2 块活检组织、胃体黏膜取 2 块活检组织。同时从每位个体抽取 2 管静脉血样本(1 管用于研究遗传标志物,1 管用于分析 CYP2C19 多态性)。
女性的平均年龄为 42.3±17.6 岁,男性为 34.66±11.2 岁。使用泮托拉唑、埃索美拉唑、雷贝拉唑和兰索拉唑制剂进行治疗。在治疗前,组织和血液样本中的 ATF-6、XBP-1、DDIT-3、DNAJC-10 和 EIF-2-AK 面板基因无显著差异。治疗后,血液中 ATF-6、XBP-1、DNAJC-9、EIF2-AK 和 NF-2L-2 基因水平显著下降。质子泵抑制剂比较显示,治疗后个体血液中 ATF-6、XBP-1 和 DNAJC-9 mRNA 的表达均显著下降。
内质网应激可用于评估胃食管反流病的临床改善和治疗效果。