Difference of Helicobacter pylori eradication rate between patients with atrophic gastritis and non-atrophic gastritis
-
摘要:
目的 探究萎缩性与非萎缩性胃炎患者中幽门螺杆菌(Hp)根除率的差异以及胃窦黏膜萎缩、肠化生和Hp密度分级是否影响Hp根除结果。 方法 纳入2021年1—12月在上海市第五人民医院消化内科门诊接受阿莫西林联合克拉霉素治疗的505例Hp阳性初治患者,根据内镜下的组织病理学结果分为萎缩性胃炎和非萎缩性胃炎2组。采用倾向性评分匹配(PSM)平衡组间人口学变量后比较组间Hp根除失败率,并进行logistic回归分析。 结果 PSM后萎缩性胃炎组患者的Hp根除失败率显著高于非萎缩性胃炎组(16.3% vs. 7.8%,P=0.023),这种差异在男性中显著(21.2% vs. 7.1%,P=0.008),在女性中不显著(P>0.05)。通过logistic回归分析发现,Hp根除失败与胃窦黏膜轻度(病理分级+)萎缩/肠化生呈正相关性(OR=2.614,95% CI:1.227~5.571,P=0.013;OR=2.882,95% CI:1.310~6.338,P=0.009),而与中重度(病理分级++~+++)萎缩/肠化生无关(均P>0.05)。此外,Hp根除失败与胃窦黏膜Hp密度分级无关(P>0.05)。 结论 萎缩性胃炎患者的Hp根除失败率显著高于非萎缩性胃炎患者,这种差异在男性中显著而在女性中不显著;Hp根除失败只与轻度胃窦黏膜萎缩/肠化生有关而与中重度萎缩/肠化生无关;Hp根除失败与胃窦黏膜Hp密度分级无关。 Abstract:Objective To investigate the difference of Helicobacter pylori (Hp) eradication rate between patients with atrophic gastritis and non-atrophic gastritis, and to analyze the relationship of the degree of gastric antrum atrophy, intestinal metaplasia and Hp density with Hp eradication rate. Methods A total of 505 Hp-positive patients who initially received amoxicillin combined with clarithromycin regimen in Fudan University Affiliated Shanghai Fifth People' s Hospital from January to December 2021 were enrolled and divided into two groups on the basis of pathological features in endoscopy, namely atrophic gastritis and non-atrophic gastritis. Propensity score matching (PSM) was used to reduce bias in the comparison of Hp eradication rates between two groups, followed by logistic regression analysis. Results After PSM, the failure rate of Hp eradication in atrophic gastritis group was significantly higher than that in non-atrophic gastritis group (16.3% vs. 7.8%, P=0.023), and the difference was significant in male (21.2% vs. 7.1%, P=0.008), but not in female (P > 0.05). Logistic regression analysis showed that the failure rate of Hp eradication was positively correlated with mild (pathological grade +) antral atrophy/intestinal metaplasia (OR=2.614, 95% CI: 1.227-5.571, P=0.013; OR=2.882, 95% CI: 1.310-6.338, P=0.009), but not associated with moderate to severe (pathological grade ++ to +++) antral atrophy/intestinal metaplasia (all P > 0.05). Moreover, Hp eradication failure was independent of antral Hp density (P > 0.05). Conclusion The failure rate of Hp eradication in patients with atrophic gastritis is significantly higher than that in patients with non-atrophic gastritis, and the difference is significant in males but not in females. In addition, Hp eradication failure increases only in patients with mild antral atrophy/intestinal metaplasia and doesn' t increase with the severity of antral atrophy/intestinal metaplasia. Moreover, Hp eradication failure is independent of antral Hp density. -
Key words:
- Atrophic gastritis /
- Helicobacter pylori /
- Amoxicillin /
- Clarithromycin /
- Propensity score matching
-
表 1 萎缩性与非萎缩性胃炎患者人口学、病理学特征和Hp根除结果的比较
Table 1. Comparison of demographic, pathological features and Hp eradication results in patients with atrophic and nonatrophic gastritis
组别 例数 年龄(x±s,岁) 性别(例) 萎缩分级[例(%)] 肠化生分级[例(%)] Hp密度分级[例(%)] Hp根除结果[例(%)] 男性 女性 0 + ++~+++ 0 + ++~+++ 0 + ++~+++ 成功 失败 萎缩性胃炎 153 53.21±11.79 85 68 0 115(75.2) 38(24.8) 4(2.6) 111(72.5) 38(24.8) 16(10.4) 76(49.7) 61(39.9) 128(83.7) 25(16.3) 非萎缩性胃炎 352 43.99±12.10 162 190 352(100.0) 0 0 332(94.3) 20(5.7) 0 17(4.8) 178(50.6) 157(44.6) 317(90.1) 35(9.9) 统计量 -8.010a 3.878b -22.179c -20.066c -0.729c 4.168b P值 <0.001 0.049 <0.001 <0.001 0.466 0.041 注:a为t值,b为χ2值,c为Z值。 表 2 PSM之后2组患者间人口学特征及Hp根除结果的比较
Table 2. Comparison of demographic characteristics and Hp eradication results between 2 groups after PSM
组别 例数 年龄(x±s,岁) 性别(男/女,例) Hp根除结果[例(%)] 成功 失败 萎缩性胃炎 153 53.21±11.79 85/68 128(83.7) 25(16.3) 非萎缩性胃炎 153 52.27±10.76 80/73 141(92.2) 12(7.8) 统计量 -0.724a 0.329b 5.200b P值 0.469 0.566 0.023 注:a为t值,b为χ2值。 表 3 男性患者中2组之间年龄和Hp根除结果的比较
Table 3. Comparison of age and Hp eradication outcomes between 2 groups in male patients
组别 例数 年龄(x±s,岁) Hp根除结果[例(%)] 成功 失败 萎缩性胃炎 85 52.53±11.86 67(78.8) 18(21.2) 非萎缩性胃炎 162 46.35±11.65 148(91.4) 14(8.6) 统计量 -3.916a 7.767b P值 <0.001 0.005 注:a为t值,b为χ2值。 表 4 女性患者中2组之间年龄和Hp根除结果的比较
Table 4. Comparison of age and Hp eradication outcomes between 2 groups in female patients
组别 例数 年龄(x±s,岁) Hp根除结果[例(%)] 成功 失败 萎缩性胃炎 68 54.06±11.73 61(89.7) 7(10.3) 非萎缩性胃炎 190 41.98±12.14 169(88.9) 21(11.1) 统计量 -7.218a 0.030b P值 <0.001 0.863 注:a为t值,b为χ2值。 表 5 PSM后男性患者中2组之间年龄和Hp根除结果的比较
Table 5. Comparison of age and Hp eradication outcomes between 2 groups in male patients after PSM
组别 例数 年龄(x±s,岁) Hp根除结果[例(%)] 成功 失败 萎缩性胃炎 85 52.53±11.86 67(78.8) 18(21.2) 非萎缩性胃炎 85 51.91±11.41 79(92.9) 6(7.1) 统计量 -0.349a 6.986b P值 0.727 0.008 注:a为t值,b为χ2值。 表 6 PSM后女性患者中2组之间年龄和Hp根除结果的比较
Table 6. Comparison of age and Hp eradication outcomes between the two groups in female patients after PSM
组别 例数 年龄(x±s,岁) Hp根除结果[例(%)] 成功 失败 萎缩性胃炎 68 54.06±11.73 61(89.7) 7(10.3) 非萎缩性胃炎 68 52.44±10.05 59(86.8) 9(13.2) 统计量 -0.863a 0.283b P值 0.389 0.595 注:a为t值,b为χ2值。 表 7 胃窦黏膜萎缩、肠化生和Hp密度的病理分级与Hp根除失败的logistic回归分析
Table 7. Logistic regression analysis of pathological grade of antral mucosa atrophy, intestinal metaplasia and Hp density and Hp eradication failure
变量 β SE Waldχ2 P值 OR 95% CI 萎缩分级a + 0.961 0.386 6.198 0.013 2.614 1.227~5.571 ++~+++ 0.296 0.612 0.234 0.629 1.344 0.405~4.462 肠化生分级b + 1.058 0.402 6.927 0.009 2.882 1.310~6.338 ++~+++ 0.395 0.625 0.310 0.528 1.484 0.436~5.055 Hp密度分级c ++~+++ 0.543 0.381 2.031 0.154 1.721 0.816~3.629 0 1.198 0.596 4.040 0.044 3.315 1.031~10.662 注:a萎缩分级以“0级”作为参照;b肠化生分级以“0级”作为参照;cHp密度分级以“+级”作为参照。各变量赋值情况如下, Hp根除结果(因变量),Hp根除失败=1,成功=0;萎缩分级,0级=0,+级=1,++~+++级=2;肠化生分级,0级=0,+级=1,++~+++级=2;Hp密度分级,0级=0,+级=1,++~+++级=2。 -
[1] ZAMANI M, EBRAHIMTABAR F, ZAMANI V, et al. Systematic review with meta-analysis: the worldwide prevalence of Helicobacter pylori infection[J]. Aliment Pharmacol Ther, 2018, 47(7): 868-876. doi: 10.1111/apt.14561 [2] REN S, CAI P, LIU Y, et al. Prevalence of Helicobacter pylori infection in China: a systematic review and meta-analysis[J]. J Gastroenterol Hepatol, 2022, 37(3): 464-470. doi: 10.1111/jgh.15751 [3] 张明伟, 汪建超, 王启之, 等. 安徽中南部地区幽门螺杆菌流行病学调查[J]. 中华全科医学, 2020, 18(8): 1395-1398. doi: 10.16766/j.cnki.issn.1674-4152.001516ZHANG M W, WANG J C, WANG Q Z, et al. Epidemiological investigation of Helicobacter pylori in central and southern area of Anhui province[J]. Chinese Journal of General Practice, 2020, 18(8): 1395-1398. doi: 10.16766/j.cnki.issn.1674-4152.001516 [4] MALFERTHEINER P, MEGRAUD F, ROKKAS T, et al. Management of Helicobacter pylori infection: the Maastricht VI/Florence consensus report[J]. Gut, 2022, 71(9): 1724-1762. doi: 10.1136/gutjnl-2022-327745 [5] 中华医学会消化病学分会幽门螺杆菌学组. 2022中国幽门螺杆菌感染治疗指南[J]. 中华消化杂志, 2022, 42(11): 745-756. doi: 10.3760/cma.j.cn311367-20220929-00479Helicobacter pylori Group, Chinese Society of Gastroenterology. 2022 Chinese national clinical practice guideline on Helicobacter pylori eradication treatment[J]. Chinese Journal of Digestion, 2022, 42(11): 745-756. doi: 10.3760/cma.j.cn311367-20220929-00479 [6] NYSSEN O P, BORDIN D, TEPES B, et al. European Registry on Helicobacter pylori management (Hp-EuReg): patterns and trends in first-line empirical eradication prescription and outcomes of 5 years and 21 533 patients[J]. Gut, 2021, 70(1): 40-54. doi: 10.1136/gutjnl-2020-321372 [7] NYSSEN O P, PEREZ-AISA A, CASTRO-FERNANDEZ M, et al. European Registry on Helicobacter pylori management: Single-capsule bismuth quadruple therapy is effective in real-world clinical practice[J]. United European Gastroenterol J, 2021, 9(1): 38-46. doi: 10.1177/2050640620972615 [8] GU L, LI S, HE Y, et al. Bismuth, rabeprazole, amoxicillin, and doxycycline as first-line Helicobacter pylori therapy in clinical practice: a pilot study[J]. Helicobacter, 2019, 24(4): e12594. DOI: 10.1111/hel.12594. [9] YI D M, YANG T T, CHAO S H, et al. Comparison the cost-efficacy of furazolidone-based versus clarithromycin-based quadruple therapy in initial treatment of Helicobacter pylori infection in a variable clarithromycin drug-resistant region, a single-center, prospective, randomized, open-label study[J]. Medicine (Baltimore), 2019, 98(6): e14408. DOI: 10.1097/MD.0000000000014408. [10] QIAO C, LI Y, LIU J, et al. Clarithromycin versus furazolidone for naive Helicobacter pylori infected patients in a high clarithromycin resistance area[J]. J Gastroenterol Hepatol, 2021, 36(9): 2383-2388. doi: 10.1111/jgh.15468 [11] 郭涛, 王强, 吴晰, 等. 阿莫西林和克拉霉素的铋剂四联方案作为初次根除幽门螺杆菌治疗的1年随访结果[J]. 中国医学科学院学报, 2019, 41(1): 75-79. https://www.cnki.com.cn/Article/CJFDTOTAL-ZYKX201901011.htmGUO T, WANG Q, WU X, et al. Amoxicillin-Clarithromycin-Containing bismuth quadruple therapy for primary eradication of Helicobacter pylori[J]. Acta Academiae Medicinae Sinicae, 2019, 41(1): 75-79. https://www.cnki.com.cn/Article/CJFDTOTAL-ZYKX201901011.htm [12] 房静远, 杜奕奇, 刘文忠, 等. 中国慢性胃炎共识意见精简版(2017年, 上海)[J]. 上海医学, 2017, 40(12): 705-708. https://www.cnki.com.cn/Article/CJFDTOTAL-SHYX201712001.htmFANG J Y, DU Y Q, LIU W Z, et al. Consensus on chronic gastritis in China(condensed edition)(2017, Shanghai)[J]. Shanghai Medical Journal, 2017, 40(12): 705-708. https://www.cnki.com.cn/Article/CJFDTOTAL-SHYX201712001.htm [13] DIXON M F, GENTA R M, YARDLEY J H, et al. Classification and grading of gastritis. The updated Sydney System. International Workshop on the Histopathology of Gastritis, Houston 1994[J]. Am J Surg Pathol, 1996, 20(10): 1161-1181. doi: 10.1097/00000478-199610000-00001 [14] 高文, 成虹, 胡伏莲, 等. 含艾普拉唑四联七天疗法根除幽门螺杆菌的全国多中心临床研究[J]. 中华医学杂志, 2012, 92(30): 2108-2112.GAO W, CHENG H, HU F L, et al. llaprazole based bismuth-containing quadruple regimen for the first-line treatment of Helicobacterpriori infection: a multicenter, randomized, controlled clinical study[J]. National Medical Journal of China, 2012, 92(30): 2108-2112. [15] LI B, LAN X, WANG L, et al. Proton-pump inhibitor and amoxicillin-based triple therapy containing clarithromycin versus metronidazole for Helicobacter pylori: a meta-analysis[J]. Microb Pathog, 2020, 142: 104075. DOI: 10.1016/j.micpath.2020.104075. [16] CHITAPANARUX T, KONGKARNKA S, WANNASAI K, et al. Prevalence and factors associated with atrophic gastritis and intestinal metaplasia: a multivariate, hospital-based, statistical analysis[J]. Cancer Epidemiol, 2023, 82: 102309. DOI: 10.1016/j.canep.2022.102309. [17] KALKAN I H, SAPMAZ F, GULITER S, et al. Severe gastritis decreases success rate of Helicobacter pylori eradication[J]. Wien Klin Wochenschr, 2016, 128(9-10): 329-334. doi: 10.1007/s00508-015-0896-2 [18] GONI E, TAMMER I, SCHUTTE K, et al. The influence of gastric atrophy on Helicobacter pylori antibiotics resistance in therapy-naive patients[J]. Front Microbiol, 2022, 13: 938676. DOI: 10.3389/fmicb.2022.938676. [19] YU J, YANG P, QIN X, et al. Impact of smoking on the eradication of Helicobacter pylori[J]. Helicobacter, 2022, 27(1): e12860. DOI: 10.1111/hel.12860. [20] OZEKI K, FURUTA T, HADA K, et al. Relationship of the difficulty of Helicobacter pylori eradication with drinking habits and allergic disease[J]. Microorganisms, 2022, 10(5): 1029. DOI: 10.3390/microorganisms10051029. [21] LERTPIRIYAPONG K, WHARY M T, MUTHUPALANI S, et al. Gastric colonisation with a restricted commensal microbiota replicates the promotion of neoplastic lesions by diverse intestinal microbiota in the Helicobacter pylori INS-GAS mouse model of gastric carcinogenesis[J]. Gut, 2014, 63(1): 54-63. doi: 10.1136/gutjnl-2013-305178 [22] 张明君, 赵静, 梁晗玮, 等. 13C尿素呼气试验检测值的判读价值[J]. 临床内科杂志, 2022, 39(4): 246-250. https://www.cnki.com.cn/Article/CJFDTOTAL-LCLZ202204019.htmZHANG M J, ZHAO J, LIANG H W, et al. Prognostic value of 13C-urea breath test[J]. Journal of Clinical Internal Medicine, 2022, 39(4): 246-250. https://www.cnki.com.cn/Article/CJFDTOTAL-LCLZ202204019.htm [23] MUKAISHO K, HAGIWARA T, NAKAYAMA T, et al. Potential mechanism of corpus-predominant gastritis after PPI therapy in Helicobacter pylori-positive patients with GERD[J]. World J Gastroenterol, 2014, 20(34): 11962-11965. doi: 10.3748/wjg.v20.i34.11962 [24] ZHAO X, ZHANG Z, LU F, et al. Effects of CYP2C19 genetic polymorphisms on the cure rates of H. pylori in patients treated with the proton pump inhibitors: an updated meta-analysis[J]. Front Pharmacol, 2022, 13: 938419. DOI: 10.3389/fphar.2022.938419. [25] DEAN L, KANE M. Omeprazole Therapy and CYP2C19 Genotype[M]. Bethesda (MD): National Center for Biotechnology Information(US), 2012.
计量
- 文章访问数: 170
- HTML全文浏览量: 93
- PDF下载量: 5
- 被引次数: 0