新型胃癌筛查评分系统在胃癌筛查及癌前病变风险评估中的价值
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1.嘉兴市第一医院消化内科;2.浙江中医药大学附属第一医院消化内科

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嘉兴市科技计划项目(2018AD32079);嘉兴市第一医院壹计划项目(2019-YA-14)


Evaluation of the new scoring system for gastric cancer screening and risk assessment of gastric precancerous lesions
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Science and Technology Project of Jiaxing (2018AD32079); First Program of The First Hospital of Jiaxing (2019-YA-14)

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    摘要:

    目的 评估新型胃癌筛查评分系统在胃癌筛查及癌前病变风险评估中的价值。方法 纳入2018年3月—2019年9月因胃部不适在嘉兴市第一医院行胃镜检查的患者共442例。内镜检查前患者根据新型胃癌筛查评分系统分为3组:低危组(0~11分)、中危组(12~16分)和高危组(17~23分),分析3组胃癌及萎缩性胃炎检出情况。根据胃黏膜萎缩及肠化的范围和程度,按照慢性胃炎分级评估系统(operative link for gastritis assessment,OLGA)及慢性胃炎肠化分级评估系统(operative link for gastritis intestinal metaplasia,OLGIM)将患者分为相应的0~Ⅳ级5组,比较新型胃癌筛查评分系统与OLGA、OLGIM系统在癌前病变风险评估中的联系。结果 442例患者根据新型胃癌筛查评分系统分组,低危组211例,中危组207例,高危组24例;按OLGA分组,0级241例,Ⅰ级105例,Ⅱ级58例,Ⅲ级27例,Ⅳ级11例;按OLGIM分组,0级224例,Ⅰ级113例,Ⅱ级61例,Ⅲ级31例,Ⅳ级13例。胃蛋白酶原Ⅰ水平(F=2.844,P=0.027)和胃蛋白酶原比值(F=5.435,P=0.001)在OLGA分级标准下5组间比较差异有统计学意义,其中Ⅲ级和Ⅳ级组明显低于其他3组(P均<0.001)。胃蛋白酶原比值在OLGIM分级标准下5组间比较差异有统计学意义(F=3.887,P=0.008),其中Ⅳ级组明显低于其他各组(P均<0.001)。Gamma系数检验及Kendall""s tau-b检验显示OLGA、OLGIM系统与新型胃癌筛查评分系统之间存在较强的一致性(P<0.001)。结论 新型胃癌筛查评分系统有助于胃癌筛查,同时与OLGA、OLGIM在胃癌前病变风险评估方面存在密切联系,可应用于我国胃癌前病变风险评估。

    Abstract:

    Objective To evaluate the new scoring system for gastric cancer screening and risk assessment of gastric precancerous lesions. Methods A total of 442 patients who underwent endoscopy due to stomach discomfort at the First Hospital of Jiaxing from March 2018 to September 2019 were enrolled. The patients were divided into three groups based on the new scoring system for gastric cancer screening before endoscopy: low-risk group (0-11 points), median-risk group (12-16 points) and high-risk group (17-23 points). The detection rates of gastric cancer and atrophic gastritis in three groups were analyzed. According to the range or degree of atrophy or intestinal metaplasia, patients were divided into five groups of stage 0 to Ⅳ based on the operative link for gastritis assessment (OLGA) or operative link for gastritis intestinal metaplasia (OLGIM). The correlation between the new gastric cancer screening scoring system and OLGA or OLGIM staging system were evaluated. Results Among 442 patients, 211 were assigned to low-risk group, 207 median-risk group and 24 high-risk group according to the new scoring system. For OLGA staging system, there were 241 cases of stage-0, 105 of stage-Ⅰ, 58 stage-Ⅱ, 27 stage-Ⅲ and 11 stage-Ⅳ. For OLGIM staging system, there were 224 cases of stage-0, 113 stage-Ⅰ, 61 stage-Ⅱ, 31 stage-Ⅲ and 13 stage-Ⅳ. The pepsinogen (PG) Ⅰ and pepsinogen ratio (PGR) levels had differences among different OLGA stages (F=2.844, P=0.027; F=5.435, P=0.001), and these two variables at Stage-Ⅲ and Ⅳ were significantly lower than three other OLGA stages (all P<0.001). The PGR level had differences among different OLGIM stages (F=3.887, P=0.008), which was significantly lower at Stage-Ⅳ than at other OLGIM stages (all P<0.001). Gamma coefficient analysis and Kendall""s tau-b analysis showed significant correlations between OLGA/OLGIM staging system and new gastric cancer screening scoring system (P<0.001). Conclusion The new scoring system is reliable for gastric cancer screening, and is closely linked with OLGA/OLGIM staging system in the risk assessment of gastric precancerous lesions.

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王霄腾,冀子中,韩丰,等.新型胃癌筛查评分系统在胃癌筛查及癌前病变风险评估中的价值[J].中华消化内镜杂志,2021,38(5):379-383.

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  • 收稿日期:2020-02-18
  • 最后修改日期:2021-03-23
  • 录用日期:2020-05-09
  • 在线发布日期: 2021-05-27
  • 出版日期: 2021-05-29
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