[1]张汗磊,王 松,陈 思,等.粪便肿瘤M2型丙酮酸激酶在结直肠癌和腺瘤性息肉中的诊断价值[J].医学信息,2021,34(12):78-81.[doi:10.3969/j.issn.1006-1959.2021.12.021]
 ZHANG Han-lei,WANG Song,CHEN Si,et al.The Diagnostic Value of Stool Tumor M2 Pyruvate Kinase in Colorectal Cancer and Adenomatous Polyps[J].Medical Information,2021,34(12):78-81.[doi:10.3969/j.issn.1006-1959.2021.12.021]
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粪便肿瘤M2型丙酮酸激酶在结直肠癌和腺瘤性息肉中的诊断价值()
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医学信息[ISSN:1006-1959/CN:61-1278/R]

卷:
34卷
期数:
2021年12期
页码:
78-81
栏目:
论著
出版日期:
2021-06-15

文章信息/Info

Title:
The Diagnostic Value of Stool Tumor M2 Pyruvate Kinase in Colorectal Cancer and Adenomatous Polyps
文章编号:
1006-1959(2021)12-0078-04
作者:
张汗磊王 松陈 思
(安徽医科大学附属省立医院消化内科,安徽 合肥 230001)
Author(s):
ZHANG Han-leiWANG SongCHEN Siet al
(Department of Gastroenterology,Provincial Hospital Affiliated to Anhui Medical University,Hefei 230001,Anhui,China)
关键词:
结直肠癌腺瘤性息肉粪便肿瘤M2型丙酮酸激酶
Keywords:
Colorectal cancerAdenomatous polypsStool tumor M2 pyruvate kinase
分类号:
R735.3
DOI:
10.3969/j.issn.1006-1959.2021.12.021
文献标志码:
A
摘要:
目的 探讨粪便肿瘤M2型丙酮酸激酶(Tu M2-PK)浓度在结直肠癌和腺瘤性息肉中的诊断价值。方法 收集2019年10月~2020年8月在安徽省立医院经术后病理明确诊断的结直肠癌患者50例,腺瘤性息肉患者47例,以及正常人群31例粪便标本,采用粪便Tu M2-PK酶联免疫快速试剂检测粪便标本中Tu M2-PK浓度,并分析Tu M2-PK浓度与结直肠癌的分期、位置和腺瘤性息肉的数目、大小的关系,评估TU M2-PK在结直肠癌和腺瘤性息肉发展和诊断中的作用。结果 粪便TuM2-PK在结直肠癌患者中的浓度高于腺瘤性息肉组和正常对照组,差异有统计学意义(P<0.05);以浓度大于4U/ml为诊断结直肠癌的cut-off值,在诊断结直肠癌的阳性率为82%;Tu M2-PK水平与结直肠癌的分期可能有关(P<0.05),与结直肠癌的位置无关,ROC曲线确定Tu M2-PK诊断腺瘤性息肉的最佳截断值为2.62 U/ml,敏感度为51.06%,特异度为80.65%,约登指数为0.317。浓度与腺瘤性息肉的数目和大小无关,ROC曲线下面积为0.704(95%CI 0.588~0.819)。结论 粪便TU M2-PK在腺瘤性息肉中无特异性诊断价值,在结直肠癌中浓度升高明显,是一种良好的肿瘤标志物,其可能参与结直肠癌的发生、发展过程。
Abstract:
Objective To investigate the diagnostic value of fecal tumor M2 pyruvate kinase (Tu M2-PK) concentration in colorectal cancer and adenomatous polyps.Methods From October 2019 to August 2020, 50 cases of colorectal cancer patients, 47 cases of adenomatous polyps, and 31 fecal specimens of normal people who were diagnosed by pathology in Anhui Provincial Hospital from October 2019 to August 2020 were collected.The fecal Tu M2-PK enzyme-linked immunoassay rapid reagent was used to detect the concentration of Tu M2-PK in stool samples, and the relationship between the concentration of Tu M2-PK and the stage and location of colorectal cancer and the number and size of adenomatous polyps was analyzed.To evaluate the role of TU M2-PK in the development and diagnosis of colorectal cancer and adenomatous polyps.Results The concentration of TuM2-PK in stool in patients with colorectal cancer was higher than that in the adenomatous polyp group and the normal control group,the difference was statistically significant (P<0.05);Taking a concentration greater than 4 U/ml as the cut-off value for the diagnosis of colorectal cancer, the positive rate in the diagnosis of colorectal cancer was 82%; Tu M2-PK level may be related to the staging of colorectal cancer (P<0.05),regardless of the location of colorectal cancer, the ROC curve determined that the best cut-off value of Tu M2-PK for the diagnosis of adenomatous polyps was 2.62 U/ml, the sensitivity was 51.06%, the specificity was 80.65%, and the Youden index was 0.317.The concentration had nothing to do with the number and size of adenomatous polyps, and the area under the ROC curve was 0.704 (95% CI 0.588~0.819).Conclusion Stool TU M2-PK has no specific diagnostic value in adenomatous polyps. It has a significant increase in concentration in colorectal cancer. It is a good tumor marker and may be involved in the occurrence and development of colorectal cancer.

参考文献/References:

[1]Bray F,Ferlay J,Soerjomataram I,et al.Global cancer statistics 2018:GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries[J].CA Cancer J Clin,2018,68(6):394-424. [2]Fitzmaurice C,Allen C,Barber RM,et al.Global, Regional, and National Cancer Incidence,Mortality,Years of Life Lost,Years Lived With Disability,and Disability-Adjusted Life-years for 32 Cancer Groups,1990 to 2015:A Systematic Analysis for the Global Burden of Disease Study[J].JAMA Oncol,2017,3(4):524-548. [3]Allemani C,Matsuda T,Di CV,et al.Global surveillance of trends in cancer survival 2000-14(CONCORD-3):analysis of individual records for 37 513 025 patients diagnosed with one of 18 cancers from 322 population-based registries in 71 countries[J].Lancet,2018,391(10125):1023-1075. [4]Hardt PD,Toepler M,Ngoumou BK,et al.Measurement of fecal pyruvate kinase type M2(tumor M2-PK)concentrations in patients with gastric cancer,colorectal cancer,colorectal adenomas and controls[J].Anticancer Research,2003,23(2A):851. [5]Rigi F,Jannatabad A,Izanloo A,et al.Expression of tumor pyruvate kinase M2 isoform in plasma and stool of patients with colorectal cancer or adenomatous polyps[J].BMC Gastroenterology,2020,20(1):241. [6]Lee JK,Liles EG,Bent S,et al.Accuracy of fecal immunochemical tests for colorectal cancer:systematic review and meta-analysis[J].Annals of Internal Medicine,2014,160(3):171. [7]Katsoula A,Paschos P,Haidich AB,et al.Diagnostic Accuracy of Fecal Immunochemical Test in Patients at Increased Risk for Colorectal Cancer:A Meta-analysis[J].Jama Internal Medicine,2017,177(8):1110-1118. [8]Zaccaro C,Saracino IM,Fiorini G,et al.Power of screening tests for colorectal cancer enhanced by high levels of M2-PK in addition to FOBT[J].Internal&Emergency Medicine,2017,12(3):1-7. [9]Leen R,Seng-Lee C,Holleran G,et al.Comparison of faecal M2-PK and FIT in a population-based bowel cancer screening cohort[J].Eur J Gastroenterol Hepatol,2014,26(5):514-518. [10]Yong CK,Kim JH,Cheung DY,et al.The Usefulness of a Novel Screening Kit for Colorectal Cancer Using the Immunochromatographic Fecal Tumor M2 Pyruvate Kinase Test[J].Gut and Liver,2015,9(5):641-648. [11]Tonus C,Sellinger M,Koss K,et al.Faecal pyruvate kinase isoenzyme type M2 for colorectal cancer screening:A meta-analysis[J].World Journal of Gastroenterology,2012,18(30):4004-4011. [12]Bond AD,Burkitt MD,Sawbridge D,et al.Correlation between Faecal Tumour M2 Pyruvate Kinase and Colonoscopy for the Detection of Adenomatous Neoplasia in a Secondary Care Cohort[J].J Gastrointestin Liver Dis,2016,25(1):71-77. [13]Keenan J, Aitchison A, Leaman J,et al.Faecal biomarkers do not always identify pre-cancerous lesions in patients who present in primary care with bowel symptoms[J].The New Zealand Medical Journal,2019,132(1501):48-56.

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更新日期/Last Update: 1900-01-01