Riesgo de cáncer gástrico en pacientes con gastritis atrófica y metaplasia intestinal en estadios OLGA y OLGIM III y IV: revisión sistemática y metanálisis
dc.contributor.advisor | Otero Regino, William Alberto | spa |
dc.contributor.author | Frias Ordoñez, Juan Sebastian | spa |
dc.contributor.cvlac | https://scienti.minciencias.gov.co/cvlac/visualizador/generarCurriculoCv.do?cod_rh=0001772314 | spa |
dc.contributor.googlescholar | https://scholar.google.com/citations?user=fV--MAwAAAAJ&hl=es&oi=ao | spa |
dc.contributor.orcid | Frias Ordoñez, Juan Sebastian [0000000327352922] | spa |
dc.contributor.researchgate | https://www.researchgate.net/profile/Juan-Frias-Ordonez | spa |
dc.contributor.scopus | Frias Ordoñez, Juan Sebastian [57193738162] | spa |
dc.date.accessioned | 2024-12-11T13:41:54Z | |
dc.date.available | 2024-12-11T13:41:54Z | |
dc.date.issued | 2024 | |
dc.description | ilustraciones, diagramas | spa |
dc.description.abstract | Introducción y objetivo: Estudios recientes han encontrado que pacientes con OLGA II, también pueden tener riesgo de cáncer gástrico (CG) a largo plazo y más aún si tienen familiares de primer grado con CG. El objetivo del presente metaanálisis es determinar si los estadios de OLGA II-IV tienen riesgo de CG y cuál es su magnitud, así como también estimar si el riesgo aumenta cuando hay familiares de primer grado con CG. Metodología: Revisión sistemática y metaanálisis. Se buscarán en varias bases de datos, incluyendo PubMed, EMBASE, Medline y la biblioteca Cochrane, artículos publicados en los últimos 10 años hasta mayo de 2024 sobre la asociación entre los diferentes estadios OLGA/OLGIM y el riesgo de GC. Análisis estadístico con estimación del efecto en términos de Odds Ratio (OR), riesgo relativo (RR) e intervalo de confianza del 95%. La heterogeneidad se estimará con I2 y Chi2. Resultados: De 273 artículos recuperados mediante nuestra búsqueda bibliográfica, se incluyeron un total 28 estudios que comprendían 23390 pacientes, se incluyeron 15 estudios de casos y controles, corte transversal, y 13 estudios de cohortes. El metaanálisis demostró una asociación significativa entre los estadios II-IV de OLGA/OLGIM y cáncer gástrico. El análisis de subgrupos en poblaciones con baja prevalencia de infección por H. pylori no encontró asociación del puntaje OLGIM en los estudios de cohorte. Conclusiones: Se presenta una versión resumida de las asociaciones estimadas de los diferentes estadios de OLGA/OLGIM y riesgo de CG (Texto tomado de la fuente). | spa |
dc.description.abstract | Introduction and objective: Recent studies have found that patients with OLGA II may also be at risk of gastric cancer (GC) in the long term and even more so if they have first-degree relatives with GC. The aim of the present meta-analysis is to determine whether OLGA stages II-IV are at risk of GC and what is its magnitude, as well as to estimate whether the risk increases when there are first-degree relatives with GC. Methodology: Systematic review and meta-analysis. Several databases, including PubMed, EMBASE, Medline and Cochrane library, will be searched for articles published in the last 10 years until May 2024 on the association between different OLGA/OLGIM stages and GC risk. Statistical analysis with estimation of effect in terms of Odds Ratio (OR), relative risk (RR) and 95% confidence interval. Heterogeneity will be estimated with I2 and Chi2. Results: Of 273 articles retrieved through our literature search, a total of 28 studies comprising 23390 patients were included, 15 case-control, cross-sectional, and 13 cohort studies. The meta-analysis demonstrated a significant association between OLGA/OLGIM stages II-IV and gastric cancer. Subgroup analysis in populations with low prevalence of H. pylori infection found no association of OLGIM score in cohort studies. Conclusions: A summarized version of the estimated associations of different OLGA/OLGIM stages and GC risk is presented. | eng |
dc.description.degreelevel | Especialidades Médicas | spa |
dc.description.degreename | Especialista en Gastroenterología | spa |
dc.description.methods | Revisión sistemática y metaanálisis. Se buscarán en varias bases de datos, incluyendo PubMed, EMBASE, Medline y la biblioteca Cochrane, artículos publicados en los últimos 10 años hasta mayo de 2024 sobre la asociación entre los diferentes estadios OLGA/OLGIM y el riesgo de GC. Análisis estadístico con estimación del efecto en términos de Odds Ratio (OR), riesgo relativo (RR) e intervalo de confianza del 95%. La heterogeneidad se estimará con I2 y Chi2. | spa |
dc.description.researcharea | Cáncer gástrico | spa |
dc.format.extent | 59 páginas + anexos | spa |
dc.format.mimetype | application/pdf | spa |
dc.identifier.instname | Universidad Nacional de Colombia | spa |
dc.identifier.reponame | Repositorio Institucional Universidad Nacional de Colombia | spa |
dc.identifier.repourl | https://repositorio.unal.edu.co/ | spa |
dc.identifier.uri | https://repositorio.unal.edu.co/handle/unal/87287 | |
dc.language.iso | spa | spa |
dc.publisher | Universidad Nacional de Colombia | spa |
dc.publisher.branch | Universidad Nacional de Colombia - Sede Bogotá | spa |
dc.publisher.faculty | Facultad de Medicina | spa |
dc.publisher.place | Bogotá, Colombia | spa |
dc.publisher.program | Bogotá - Medicina - Especialidad en Gastroenterología | spa |
dc.relation.references | 2. P C. Human gastric carcinogenesis: a multistep and multifactorial process--First American Cancer Society Award Lecture on Cancer Epidemiology and Prevention. Cancer Res [Internet]. 1992;52(24):6735–40. Available from: https://pubmed.ncbi.nlm.nih.gov/1458460/ | spa |
dc.relation.references | 3. Lahner E, Bordi C, Cattaruzza MS, Iannoni C, Milione M, Delle Fave G, et al. Long-term follow-up in atrophic body gastritis patients: Atrophy and intestinal metaplasia are persistent lesions irrespective of Helicobacter pylori infection. Aliment Pharmacol Ther. 2005;22(5):471–81. | spa |
dc.relation.references | 4. De Vries AC, Haringsma J, Kuipers EJ. The detection, surveillance and treatment of premalignant gastric lesions related to Helicobacter pylori infection. Helicobacter. 2007;12(1):1–15. | spa |
dc.relation.references | 5. Filipe MI, Muñoz N, Matko I, Kato I, Pompe‐Kirn V, Jutersek A, et al. Intestinal metaplasia types and the risk of gastric cancer: A cohort study in Slovenia. Int J Cancer. 1994;57(3):324–9. | spa |
dc.relation.references | 6. Uemura N, Okamoto S, Yamamoto S, Matsumura N, Yamaguchi S, Yamakido M, Taniyama K, et al. Helicobacter pylori infection and the development of gastric cancer. N Engl J Med. 2001 Sep 13;345(11):784-9. doi: 10.1056/NEJMoa001999. | spa |
dc.relation.references | 7. Rokkas T, Filipe MI, Sladen GE. Detection of an increased incidence of early gastric cancer in patients with intestinal metaplasia type III who are closely followed up. Gut. 1991;32(10):1110–3. | spa |
dc.relation.references | 8. Engevik AC, Kaji I, Goldenring JR. The physiology of the gastric parietal cell. Physiol Rev. 2020;100(2):573–602. | spa |
dc.relation.references | 9. Rugge M, De Boni M, Pennelli G, De Bona M, Giacomelli L, Fassan M, et al. Gastritis OLGA-staging and gastric cancer risk: A twelve-year clinico-pathological follow-up study. Aliment Pharmacol Ther. 2010;31(10):1104–11. | spa |
dc.relation.references | 10. Park YH, Kim N. Review of Atrophic Gastritis and Intestinal Metaplasia as a Premalignant Lesion of Gastric Cancer. J Cancer Prev. 2015;20(1):25–40. | spa |
dc.relation.references | 11. Cho SJ, Choi IJ, Kook MC, Nam BH, Kim CG, Lee JY, et al. Staging of intestinal- and diffuse-type gastric cancers with the OLGA and OLGIM staging systems. Aliment Pharmacol Ther. 2013;38(10):1292–302. | spa |
dc.relation.references | 12. Capelle LG, de Vries AC, Haringsma J, Ter Borg F, de Vries RA, Bruno MJ, et al. The staging of gastritis with the OLGA system by using intestinal metaplasia as an accurate alternative for atrophic gastritis. Gastrointest Endosc. 2010;71(7):1150–8. | spa |
dc.relation.references | 13. Rugge M, Correa P, Di Mario F, El-Omar E, Fiocca R, Geboes K, et al. OLGA staging for gastritis: A tutorial. Dig Liver Dis. 2008;40(8):650–8. | spa |
dc.relation.references | 14. Dinis-Ribeiro M, Areia M, De Vries AC, Marcos-Pinto R, Monteiro-Soares M, Oconnor A, et al. Management of precancerous conditions and lesions in the stomach (MAPS): Guideline from the European Society of Gastrointestinal Endoscopy (ESGE), European Helicobacter Study Group (EHSG), European Society of Pathology (ESP), and the Sociedade Portuguesa . Endoscopy. 2012;44(1):74–94. | spa |
dc.relation.references | 15. De Re V, Orzes E, Canzonieri V, Maiero S, Fornasarig M, Alessandrini L, et al. Pepsinogens to distinguish patients with gastric intestinal metaplasia and helicobacter pylori infection among populations at risk for gastric cancer. Clin Transl Gastroenterol. 2016;7(7):1–2. | spa |
dc.relation.references | 16. Yue H, Shan L, Bin L. The significance of OLGA and OLGIM staging systems in the risk assessment of gastric cancer: a systematic review and meta-analysis. Gastric Cancer. 2018;21(4):579–87. | spa |
dc.relation.references | 17. Molaei M, Ehtiati A, Mashayekhi R, Rafizadeh M, Zojaji H, Mirsattari D, et al. Gastric atrophy: Use of OLGA staging system in practice. Gastroenterol Hepatol from Bed to Bench. 2016;9(1):25–9. | spa |
dc.relation.references | 18. Correa P, Piazuelo MB, Wilson KT. Pathology of gastric intestinal metaplasia: Clinical implications. Am J Gastroenterol. 2010;105(3):493–8. | spa |
dc.relation.references | 19. Gastric cancer . National Cancer Institute (consultado el 15/05/2024 en: https://www.cancer.gov/types/stomach. | spa |
dc.relation.references | 20. Murakami T. Pathomorphological diagnosis: definition and gross classification of early gastric cancer. Gann Monogr Cancer Res. 1971;11:53-55. | spa |
dc.relation.references | 21. Morson BC, Sobin LH, Grundmann E, Johansen A, Nagayo T, Serck-Hanssen A. Precancerous conditions and epithelial dysplasia in the stomach. J Clin Pathol. 1980;33(8):711–21. | spa |
dc.relation.references | 22. WHO Classification of tumors. Digestive system tumors. Tumors of the stomach. WHO Classification of Tumors Editorial Board. 5th Ed. Lyon: IARC press; 2019, pp. 59-110. | spa |
dc.relation.references | 23. Karimi P, Islami F, Anandasabapathy S, Freedman ND, Kamangar F. Gastric cancer: Descriptive epidemiology, risk factors, screening, and prevention. Cancer Epidemiol Biomarkers Prev. 2014;23(5):700–13. | spa |
dc.relation.references | 24. Marques-Silva L, Areia M, Elvas L, Dinis-Ribeiro M. Prevalence of gastric precancerous conditions: A systematic review and meta-analysis. Eur J Gastroenterol Hepatol. 2014;26(4):378–87. | spa |
dc.relation.references | 25. Liang B, Yuan Y, Peng XJ, Liu XL, Hu XK, Xing DM. Current and future perspectives for Helicobacter pylori treatment and management: From antibiotics to probiotics. Front Cell Infect Microbiol. 2022;12:20–1. | spa |
dc.relation.references | 26. Clinical Guidelines on the Identification, Evaluation, and Treatment of Overweight and Obesity in Adults--The Evidence Report. National Institutes of Health. Obes Res. 1998;6 Suppl 2:9813653. | spa |
dc.relation.references | 27. WHO global report on trends in prevalence of tobacco use 2000-2025, fourth edition. WHO, Geneva, 2021. | spa |
dc.relation.references | 28. Mccarron DA, Kazaks AG, Geerling JC, Stern JS, Graudal NA. Normal range of human dietary sodium intake: A perspective based on 24-hour urinary sodium excretion worldwide. Am J Hypertens. 2013;26(10):1218–23. | spa |
dc.relation.references | 29. Beard JC, Swager TM. An Organic Chemist’s Guide to N-Nitrosamines: Their Structure, Reactivity, and Role as Contaminants. J Org Chem. 2021;86(3):2037–57. | spa |
dc.relation.references | 30. Naeher LP, Brauer M, Lipsett M, Zelikoff JT, Simpson CD, Koenig JQ, et al. Woodsmoke health effects: A review. Inhal Toxicol. 2007;19(1):67–106. | spa |
dc.relation.references | 31. Wu GA, Terol J, Ibanez V, López-García A, Pérez-Román E, Borredá C, et al. Genomics of the origin and evolution of Citrus. Nature. 2018;554(7692):311–6. | spa |
dc.relation.references | 32. Stanaway JD, Afshin A, Ashbaugh C, Bisignano C, Brauer M, Ferrara G, et al. Health effects associated with vegetable consumption: a Burden of Proof study. Nat Med. 2022;28(10):2066–74. | spa |
dc.relation.references | 33. Alcohol’s Effects on Health.National Institute on Alcohol Abuse and Alcoholism. (Consultado el 15/05/2024 en: https://www.niaaa.nih.gov/alcohol-health/overview-alcohol-consumption/moderate-binge-drinking). | spa |
dc.relation.references | 34. Laporte RE, Montoye HJ, Caspersen CJ. Physical Activity, Exercise, and Physical Fitness: Definitions and Distinctions for Health-Related Research Synopsis. Public Health Rep. 1985;100(2):126–31. | spa |
dc.relation.references | 35. Peavitt, Helen (15 November 2017). Refrigerator: The Story of Cool in the Kitchen. Reaktion Books. p. 8. ISBN 978-1-78023-797-8. | spa |
dc.relation.references | 36. Liu Q, Ding L, Qiu X, Meng F. Updated evaluation of endoscopic submucosal dissection versus surgery for early gastric cancer: A systematic review and meta-analysis. Int J Surg. 2020;73:28–41. | spa |
dc.relation.references | 37. Ho SWT, Tan P. Dissection of gastric cancer heterogeneity for precision oncology. Cancer Sci. 2019;110(11):3405–14. | spa |
dc.relation.references | 38. Koulis A, Buckle A, Boussioutas A. Premalignant lesions and gastric cancer: Current understanding. World J Gastrointest Oncol. 2019;11(9):665–78. | spa |
dc.relation.references | 39. Bonelli P, Borrelli A, Tuccillo FM, Silvestro L, Palaia R, Buonaguro FM. Precision medicine in gastric cancer. World J Gastrointest Oncol. 2019;11(10):804–29. | spa |
dc.relation.references | 40. Asaka M, Mabe K. Strategies for eliminating death from gastric cancer in Japan. Proc Japan Acad Ser B Phys Biol Sci. 2014;90(7):251–8. | spa |
dc.relation.references | 41. Wang X, Zhao J, Shen Z, Fairweather M, Enzinger PC, Sun Y, et al. Multidisciplinary Approach in Improving Survival Outcome of Early-Stage Gastric Cancer. J Surg Res. 2020;255:285–96. | spa |
dc.relation.references | 42. Mickevicius A, Ignatavicius P, Markelis R, Parseliunas A, Butkute D, Kiudelis M, et al. Trends and results in treatment of gastric cancer over last two decades at single East European centre: A cohort study. BMC Surg. 2014;14(1):1–2. | spa |
dc.relation.references | 43. Oh SE, An JY, Choi MG, Sohn TS, Bae JM, Kim S, et al. Long term oncological outcome of patients with grossly early gastric cancer-mimicking advanced gastric cancer. Eur J Surg Oncol. 2020;46(7):1262–8. | spa |
dc.relation.references | 44. Estimated number of new cases in 2020, world, both sexes, all ages [Internet]. International Agency for Research/World Health Organization (IARC/WHO); 2021 [consultado el 15 de mayo de 2024]. Disponible en: https://gco.iarc.fr/today/online-analysis-pie?v=. | spa |
dc.relation.references | 45. Bae JM, Kim EH. Epstein-Barr virus and gastric cancer risk: A metaanalysis with meta-regression of case-control studies. J Prev Med Public Heal. 2016;49(2):97–107. | spa |
dc.relation.references | 46. Wroblewski LE, Peek RM, Wilson KT. Helicobacter pylori and gastric cancer: Factors that modulate disease risk. Clin Microbiol Rev. 2010;23(4):713–39. | spa |
dc.relation.references | 47. Cats A, Meuwissen SGM, Forman D, Craanen ME, Kuipers EJ. Helicobacter pylori: A true carcinogen? Eur J Gastroenterol Hepatol. 1998;10(6):447–50. | spa |
dc.relation.references | 48. Conteduca V, Sansonno D, Lauletta G, Russi S, Ingravallo G, Dammacco F. H. pylori infection and gastric cancer: State of the art (Review). Int J Oncol. 2013;42(1):5–18. | spa |
dc.relation.references | 49. Rick JR, Goldman M, Semino-Mora C, Liu H, Olsen C, Rueda-Pedraza E, et al. In situ expression of cagA and risk of gastroduodenal disease in helicobacter pylori-infected children. J Pediatr Gastroenterol Nutr. 2010;50(2):167–72. | spa |
dc.relation.references | 50. Hatakeyama M. Oncogenic mechanisms of the Helicobacter pylori CagA protein. Nat Rev Cancer. 2004;4(9):688–94. | spa |
dc.relation.references | 51. Iizasa H, Nanbo A, Nishikawa J, Jinushi M, Yoshiyama H. Epstein-barr virus (EBV)-associated gastric carcinoma. Viruses. 2012;4(12):3420–39. | spa |
dc.relation.references | 52. Kim YS, Paik SR, Kim HK, Yeom BW, Kim I, Lee D. Epstein-Barr virus and CD21 expression in gastrointestinal tumors. Pathol Res Pract. 1998;194(10):705–11. | spa |
dc.relation.references | 53. Kim J, Cho YA, Choi WJ, Jeong SH. Gene-diet interactions in gastric cancer risk: A systematic review. World J Gastroenterol. 2014;20(28):9600–10. | spa |
dc.relation.references | 54. Zhang Z, Zhang X. Salt taste preference, sodium intake and gastric cancer in China. Asian Pacific J Cancer Prev. 2011;12(5):1207–10. | spa |
dc.relation.references | 55. Keszei AP, Goldbohm RA, Schouten LJ, Jakszyn P, Van Den Brandt PA. Dietary N-nitroso compounds, endogenous nitrosation, and the risk of esophageal and gastric cancer subtypes in the Netherlands Cohort Study. Am J Clin Nutr. 2013;97(1):135–46. | spa |
dc.relation.references | 56. Moy KA, Fan Y, Wang R, Gao YT, Yu MC, Yuan JM. Alcohol and tobacco use in relation to gastric cancer: A prospective study of men in Shanghai, China. Cancer Epidemiol Biomarkers Prev. 2010;19(9):2287–97. | spa |
dc.relation.references | 57. Duell EJ, Travier N, Lujan-Barroso L, Clavel-Chapelon F, Boutron-Ruault MC, Morois S, et al. Alcohol consumption and gastric cancer risk in the European Prospective Investigation into Cancer and Nutrition (EPIC) cohort. Am J Clin Nutr. 2011;94(5):1266–75. | spa |
dc.relation.references | 58. Vogelaar IP, van der Post RS, Bisseling TM, van Krieken JHJM, Ligtenberg MJL, Hoogerbrugge N. Familial gastric cancer: Detection of a hereditary cause helps to understand its etiology. Hered Cancer Clin Pract. 2012;10(1):1–2. | spa |
dc.relation.references | 59. Pinheiro H, Oliveira C, Seruca R, Carneiro F. Hereditary diffuse gastric cancer - Pathophysiology and clinical management. Best Pract Res Clin Gastroenterol. 2014;28(6):1055–68. | spa |
dc.relation.references | 60. Lim SH, Kwon JW, Kim N, Kim GH, Kang JM, Park MJ, et al. Prevalence and risk factors of Helicobacter pylori infection in Korea: Nationwide multicenter study over 13 years. BMC Gastroenterol. 2013;13(1):1–2. | spa |
dc.relation.references | 61. Corso G, Marrelli D. Frequency of familial gastric cancer. Spotlight Fam Hered Gastric Cancer. 2013;11–8. | spa |
dc.relation.references | 62. Kahrilas PJ, Kishk SM, Helm JF, Dodds WJ, Harig JM, Hogan WJ. Comparison of pseudoachalasia and achalasia. Am J Med. 1987;82(3):439–46. | spa |
dc.relation.references | 63. Wanebo HJ, Kennedy BJ, Chmiel J, Steele G, Winchester D, Osteen R. Cancer of the stomach A patient care study by the American college of surgeons. Ann Surg. 1993;218(5):583–92. | spa |
dc.relation.references | 64. Sawyers JL. Gastric carcinoma. Curr Probl Surg. 1995;32(2):7776992. | spa |
dc.relation.references | 65. Zagari RM, Rabitti S, Greenwood DC, Eusebi LH, Vestito A, Bazzoli F. Systematic review with meta-analysis: diagnostic performance of the combination of pepsinogen, gastrin-17 and anti-Helicobacter pylori antibodies serum assays for the diagnosis of atrophic gastritis. Aliment Pharmacol Ther. 2017;46(7):657–67. | spa |
dc.relation.references | 66. Hwang YJ, Kim N, Lee HS, Lee JB, Choi YJ, Yoon H, et al. Reversibility of atrophic gastritis and intestinal metaplasia after Helicobacter pylori eradication - a prospective study for up to 10 years. Aliment Pharmacol Ther. 2018;47(3):380–90. | spa |
dc.relation.references | 67. Zhao Z, Yin Z, Wang S, Wang J, Bai B, Qiu Z, et al. Meta-analysis: The diagnostic efficacy of chromoendoscopy for early gastric cancer and premalignant gastric lesions. J Gastroenterol Hepatol. 2016;31(9):1539–45. | spa |
dc.relation.references | 68. Anagnostopoulos GK, Yao K, Kaye P, Fogden E, Fortun P, Shonde A, et al. High-resolution magnification endoscopy can reliably identify normal gastric mucosa, Helicobacter pylori-associated gastritis, and gastric atrophy. Endoscopy. 2007;39(3):202–7. | spa |
dc.relation.references | 69. Ang TL, Pittayanon R, Lau JYW, Rerknimitr R, Ho SH, Singh R, et al. A multicenter randomized comparison between high-definition white light endoscopy and narrow band imaging for detection of gastric lesions. Eur J Gastroenterol Hepatol. 2015;27(12):1473–8. | spa |
dc.relation.references | 70. Ezoe Y, Muto M, Uedo N, Doyama H, Yao K, Oda I, et al. Magnifying narrowband imaging is more accurate than conventional white-light imaging in diagnosis of gastric mucosal cancer. Gastroenterology. 2011;141(6):4–5. | spa |
dc.relation.references | 71. Isajevs S, Liepniece-Karele I, Janciauskas D, Moisejevs G, Funka K, Kikuste I, et al. The effect of incisura angularis biopsy sampling on the assessment of gastritis stage. Eur J Gastroenterol Hepatol. 2014;26(5):510–3. | spa |
dc.relation.references | 72. Varbanova M, Wex T, Jechorek D, Röhl FW, Langner C, Selgrad M, et al. Impact of the angulus biopsy for the detection of gastric preneoplastic conditions and gastric cancer risk assessment. J Clin Pathol. 2016;69(1):19–25. | spa |
dc.relation.references | 73. Evans JA, Chandrasekhara V, Chathadi K V., Decker GA, Early DS, Fisher DA, et al. The role of endoscopy in the management of premalignant and malignant conditions of the stomach. Gastrointest Endosc. 2015;82(1):1–8. | spa |
dc.relation.references | 74. Matysiak-Budnik T, Camargo MC, Piazuelo MB, Leja M. Recent Guidelines on the Management of Patients with Gastric Atrophy: Common Points and Controversies. Dig Dis Sci. 2020;65(7):1899–903. | spa |
dc.relation.references | 75. Isajevs S, Liepniece-Karele I, Janciauskas D, Moisejevs G, Putnins V, Funka K, et al. Gastritis staging: Interobserver agreement by applying OLGA and OLGIM systems. Virchows Arch. 2014;464(4):403–7. | spa |
dc.relation.references | 76. Rugge M, Meggio A, Pennelli G, Piscioli F, Giacomelli L, De Pretis G, et al. Gastritis staging in clinical practice: The OLGA staging system. Gut. 2007;56(5):631–6. | spa |
dc.relation.references | 77. Mera RM, Bravo LE, Constanza Camargo M, Bravo JC, Delgado AG, Romero-Gallo J, et al. Dynamics of Helicobacter pylori infection as a determinant of progression of gastric precancerous lesions: 16-year follow-up of an eradication trial. Gut. 2018;67(7):1239–46. | spa |
dc.relation.references | 78. Correa P. Clinical implications of recent developments in gastric cancer pathology and epidemiology. Semin Oncol. 1985;12(1):2–10. | spa |
dc.relation.references | 79. Lauren P. the Two Histological Main Types of Gastric Carcinoma: Diffuse and So-Called Intestinal-Type Carcinoma. an Attempt At a Histo-Clinical Classification. Acta Pathol Microbiol Scand. 1965;64:31–49. | spa |
dc.relation.references | 80. Kong YJ, Yi HG, Dai JC, Wei MX. Histological changes of gastric mucosa after Helicobacter pylori eradication: A systematic review and meta-analysis. World J Gastroenterol. 2014;20(19):5903–11. | spa |
dc.relation.references | 81. Chen HN, Wang Z, Li X, Zhou ZG. Helicobacter pylori eradication cannot reduce the risk of gastric cancer in patients with intestinal metaplasia and dysplasia: evidence from a meta-analysis. Gastric Cancer. 2016;19(1):166–75. | spa |
dc.relation.references | 82. Rokkas T, Rokka A, Portincasa P. A systematic review and meta-analysis of the role of Helicobacter pylori eradication in preventing gastric cancer. Ann Gastroenterol. 2017;30(4):414–23. | spa |
dc.relation.references | 83. Choi IJ, Kook M-C, Kim Y-I, Cho S-J, Lee JY, Kim CG, et al. Helicobacter pylori Therapy for the Prevention of Metachronous Gastric Cancer . N Engl J Med. 2018;378(12):1085–95. | spa |
dc.relation.references | 84. Wong BCY, Zhang L, Ma JL, Pan KF, Li JY, Shen L, et al. Effects of selective COX-2 inhibitor and Helicobacter pylori eradication on precancerous gastric lesions. Gut. 2012;61(6):812–8. | spa |
dc.relation.references | 85. Huang XZ, Chen Y, Wu J, Zhang X, Wu CC, Zhang CY, et al. Aspirin and non-steroidal anti-inflammatory drugs use reduce gastric cancer risk: A dose-response meta-analysis. Oncotarget. 2017;8(3):4781–95. | spa |
dc.relation.references | 86. Hirasawa T, Gotoda T, Miyata S, Kato Y, Shimoda T, Taniguchi H, et al. Incidence of lymph node metastasis and the feasibility of endoscopic resection for undifferentiated-type early gastric cancer. Gastric Cancer. 2009;12(3):148–52. | spa |
dc.relation.references | 87. Ferlay J, Soerjomataram I, Dikshit R, Eser S, Mathers C, Rebelo M, et al. Cancer incidence and mortality worldwide: Sources, methods and major patterns in GLOBOCAN 2012. Int J Cancer. 2015;136(5):E359–86. | spa |
dc.relation.references | 88. Karim-Kos HE, de Vries E, Soerjomataram I, Lemmens V, Siesling S, Coebergh JWW. Recent trends of cancer in Europe: A combined approach of incidence, survival and mortality for 17 cancer sites since the 1990s. Eur J Cancer. 2008;44(10):1345–89. | spa |
dc.relation.references | 89. Correa P, Haenszel W, Cuello C, Tannenbaum S, Archer M. a Model for Gastric Cancer Epidemiology. Lancet. 1975;306(7924):58–60. | spa |
dc.relation.references | 90. Correa P. Gastric cancer: Two epidemics? Dig Dis Sci. 2011;56(5):1585–6. | spa |
dc.relation.references | 91. Pasechnikov V, Chukov S, Fedorov E, Kikuste I, Leja M. Gastric cancer: Prevention, screening and early diagnosis. World J Gastroenterol. 2014;20(38):13842–62. | spa |
dc.relation.references | 92. Shiotani A, Haruma K, Uedo N, Iishi H, Ishihara R, Tatsuta M, et al. Histological risk markers for non-cardia early gastric cancer: Pattern of mucin expression and gastric cancer. Virchows Arch. 2006;449(6):652–9. | spa |
dc.relation.references | 93. Lee JWJ, Zhu F, Srivastava S, Tsao SKK, Khor C, Ho KY, et al. Severity of gastric intestinal metaplasia predicts the risk of gastric cancer: a prospective multicentre cohort study (GCEP). Gut. 2022;71(5):854–63. | spa |
dc.relation.references | 94. Mansour-Ghanaei F, Joukar F, Yeganeh S, Sadeghi M, Daryakar A, Sepehrimanesh M. OLGA- and OLGIM-Based Staging in the Patients with Gastritis and Endoscopy Indications. Turkish J Gastroenterol. 2022;33(2):95–102. | spa |
dc.relation.references | 95. Wu M, Feng S, Qian M, Wang S, Zhang K. Helicobacter pylori Infection Combined with OLGA and OLGIM Staging Systems for Risk Assessment of Gastric Cancer: A Retrospective Study in Eastern China. Risk Manag Healthc Policy. 2022;15:2243–55. | spa |
dc.relation.references | 96. Carlosama YH, Acosta CP, Sierra CH, Rosero CY, Bolaños HJ. The Operative Link on Gastritis Assessment (OLGA) system as a marker for gastric cancer and dysplasia in a Colombian population at risk: A multicenter study. Biomedica. 2023;43:30–40. | spa |
dc.relation.references | 97. Zhou Y, Li HY, Zhang JJ, Chen XY, Ge ZZ, Li XB. Operative link on gastritis assessment stage is an appropriate predictor of early gastric cancer. World J Gastroenterol. 2016;22(13):3670–8. | spa |
dc.relation.references | 98. Chen M, Liu XL, Zhu XJ, Wu SR, Wang N, Li SB, et al. Endoscopic grading of gastric atrophy and histological gastritis staging on risk assessment for early gastric cancer: A case–control study. J Dig Dis. 2023;24(4):262–70. | spa |
dc.relation.references | 99. Piazuelo MB, Bravo LE, Mera RM, Camargo MC, Bravo JC, Delgado AG, et al. The Colombian Chemoprevention Trial: 20-Year Follow-Up of a Cohort of Patients With Gastric Precancerous Lesions. Gastroenterology. 2021;160(4):1106-1117.e3. | spa |
dc.relation.references | 100. Den Hollander WJ, Holster IL, Den Hoed CM, Capelle LG, Tang TJ, Anten MP, et al. Surveillance of premalignant gastric lesions: A multicentre prospective cohort study from low incidence regions. Gut. 2019;68(4):585–93. | spa |
dc.relation.references | 101. Kodama M, Murakami K, Okimoto T, Abe H, Sato R, Ogawa R, et al. Histological characteristics of gastric mucosa prior to Helicobacter pylori eradication may predict gastric cancer. Scand J Gastroenterol. 2013;48(11):1249–56. | spa |
dc.relation.references | 102. Tsai YC, Hsiao WH, Yang HB, Cheng HC, Chang WL, Lu CC, et al. The corpus-predominant gastritis index may serve as an early marker of helicobacter pylori-infected patients at risk of gastric cancer. Aliment Pharmacol Ther. 2013;37(10):969–78. | spa |
dc.relation.references | 103. Yun CY, Kim N, Lee J, Lee JY, Hwang YJ, Lee HS, et al. Usefulness of OLGA and OLGIM system not only for intestinal type but also for diffuse type of gastric cancer, and no interaction among the gastric cancer risk factors. Helicobacter. 2018;23(6):12–3. | spa |
dc.relation.references | 104. Rugge M, Genta RM, Fassan M, Valentini E, Coati I, Guzzinati S, et al. OLGA Gastritis Staging for the Prediction of Gastric Cancer Risk: A Long-term Follow-up Study of 7436 Patients. Am J Gastroenterol. 2018;113(11):1621–8. | spa |
dc.relation.references | 105. Huang Y, Chen J, Guo Y, Ding Z, Liang X, Zhang W, et al. Staging of operative link on gastritis assessment and operative link on gastric intestinal metaplasia systems for risk assessment of early gastric cancer: a case-control study. J Clin Pathol. 2023;12–3. | spa |
dc.relation.references | 106. Marcos P, Brito-Gonçalves G, Libânio D, Pita I, Castro R, Sá I, et al. Endoscopic grading of gastric intestinal metaplasia on risk assessment for early gastric neoplasia: Can we replace histology assessment also in the West? Gut. 2020;69(10):1762–8. | spa |
dc.relation.references | 107. Choi I, Cho S, Kook M, Kim C, Lee J. Validaton of gastritis OLGA-staging system for gastric cancer risk in a region of high prevalence: a case-control study. Helicobacter. 2012;17:76. | spa |
dc.relation.references | 108. Nieminen AA, Kontto J, Puolakkainen P, Virtamo J, Kokkola A. Comparison of operative link for gastritis assessment, operative link on gastric intestinal metaplasia assessment, and TAIM stagings among men with atrophic gastritis. World J Gastroenterol. 2020;26(24):3447–57. | spa |
dc.relation.references | 109. Satoh K, Osawa H, Yoshizawa M, Nakano H, Hirasawa T, Kihira K, et al. Assessment of atrophic gastritis using the OLGA system. Helicobacter. 2008;13(3):225–9. | spa |
dc.relation.references | 110. Chapelle N, Péron M, Quénéhervé L, Bourget A, Leroy M, Touchefeu Y, et al. Long-Term Follow-up of Gastric Precancerous Lesions in a Low GC Incidence Area. Clin Transl Gastroenterol. 2020;11(12):e00237. | spa |
dc.relation.references | 111. Esposito G, Dilaghi E, Cazzato M, Pilozzi E, Conti L, Carabotti M, et al. Endoscopic surveillance at 3 years after diagnosis, according to European guidelines, seems safe in patients with atrophic gastritis in a low-risk region. Dig Liver Dis. 2021;53(4):467–73. | spa |
dc.relation.references | 112. Latorre G, Silva F, Montero I, Bustamante M, Dukes E, Uribe J, et al. Comparison of OLGA and OLGIM as predictors of gastric cancer in a Latin American population: the ECHOS Study. Gut. 2024;73(10):e18. | spa |
dc.relation.references | 113. Kawamura M, Uedo N, Yao K, Koike T, Kanesaka T, Hatta W, et al. Endoscopic and histological risk stratification for gastric cancer using gastric intestinal metaplasia. J Gastroenterol Hepatol. 2024;1–2. | spa |
dc.relation.references | 114. Wang X, Han F, Wang C, Lyu B. The value of OLGA staging system in risk assessment of gastric precancerous states and precancerous lesions. Natl Med J China. 2022;102(12):853–7. | spa |
dc.relation.references | 115. Sun L, Jin X, Huang L, Zhao J, Jin H, Chen M, et al. Risk of progression in patients with chronic atrophic gastritis: A retrospective study. Front Oncol. 2022;12:1–2. | spa |
dc.relation.references | 116. Malfertheiner P, Megraud F, Rokkas T, et al. Management of Helicobacter pylori infection: the Maastricht VI/Florence consensus report. Gut. Published online August 8, 2022. doi:10.1136/gutjnl-2022-327745. | spa |
dc.relation.references | 117. Liou JM, Malfertheiner P, Smith SI, El-Omar EM, Wu MS. 40 years after the discovery of Helicobacter pylori: towards elimination of H pylori for gastric cancer prevention. Lancet. 2024;403(10444):2570–2. | spa |
dc.rights.accessrights | info:eu-repo/semantics/openAccess | spa |
dc.rights.license | Atribución-NoComercial-SinDerivadas 4.0 Internacional | spa |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | spa |
dc.subject.ddc | 610 - Medicina y salud::616 - Enfermedades | spa |
dc.subject.ddc | 610 - Medicina y salud::615 - Farmacología y terapéutica | spa |
dc.subject.decs | Neoplasias Intestinales | spa |
dc.subject.decs | Intestinal Neoplasms | eng |
dc.subject.decs | Metaanálisis como Asunto | spa |
dc.subject.decs | Meta-Analysis as Topic | eng |
dc.subject.decs | Enfermedades Genéticas Congénitas | spa |
dc.subject.decs | Genetic Diseases, Inborn | eng |
dc.subject.proposal | Neoplasias Gástricas | spa |
dc.subject.proposal | Gastritis Atrófica | spa |
dc.subject.proposal | Metaplasia | spa |
dc.subject.proposal | Factores de Riesgo | spa |
dc.subject.proposal | Metaanálisis | spa |
dc.subject.proposal | Revisión Sistemática | spa |
dc.subject.proposal | Stomach Neoplasms | eng |
dc.subject.proposal | Gastritis | eng |
dc.subject.proposal | Atrophic | eng |
dc.subject.proposal | Metaplasia | eng |
dc.subject.proposal | Risk factors | eng |
dc.subject.proposal | Meta-Analysis | eng |
dc.subject.proposal | Systematic review | eng |
dc.title | Riesgo de cáncer gástrico en pacientes con gastritis atrófica y metaplasia intestinal en estadios OLGA y OLGIM III y IV: revisión sistemática y metanálisis | spa |
dc.title.translated | Gastric cancer risk in patients with atrophic gastritis and intestinal metaplasia in OLGA and OLGIM stages III and IV: systematic review and meta-analysis | eng |
dc.type | Trabajo de grado - Especialidad Médica | spa |
dc.type.coar | http://purl.org/coar/resource_type/c_bdcc | spa |
dc.type.coarversion | http://purl.org/coar/version/c_ab4af688f83e57aa | spa |
dc.type.content | Text | spa |
dc.type.driver | info:eu-repo/semantics/masterThesis | spa |
dc.type.redcol | http://purl.org/redcol/resource_type/TM | spa |
dc.type.version | info:eu-repo/semantics/acceptedVersion | spa |
dcterms.audience.professionaldevelopment | Investigadores | spa |
oaire.accessrights | http://purl.org/coar/access_right/c_abf2 | spa |
Archivos
Bloque original
Bloque de licencias
1 - 1 de 1
No hay miniatura disponible
- Nombre:
- license.txt
- Tamaño:
- 5.74 KB
- Formato:
- Item-specific license agreed upon to submission
- Descripción: