ECOLOGICAL AND DIAGNOSTIC ASPECTS OF URINARY SCHISTOSOMIASIS AS PRECANCER (Literature review)


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Abstract

The article has included the issues of modern approaches to diagnosis and treatment of urinary schistosomiasis, a common parasitic disease. Numerous studies of pathogenesis, clinical manifestations and further development of urinary schistosomiasis allow us to consider this parasitosis as a precancerous disease. Due to the high rates of modern population igration, the widened area of schistosomiasis spreading and young age of patients, this subject is characterized by high medical and social significance. Despite the development of modern science, issues of diagnosis of this disease are relevant. We have an unresolved problem of verification of hidden forms, and the lack of effective screening complicates activity of the medical systems of the countries located in endemic areas. Also, the issues of early detection of the bladder cancer associated with urinary schistosomiasis that manifests itself in decades after the primary infection are pressing. The article has given an overview of original research works carried out over the last 30 years dedicated to epidemiology of urinary schistosomiasis and specific features of clinical and laboratory diagnosis of the bladder cancer caused by schistosomiasis: from clinical symptoms to high-precision molecular studies. We have identified shortcomings of existing research techniques and have planned the ways to improve verification of urinary schistosomiasis taking into account high carcinogenic activity of the pathogen and growth of medical-statistical indices in patients with the bladder cancer among residents of different countries.

About the authors

V Yu Startsev

Saint-Petersburg State Pediatric Medical University

Email: vlad_startsev@mail.ru
доктор медицинских наук, профессор кафедры онкологии с курсом лучевой диагностики и лучевой терапии ГБОУ ВПО «Санкт-Петербургский государственный педиатрический медицинский университет» Министерства здравоохранения Российской Федерации 194100, г. Санкт-Петербург, ул. Литовская, д. 2

A Yu Kolmakov

Lobitu Clinical Hospital

Lobitu, prov. Bengela, Angola

References

  1. Бронштейн А.М., Малышев Н.А., Жаров С.Н. Острый мочеполовой шистосомоз у туриста, посетившего Уганду и Кению: описание случая и обзор литературы // Эпидемиология и инфекционные болезни. 2012. № 5. С. 47-50.
  2. Катаханова Л.Л., Савин В.А., Исаева Я.В., Болоцкая Т.Г. Случай мочеполового шистосомоза у ребенка 10 лет // Вестник Сургута. 2013. № 1 (15). С. 59-61.
  3. Лопаткин Н.А., Пугачев А.Г., Аполихин О.А. Урология. М.: ГЭОТАР-медиа, 2010. 520 с.
  4. Abdel-Halim R.E., Al-Mashad S., Al-Dabbagh A. Fluoroscopic assessment of bilharzial ureteropathy // Clin. Radiol. 1995. Vol. 31. Р 36-89.
  5. Abdel-Fattah M., Al-Sherbiny M., Osman A. et al. Improving the detection limit of quantitative diagnosis of anti-S. haematobium antibodies using Falcon Assay Screening Test (FAST) ELISA by developing a new standard curve // Parasitol. Res. 2011. Vol. 108. Р 1457-1463.
  6. Abdulamir A.S., Hafidh R.R., Kadhim H.S. et al. Tumor markers of bladder cancers: the schistosomal bladder tumors versus nonschistosomal bladder tumors // J. Exp. Clin. Cancer Res. 2009. Vol. 28. Р. 28-37.
  7. Al-Sherbiny M.M., Osman A.M., Hancock K. et al. Application of immunodiagnostic assays: detection of antibodies and circulating antigens in human schistosomiasis and correlation with clinical findings // Am. J. Trop. Med. Hyg. 1999. Vol. 60. P 960-966.
  8. Ayele B., Erko B., Legesse M. et al. Evaluation of circulating cathodic antigen (CCA) strip for diagnosis of urinary schistosomiasis in Hassoba school children, Afar, Ethiopia // Parasite. 2008. Vol. 15. P. 69-75.
  9. Aryeetey Y.A., Essien-Baidoo S., Larbi I. A. et al. Molecular diagnosis of Schistosoma infections in urine samples of school children in Ghana // Am. J. Trop. Med. Hyg. 2013. Vol. 88. P. 1028-1031.
  10. Baguley B., Barrett-Connor E., Beland F. et al. Biological agents: a review of human carcinogens // Eval. Carcinog. Risks Hum. 2012. Vol. 100. P. 1 - 14.
  11. Bichler K-H., Feil G., Zumbragel A. et al. S. Schistosomiasis: a critical review // Curr. Opin. Urol. 2001. Vol. 11. P. 97-101.
  12. Botelho M., Santos J., Gouveia M. et al. Urinary Estrogen Metabolites and Self-Reported Infertility in Women Infected with Schistosoma haematobium // Plos One J. 2014. Vol. 10. P 32-35.
  13. Braun-Munzinger R.A., Southgate B. A. Repeatability and reproducibility of egg counts of Schistosoma haematobium in urine // Trop. Med. Parasitol. 1992. Vol. 43. P. 149-154.
  14. De Brito P.A., Kazura J.W., Mahmoud A. A. Host granulomatous response in Schistosomiasis mansoni Antibody and cell-mediated damage of parasite eggs in vitro // J. Clin. Invest., 1984. Vol. 74, N 5. P. 1715-1723.
  15. Jonge de N., Kremsner P.G., Krijger F.W. et al. Detection of the schistosome circulating cathodic antigen by enzyme immunoassay using biotinylated monoclonal antibodies // Trans. R. Soc. Trop. Med. Hyg. 1990. Vol. 84. P. 815-818.
  16. Doenhoff M.J., Butterworth A. E., Hayes R. J. et al. Seroepidemiology and serodiagnosis of schistosomiasis in Kenya using crude and purified egg antigens of Schistosoma mansoni in ELISA // Transactions of the Royal Society of Tropical Medicine and Hygiene, 1993. Vol. 87. P. 42-48.
  17. Downs J.A., Van Lieshout L., Verweij J.J. Persistence of Schistosome DNA and cervical abnormalities following standard treatment for female urogenital schistosomiasis // Trop. Med. Int. Health. 2013. Vol. 18. P. 28-33.
  18. El-Mawla N.G., El-Bolkainy M.N., Khaled H.M. Bladder cancer in Africa: update // Semin. Oncol. 2001. Vol. 28. P 174-178.
  19. Ghoneim M.A., El-Mekresh M.M., El-Baz M.A. et al. Radical cystectomy for carcinoma of the bladder, critical evaluation of the results in 1026 cases // J. Urol. 1997. Vol. 158, N 2. P. 393-399.
  20. Gouda I., Mokhtar N., Bilal D. et al. Bilharziasis and bladder cancer: a time trend analysis of 9843 patients // J. Egypt. Natl. Canc. Inst. 2007. Vol. 19, N 2. P. 158-162.
  21. Gryseels B., Polman K., Clerinx J. et al. Human schistosomiasis // Lancet. 2006. Vol. 368. P. 1106-1118.
  22. Hasab A.A., El-Nimr N.A., Al-Shibani L.A. et al. Rapid diagnosis of schistosomiasis in Yemen using a simple questionnaire and urine reagent strips // East. Mediterran. Health J. 2014. Vol. 20, N. 4. P. 242-249.
  23. Hicks R.M., James C., Webbe G. Effect of Schistosoma haematobium and N-butyl-N-14-hydroxybutylnitrosamine on the development of urothelial neoplasia in the baboon // Brit. J. Cancer. 1980. Vol. 42, N 5. P. 730-755.
  24. Hugosson C. O. Striation of the renal pelvis and ureter bilharziasis // Clin. Radiol. 1987. Vol. 38. P. 407.
  25. IARC Working Group on the Evaluation of Cardiogenic Risks to Humanos. Schistosomes, liver flukes and Helicobacter pylori // IARC Monogr Eval Carcinog Risks Hum. 1994. Vol. 61. P. 1-241.
  26. Jorulf H., Linstedt E. Urogenital schistosomiasis: CT evaluation // Radiology. 1985. Vol. 157. P. 745-749.
  27. King C.H. Parasites and poverty: the case of schistosomiasis // Acta Trop. 2010. Vol. 113. P. 95-104.
  28. Legesse M., Erko B. Field-based evaluation of a reagent strip test for diagnosis of schistosomiasis mansoni by detecting circulating cathodic antigen (CCA) in urine in low endemic area in Ethiopia // Parasite. 2008. Vol. 15. P. 151 - 155.
  29. Lodh N., Mwansa J.C., Mutengo M.M. et al. Diagnosis of Schistosoma mansoni without the stool: comparison of three diagnostic tests to detect Schistosoma mansoni infection from filtered urine in Zambia // Am. J. Trop. Med. Hyg. 2013. Vol. 89. P. 46-50.
  30. Melman S.D., Steinauer M.L., Cunningham C. et al. Reduced susceptibility to praziquantel among naturally occurring Kenyan isolates of Schistosoma mansoni // PLoS Negl. Trop. Dis. 2009. Vol. 3. P. 73-79.
  31. Navarro-Cabanas G., Garcia-Sànchez N., Rubio-Rubio R. et al. Esquistosomiasis urogenital: un diagnôstico sencillo // An. Esp. Pediatr. 2006. Vol. 64. P. 282-284.
  32. Obeng B.B., Aryeetey Y.A., Dood de C.J., et al. Application of a circulating-cathodic-antigen (CCA) strip test and real-time PCR, in comparison with microscopy, for the detection of Schistosoma haematobium in urine samples from Ghana // Ann. Trop. Med. Parasitol. 2008. Vol. 102. P. 625-633.
  33. Parkin D.M. The global health burden of infection-associated cancers in the year 2002 // Int. J. Cancer. 2006. Vol. 118. P. 3030-3044.
  34. Polman K., Meremarie M., Dirk E. et al. Specificity of circulating antigen detection for schistosomiasis mansoni in Senegal and Burundi // Trop. Med. Intern. Health. 2000. Vol. 5, iss. 8. P. 534-537.
  35. Poggensee G., Feldmeier H., Krantz I. Schistosomiasis of the female genital tract: public health aspects // Parasitol. Today. 1999. Vol. 15. P. 378-381.
  36. Polman K., Stelma F.F., Gryseels B. et al. Epidemiologic application of circulating antigen detection in a recent Schistosoma mansoni focus in northern Senegal // Am. J. Trop. Med. Hyg. 1995. Vol. 53. P. 152-157.
  37. Rashad S.B. Schistosomiasis: Current Status and Recent Updates Urinary Schistosomiasis Review // J. Adv. Res. 2013. Vol. 4. P. 453-459.
  38. Savioli L., Renganathan E., Montresor A. et al. Division of Control of Tropical Diseases, Schistomiasis and Intestinal Parasites Unit, World Health Organization. Control of schistosomiasis - a global picture // Parasitol. Today. 1997. Vol. 13. P. 444-448.
  39. Shiff C., Naples J.M., Isharwal S. et al. Non-invasive methods to detect schistosome-based bladder cancer: Is the association sufficient for epidemiological use? // Trans. R. Soc. Trop. Med. Hyg. 2010. Vol. 104, N 1. P. 3-5.
  40. Shiff C., Veltri R., Naples J. et al. Ultrasound verification of bladder damage is associated with known biomarkers of bladder cancer in adults chronically infected with Schistosoma haematobium in Ghana // Trans. R. Soc. Trop. Med. Hyg. 2006. Vol. 100. P. 847-854.
  41. Standley C.J., Adriko M., Arinaitwe M. et al. Epidemiology and control of intestinal schistosomiasis on the Sesse Islands, Uganda: integrating malacology and parasitology to tailor local treatment recommendations // Parasit. Vectors. 2010. Vol. 3. P. 64.
  42. Standley C.J., Lwambo N., Lange C. et al. Performance of circulating cathodic antigen (CCA) urine-dipsticks for rapid detection of intestinal schistosomiasis in schoolchildren from shoreline communities of Lake Victoria // Parasit. Vectors. 2010. Vol. 3. P. 7.
  43. Stothard J.R., Sousa-Figueiredo J.C., Standley A. et al. An evaluation of urine-CCA strip test and fingerprick blood SEA-ELISA for detection of urinary schistosomiasis in schoolchildren in Zanzibar // Acta Trop. 2009. Vol. 111. P. 64 - 70.
  44. Tsang V.C., Hancock K., Kelly M.A. et al. Schistosoma mansoni adult microsomal antigens, a serologic reagent. II. Specificity of antibody responses to the S. mansoni microsomal antigen (MAMA) // J. of Immun. 1983. Vol. 130. P. 1366-1370.
  45. Van Dam G.J., Wichers J.H., Ferreira T.M. et al. Diagnosis of schistosomiasis by reagent strip test for detection of circulating cathodic antigen // J. Clin. Microbiol. 2004. Vol. 42. P. 5458-5461.
  46. Van der Werf M.J., Vlas de S.J., Brooker S. et al. Quantification of clinical morbidity associated with schistosome infection in sub-Saharan Africa // Acta Trop. 2003. Vol. 86. P. 125-139.
  47. Van Lieshout L., Polderman A.M., Deelder A.M. Immunodiagnosis of schistosomiasis by determination of the circulating antigens CAA and CCA, in particular in individuals with recent or light infections // Acta Trop. 2000. Vol. 77. P. 69-80.
  48. Van Lieshout L., Polderman A.M., Vlas de S.J. et al. Analysis of worm burden variation in human Schistosoma mansoni infections by determination of serum levels of circulating anodic antigen and circulating cathodic antigen // J. Infect. Dis. 1995. Vol. 172. P. 1336-1342.
  49. Wilson R.A., Curwen R.S., Braschi S. et al. From genomes to vaccines via the proteome // Mem. Inst. Oswaldo Cruz. 2004. Vol. 99. P. 45-50.
  50. Schistosomiasis. WHO recommendations, updated February 2014: http://www.who.int/mediacentre/factsheets/fs115/en.

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