Full-text resources of PSJD and other databases are now available in the new Library of Science.
Visit https://bibliotekanauki.pl

PL EN


Preferences help
enabled [disable] Abstract
Number of results
2016 | 63 | 1 | 127-130

Article title

Conflicting results of non-invasive methods for detection of Helicobacter pylori infection in children with celiac disease - a preliminary study

Content

Title variants

Languages of publication

EN

Abstracts

EN
Background: There are no data addressing the usefulness of non-invasive tests for the detection of Helicobacter pylori (HP) infection in celiac disease (CD). Aim: The aim of this study was to compare two most sensitive and specific tests - urea breath test (UBT) and fecal antigen test (FAT) in HP diagnosis in CD patients. Materials and Methods: The study comprised of 76 CD patients, 49 healthy subjects (HS) and 35 patients who underwent differential diagnosis due to abdominal pain (AP patients). The presence of HP infection was evaluated using the 13C isotope-labeled UBT and FAT (ELISA). Results: HP infection was diagnosed based on UBT and FAT in 8 (16.3%) and 7 (14.3%) HS, and in 8 (10.5%) CD patients and 12 (34.3%) AP patients, respectively, using both tests. The prevalence of conflicting results in comparison with positive results (obtained with any of the two tests) was distinctly higher (54.5%) in CD group than in other subjects (23.3%); however, due to low HP prevalence, it did not reach the level of significance (p<0.1759). Conclusion: CD may increase the risk of divergent results of non-invasive tests used for the detection of HP infection in children. Since UBT is the most reliable test, we suggest its standard use as a method of choice in pediatric CD - at least until new evidence emerges supporting a different approach.

Year

Volume

63

Issue

1

Pages

127-130

Physical description

Dates

published
2016
received
2015-06-22
revised
2015-09-30
accepted
2015-12-21
(unknown)
2016-01-27

Contributors

  • Pediatric Department with Children's Cardiologic Subunit, Specialist Hospital of Holy Spirit in Sandomierz, Sandomierz, Poland
author
  • Department of Physiology, Poznan University of Medical Sciences, Poznań, Poland
author
  • Department of Pediatric Gastroenterology and Metabolic Diseases, Poznan University of Medical Sciences, Poznań, Poland
  • Department of Pediatric Gastroenterology and Metabolic Diseases, Poznan University of Medical Sciences, Poznań, Poland
  • Department of Pediatric Gastroenterology and Metabolic Diseases, Poznan University of Medical Sciences, Poznań, Poland
  • Department of General, Gastroenterological and Endocrinological Surgery, Poznan University of Medical Sciences, Poznań, Poland
  • Institute of Human Genetics, Polish Academy of Sciences, Poznań, Poland
  • Department of Pediatrics, The School of Medicine and Division of Dentistry in Zabrze, Medical University of Silesia in Katowice, Zabrze, Poland
  • Department of Pediatric Gastroenterology and Metabolic Diseases, Poznan University of Medical Sciences, Poznań, Poland

References

  • Kusters JG, Vliet AH, Kuipers EJ (2006) Pathogenesis of Helicobacter pylori infection. Clin Microbiol Rev 19: 449-490.
  • Ekstrom AM, Held M, Hansson LE, Engstrand L, Nyren O (2001) Helicobacter pylori in gastric cancer established by CagA immunoblot as a marker of past infection. Gastroenterology 121: 784-791.
  • WHO International Agency for Research on Cancer web side. Monographs on the evaluation of carcinogenic risks to humans. 1994; 61: schistosomes, liver flukes and Helicobacter pylori. http://monographs.iarc.fr/ENG/Monographs/. Access March 16th 2014.
  • Drzymała-Czyż S, Kwiecień J, Pogorzelski A, Rachel M, Banasiewicz T, Pławski A, Szczawińska-Popłonyk A, Herzig KH, Walkowiak J (2013) Prevalence of Helicobacter pylori infection in patients with cystic fibrosis. J Cyst Fibros 12: 761-765.
  • Jozefczuk J, Bancerz B, Walkowiak M, Glapa A, Nowak J, Piescikowska J, Kwiecień J, Walkowiak J (2015) Prevalence of Helicobacter pylori infection in pediatric celiac disease. Eur Rev Med Pharmacol Sci 19: 2031-2035.
  • Żabka A, Kwiecień J, Bąk-Drabik K, Krzywicka A, Porębska J, Pieniążek W (2010) Does frequency of H. pylori in children 3-18 years old decrease? (Preliminary report). Probl Med Rodz 2: 18-20 (in Polish?).
  • Husby S, Koletzko S, Korponay-Szabó IR, Mearin ML, Phillips A, Shamir R, Troncone R, Giersiepen K, Branski D, Catassi C, Lelgeman M, Mäki M, Ribes-Koninckx C, Ventura A, Zimmer KP; ESPGHAN Working Group on Coeliac Disease Diagnosis; ESPGHAN Gastroenterology Committee (2012) European Society for Pediatric Gastroenterology, Hepatology, and Nutrition guidelines for the diagnosis of coeliac disease. J Pediatr Gastroenterol Nutr 54: 136-160.
  • Dzierzanowska-Fangrat K, Lehours P, Mégraud F, Dzierzanowska D (2006) Diagnosis of Helicobacter pylori infection. Helicobacter 11: 6-13.
  • Asaka M, Kato M, Takahashi S, Fukuda Y, Sugiyama T, Ota H, Uemura N, Murakami K, Satoh K, Sugano K (2010) Guidelines for the management of Helicobacter pylori infection in Japan: 2009 revised edition. Helicobacter 15: 1-20.
  • Malfertheiner P1, Megraud F, O'Morain CA, Atherton J, Axon AT, Bazzoli F, Gensini GF, Gisbert JP, Graham DY, Rokkas T, El-Omar EM, Kuipers EJ; European Helicobacter Study Group (2012) Management of Helicobacter pylori infection-the Maastricht IV/Florence Consensus Report. Gut 61: 646-664.
  • Masoero G, Lombardo L, Della Monica P, Vicari S, Crocilla C, Duglio A, Pera A (2000) Discrepancy between Helicobacter pylori stool antigen assay and urea breath test in the detection of Helicobacter pylori infection. Dig Liver Dis 32: 285-290.
  • Andersen LP, Rasmussen L (2009) Helicobacter pylori-coccoid forms and biofilm formation. FEMS Immunol Med Microbiol 56: 112-115.
  • Casasola-Rodriguez B, Orta de Velasquez MT, Luqueño-Martinez VG, Monje-Ramirez I (2013) Quantification of Helicobacter pylori in the viable but nonculturable state by quantitative PCR in water disinfected with ozone. Water Sci Technol 68: 2468-2472.
  • Azevedo, NF, Almeida C, Keevil CW, Vieira MJ (2006) Coccoid morphology as a possible manifestation of Helicobacter pylori adaptation to adverse environments. Helicobacter 11: 342-343.
  • Shimoyama T (2013) Stool antigen tests for the management of Helicobacter pylori infection. World J Gastroenterol 19: 8188-8191.
  • Pinto-Sanchez MI, Bercik P, Verdu EF (2015) Motility alterations in celiac disease and non-celiac gluten sensitivity. Dig Dis 33: 200-207.
  • Nenna R, Magliocca FM, Tiberti C, Mastrogiorgio G, Petrarca L, Mennini M, Lucantoni F, Luparia RP, Bonamico M (2012) J Pediatr Gastroenterol Nutr 55: 728-732.
  • Ferwana M, Abdulmajeed I, Alhajiahmed A, Madani W, Firwana B, Hasan R, Altayar O, Limburg PJ, Murad MH, Knawy B (2015) Accuracy of urea breath test in Helicobacter pylori infection: Meta-analysis. World J Gastroenterol 21: 1305-1314.
  • Leal YA, Flores LL, Fuentes-Panana EM, Cedillo-Rivera R, Torres J (2011) 13C-urea breath test for the diagnosis of Helicobacter pylori infection in children: a systematic review and meta-analysis. Helicobacter 16: 327-337
  • Zhou X, Su J, Xu G, Zhang G (2014) Accuracy of stool antigen test for the diagnosis of Helicobacter pylori infection in children: a meta-analysis. Clin Res Hepatol Gastroenterol 38: 629-638.
  • Gisbert JP, de la Morena F, Abraira V (2006) Accuracy of monoclonal stool antigen test for the diagnosis of H. pylori infection: a systematic review and meta-analysis. Am J Gastroenterol 101: 1921-1930.
  • Drzymała-Czyż S, Stawinska-Witoszynska B, Mądry E, Krzywinska-Wiewiórowska M, Szczepanik M, Walkowiak J, Kwiecień J (2014) Non-invasive detection of Helicobacter pylori in cystic fibrosis - the fecal test vs. the urea breath test. Eur Rev Med Pharmacol Sci 18: 2343-2348.

Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.bwnjournal-article-abpv63p127kz
JavaScript is turned off in your web browser. Turn it on to take full advantage of this site, then refresh the page.