Detection of Helicobacter pylori in adenotonsillar tissue of children with chronic adenotonsillitis using rapid urease test, PCR and blood serology: A prospective study
Abstract Objective Contradictory results have been reported regarding Helicobacter pylori ( H. pylori ) detection in adenotonsillar tissue. The aims of this study were to investigate whether adenotonsillar tissue of symptomatic children with chronic adenotonsillitis harbors the H. pylori organism, u...
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Veröffentlicht in: | International journal of pediatric otorhinolaryngology 2011-04, Vol.75 (4), p.568-572 |
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description | Abstract Objective Contradictory results have been reported regarding Helicobacter pylori ( H. pylori ) detection in adenotonsillar tissue. The aims of this study were to investigate whether adenotonsillar tissue of symptomatic children with chronic adenotonsillitis harbors the H. pylori organism, using two biopsy-based invasive methods namely; rapid urease test (RUT) and polymerase chain reaction (PCR) as well as blood serology and to compare the results obtained from each of these methods to the “gold standard”. Methods This prospective clinical study was carried out on 20 children aged between 2 and 10 years scheduled for tonsillectomy +/− adenoidectomy in a tertiary referral center. Exclusion criteria included: use of antacids, H2 blockers or antibiotics during the previous month before surgery and adenotonsillectomy for obstructive sleep apnea. Core biopsy samples from resected adenotonsillar tissue was tested for H. pylori detection using both RUT and PCR assay for the ureC gene. Preoperative patient venous blood samples were also tested for H. pylori IgG antibodies. As a “gold standard”, examined tissue was considered to be H. pylori infected if the two biopsy specimen-based methods (RUT and PCR) yielded positive results. Results Thirty adenotonsillectomy specimens were tested (20 tonsils and 10 adenoids). RUT was positive in 16 (53.3%) specimens (12 tonsils and 4 adenoids). According to the “gold standard”, 11/16 were considered false-positive, yielding this test sensitivity 100% and specificity 56%. The ureC gene sequence was detected by PCR in 5 (16.6%) specimens (3 tonsils and 2 adenoids), all of which were also positive by RUT, thus were considered H. pylori infected. Accordingly, PCR had a 100% sensitivity and specificity. Serology testing was positive for H. pylori IgG antibodies in 4/20 patients (20%), only two of them were found to have H. pylori infected adenotonsillar tissue. Conclusions Based on our findings it seems that adenotonsillar tissue may constitute an extra-gastric reservoir for H. pylori in symptomatic children with chronic adenotonsillitis. RUT was found to be of less accuracy than PCR in H. pylori detection in an extra-gastric location, thus results of previous studies using this test alone for detection of oral H. pylori should be treated with caution. |
doi_str_mv | 10.1016/j.ijporl.2011.01.021 |
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The aims of this study were to investigate whether adenotonsillar tissue of symptomatic children with chronic adenotonsillitis harbors the H. pylori organism, using two biopsy-based invasive methods namely; rapid urease test (RUT) and polymerase chain reaction (PCR) as well as blood serology and to compare the results obtained from each of these methods to the “gold standard”. Methods This prospective clinical study was carried out on 20 children aged between 2 and 10 years scheduled for tonsillectomy +/− adenoidectomy in a tertiary referral center. Exclusion criteria included: use of antacids, H2 blockers or antibiotics during the previous month before surgery and adenotonsillectomy for obstructive sleep apnea. Core biopsy samples from resected adenotonsillar tissue was tested for H. pylori detection using both RUT and PCR assay for the ureC gene. Preoperative patient venous blood samples were also tested for H. pylori IgG antibodies. As a “gold standard”, examined tissue was considered to be H. pylori infected if the two biopsy specimen-based methods (RUT and PCR) yielded positive results. Results Thirty adenotonsillectomy specimens were tested (20 tonsils and 10 adenoids). RUT was positive in 16 (53.3%) specimens (12 tonsils and 4 adenoids). According to the “gold standard”, 11/16 were considered false-positive, yielding this test sensitivity 100% and specificity 56%. The ureC gene sequence was detected by PCR in 5 (16.6%) specimens (3 tonsils and 2 adenoids), all of which were also positive by RUT, thus were considered H. pylori infected. Accordingly, PCR had a 100% sensitivity and specificity. Serology testing was positive for H. pylori IgG antibodies in 4/20 patients (20%), only two of them were found to have H. pylori infected adenotonsillar tissue. Conclusions Based on our findings it seems that adenotonsillar tissue may constitute an extra-gastric reservoir for H. pylori in symptomatic children with chronic adenotonsillitis. RUT was found to be of less accuracy than PCR in H. pylori detection in an extra-gastric location, thus results of previous studies using this test alone for detection of oral H. pylori should be treated with caution.</description><identifier>ISSN: 0165-5876</identifier><identifier>EISSN: 1872-8464</identifier><identifier>DOI: 10.1016/j.ijporl.2011.01.021</identifier><identifier>PMID: 21324534</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>Adenoidectomy - methods ; Adenoids ; Adenoids - microbiology ; Adenoids - physiopathology ; Adenoids - surgery ; Child ; Child, Preschool ; Chronic Disease ; Cohort Studies ; Female ; Helicobacter Infections - blood ; Helicobacter Infections - diagnosis ; Helicobacter pylori ; Helicobacter pylori - isolation & purification ; Humans ; Immunohistochemistry ; Lymphadenitis - diagnosis ; Lymphadenitis - microbiology ; Lymphadenitis - surgery ; Male ; Otolaryngology ; Pediatrics ; Polymerase chain reaction ; Polymerase Chain Reaction - methods ; Predictive Value of Tests ; Prospective Studies ; Rapid urease test ; Risk Assessment ; Sensitivity and Specificity ; Serologic Tests - methods ; Serological test ; Tonsillectomy - methods ; Tonsillitis - diagnosis ; Tonsillitis - microbiology ; Tonsillitis - surgery ; Tonsils ; Urease - analysis</subject><ispartof>International journal of pediatric otorhinolaryngology, 2011-04, Vol.75 (4), p.568-572</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2011 Elsevier Ireland Ltd</rights><rights>Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-3a8ecc0d03df1657bed9558f583b701aa759e3fc55893f2672dd1ac0320d52753</citedby><cites>FETCH-LOGICAL-c448t-3a8ecc0d03df1657bed9558f583b701aa759e3fc55893f2672dd1ac0320d52753</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0165587611000267$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21324534$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Abdel-Monem, Mohamed H</creatorcontrib><creatorcontrib>Magdy, Emad A</creatorcontrib><creatorcontrib>Nour, Yasser A</creatorcontrib><creatorcontrib>Harfoush, Reem A</creatorcontrib><creatorcontrib>Ibreak, Alnagy</creatorcontrib><title>Detection of Helicobacter pylori in adenotonsillar tissue of children with chronic adenotonsillitis using rapid urease test, PCR and blood serology: A prospective study</title><title>International journal of pediatric otorhinolaryngology</title><addtitle>Int J Pediatr Otorhinolaryngol</addtitle><description>Abstract Objective Contradictory results have been reported regarding Helicobacter pylori ( H. pylori ) detection in adenotonsillar tissue. The aims of this study were to investigate whether adenotonsillar tissue of symptomatic children with chronic adenotonsillitis harbors the H. pylori organism, using two biopsy-based invasive methods namely; rapid urease test (RUT) and polymerase chain reaction (PCR) as well as blood serology and to compare the results obtained from each of these methods to the “gold standard”. Methods This prospective clinical study was carried out on 20 children aged between 2 and 10 years scheduled for tonsillectomy +/− adenoidectomy in a tertiary referral center. Exclusion criteria included: use of antacids, H2 blockers or antibiotics during the previous month before surgery and adenotonsillectomy for obstructive sleep apnea. Core biopsy samples from resected adenotonsillar tissue was tested for H. pylori detection using both RUT and PCR assay for the ureC gene. Preoperative patient venous blood samples were also tested for H. pylori IgG antibodies. As a “gold standard”, examined tissue was considered to be H. pylori infected if the two biopsy specimen-based methods (RUT and PCR) yielded positive results. Results Thirty adenotonsillectomy specimens were tested (20 tonsils and 10 adenoids). RUT was positive in 16 (53.3%) specimens (12 tonsils and 4 adenoids). According to the “gold standard”, 11/16 were considered false-positive, yielding this test sensitivity 100% and specificity 56%. The ureC gene sequence was detected by PCR in 5 (16.6%) specimens (3 tonsils and 2 adenoids), all of which were also positive by RUT, thus were considered H. pylori infected. Accordingly, PCR had a 100% sensitivity and specificity. Serology testing was positive for H. pylori IgG antibodies in 4/20 patients (20%), only two of them were found to have H. pylori infected adenotonsillar tissue. Conclusions Based on our findings it seems that adenotonsillar tissue may constitute an extra-gastric reservoir for H. pylori in symptomatic children with chronic adenotonsillitis. RUT was found to be of less accuracy than PCR in H. pylori detection in an extra-gastric location, thus results of previous studies using this test alone for detection of oral H. pylori should be treated with caution.</description><subject>Adenoidectomy - methods</subject><subject>Adenoids</subject><subject>Adenoids - microbiology</subject><subject>Adenoids - physiopathology</subject><subject>Adenoids - surgery</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Chronic Disease</subject><subject>Cohort Studies</subject><subject>Female</subject><subject>Helicobacter Infections - blood</subject><subject>Helicobacter Infections - diagnosis</subject><subject>Helicobacter pylori</subject><subject>Helicobacter pylori - isolation & purification</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Lymphadenitis - diagnosis</subject><subject>Lymphadenitis - microbiology</subject><subject>Lymphadenitis - surgery</subject><subject>Male</subject><subject>Otolaryngology</subject><subject>Pediatrics</subject><subject>Polymerase chain reaction</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Predictive Value of Tests</subject><subject>Prospective Studies</subject><subject>Rapid urease test</subject><subject>Risk Assessment</subject><subject>Sensitivity and Specificity</subject><subject>Serologic Tests - methods</subject><subject>Serological test</subject><subject>Tonsillectomy - methods</subject><subject>Tonsillitis - diagnosis</subject><subject>Tonsillitis - microbiology</subject><subject>Tonsillitis - surgery</subject><subject>Tonsils</subject><subject>Urease - analysis</subject><issn>0165-5876</issn><issn>1872-8464</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkl2L1DAUhoMo7jj6D0Ry540dk7SZpl4Iy_ixwoLix3VIk9Pd1ExSk3Sl_8ifacqsgt4sHAgJT87H-x6EnlKyo4TuX447O04huh0jlO5ICUbvoQ0VLatEs2_uo03BeMVFuz9Dj1IaCaEt4fwhOmO0Zg2vmw369QYy6GyDx2HAF-CsDr3SGSKeFheixdZjZcCHHHyyzqmIs01phpXX19aZCB7_tPm63GLwVv-D2wLjOVl_haOarMFzBJUAZ0j5Bf50-IyVN7h3IRicIAYXrpZX-BxPMaRpbewGcMqzWR6jB4NyCZ7cnlv07d3br4eL6vLj-w-H88tKN43IVa0EaE0Mqc1Qpm97MB3nYuCi7ltClWp5B_Wgy1tXD2zfMmOo0qRmxHDW8nqLnp_ylg5-zKVLebRJQxncQ5iTFEKQTnBB7ia5YIIz3hWyOZG6TJUiDHKK9qjiIimRq5lylCcz5WqmJCWKRVv07LbA3B_B_P30x70CvD4BUAS5sRBl0ha8BmNj0U6aYO-q8H8C7WyxULnvsEAawxx9EVtSmZgk8su6UOs-UUoIKeLVvwG2Ysqn</recordid><startdate>20110401</startdate><enddate>20110401</enddate><creator>Abdel-Monem, Mohamed H</creator><creator>Magdy, Emad A</creator><creator>Nour, Yasser A</creator><creator>Harfoush, Reem A</creator><creator>Ibreak, Alnagy</creator><general>Elsevier Ireland Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QL</scope><scope>C1K</scope></search><sort><creationdate>20110401</creationdate><title>Detection of Helicobacter pylori in adenotonsillar tissue of children with chronic adenotonsillitis using rapid urease test, PCR and blood serology: A prospective study</title><author>Abdel-Monem, Mohamed H ; Magdy, Emad A ; Nour, Yasser A ; Harfoush, Reem A ; Ibreak, Alnagy</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-3a8ecc0d03df1657bed9558f583b701aa759e3fc55893f2672dd1ac0320d52753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adenoidectomy - methods</topic><topic>Adenoids</topic><topic>Adenoids - microbiology</topic><topic>Adenoids - physiopathology</topic><topic>Adenoids - surgery</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Chronic Disease</topic><topic>Cohort Studies</topic><topic>Female</topic><topic>Helicobacter Infections - blood</topic><topic>Helicobacter Infections - diagnosis</topic><topic>Helicobacter pylori</topic><topic>Helicobacter pylori - isolation & purification</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Lymphadenitis - diagnosis</topic><topic>Lymphadenitis - microbiology</topic><topic>Lymphadenitis - surgery</topic><topic>Male</topic><topic>Otolaryngology</topic><topic>Pediatrics</topic><topic>Polymerase chain reaction</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Predictive Value of Tests</topic><topic>Prospective Studies</topic><topic>Rapid urease test</topic><topic>Risk Assessment</topic><topic>Sensitivity and Specificity</topic><topic>Serologic Tests - methods</topic><topic>Serological test</topic><topic>Tonsillectomy - methods</topic><topic>Tonsillitis - diagnosis</topic><topic>Tonsillitis - microbiology</topic><topic>Tonsillitis - surgery</topic><topic>Tonsils</topic><topic>Urease - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Abdel-Monem, Mohamed H</creatorcontrib><creatorcontrib>Magdy, Emad A</creatorcontrib><creatorcontrib>Nour, Yasser A</creatorcontrib><creatorcontrib>Harfoush, Reem A</creatorcontrib><creatorcontrib>Ibreak, Alnagy</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>International journal of pediatric otorhinolaryngology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Abdel-Monem, Mohamed H</au><au>Magdy, Emad A</au><au>Nour, Yasser A</au><au>Harfoush, Reem A</au><au>Ibreak, Alnagy</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Detection of Helicobacter pylori in adenotonsillar tissue of children with chronic adenotonsillitis using rapid urease test, PCR and blood serology: A prospective study</atitle><jtitle>International journal of pediatric otorhinolaryngology</jtitle><addtitle>Int J Pediatr Otorhinolaryngol</addtitle><date>2011-04-01</date><risdate>2011</risdate><volume>75</volume><issue>4</issue><spage>568</spage><epage>572</epage><pages>568-572</pages><issn>0165-5876</issn><eissn>1872-8464</eissn><abstract>Abstract Objective Contradictory results have been reported regarding Helicobacter pylori ( H. pylori ) detection in adenotonsillar tissue. The aims of this study were to investigate whether adenotonsillar tissue of symptomatic children with chronic adenotonsillitis harbors the H. pylori organism, using two biopsy-based invasive methods namely; rapid urease test (RUT) and polymerase chain reaction (PCR) as well as blood serology and to compare the results obtained from each of these methods to the “gold standard”. Methods This prospective clinical study was carried out on 20 children aged between 2 and 10 years scheduled for tonsillectomy +/− adenoidectomy in a tertiary referral center. Exclusion criteria included: use of antacids, H2 blockers or antibiotics during the previous month before surgery and adenotonsillectomy for obstructive sleep apnea. Core biopsy samples from resected adenotonsillar tissue was tested for H. pylori detection using both RUT and PCR assay for the ureC gene. Preoperative patient venous blood samples were also tested for H. pylori IgG antibodies. As a “gold standard”, examined tissue was considered to be H. pylori infected if the two biopsy specimen-based methods (RUT and PCR) yielded positive results. Results Thirty adenotonsillectomy specimens were tested (20 tonsils and 10 adenoids). RUT was positive in 16 (53.3%) specimens (12 tonsils and 4 adenoids). According to the “gold standard”, 11/16 were considered false-positive, yielding this test sensitivity 100% and specificity 56%. The ureC gene sequence was detected by PCR in 5 (16.6%) specimens (3 tonsils and 2 adenoids), all of which were also positive by RUT, thus were considered H. pylori infected. Accordingly, PCR had a 100% sensitivity and specificity. Serology testing was positive for H. pylori IgG antibodies in 4/20 patients (20%), only two of them were found to have H. pylori infected adenotonsillar tissue. Conclusions Based on our findings it seems that adenotonsillar tissue may constitute an extra-gastric reservoir for H. pylori in symptomatic children with chronic adenotonsillitis. RUT was found to be of less accuracy than PCR in H. pylori detection in an extra-gastric location, thus results of previous studies using this test alone for detection of oral H. pylori should be treated with caution.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>21324534</pmid><doi>10.1016/j.ijporl.2011.01.021</doi><tpages>5</tpages></addata></record> |
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subjects | Adenoidectomy - methods Adenoids Adenoids - microbiology Adenoids - physiopathology Adenoids - surgery Child Child, Preschool Chronic Disease Cohort Studies Female Helicobacter Infections - blood Helicobacter Infections - diagnosis Helicobacter pylori Helicobacter pylori - isolation & purification Humans Immunohistochemistry Lymphadenitis - diagnosis Lymphadenitis - microbiology Lymphadenitis - surgery Male Otolaryngology Pediatrics Polymerase chain reaction Polymerase Chain Reaction - methods Predictive Value of Tests Prospective Studies Rapid urease test Risk Assessment Sensitivity and Specificity Serologic Tests - methods Serological test Tonsillectomy - methods Tonsillitis - diagnosis Tonsillitis - microbiology Tonsillitis - surgery Tonsils Urease - analysis |
title | Detection of Helicobacter pylori in adenotonsillar tissue of children with chronic adenotonsillitis using rapid urease test, PCR and blood serology: A prospective study |
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