Adenovirus-Associated Acute Appendicitis: An Under-Recognized Relationship?
Acute appendicitis (AA) is one of the most common causes of a surgical abdomen worldwide, occurring most frequently in those age 10 to 29 years. Adenovirus (ADV) is a rare but reported cause of AA in children and a well-recognized cause of intussusception in infants and young children. Annually, abo...
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description | Acute appendicitis (AA) is one of the most common causes of a surgical abdomen worldwide, occurring most frequently in those age 10 to 29 years. Adenovirus (ADV) is a rare but reported cause of AA in children and a well-recognized cause of intussusception in infants and young children. Annually, about 36,000 basic military trainees (BMTs) undergo initial training at Joint Base San Antonio Lackland, Texas. Before reintroduction of the ADV 4/7 vaccine in November 2011, one-third of BMTs developed an adenoviral upper respiratory tract infection (URI) during the 8.5 weeks of training. We hypothesized that ADV may be a common cause of AA in the BMT population given their young age and high incidence of adenoviral URIs. The objective of this study was to determine the frequency with which ADV, cytomegalovirus (CMV), Epstein-Barr virus (EBV), and enterovirus were associated with AA in a population of young adults.
This study was a retrospective review of patient charts and existing pathological tissue specimens of all BMTs who underwent appendectomy at the Wilford Hall Medical Center from January 1, 2003, to August 31, 2011. Pathological tissue samples from 112 BMTs were assayed by quantitative polymerase chain reaction (qPCR) and immunohistochemistry (IHC) for viral targets.
ADV DNA was detected in 16 of 112 samples (14%) via qPCR: ADV 4 in 13 cases, ADV B14 in 1 case, and nontypable ADV in 2 cases. IHC was positive in only the ADV B14 case (0.9%). All cases were negative for CMV, EBV, and enterovirus.
By using qPCR, this study demonstrated an association between ADV and AA higher than has been previously reported: ADV was detected in 14% of AA cases in this series versus in only 0.23% of AA cases in previous studies (p < 0.01). There was no evidence of CMV, EBV, or enterovirus association with AA in this study. Comparison of qPCR to IHC shows that histologic analysis may overlook evidence of ADV in appendiceal tissue: qPCR is significantly more sensitive than light microscopy and IHC for detecting ADV in this setting. Because ADV 4 was detected in 81% of those with positive qPCR, the recently licensed live oral ADV vaccine might be useful for primary prevention against AA. Prospective studies evaluating young adults presenting with AA for evidence of infection with ADV are needed to determine if a causal relationship exists. |
doi_str_mv | 10.7205/MILMED-D-16-00308 |
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This study was a retrospective review of patient charts and existing pathological tissue specimens of all BMTs who underwent appendectomy at the Wilford Hall Medical Center from January 1, 2003, to August 31, 2011. Pathological tissue samples from 112 BMTs were assayed by quantitative polymerase chain reaction (qPCR) and immunohistochemistry (IHC) for viral targets.
ADV DNA was detected in 16 of 112 samples (14%) via qPCR: ADV 4 in 13 cases, ADV B14 in 1 case, and nontypable ADV in 2 cases. IHC was positive in only the ADV B14 case (0.9%). All cases were negative for CMV, EBV, and enterovirus.
By using qPCR, this study demonstrated an association between ADV and AA higher than has been previously reported: ADV was detected in 14% of AA cases in this series versus in only 0.23% of AA cases in previous studies (p < 0.01). There was no evidence of CMV, EBV, or enterovirus association with AA in this study. Comparison of qPCR to IHC shows that histologic analysis may overlook evidence of ADV in appendiceal tissue: qPCR is significantly more sensitive than light microscopy and IHC for detecting ADV in this setting. Because ADV 4 was detected in 81% of those with positive qPCR, the recently licensed live oral ADV vaccine might be useful for primary prevention against AA. Prospective studies evaluating young adults presenting with AA for evidence of infection with ADV are needed to determine if a causal relationship exists.</description><identifier>ISSN: 0026-4075</identifier><identifier>EISSN: 1930-613X</identifier><identifier>DOI: 10.7205/MILMED-D-16-00308</identifier><identifier>PMID: 29087922</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Academic Medical Centers - organization & administration ; Acute Disease - epidemiology ; Adenoviridae - pathogenicity ; Adenovirus Infections, Human - complications ; Adenovirus Infections, Human - epidemiology ; Adenovirus Vaccines - therapeutic use ; Adolescent ; Adult ; Age ; Appendectomy ; Appendicitis ; Appendicitis - epidemiology ; Appendicitis - etiology ; Cytomegalovirus ; Education - organization & administration ; Education - statistics & numerical data ; Female ; Humans ; Infections ; Male ; Polymerase chain reaction ; Respiratory diseases ; Texas - epidemiology ; Viral infections ; Young adults</subject><ispartof>Military medicine, 2017-05, Vol.182 (5), p.e1765-e1768</ispartof><rights>Reprint & Copyright © 2017 Association of Military Surgeons of the U.S.</rights><rights>Copyright Association of Military Surgeons of the United States May/Jun 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-c33ddddc564a03977bf3bf966ac44de708b6af38f5ee0fa0e00e4b9cbebf75533</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29087922$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lynch, David T</creatorcontrib><creatorcontrib>Lott, Lisa</creatorcontrib><creatorcontrib>Cebe, Katherine</creatorcontrib><creatorcontrib>McDonald, J Matthew</creatorcontrib><creatorcontrib>Abplanalp, Allison</creatorcontrib><creatorcontrib>Tully, Charla</creatorcontrib><creatorcontrib>Trujillo-Lopez, Elizabeth</creatorcontrib><creatorcontrib>Danaher, Patrick J</creatorcontrib><title>Adenovirus-Associated Acute Appendicitis: An Under-Recognized Relationship?</title><title>Military medicine</title><addtitle>Mil Med</addtitle><description>Acute appendicitis (AA) is one of the most common causes of a surgical abdomen worldwide, occurring most frequently in those age 10 to 29 years. Adenovirus (ADV) is a rare but reported cause of AA in children and a well-recognized cause of intussusception in infants and young children. Annually, about 36,000 basic military trainees (BMTs) undergo initial training at Joint Base San Antonio Lackland, Texas. Before reintroduction of the ADV 4/7 vaccine in November 2011, one-third of BMTs developed an adenoviral upper respiratory tract infection (URI) during the 8.5 weeks of training. We hypothesized that ADV may be a common cause of AA in the BMT population given their young age and high incidence of adenoviral URIs. The objective of this study was to determine the frequency with which ADV, cytomegalovirus (CMV), Epstein-Barr virus (EBV), and enterovirus were associated with AA in a population of young adults.
This study was a retrospective review of patient charts and existing pathological tissue specimens of all BMTs who underwent appendectomy at the Wilford Hall Medical Center from January 1, 2003, to August 31, 2011. Pathological tissue samples from 112 BMTs were assayed by quantitative polymerase chain reaction (qPCR) and immunohistochemistry (IHC) for viral targets.
ADV DNA was detected in 16 of 112 samples (14%) via qPCR: ADV 4 in 13 cases, ADV B14 in 1 case, and nontypable ADV in 2 cases. IHC was positive in only the ADV B14 case (0.9%). All cases were negative for CMV, EBV, and enterovirus.
By using qPCR, this study demonstrated an association between ADV and AA higher than has been previously reported: ADV was detected in 14% of AA cases in this series versus in only 0.23% of AA cases in previous studies (p < 0.01). There was no evidence of CMV, EBV, or enterovirus association with AA in this study. Comparison of qPCR to IHC shows that histologic analysis may overlook evidence of ADV in appendiceal tissue: qPCR is significantly more sensitive than light microscopy and IHC for detecting ADV in this setting. Because ADV 4 was detected in 81% of those with positive qPCR, the recently licensed live oral ADV vaccine might be useful for primary prevention against AA. Prospective studies evaluating young adults presenting with AA for evidence of infection with ADV are needed to determine if a causal relationship exists.</description><subject>Academic Medical Centers - organization & administration</subject><subject>Acute Disease - epidemiology</subject><subject>Adenoviridae - pathogenicity</subject><subject>Adenovirus Infections, Human - complications</subject><subject>Adenovirus Infections, Human - epidemiology</subject><subject>Adenovirus Vaccines - therapeutic use</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Age</subject><subject>Appendectomy</subject><subject>Appendicitis</subject><subject>Appendicitis - epidemiology</subject><subject>Appendicitis - etiology</subject><subject>Cytomegalovirus</subject><subject>Education - organization & administration</subject><subject>Education - statistics & numerical data</subject><subject>Female</subject><subject>Humans</subject><subject>Infections</subject><subject>Male</subject><subject>Polymerase chain reaction</subject><subject>Respiratory diseases</subject><subject>Texas - epidemiology</subject><subject>Viral infections</subject><subject>Young adults</subject><issn>0026-4075</issn><issn>1930-613X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><recordid>eNpdkMFKw0AQhhdRbK0-gBcpePGyOpvdbLJeJLRViy1CseBt2WwmuqVNYjYR9OmNtnpwDjOX7_8ZPkJOGVxGAYRX8-lsPhnTMWWSAnCI90ifKQ5UMv68T_oAgaQCorBHjrxfATChYnZIeoGCOFJB0CcPSYZF-e7q1tPE-9I602A2TGzb4DCpKiwyZ13j_PUwKYbLIsOaLtCWL4X77LgFrk3jysK_uurmmBzkZu3xZHcHZHk7eRrd09nj3XSUzKjlUdB0m2fd2FAKA1xFUZrzNFdSGitEhhHEqTQ5j_MQEXIDCIAiVTbFNI_CkPMBudj2VnX51qJv9MZ5i-u1KbBsvWYqjEMRKAUdev4PXZVtXXTfdRQEQkgp445iW8rWpfc15rqq3cbUH5qB_jatt6b1WDOpf0x3mbNdc5tuMPtL_KrlX4wDeh8</recordid><startdate>201705</startdate><enddate>201705</enddate><creator>Lynch, David T</creator><creator>Lott, Lisa</creator><creator>Cebe, Katherine</creator><creator>McDonald, J Matthew</creator><creator>Abplanalp, Allison</creator><creator>Tully, Charla</creator><creator>Trujillo-Lopez, Elizabeth</creator><creator>Danaher, Patrick J</creator><general>Oxford University Press</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>3V.</scope><scope>4T-</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88F</scope><scope>88G</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M1Q</scope><scope>M2M</scope><scope>M2P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope></search><sort><creationdate>201705</creationdate><title>Adenovirus-Associated Acute Appendicitis: An Under-Recognized Relationship?</title><author>Lynch, David T ; Lott, Lisa ; Cebe, Katherine ; McDonald, J Matthew ; Abplanalp, Allison ; Tully, Charla ; Trujillo-Lopez, Elizabeth ; Danaher, Patrick J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c372t-c33ddddc564a03977bf3bf966ac44de708b6af38f5ee0fa0e00e4b9cbebf75533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Academic Medical Centers - organization & administration</topic><topic>Acute Disease - epidemiology</topic><topic>Adenoviridae - pathogenicity</topic><topic>Adenovirus Infections, Human - complications</topic><topic>Adenovirus Infections, Human - epidemiology</topic><topic>Adenovirus Vaccines - therapeutic use</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Age</topic><topic>Appendectomy</topic><topic>Appendicitis</topic><topic>Appendicitis - epidemiology</topic><topic>Appendicitis - etiology</topic><topic>Cytomegalovirus</topic><topic>Education - organization & administration</topic><topic>Education - statistics & numerical data</topic><topic>Female</topic><topic>Humans</topic><topic>Infections</topic><topic>Male</topic><topic>Polymerase chain reaction</topic><topic>Respiratory diseases</topic><topic>Texas - epidemiology</topic><topic>Viral infections</topic><topic>Young adults</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lynch, David T</creatorcontrib><creatorcontrib>Lott, Lisa</creatorcontrib><creatorcontrib>Cebe, Katherine</creatorcontrib><creatorcontrib>McDonald, J Matthew</creatorcontrib><creatorcontrib>Abplanalp, Allison</creatorcontrib><creatorcontrib>Tully, Charla</creatorcontrib><creatorcontrib>Trujillo-Lopez, Elizabeth</creatorcontrib><creatorcontrib>Danaher, Patrick J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>Proquest Nursing & Allied Health Source</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Military Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>eLibrary</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Military Database</collection><collection>ProQuest Psychology</collection><collection>Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><jtitle>Military medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lynch, David T</au><au>Lott, Lisa</au><au>Cebe, Katherine</au><au>McDonald, J Matthew</au><au>Abplanalp, Allison</au><au>Tully, Charla</au><au>Trujillo-Lopez, Elizabeth</au><au>Danaher, Patrick J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adenovirus-Associated Acute Appendicitis: An Under-Recognized Relationship?</atitle><jtitle>Military medicine</jtitle><addtitle>Mil Med</addtitle><date>2017-05</date><risdate>2017</risdate><volume>182</volume><issue>5</issue><spage>e1765</spage><epage>e1768</epage><pages>e1765-e1768</pages><issn>0026-4075</issn><eissn>1930-613X</eissn><abstract>Acute appendicitis (AA) is one of the most common causes of a surgical abdomen worldwide, occurring most frequently in those age 10 to 29 years. Adenovirus (ADV) is a rare but reported cause of AA in children and a well-recognized cause of intussusception in infants and young children. Annually, about 36,000 basic military trainees (BMTs) undergo initial training at Joint Base San Antonio Lackland, Texas. Before reintroduction of the ADV 4/7 vaccine in November 2011, one-third of BMTs developed an adenoviral upper respiratory tract infection (URI) during the 8.5 weeks of training. We hypothesized that ADV may be a common cause of AA in the BMT population given their young age and high incidence of adenoviral URIs. The objective of this study was to determine the frequency with which ADV, cytomegalovirus (CMV), Epstein-Barr virus (EBV), and enterovirus were associated with AA in a population of young adults.
This study was a retrospective review of patient charts and existing pathological tissue specimens of all BMTs who underwent appendectomy at the Wilford Hall Medical Center from January 1, 2003, to August 31, 2011. Pathological tissue samples from 112 BMTs were assayed by quantitative polymerase chain reaction (qPCR) and immunohistochemistry (IHC) for viral targets.
ADV DNA was detected in 16 of 112 samples (14%) via qPCR: ADV 4 in 13 cases, ADV B14 in 1 case, and nontypable ADV in 2 cases. IHC was positive in only the ADV B14 case (0.9%). All cases were negative for CMV, EBV, and enterovirus.
By using qPCR, this study demonstrated an association between ADV and AA higher than has been previously reported: ADV was detected in 14% of AA cases in this series versus in only 0.23% of AA cases in previous studies (p < 0.01). There was no evidence of CMV, EBV, or enterovirus association with AA in this study. Comparison of qPCR to IHC shows that histologic analysis may overlook evidence of ADV in appendiceal tissue: qPCR is significantly more sensitive than light microscopy and IHC for detecting ADV in this setting. Because ADV 4 was detected in 81% of those with positive qPCR, the recently licensed live oral ADV vaccine might be useful for primary prevention against AA. Prospective studies evaluating young adults presenting with AA for evidence of infection with ADV are needed to determine if a causal relationship exists.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>29087922</pmid><doi>10.7205/MILMED-D-16-00308</doi><oa>free_for_read</oa></addata></record> |
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subjects | Academic Medical Centers - organization & administration Acute Disease - epidemiology Adenoviridae - pathogenicity Adenovirus Infections, Human - complications Adenovirus Infections, Human - epidemiology Adenovirus Vaccines - therapeutic use Adolescent Adult Age Appendectomy Appendicitis Appendicitis - epidemiology Appendicitis - etiology Cytomegalovirus Education - organization & administration Education - statistics & numerical data Female Humans Infections Male Polymerase chain reaction Respiratory diseases Texas - epidemiology Viral infections Young adults |
title | Adenovirus-Associated Acute Appendicitis: An Under-Recognized Relationship? |
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