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Natural History of HPV Infection across the Lifespan: Role of Viral Latency
Large-scale epidemiologic studies have been invaluable for elaboration of the causal relationship between persistent detection of genital human papillomavirus (HPV) infection and the development of invasive cervical cancer. However, these studies provide limited data to adequately inform models of t...
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Published in: | Viruses 2017-09, Vol.9 (10), p.267 |
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description | Large-scale epidemiologic studies have been invaluable for elaboration of the causal relationship between persistent detection of genital human papillomavirus (HPV) infection and the development of invasive cervical cancer. However, these studies provide limited data to adequately inform models of the individual-level natural history of HPV infection over the course of a lifetime, and particularly ignore the biological distinction between HPV-negative tests and lack of infection (i.e., the possibility of latent, undetectable HPV infection). Using data from more recent epidemiological studies, this review proposes an alternative model of the natural history of genital HPV across the life span. We argue that a more complete elucidation of the age-specific probabilities of the alternative transitions is highly relevant with the expanded use of HPV testing in cervical cancer screening. With routine HPV testing in cervical cancer screening, women commonly transition in and out of HPV detectability, raising concerns for the patient and the provider regarding the source of the positive test result, its prognosis, and effective strategies to prevent future recurrence. Alternative study designs and analytic frameworks are proposed to better understand the frequency and determinants of these transition pathways. |
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However, these studies provide limited data to adequately inform models of the individual-level natural history of HPV infection over the course of a lifetime, and particularly ignore the biological distinction between HPV-negative tests and lack of infection (i.e., the possibility of latent, undetectable HPV infection). Using data from more recent epidemiological studies, this review proposes an alternative model of the natural history of genital HPV across the life span. We argue that a more complete elucidation of the age-specific probabilities of the alternative transitions is highly relevant with the expanded use of HPV testing in cervical cancer screening. With routine HPV testing in cervical cancer screening, women commonly transition in and out of HPV detectability, raising concerns for the patient and the provider regarding the source of the positive test result, its prognosis, and effective strategies to prevent future recurrence. Alternative study designs and analytic frameworks are proposed to better understand the frequency and determinants of these transition pathways.</description><identifier>ISSN: 1999-4915</identifier><identifier>EISSN: 1999-4915</identifier><identifier>DOI: 10.3390/v9100267</identifier><identifier>PMID: 28934151</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Adult ; Age ; Age Factors ; Cancer screening ; Cervical cancer ; Cervical Intraepithelial Neoplasia - diagnosis ; Cervical Intraepithelial Neoplasia - epidemiology ; Cervical Intraepithelial Neoplasia - virology ; Cervix ; Female ; Human papillomavirus ; Human Papillomavirus DNA Tests ; Humans ; Infections ; Invasiveness ; Latency ; Life span ; Longevity ; Medical screening ; Middle Aged ; Natural history ; Papillomaviridae - physiology ; papillomavirus ; Papillomavirus Infections - complications ; Papillomavirus Infections - diagnosis ; Papillomavirus Infections - epidemiology ; Papillomavirus Infections - prevention & control ; Papillomavirus Vaccines - therapeutic use ; Prognosis ; Recurrence ; Review ; Risk Factors ; Studies ; Uterine Cervical Neoplasms - diagnosis ; Uterine Cervical Neoplasms - epidemiology ; Uterine Cervical Neoplasms - virology ; Virus Latency</subject><ispartof>Viruses, 2017-09, Vol.9 (10), p.267</ispartof><rights>Copyright MDPI AG 2017</rights><rights>2017 by the authors. 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c532t-f531be05af7edbb377153a7795f1fc317dd09c1ee4bcc32ccb0e09cd2f0e3793</citedby><cites>FETCH-LOGICAL-c532t-f531be05af7edbb377153a7795f1fc317dd09c1ee4bcc32ccb0e09cd2f0e3793</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1965584038/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1965584038?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28934151$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gravitt, Patti E</creatorcontrib><creatorcontrib>Winer, Rachel L</creatorcontrib><title>Natural History of HPV Infection across the Lifespan: Role of Viral Latency</title><title>Viruses</title><addtitle>Viruses</addtitle><description>Large-scale epidemiologic studies have been invaluable for elaboration of the causal relationship between persistent detection of genital human papillomavirus (HPV) infection and the development of invasive cervical cancer. However, these studies provide limited data to adequately inform models of the individual-level natural history of HPV infection over the course of a lifetime, and particularly ignore the biological distinction between HPV-negative tests and lack of infection (i.e., the possibility of latent, undetectable HPV infection). Using data from more recent epidemiological studies, this review proposes an alternative model of the natural history of genital HPV across the life span. We argue that a more complete elucidation of the age-specific probabilities of the alternative transitions is highly relevant with the expanded use of HPV testing in cervical cancer screening. With routine HPV testing in cervical cancer screening, women commonly transition in and out of HPV detectability, raising concerns for the patient and the provider regarding the source of the positive test result, its prognosis, and effective strategies to prevent future recurrence. Alternative study designs and analytic frameworks are proposed to better understand the frequency and determinants of these transition pathways.</description><subject>Adult</subject><subject>Age</subject><subject>Age Factors</subject><subject>Cancer screening</subject><subject>Cervical cancer</subject><subject>Cervical Intraepithelial Neoplasia - diagnosis</subject><subject>Cervical Intraepithelial Neoplasia - epidemiology</subject><subject>Cervical Intraepithelial Neoplasia - virology</subject><subject>Cervix</subject><subject>Female</subject><subject>Human papillomavirus</subject><subject>Human Papillomavirus DNA Tests</subject><subject>Humans</subject><subject>Infections</subject><subject>Invasiveness</subject><subject>Latency</subject><subject>Life span</subject><subject>Longevity</subject><subject>Medical screening</subject><subject>Middle Aged</subject><subject>Natural history</subject><subject>Papillomaviridae - physiology</subject><subject>papillomavirus</subject><subject>Papillomavirus Infections - complications</subject><subject>Papillomavirus Infections - diagnosis</subject><subject>Papillomavirus Infections - epidemiology</subject><subject>Papillomavirus Infections - prevention & control</subject><subject>Papillomavirus Vaccines - therapeutic use</subject><subject>Prognosis</subject><subject>Recurrence</subject><subject>Review</subject><subject>Risk Factors</subject><subject>Studies</subject><subject>Uterine Cervical Neoplasms - diagnosis</subject><subject>Uterine Cervical Neoplasms - epidemiology</subject><subject>Uterine Cervical Neoplasms - virology</subject><subject>Virus Latency</subject><issn>1999-4915</issn><issn>1999-4915</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkU1rGzEQhkVpqZO00F8QFnrJxam0klarHAohJLGpSUsJuQpJO7Jl1itX0gb877Obrzo5SYwePczMi9A3gk8plfjHvSQYl5X4gA6IlHLKJOEf9-4TdJjSGuOqklh8RpOylpQRTg7Qrxud-6jbYuZTDnFXBFfM_twV886BzT50hbYxpFTkFRQL7yBtdXdW_A0tjOidH_8udIbO7r6gT063Cb4-n0fo9ury9mI2Xfy-nl-cL6aW0zJPHafEAObaCWiMoUIQTrUQkjviLCWiabC0BIAZa2lprcEwFJrSYaBC0iM0f9I2Qa_VNvqNjjsVtFePhRCXSsfsbQtKN8C1YKV2ljEjuBElYcxy19QgbGUG188n17Y3G2gsdHkY6I307UvnV2oZ7hWvJKnI2MzJsyCGfz2krDY-WWhb3UHokyKSDbnUtRzR7-_QdehjN2xqoCrOa4Zp_V_4uPYI7rUZgtUYtnoJe0CP95t_BV_SpQ9u4qRo</recordid><startdate>20170921</startdate><enddate>20170921</enddate><creator>Gravitt, Patti E</creator><creator>Winer, Rachel L</creator><general>MDPI AG</general><general>MDPI</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>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20170921</creationdate><title>Natural History of HPV Infection across the Lifespan: Role of Viral Latency</title><author>Gravitt, Patti E ; 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However, these studies provide limited data to adequately inform models of the individual-level natural history of HPV infection over the course of a lifetime, and particularly ignore the biological distinction between HPV-negative tests and lack of infection (i.e., the possibility of latent, undetectable HPV infection). Using data from more recent epidemiological studies, this review proposes an alternative model of the natural history of genital HPV across the life span. We argue that a more complete elucidation of the age-specific probabilities of the alternative transitions is highly relevant with the expanded use of HPV testing in cervical cancer screening. With routine HPV testing in cervical cancer screening, women commonly transition in and out of HPV detectability, raising concerns for the patient and the provider regarding the source of the positive test result, its prognosis, and effective strategies to prevent future recurrence. 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subjects | Adult Age Age Factors Cancer screening Cervical cancer Cervical Intraepithelial Neoplasia - diagnosis Cervical Intraepithelial Neoplasia - epidemiology Cervical Intraepithelial Neoplasia - virology Cervix Female Human papillomavirus Human Papillomavirus DNA Tests Humans Infections Invasiveness Latency Life span Longevity Medical screening Middle Aged Natural history Papillomaviridae - physiology papillomavirus Papillomavirus Infections - complications Papillomavirus Infections - diagnosis Papillomavirus Infections - epidemiology Papillomavirus Infections - prevention & control Papillomavirus Vaccines - therapeutic use Prognosis Recurrence Review Risk Factors Studies Uterine Cervical Neoplasms - diagnosis Uterine Cervical Neoplasms - epidemiology Uterine Cervical Neoplasms - virology Virus Latency |
title | Natural History of HPV Infection across the Lifespan: Role of Viral Latency |
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