Community HIV‐1 drug resistance is associated with transmitted drug resistance

Objectives As community viral load (CVL) measurements are associated with the incidence of new HIV‐1 infections in a population, we hypothesized that similarly measured community drug resistance (CDR) could predict the prevalence of transmitted drug resistance (TDR). Methods Between 2001 and 2011, t...

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Veröffentlicht in:HIV medicine 2014-07, Vol.15 (6), p.339-346
Hauptverfasser: Tilghman, MW, Pérez‐Santiago, J, Osorio, G, Little, SJ, Richman, DD, Mathews, WC, Haubrich, RH, Smith, DM
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container_end_page 346
container_issue 6
container_start_page 339
container_title HIV medicine
container_volume 15
creator Tilghman, MW
Pérez‐Santiago, J
Osorio, G
Little, SJ
Richman, DD
Mathews, WC
Haubrich, RH
Smith, DM
description Objectives As community viral load (CVL) measurements are associated with the incidence of new HIV‐1 infections in a population, we hypothesized that similarly measured community drug resistance (CDR) could predict the prevalence of transmitted drug resistance (TDR). Methods Between 2001 and 2011, the prevalences of HIV‐1 drug resistance for patients with established infection receiving HIV care (i.e. CDR) and TDR in recently infected patients were determined in San Diego. At each position in HIV‐1 reverse transcriptase (RT) and protease (pro), drug resistance was evaluated both as the overall prevalence of resistance‐associated mutations and by weighting each resistance position to the concurrent viral load of the patient and its proportion to the total viral load of the clinic (CVL). The weighting was the proportion of the CVL associated with patients identified with resistance at each residue. Spearman ranked correlation coefficients were used to determine associations between CDR and TDR. Results We analysed 1088 resistance tests for 971 clinic patients and baseline resistance tests for 542 recently infected patients. CDR at positions 30, 46, and 88 in pro was associated with TDR between 2001 and 2011. When CDR was weighted by the viral load of patients, CDR was associated with TDR at position 103 in RT. Each of these associations was corroborated at least once using shorter measurement intervals. Conclusions Despite evaluation of a limited percentage of chronically infected patients in San Diego, CDR correlated with TDR at key resistance positions and therefore may be a useful tool with which to predict the prevalence of TDR.
doi_str_mv 10.1111/hiv.12122
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Methods Between 2001 and 2011, the prevalences of HIV‐1 drug resistance for patients with established infection receiving HIV care (i.e. CDR) and TDR in recently infected patients were determined in San Diego. At each position in HIV‐1 reverse transcriptase (RT) and protease (pro), drug resistance was evaluated both as the overall prevalence of resistance‐associated mutations and by weighting each resistance position to the concurrent viral load of the patient and its proportion to the total viral load of the clinic (CVL). The weighting was the proportion of the CVL associated with patients identified with resistance at each residue. Spearman ranked correlation coefficients were used to determine associations between CDR and TDR. Results We analysed 1088 resistance tests for 971 clinic patients and baseline resistance tests for 542 recently infected patients. CDR at positions 30, 46, and 88 in pro was associated with TDR between 2001 and 2011. When CDR was weighted by the viral load of patients, CDR was associated with TDR at position 103 in RT. Each of these associations was corroborated at least once using shorter measurement intervals. Conclusions Despite evaluation of a limited percentage of chronically infected patients in San Diego, CDR correlated with TDR at key resistance positions and therefore may be a useful tool with which to predict the prevalence of TDR.</description><identifier>ISSN: 1464-2662</identifier><identifier>EISSN: 1468-1293</identifier><identifier>DOI: 10.1111/hiv.12122</identifier><identifier>PMID: 24417811</identifier><language>eng</language><publisher>England</publisher><subject>Adult ; Analysis of Variance ; Anti-HIV Agents - therapeutic use ; California - epidemiology ; CD4 Lymphocyte Count ; Cohort Studies ; Drug Resistance, Viral - genetics ; Female ; genotype ; highly active antiretroviral therapy ; HIV ; HIV Infections - drug therapy ; HIV Infections - epidemiology ; HIV Infections - genetics ; HIV Infections - virology ; HIV Protease - genetics ; HIV-1 - drug effects ; Human immunodeficiency virus 1 ; Humans ; Male ; Middle Aged ; Mutation ; Prevalence ; RNA, Viral - genetics ; RNA-Directed DNA Polymerase - genetics ; viral drug resistance ; Viral Load</subject><ispartof>HIV medicine, 2014-07, Vol.15 (6), p.339-346</ispartof><rights>2014 British HIV Association</rights><rights>2014 British HIV Association.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4482-69487ccd7b9ba4c596461b1b0bed039b5dd397ab2b594d6ca2db5d25f0345b243</citedby><cites>FETCH-LOGICAL-c4482-69487ccd7b9ba4c596461b1b0bed039b5dd397ab2b594d6ca2db5d25f0345b243</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fhiv.12122$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fhiv.12122$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24417811$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tilghman, MW</creatorcontrib><creatorcontrib>Pérez‐Santiago, J</creatorcontrib><creatorcontrib>Osorio, G</creatorcontrib><creatorcontrib>Little, SJ</creatorcontrib><creatorcontrib>Richman, DD</creatorcontrib><creatorcontrib>Mathews, WC</creatorcontrib><creatorcontrib>Haubrich, RH</creatorcontrib><creatorcontrib>Smith, DM</creatorcontrib><title>Community HIV‐1 drug resistance is associated with transmitted drug resistance</title><title>HIV medicine</title><addtitle>HIV Med</addtitle><description>Objectives As community viral load (CVL) measurements are associated with the incidence of new HIV‐1 infections in a population, we hypothesized that similarly measured community drug resistance (CDR) could predict the prevalence of transmitted drug resistance (TDR). Methods Between 2001 and 2011, the prevalences of HIV‐1 drug resistance for patients with established infection receiving HIV care (i.e. CDR) and TDR in recently infected patients were determined in San Diego. At each position in HIV‐1 reverse transcriptase (RT) and protease (pro), drug resistance was evaluated both as the overall prevalence of resistance‐associated mutations and by weighting each resistance position to the concurrent viral load of the patient and its proportion to the total viral load of the clinic (CVL). The weighting was the proportion of the CVL associated with patients identified with resistance at each residue. Spearman ranked correlation coefficients were used to determine associations between CDR and TDR. Results We analysed 1088 resistance tests for 971 clinic patients and baseline resistance tests for 542 recently infected patients. CDR at positions 30, 46, and 88 in pro was associated with TDR between 2001 and 2011. When CDR was weighted by the viral load of patients, CDR was associated with TDR at position 103 in RT. Each of these associations was corroborated at least once using shorter measurement intervals. Conclusions Despite evaluation of a limited percentage of chronically infected patients in San Diego, CDR correlated with TDR at key resistance positions and therefore may be a useful tool with which to predict the prevalence of TDR.</description><subject>Adult</subject><subject>Analysis of Variance</subject><subject>Anti-HIV Agents - therapeutic use</subject><subject>California - epidemiology</subject><subject>CD4 Lymphocyte Count</subject><subject>Cohort Studies</subject><subject>Drug Resistance, Viral - genetics</subject><subject>Female</subject><subject>genotype</subject><subject>highly active antiretroviral therapy</subject><subject>HIV</subject><subject>HIV Infections - drug therapy</subject><subject>HIV Infections - epidemiology</subject><subject>HIV Infections - genetics</subject><subject>HIV Infections - virology</subject><subject>HIV Protease - genetics</subject><subject>HIV-1 - drug effects</subject><subject>Human immunodeficiency virus 1</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mutation</subject><subject>Prevalence</subject><subject>RNA, Viral - genetics</subject><subject>RNA-Directed DNA Polymerase - genetics</subject><subject>viral drug resistance</subject><subject>Viral Load</subject><issn>1464-2662</issn><issn>1468-1293</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkctKAzEUhoMo3he-gMxSF9PmcjKXjSDFGwi6ULcht9rIXOpkpqU7H8Fn9ElMOyoqCGaTcPLx8Sc_QgcED0hYw4mbDQgllK6hbQJJFhOas_XVGWKaJHQL7Xj_hDFJWY430RYFIGlGyDa6HdVl2VWuXUSXVw9vL68kMk33GDXWO9_KStvI-Uh6X2snW2uiuWsnUdvIypeuXQ5-4XtoYywLb_c_9l10f352N7qMr28urkan17EGyGic5JClWptU5UqC5nkCCVFEYWUNZrnixrA8lYoqnoNJtKQmzCgfYwZcUWC76KT3TjtVWqNtFUIVYtq4UjYLUUsnft5UbiIe65kAzHkKaRAcfQia-rmzvhWl89oWhaxs3XlBOGBKGQb2D5Tx8P0JLGMd96huau8bO_5KRLBYliVCWWJVVmAPvz_hi_xsJwDDHpi7wi7-NolQXa98B8kFoDg</recordid><startdate>201407</startdate><enddate>201407</enddate><creator>Tilghman, MW</creator><creator>Pérez‐Santiago, J</creator><creator>Osorio, G</creator><creator>Little, SJ</creator><creator>Richman, DD</creator><creator>Mathews, WC</creator><creator>Haubrich, RH</creator><creator>Smith, DM</creator><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>7U9</scope><scope>H94</scope><scope>5PM</scope></search><sort><creationdate>201407</creationdate><title>Community HIV‐1 drug resistance is associated with transmitted drug resistance</title><author>Tilghman, MW ; Pérez‐Santiago, J ; Osorio, G ; Little, SJ ; Richman, DD ; Mathews, WC ; Haubrich, RH ; Smith, DM</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4482-69487ccd7b9ba4c596461b1b0bed039b5dd397ab2b594d6ca2db5d25f0345b243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>Analysis of Variance</topic><topic>Anti-HIV Agents - therapeutic use</topic><topic>California - epidemiology</topic><topic>CD4 Lymphocyte Count</topic><topic>Cohort Studies</topic><topic>Drug Resistance, Viral - genetics</topic><topic>Female</topic><topic>genotype</topic><topic>highly active antiretroviral therapy</topic><topic>HIV</topic><topic>HIV Infections - drug therapy</topic><topic>HIV Infections - epidemiology</topic><topic>HIV Infections - genetics</topic><topic>HIV Infections - virology</topic><topic>HIV Protease - genetics</topic><topic>HIV-1 - drug effects</topic><topic>Human immunodeficiency virus 1</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Mutation</topic><topic>Prevalence</topic><topic>RNA, Viral - genetics</topic><topic>RNA-Directed DNA Polymerase - genetics</topic><topic>viral drug resistance</topic><topic>Viral Load</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tilghman, MW</creatorcontrib><creatorcontrib>Pérez‐Santiago, J</creatorcontrib><creatorcontrib>Osorio, G</creatorcontrib><creatorcontrib>Little, SJ</creatorcontrib><creatorcontrib>Richman, DD</creatorcontrib><creatorcontrib>Mathews, WC</creatorcontrib><creatorcontrib>Haubrich, RH</creatorcontrib><creatorcontrib>Smith, DM</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>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>HIV medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tilghman, MW</au><au>Pérez‐Santiago, J</au><au>Osorio, G</au><au>Little, SJ</au><au>Richman, DD</au><au>Mathews, WC</au><au>Haubrich, RH</au><au>Smith, DM</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Community HIV‐1 drug resistance is associated with transmitted drug resistance</atitle><jtitle>HIV medicine</jtitle><addtitle>HIV Med</addtitle><date>2014-07</date><risdate>2014</risdate><volume>15</volume><issue>6</issue><spage>339</spage><epage>346</epage><pages>339-346</pages><issn>1464-2662</issn><eissn>1468-1293</eissn><abstract>Objectives As community viral load (CVL) measurements are associated with the incidence of new HIV‐1 infections in a population, we hypothesized that similarly measured community drug resistance (CDR) could predict the prevalence of transmitted drug resistance (TDR). Methods Between 2001 and 2011, the prevalences of HIV‐1 drug resistance for patients with established infection receiving HIV care (i.e. CDR) and TDR in recently infected patients were determined in San Diego. At each position in HIV‐1 reverse transcriptase (RT) and protease (pro), drug resistance was evaluated both as the overall prevalence of resistance‐associated mutations and by weighting each resistance position to the concurrent viral load of the patient and its proportion to the total viral load of the clinic (CVL). The weighting was the proportion of the CVL associated with patients identified with resistance at each residue. Spearman ranked correlation coefficients were used to determine associations between CDR and TDR. Results We analysed 1088 resistance tests for 971 clinic patients and baseline resistance tests for 542 recently infected patients. CDR at positions 30, 46, and 88 in pro was associated with TDR between 2001 and 2011. When CDR was weighted by the viral load of patients, CDR was associated with TDR at position 103 in RT. Each of these associations was corroborated at least once using shorter measurement intervals. Conclusions Despite evaluation of a limited percentage of chronically infected patients in San Diego, CDR correlated with TDR at key resistance positions and therefore may be a useful tool with which to predict the prevalence of TDR.</abstract><cop>England</cop><pmid>24417811</pmid><doi>10.1111/hiv.12122</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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ispartof HIV medicine, 2014-07, Vol.15 (6), p.339-346
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language eng
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source MEDLINE; Access via Wiley Online Library; EZB-FREE-00999 freely available EZB journals; Wiley Online Library (Open Access Collection)
subjects Adult
Analysis of Variance
Anti-HIV Agents - therapeutic use
California - epidemiology
CD4 Lymphocyte Count
Cohort Studies
Drug Resistance, Viral - genetics
Female
genotype
highly active antiretroviral therapy
HIV
HIV Infections - drug therapy
HIV Infections - epidemiology
HIV Infections - genetics
HIV Infections - virology
HIV Protease - genetics
HIV-1 - drug effects
Human immunodeficiency virus 1
Humans
Male
Middle Aged
Mutation
Prevalence
RNA, Viral - genetics
RNA-Directed DNA Polymerase - genetics
viral drug resistance
Viral Load
title Community HIV‐1 drug resistance is associated with transmitted drug resistance
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