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Faster Progression to AIDS and AIDS-Related Death Among Seroincident Individuals Infected With Recombinant HIV-1 A3/CRF02_AG Compared With Sub-subtype A3
Background. Human immunodeficiency virus type 1 (HIV-1) is divided into subtypes and circulating recombinant forms (CRFs) but the impact of subtype/CRF on disease progression is not fully understood. Methods. We determined the HIV-1 subtype/CRF of 152 seroincident individuals from Guinea-Bissau, bas...
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Published in: | The Journal of infectious diseases 2014-03, Vol.209 (5), p.721-728 |
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creator | Palm, Angelica A. Esbjörnsson, Joakim Månsson, Fredrik Kvist, Anders Isberg, Per-Erik Biague, Antonio da Silva, Zacarias José Jansson, Marianne Norrgren, Hans Medstrand, Patrik |
description | Background. Human immunodeficiency virus type 1 (HIV-1) is divided into subtypes and circulating recombinant forms (CRFs) but the impact of subtype/CRF on disease progression is not fully understood. Methods. We determined the HIV-1 subtype/CRF of 152 seroincident individuals from Guinea-Bissau, based on the C2-V3 region of env. Disease progression was measured as time from estimated seroconversion to AIDS and AIDS-related death. Hazard ratios (HRs) were calculated using a Cox proportional hazard model, adjusting for gender and age at seroconversion. Results. The major subtypes/CRFs identified were CRF02_ AG (53%), A3 (29%), and A3/02 (a recombinant of A3 and CRF02_ AG) (13%). Infection with A3/02 was associated with a close to 3-fold increased risk of AIDS and AIDS-related death compared to A3 (HR = 2.6 [P = 0.011] and 2.9 [P = 0.032], respectively). The estimated time from seroconversion to AIDS and AIDS-related death was 5.0 and 8.0 years for A3/02, 6.2 and 9.0 years for CRF02_ AG, and 7.2 and 11.3 years for A3. Conclusion. Our results show that there are differences in disease progression between HIV-1 A-like subtypes/CRFs. Individuals infected with A3/02 have among the fastest progression rates to AIDS reported to date. Determining the HIV-1 subtype of infected individuals could be important in the management of HIV-1 infections. |
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Human immunodeficiency virus type 1 (HIV-1) is divided into subtypes and circulating recombinant forms (CRFs) but the impact of subtype/CRF on disease progression is not fully understood. Methods. We determined the HIV-1 subtype/CRF of 152 seroincident individuals from Guinea-Bissau, based on the C2-V3 region of env. Disease progression was measured as time from estimated seroconversion to AIDS and AIDS-related death. Hazard ratios (HRs) were calculated using a Cox proportional hazard model, adjusting for gender and age at seroconversion. Results. The major subtypes/CRFs identified were CRF02_ AG (53%), A3 (29%), and A3/02 (a recombinant of A3 and CRF02_ AG) (13%). Infection with A3/02 was associated with a close to 3-fold increased risk of AIDS and AIDS-related death compared to A3 (HR = 2.6 [P = 0.011] and 2.9 [P = 0.032], respectively). The estimated time from seroconversion to AIDS and AIDS-related death was 5.0 and 8.0 years for A3/02, 6.2 and 9.0 years for CRF02_ AG, and 7.2 and 11.3 years for A3. Conclusion. Our results show that there are differences in disease progression between HIV-1 A-like subtypes/CRFs. Individuals infected with A3/02 have among the fastest progression rates to AIDS reported to date. Determining the HIV-1 subtype of infected individuals could be important in the management of HIV-1 infections.</description><identifier>ISSN: 0022-1899</identifier><identifier>EISSN: 1537-6613</identifier><identifier>DOI: 10.1093/infdis/jit416</identifier><identifier>PMID: 23935204</identifier><identifier>CODEN: JIDIAQ</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Acquired Immunodeficiency Syndrome - drug therapy ; Acquired Immunodeficiency Syndrome - mortality ; Acquired Immunodeficiency Syndrome - pathology ; Acquired Immunodeficiency Syndrome - virology ; Adult ; AIDS ; Analytical estimating ; Antiretroviral Therapy, Highly Active - methods ; Biological and medical sciences ; CD4-Positive T-Lymphocytes - immunology ; CD4-Positive T-Lymphocytes - virology ; CD8-Positive T-Lymphocytes - immunology ; CD8-Positive T-Lymphocytes - virology ; Disease Progression ; Female ; Fundamental and applied biological sciences. Psychology ; Guinea-Bissau ; HIV ; HIV 1 ; HIV infections ; HIV Infections - drug therapy ; HIV Infections - mortality ; HIV Infections - pathology ; HIV Infections - virology ; HIV-1 - drug effects ; HIV-1 - genetics ; HIV/AIDS ; Human genetics ; Human immunodeficiency virus 1 ; Human viral diseases ; Humans ; Infectious diseases ; Male ; Medical sciences ; Microbiology ; Middle Aged ; Recombination, Genetic - genetics ; T lymphocytes ; Viral diseases ; Viral diseases of the lymphoid tissue and the blood. Aids ; Viral load ; Viruses</subject><ispartof>The Journal of infectious diseases, 2014-03, Vol.209 (5), p.721-728</ispartof><rights>Copyright © 2014 Oxford University Press on behalf of the Infectious Diseases Society of America</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c417t-cc3479ea2055adb072e1b2deb6c1da71a2f418f07110606b0d5ccd9a66090afb3</citedby><cites>FETCH-LOGICAL-c417t-cc3479ea2055adb072e1b2deb6c1da71a2f418f07110606b0d5ccd9a66090afb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/43707976$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/43707976$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,58238,58471</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28363968$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23935204$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Palm, Angelica A.</creatorcontrib><creatorcontrib>Esbjörnsson, Joakim</creatorcontrib><creatorcontrib>Månsson, Fredrik</creatorcontrib><creatorcontrib>Kvist, Anders</creatorcontrib><creatorcontrib>Isberg, Per-Erik</creatorcontrib><creatorcontrib>Biague, Antonio</creatorcontrib><creatorcontrib>da Silva, Zacarias José</creatorcontrib><creatorcontrib>Jansson, Marianne</creatorcontrib><creatorcontrib>Norrgren, Hans</creatorcontrib><creatorcontrib>Medstrand, Patrik</creatorcontrib><title>Faster Progression to AIDS and AIDS-Related Death Among Seroincident Individuals Infected With Recombinant HIV-1 A3/CRF02_AG Compared With Sub-subtype A3</title><title>The Journal of infectious diseases</title><addtitle>J Infect Dis</addtitle><description>Background. Human immunodeficiency virus type 1 (HIV-1) is divided into subtypes and circulating recombinant forms (CRFs) but the impact of subtype/CRF on disease progression is not fully understood. Methods. We determined the HIV-1 subtype/CRF of 152 seroincident individuals from Guinea-Bissau, based on the C2-V3 region of env. Disease progression was measured as time from estimated seroconversion to AIDS and AIDS-related death. Hazard ratios (HRs) were calculated using a Cox proportional hazard model, adjusting for gender and age at seroconversion. Results. The major subtypes/CRFs identified were CRF02_ AG (53%), A3 (29%), and A3/02 (a recombinant of A3 and CRF02_ AG) (13%). Infection with A3/02 was associated with a close to 3-fold increased risk of AIDS and AIDS-related death compared to A3 (HR = 2.6 [P = 0.011] and 2.9 [P = 0.032], respectively). The estimated time from seroconversion to AIDS and AIDS-related death was 5.0 and 8.0 years for A3/02, 6.2 and 9.0 years for CRF02_ AG, and 7.2 and 11.3 years for A3. Conclusion. Our results show that there are differences in disease progression between HIV-1 A-like subtypes/CRFs. Individuals infected with A3/02 have among the fastest progression rates to AIDS reported to date. Determining the HIV-1 subtype of infected individuals could be important in the management of HIV-1 infections.</description><subject>Acquired Immunodeficiency Syndrome - drug therapy</subject><subject>Acquired Immunodeficiency Syndrome - mortality</subject><subject>Acquired Immunodeficiency Syndrome - pathology</subject><subject>Acquired Immunodeficiency Syndrome - virology</subject><subject>Adult</subject><subject>AIDS</subject><subject>Analytical estimating</subject><subject>Antiretroviral Therapy, Highly Active - methods</subject><subject>Biological and medical sciences</subject><subject>CD4-Positive T-Lymphocytes - immunology</subject><subject>CD4-Positive T-Lymphocytes - virology</subject><subject>CD8-Positive T-Lymphocytes - immunology</subject><subject>CD8-Positive T-Lymphocytes - virology</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Guinea-Bissau</subject><subject>HIV</subject><subject>HIV 1</subject><subject>HIV infections</subject><subject>HIV Infections - drug therapy</subject><subject>HIV Infections - mortality</subject><subject>HIV Infections - pathology</subject><subject>HIV Infections - virology</subject><subject>HIV-1 - drug effects</subject><subject>HIV-1 - genetics</subject><subject>HIV/AIDS</subject><subject>Human genetics</subject><subject>Human immunodeficiency virus 1</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microbiology</subject><subject>Middle Aged</subject><subject>Recombination, Genetic - genetics</subject><subject>T lymphocytes</subject><subject>Viral diseases</subject><subject>Viral diseases of the lymphoid tissue and the blood. Aids</subject><subject>Viral load</subject><subject>Viruses</subject><issn>0022-1899</issn><issn>1537-6613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqF0U1v1DAQBmALgejScuQI8gWJS9jxR-z1Mdqy7UqVqHb5OEaO7RSvknixE6T-FP4tLtmWI6cZaR69h3kRekPgIwHFln5orU_Lgx85Ec_QgpRMFkIQ9hwtACgtyEqpM_QqpQMAcCbkS3RGmWIlBb5Avzc6jS7i2xjuokvJhwGPAVfbyz3Wg_27FDvX6dFZfOn0-ANXfRju8N7F4AfjrRtGvB2s_-XtpLuU99aZB_3dZ7xzJvSNH3RW19tvBcEVW653G6B1dYXXoT_q-Gj3U1OkqRnvjy6rC_SizXnu9Wmeo6-bT1_W18XN56vturopDCdyLIxhXCqnKZSltg1I6khDrWuEIVZLomnLyaoFSQgIEA3Y0hirtBCgQLcNO0cf5txjDD8nl8a698m4rtODC1OqieBUUCKB_Z9ypUjJGaeZFjM1MaQUXVsfo-91vK8J1A_F1XNx9Vxc9u9O0VPTO_ukH5vK4P0J6GR010adn5_-uRUTTIlVdm9nd0hjiE93ziRIJQX7A1_Pqwc</recordid><startdate>20140301</startdate><enddate>20140301</enddate><creator>Palm, Angelica A.</creator><creator>Esbjörnsson, Joakim</creator><creator>Månsson, Fredrik</creator><creator>Kvist, Anders</creator><creator>Isberg, Per-Erik</creator><creator>Biague, Antonio</creator><creator>da Silva, Zacarias José</creator><creator>Jansson, Marianne</creator><creator>Norrgren, Hans</creator><creator>Medstrand, Patrik</creator><general>Oxford University Press</general><scope>IQODW</scope><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></search><sort><creationdate>20140301</creationdate><title>Faster Progression to AIDS and AIDS-Related Death Among Seroincident Individuals Infected With Recombinant HIV-1 A3/CRF02_AG Compared With Sub-subtype A3</title><author>Palm, Angelica A. ; Esbjörnsson, Joakim ; Månsson, Fredrik ; Kvist, Anders ; Isberg, Per-Erik ; Biague, Antonio ; da Silva, Zacarias José ; Jansson, Marianne ; Norrgren, Hans ; Medstrand, Patrik</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-cc3479ea2055adb072e1b2deb6c1da71a2f418f07110606b0d5ccd9a66090afb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Acquired Immunodeficiency Syndrome - drug therapy</topic><topic>Acquired Immunodeficiency Syndrome - mortality</topic><topic>Acquired Immunodeficiency Syndrome - pathology</topic><topic>Acquired Immunodeficiency Syndrome - virology</topic><topic>Adult</topic><topic>AIDS</topic><topic>Analytical estimating</topic><topic>Antiretroviral Therapy, Highly Active - methods</topic><topic>Biological and medical sciences</topic><topic>CD4-Positive T-Lymphocytes - immunology</topic><topic>CD4-Positive T-Lymphocytes - virology</topic><topic>CD8-Positive T-Lymphocytes - immunology</topic><topic>CD8-Positive T-Lymphocytes - virology</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Guinea-Bissau</topic><topic>HIV</topic><topic>HIV 1</topic><topic>HIV infections</topic><topic>HIV Infections - drug therapy</topic><topic>HIV Infections - mortality</topic><topic>HIV Infections - pathology</topic><topic>HIV Infections - virology</topic><topic>HIV-1 - drug effects</topic><topic>HIV-1 - genetics</topic><topic>HIV/AIDS</topic><topic>Human genetics</topic><topic>Human immunodeficiency virus 1</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microbiology</topic><topic>Middle Aged</topic><topic>Recombination, Genetic - genetics</topic><topic>T lymphocytes</topic><topic>Viral diseases</topic><topic>Viral diseases of the lymphoid tissue and the blood. Aids</topic><topic>Viral load</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Palm, Angelica A.</creatorcontrib><creatorcontrib>Esbjörnsson, Joakim</creatorcontrib><creatorcontrib>Månsson, Fredrik</creatorcontrib><creatorcontrib>Kvist, Anders</creatorcontrib><creatorcontrib>Isberg, Per-Erik</creatorcontrib><creatorcontrib>Biague, Antonio</creatorcontrib><creatorcontrib>da Silva, Zacarias José</creatorcontrib><creatorcontrib>Jansson, Marianne</creatorcontrib><creatorcontrib>Norrgren, Hans</creatorcontrib><creatorcontrib>Medstrand, Patrik</creatorcontrib><collection>Pascal-Francis</collection><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><jtitle>The Journal of infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Palm, Angelica A.</au><au>Esbjörnsson, Joakim</au><au>Månsson, Fredrik</au><au>Kvist, Anders</au><au>Isberg, Per-Erik</au><au>Biague, Antonio</au><au>da Silva, Zacarias José</au><au>Jansson, Marianne</au><au>Norrgren, Hans</au><au>Medstrand, Patrik</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Faster Progression to AIDS and AIDS-Related Death Among Seroincident Individuals Infected With Recombinant HIV-1 A3/CRF02_AG Compared With Sub-subtype A3</atitle><jtitle>The Journal of infectious diseases</jtitle><addtitle>J Infect Dis</addtitle><date>2014-03-01</date><risdate>2014</risdate><volume>209</volume><issue>5</issue><spage>721</spage><epage>728</epage><pages>721-728</pages><issn>0022-1899</issn><eissn>1537-6613</eissn><coden>JIDIAQ</coden><abstract>Background. Human immunodeficiency virus type 1 (HIV-1) is divided into subtypes and circulating recombinant forms (CRFs) but the impact of subtype/CRF on disease progression is not fully understood. Methods. We determined the HIV-1 subtype/CRF of 152 seroincident individuals from Guinea-Bissau, based on the C2-V3 region of env. Disease progression was measured as time from estimated seroconversion to AIDS and AIDS-related death. Hazard ratios (HRs) were calculated using a Cox proportional hazard model, adjusting for gender and age at seroconversion. Results. The major subtypes/CRFs identified were CRF02_ AG (53%), A3 (29%), and A3/02 (a recombinant of A3 and CRF02_ AG) (13%). Infection with A3/02 was associated with a close to 3-fold increased risk of AIDS and AIDS-related death compared to A3 (HR = 2.6 [P = 0.011] and 2.9 [P = 0.032], respectively). The estimated time from seroconversion to AIDS and AIDS-related death was 5.0 and 8.0 years for A3/02, 6.2 and 9.0 years for CRF02_ AG, and 7.2 and 11.3 years for A3. Conclusion. Our results show that there are differences in disease progression between HIV-1 A-like subtypes/CRFs. Individuals infected with A3/02 have among the fastest progression rates to AIDS reported to date. Determining the HIV-1 subtype of infected individuals could be important in the management of HIV-1 infections.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>23935204</pmid><doi>10.1093/infdis/jit416</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acquired Immunodeficiency Syndrome - drug therapy Acquired Immunodeficiency Syndrome - mortality Acquired Immunodeficiency Syndrome - pathology Acquired Immunodeficiency Syndrome - virology Adult AIDS Analytical estimating Antiretroviral Therapy, Highly Active - methods Biological and medical sciences CD4-Positive T-Lymphocytes - immunology CD4-Positive T-Lymphocytes - virology CD8-Positive T-Lymphocytes - immunology CD8-Positive T-Lymphocytes - virology Disease Progression Female Fundamental and applied biological sciences. Psychology Guinea-Bissau HIV HIV 1 HIV infections HIV Infections - drug therapy HIV Infections - mortality HIV Infections - pathology HIV Infections - virology HIV-1 - drug effects HIV-1 - genetics HIV/AIDS Human genetics Human immunodeficiency virus 1 Human viral diseases Humans Infectious diseases Male Medical sciences Microbiology Middle Aged Recombination, Genetic - genetics T lymphocytes Viral diseases Viral diseases of the lymphoid tissue and the blood. Aids Viral load Viruses |
title | Faster Progression to AIDS and AIDS-Related Death Among Seroincident Individuals Infected With Recombinant HIV-1 A3/CRF02_AG Compared With Sub-subtype A3 |
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