Long-term exposure to tenofovir continuously decrease renal function in HIV-1-infected patients with low body weight: results from 10 years of follow-up
To investigate the effect of long-term tenofovir disoproxil fumarate (TDF) use on renal function, especially in patients with low body weight who are vulnerable to TDF nephrotoxicity. A single-center, observational study in Tokyo, Japan. We performed a 10 years cohort study of 792 HIV-1-infected pat...
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creator | NISHIJIMA, Takeshi KAWASAKI, Yohei TSUKADA, Kunihisa TERUYA, Katsuji KIKUCHI, Yoshimi GATANAGA, Hiroyuki OKA, Shinichi TANAKA, Noriko MIZUSHIMA, Daisuke AOKI, Takahiro WATANABE, Koji EI KINAI HONDA, Haruhito YAZAKI, Hirohisa TANUMA, Junko |
description | To investigate the effect of long-term tenofovir disoproxil fumarate (TDF) use on renal function, especially in patients with low body weight who are vulnerable to TDF nephrotoxicity.
A single-center, observational study in Tokyo, Japan.
We performed a 10 years cohort study of 792 HIV-1-infected patients. The effect of long-term TDF use on estimated glomerular filtration rate (eGFR) was investigated on treatment-naive patients who started TDF-containing antiretroviral therapy (n = 422) and those who started abacavir-containing antiretroviral therapy as control (n = 370). Three renal endpoints were examined by the logistic regression model: decrement in eGFR of higher than 10 ml/min per 1.73 m relative to the baseline, more than 25% decrement in eGFR, and eGFR lower than 60 ml/min per 1.73 m at least 3 months apart. The loss in eGFR was estimated using linear mixed models for repeated measures.
The median weight at baseline was 63 kg. TDF use increased the risk of all three renal outcomes compared with the control group: higher than 10 ml/min per 1.73 m decrement in eGFR [adjusted odds ratio (OR) = 2.1, 95% confidence interval (CI) 1.45-3.14, P < 0.001], more than 25% decrement (adjusted OR = 2.1, 95% CI 1.50-2.90, P < 0.001), and eGFR lower than 60 ml/min per 1.73 m at least 3 months apart (adjusted OR = 3.9, 95% CI 1.62-9.36, P = 0.002). The cumulative mean loss relative to the control after 1, 2, 3, 4, and 5 years of TDF exposure was -3.8, -3.6, -5.5, -6.6, and -10.3 ml/min per 1.73 m, respectively, indicating that the loss in eGFR increased over time (P < 0.001).
In this cohort of patients with low body weight, TDF exposure increased the risk of renal dysfunction. Furthermore, the loss in eGFR relative to the control increased continuously up to 5 years. |
doi_str_mv | 10.1097/QAD.0000000000000347 |
format | Article |
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A single-center, observational study in Tokyo, Japan.
We performed a 10 years cohort study of 792 HIV-1-infected patients. The effect of long-term TDF use on estimated glomerular filtration rate (eGFR) was investigated on treatment-naive patients who started TDF-containing antiretroviral therapy (n = 422) and those who started abacavir-containing antiretroviral therapy as control (n = 370). Three renal endpoints were examined by the logistic regression model: decrement in eGFR of higher than 10 ml/min per 1.73 m relative to the baseline, more than 25% decrement in eGFR, and eGFR lower than 60 ml/min per 1.73 m at least 3 months apart. The loss in eGFR was estimated using linear mixed models for repeated measures.
The median weight at baseline was 63 kg. TDF use increased the risk of all three renal outcomes compared with the control group: higher than 10 ml/min per 1.73 m decrement in eGFR [adjusted odds ratio (OR) = 2.1, 95% confidence interval (CI) 1.45-3.14, P < 0.001], more than 25% decrement (adjusted OR = 2.1, 95% CI 1.50-2.90, P < 0.001), and eGFR lower than 60 ml/min per 1.73 m at least 3 months apart (adjusted OR = 3.9, 95% CI 1.62-9.36, P = 0.002). The cumulative mean loss relative to the control after 1, 2, 3, 4, and 5 years of TDF exposure was -3.8, -3.6, -5.5, -6.6, and -10.3 ml/min per 1.73 m, respectively, indicating that the loss in eGFR increased over time (P < 0.001).
In this cohort of patients with low body weight, TDF exposure increased the risk of renal dysfunction. Furthermore, the loss in eGFR relative to the control increased continuously up to 5 years.</description><identifier>ISSN: 0269-9370</identifier><identifier>EISSN: 1473-5571</identifier><identifier>DOI: 10.1097/QAD.0000000000000347</identifier><identifier>PMID: 25259702</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Adenine - adverse effects ; Adenine - analogs & derivatives ; Adenine - therapeutic use ; Adult ; AIDS/HIV ; Anti-HIV Agents - adverse effects ; Anti-HIV Agents - therapeutic use ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Antiviral agents ; Biological and medical sciences ; Body Weight ; Cohort Studies ; Female ; Glomerular Filtration Rate - drug effects ; HIV Infections - complications ; HIV Infections - drug therapy ; HIV Infections - virology ; HIV-1 - isolation & purification ; Human immunodeficiency virus ; Human viral diseases ; Humans ; Immunodeficiencies ; Immunodeficiencies. Immunoglobulinopathies ; Immunopathology ; Infectious diseases ; Longitudinal Studies ; Male ; Medical sciences ; Organophosphonates - adverse effects ; Organophosphonates - therapeutic use ; Pharmacology. Drug treatments ; Renal Insufficiency - chemically induced ; Tenofovir ; Tokyo ; Viral diseases ; Viral diseases of the lymphoid tissue and the blood. Aids</subject><ispartof>AIDS (London), 2014-08, Vol.28 (13), p.1903-1910</ispartof><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c319t-5b3b4115ada993ab1f4660a54564841e21d1daa2d5d2b1a75b074cd33c015f2e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27915,27916</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28807165$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25259702$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>NISHIJIMA, Takeshi</creatorcontrib><creatorcontrib>KAWASAKI, Yohei</creatorcontrib><creatorcontrib>TSUKADA, Kunihisa</creatorcontrib><creatorcontrib>TERUYA, Katsuji</creatorcontrib><creatorcontrib>KIKUCHI, Yoshimi</creatorcontrib><creatorcontrib>GATANAGA, Hiroyuki</creatorcontrib><creatorcontrib>OKA, Shinichi</creatorcontrib><creatorcontrib>TANAKA, Noriko</creatorcontrib><creatorcontrib>MIZUSHIMA, Daisuke</creatorcontrib><creatorcontrib>AOKI, Takahiro</creatorcontrib><creatorcontrib>WATANABE, Koji</creatorcontrib><creatorcontrib>EI KINAI</creatorcontrib><creatorcontrib>HONDA, Haruhito</creatorcontrib><creatorcontrib>YAZAKI, Hirohisa</creatorcontrib><creatorcontrib>TANUMA, Junko</creatorcontrib><title>Long-term exposure to tenofovir continuously decrease renal function in HIV-1-infected patients with low body weight: results from 10 years of follow-up</title><title>AIDS (London)</title><addtitle>AIDS</addtitle><description>To investigate the effect of long-term tenofovir disoproxil fumarate (TDF) use on renal function, especially in patients with low body weight who are vulnerable to TDF nephrotoxicity.
A single-center, observational study in Tokyo, Japan.
We performed a 10 years cohort study of 792 HIV-1-infected patients. The effect of long-term TDF use on estimated glomerular filtration rate (eGFR) was investigated on treatment-naive patients who started TDF-containing antiretroviral therapy (n = 422) and those who started abacavir-containing antiretroviral therapy as control (n = 370). Three renal endpoints were examined by the logistic regression model: decrement in eGFR of higher than 10 ml/min per 1.73 m relative to the baseline, more than 25% decrement in eGFR, and eGFR lower than 60 ml/min per 1.73 m at least 3 months apart. The loss in eGFR was estimated using linear mixed models for repeated measures.
The median weight at baseline was 63 kg. TDF use increased the risk of all three renal outcomes compared with the control group: higher than 10 ml/min per 1.73 m decrement in eGFR [adjusted odds ratio (OR) = 2.1, 95% confidence interval (CI) 1.45-3.14, P < 0.001], more than 25% decrement (adjusted OR = 2.1, 95% CI 1.50-2.90, P < 0.001), and eGFR lower than 60 ml/min per 1.73 m at least 3 months apart (adjusted OR = 3.9, 95% CI 1.62-9.36, P = 0.002). The cumulative mean loss relative to the control after 1, 2, 3, 4, and 5 years of TDF exposure was -3.8, -3.6, -5.5, -6.6, and -10.3 ml/min per 1.73 m, respectively, indicating that the loss in eGFR increased over time (P < 0.001).
In this cohort of patients with low body weight, TDF exposure increased the risk of renal dysfunction. Furthermore, the loss in eGFR relative to the control increased continuously up to 5 years.</description><subject>Adenine - adverse effects</subject><subject>Adenine - analogs & derivatives</subject><subject>Adenine - therapeutic use</subject><subject>Adult</subject><subject>AIDS/HIV</subject><subject>Anti-HIV Agents - adverse effects</subject><subject>Anti-HIV Agents - therapeutic use</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Antiviral agents</subject><subject>Biological and medical sciences</subject><subject>Body Weight</subject><subject>Cohort Studies</subject><subject>Female</subject><subject>Glomerular Filtration Rate - drug effects</subject><subject>HIV Infections - complications</subject><subject>HIV Infections - drug therapy</subject><subject>HIV Infections - virology</subject><subject>HIV-1 - isolation & purification</subject><subject>Human immunodeficiency virus</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Immunodeficiencies</subject><subject>Immunodeficiencies. Immunoglobulinopathies</subject><subject>Immunopathology</subject><subject>Infectious diseases</subject><subject>Longitudinal Studies</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Organophosphonates - adverse effects</subject><subject>Organophosphonates - therapeutic use</subject><subject>Pharmacology. Drug treatments</subject><subject>Renal Insufficiency - chemically induced</subject><subject>Tenofovir</subject><subject>Tokyo</subject><subject>Viral diseases</subject><subject>Viral diseases of the lymphoid tissue and the blood. Aids</subject><issn>0269-9370</issn><issn>1473-5571</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkctu1TAQhi0EoofCGyDkDRKbFE98S9hV5dJKR0JIwDZy7HFrlGMH2-nhvAmPS1APF7FhNrOY75_R6CPkKbAzYL1--eH89Rn7u7jQ98gGhOaNlBrukw1rVd_0XLMT8qiULysjWdc9JCetbGWvWbsh37cpXjcV847itzmVJSOtiVaMyafbkKlNsYa4pKVMB-rQZjQFacZoJuqXaGtIkYZIL68-N9CE6NFWdHQ2NWCshe5DvaFT2tMxuQPdY7i-qa_WfFmmdepz2lFg9IAmF5o89Wla4WaZH5MH3kwFnxz7Kfn09s3Hi8tm-_7d1cX5trEc-trIkY8CQBpn-p6bEbxQihkppBKdAGzBgTOmddK1IxgtR6aFdZxbBtK3yE_Ji7u9c05fFyx12IVicZpMxPXpAbTqpO6F6v-PSqUAQGlYUXGH2pxKyeiHOYedyYcB2PBT37DqG_7Vt8aeHS8s4w7d79AvXyvw_AiYYs3ks4k2lD9c1zENSvIfg8Sj2g</recordid><startdate>20140824</startdate><enddate>20140824</enddate><creator>NISHIJIMA, Takeshi</creator><creator>KAWASAKI, Yohei</creator><creator>TSUKADA, Kunihisa</creator><creator>TERUYA, Katsuji</creator><creator>KIKUCHI, Yoshimi</creator><creator>GATANAGA, Hiroyuki</creator><creator>OKA, Shinichi</creator><creator>TANAKA, Noriko</creator><creator>MIZUSHIMA, Daisuke</creator><creator>AOKI, Takahiro</creator><creator>WATANABE, Koji</creator><creator>EI KINAI</creator><creator>HONDA, Haruhito</creator><creator>YAZAKI, Hirohisa</creator><creator>TANUMA, Junko</creator><general>Lippincott Williams & Wilkins</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>7T2</scope><scope>7T5</scope><scope>7U2</scope><scope>7U9</scope><scope>C1K</scope><scope>H94</scope></search><sort><creationdate>20140824</creationdate><title>Long-term exposure to tenofovir continuously decrease renal function in HIV-1-infected patients with low body weight: results from 10 years of follow-up</title><author>NISHIJIMA, Takeshi ; KAWASAKI, Yohei ; TSUKADA, Kunihisa ; TERUYA, Katsuji ; KIKUCHI, Yoshimi ; GATANAGA, Hiroyuki ; OKA, Shinichi ; TANAKA, Noriko ; MIZUSHIMA, Daisuke ; AOKI, Takahiro ; WATANABE, Koji ; EI KINAI ; HONDA, Haruhito ; YAZAKI, Hirohisa ; TANUMA, Junko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c319t-5b3b4115ada993ab1f4660a54564841e21d1daa2d5d2b1a75b074cd33c015f2e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adenine - adverse effects</topic><topic>Adenine - analogs & derivatives</topic><topic>Adenine - therapeutic use</topic><topic>Adult</topic><topic>AIDS/HIV</topic><topic>Anti-HIV Agents - adverse effects</topic><topic>Anti-HIV Agents - therapeutic use</topic><topic>Antibiotics. Antiinfectious agents. Antiparasitic agents</topic><topic>Antiviral agents</topic><topic>Biological and medical sciences</topic><topic>Body Weight</topic><topic>Cohort Studies</topic><topic>Female</topic><topic>Glomerular Filtration Rate - drug effects</topic><topic>HIV Infections - complications</topic><topic>HIV Infections - drug therapy</topic><topic>HIV Infections - virology</topic><topic>HIV-1 - isolation & purification</topic><topic>Human immunodeficiency virus</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Immunodeficiencies</topic><topic>Immunodeficiencies. Immunoglobulinopathies</topic><topic>Immunopathology</topic><topic>Infectious diseases</topic><topic>Longitudinal Studies</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Organophosphonates - adverse effects</topic><topic>Organophosphonates - therapeutic use</topic><topic>Pharmacology. Drug treatments</topic><topic>Renal Insufficiency - chemically induced</topic><topic>Tenofovir</topic><topic>Tokyo</topic><topic>Viral diseases</topic><topic>Viral diseases of the lymphoid tissue and the blood. Aids</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>NISHIJIMA, Takeshi</creatorcontrib><creatorcontrib>KAWASAKI, Yohei</creatorcontrib><creatorcontrib>TSUKADA, Kunihisa</creatorcontrib><creatorcontrib>TERUYA, Katsuji</creatorcontrib><creatorcontrib>KIKUCHI, Yoshimi</creatorcontrib><creatorcontrib>GATANAGA, Hiroyuki</creatorcontrib><creatorcontrib>OKA, Shinichi</creatorcontrib><creatorcontrib>TANAKA, Noriko</creatorcontrib><creatorcontrib>MIZUSHIMA, Daisuke</creatorcontrib><creatorcontrib>AOKI, Takahiro</creatorcontrib><creatorcontrib>WATANABE, Koji</creatorcontrib><creatorcontrib>EI KINAI</creatorcontrib><creatorcontrib>HONDA, Haruhito</creatorcontrib><creatorcontrib>YAZAKI, Hirohisa</creatorcontrib><creatorcontrib>TANUMA, Junko</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>Health and Safety Science Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Safety Science and Risk</collection><collection>Virology and AIDS Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>AIDS (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>NISHIJIMA, Takeshi</au><au>KAWASAKI, Yohei</au><au>TSUKADA, Kunihisa</au><au>TERUYA, Katsuji</au><au>KIKUCHI, Yoshimi</au><au>GATANAGA, Hiroyuki</au><au>OKA, Shinichi</au><au>TANAKA, Noriko</au><au>MIZUSHIMA, Daisuke</au><au>AOKI, Takahiro</au><au>WATANABE, Koji</au><au>EI KINAI</au><au>HONDA, Haruhito</au><au>YAZAKI, Hirohisa</au><au>TANUMA, Junko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long-term exposure to tenofovir continuously decrease renal function in HIV-1-infected patients with low body weight: results from 10 years of follow-up</atitle><jtitle>AIDS (London)</jtitle><addtitle>AIDS</addtitle><date>2014-08-24</date><risdate>2014</risdate><volume>28</volume><issue>13</issue><spage>1903</spage><epage>1910</epage><pages>1903-1910</pages><issn>0269-9370</issn><eissn>1473-5571</eissn><abstract>To investigate the effect of long-term tenofovir disoproxil fumarate (TDF) use on renal function, especially in patients with low body weight who are vulnerable to TDF nephrotoxicity.
A single-center, observational study in Tokyo, Japan.
We performed a 10 years cohort study of 792 HIV-1-infected patients. The effect of long-term TDF use on estimated glomerular filtration rate (eGFR) was investigated on treatment-naive patients who started TDF-containing antiretroviral therapy (n = 422) and those who started abacavir-containing antiretroviral therapy as control (n = 370). Three renal endpoints were examined by the logistic regression model: decrement in eGFR of higher than 10 ml/min per 1.73 m relative to the baseline, more than 25% decrement in eGFR, and eGFR lower than 60 ml/min per 1.73 m at least 3 months apart. The loss in eGFR was estimated using linear mixed models for repeated measures.
The median weight at baseline was 63 kg. TDF use increased the risk of all three renal outcomes compared with the control group: higher than 10 ml/min per 1.73 m decrement in eGFR [adjusted odds ratio (OR) = 2.1, 95% confidence interval (CI) 1.45-3.14, P < 0.001], more than 25% decrement (adjusted OR = 2.1, 95% CI 1.50-2.90, P < 0.001), and eGFR lower than 60 ml/min per 1.73 m at least 3 months apart (adjusted OR = 3.9, 95% CI 1.62-9.36, P = 0.002). The cumulative mean loss relative to the control after 1, 2, 3, 4, and 5 years of TDF exposure was -3.8, -3.6, -5.5, -6.6, and -10.3 ml/min per 1.73 m, respectively, indicating that the loss in eGFR increased over time (P < 0.001).
In this cohort of patients with low body weight, TDF exposure increased the risk of renal dysfunction. Furthermore, the loss in eGFR relative to the control increased continuously up to 5 years.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>25259702</pmid><doi>10.1097/QAD.0000000000000347</doi><tpages>8</tpages></addata></record> |
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subjects | Adenine - adverse effects Adenine - analogs & derivatives Adenine - therapeutic use Adult AIDS/HIV Anti-HIV Agents - adverse effects Anti-HIV Agents - therapeutic use Antibiotics. Antiinfectious agents. Antiparasitic agents Antiviral agents Biological and medical sciences Body Weight Cohort Studies Female Glomerular Filtration Rate - drug effects HIV Infections - complications HIV Infections - drug therapy HIV Infections - virology HIV-1 - isolation & purification Human immunodeficiency virus Human viral diseases Humans Immunodeficiencies Immunodeficiencies. Immunoglobulinopathies Immunopathology Infectious diseases Longitudinal Studies Male Medical sciences Organophosphonates - adverse effects Organophosphonates - therapeutic use Pharmacology. Drug treatments Renal Insufficiency - chemically induced Tenofovir Tokyo Viral diseases Viral diseases of the lymphoid tissue and the blood. Aids |
title | Long-term exposure to tenofovir continuously decrease renal function in HIV-1-infected patients with low body weight: results from 10 years of follow-up |
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