Incomplete Reversibility of Estimated Glomerular Filtration Rate Decline Following Tenofovir Disoproxil Fumarate Exposure

Background. Tenofovir disoproxil fumarate (TDF) has been linked to renal impairment, but the extent to which this impairment is reversible is unclear. We aimed to investigate the reversibility of renal decline during TDF therapy. Methods. Cox proportional hazards models assessed factors associated w...

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Veröffentlicht in:The Journal of infectious diseases 2014-08, Vol.210 (3), p.363-373
Hauptverfasser: Jose, Sophie, Hamzah, Lisa, Campbell, Lucy J., Hill, Teresa, Fisher, Martin, Leen, Clifford, Gilson, Richard, Walsh, John, Nelson, Mark, Hay, Phillip, Johnson, Margaret, Chadwick, David, Nitsch, Dorothea, Jones, Rachael, Sabin, Caroline A., Post, Frank A.
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container_end_page 373
container_issue 3
container_start_page 363
container_title The Journal of infectious diseases
container_volume 210
creator Jose, Sophie
Hamzah, Lisa
Campbell, Lucy J.
Hill, Teresa
Fisher, Martin
Leen, Clifford
Gilson, Richard
Walsh, John
Nelson, Mark
Hay, Phillip
Johnson, Margaret
Chadwick, David
Nitsch, Dorothea
Jones, Rachael
Sabin, Caroline A.
Post, Frank A.
description Background. Tenofovir disoproxil fumarate (TDF) has been linked to renal impairment, but the extent to which this impairment is reversible is unclear. We aimed to investigate the reversibility of renal decline during TDF therapy. Methods. Cox proportional hazards models assessed factors associated with discontinuing TDF in those with an exposure duration of >6 months. In those who discontinued TDF therapy, linear piecewise regression models estimated glomerular filtration rate (eGFR) slopes before initiation of, during, and after discontinuation of TDF therapy. Factors associated with not achieving eGFR recovery 6 months after discontinuing TDF were assessed using multivariable logistic regression. Results. We observed declines in the eGFR during TDF exposure (mean slopes, -15.7 mL/minute/1.73 m²/year [95% confidence interval {CI}, -20.5 to -10.9] during the first 3 months and -3.1 mL/minute/1.73 m²/year [95% CI, -4.6 to -1.7] thereafter) and evidence of eGFR increases following discontinuation of TDF therapy (mean slopes, 12.5 mL/minute/1.73 m²/year [95% CI, 8.9-16.1] during the first 3 months and 0.8 mL/minute/1.73 m²/year [95% CI, .1-1.5] thereafter). Following TDF discontinuation, 38.6% of patients with a decline in the eGFR did not experience recovery. A higher eGFR at baseline, a lower eGFR after discontinuation of TDF therapy, and more-prolonged exposure to TDF were associated with an increased risk of incomplete recovery 6 months after discontinuation of TDF therapy. Conclusions. This study shows that a decline in the eGFR during TDF therapy was not fully reversible in one third of patients and suggests that prolonged TDF exposure at a low eGFR should be avoided.
doi_str_mv 10.1093/infdis/jiu107
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Tenofovir disoproxil fumarate (TDF) has been linked to renal impairment, but the extent to which this impairment is reversible is unclear. We aimed to investigate the reversibility of renal decline during TDF therapy. Methods. Cox proportional hazards models assessed factors associated with discontinuing TDF in those with an exposure duration of &gt;6 months. In those who discontinued TDF therapy, linear piecewise regression models estimated glomerular filtration rate (eGFR) slopes before initiation of, during, and after discontinuation of TDF therapy. Factors associated with not achieving eGFR recovery 6 months after discontinuing TDF were assessed using multivariable logistic regression. Results. We observed declines in the eGFR during TDF exposure (mean slopes, -15.7 mL/minute/1.73 m²/year [95% confidence interval {CI}, -20.5 to -10.9] during the first 3 months and -3.1 mL/minute/1.73 m²/year [95% CI, -4.6 to -1.7] thereafter) and evidence of eGFR increases following discontinuation of TDF therapy (mean slopes, 12.5 mL/minute/1.73 m²/year [95% CI, 8.9-16.1] during the first 3 months and 0.8 mL/minute/1.73 m²/year [95% CI, .1-1.5] thereafter). Following TDF discontinuation, 38.6% of patients with a decline in the eGFR did not experience recovery. A higher eGFR at baseline, a lower eGFR after discontinuation of TDF therapy, and more-prolonged exposure to TDF were associated with an increased risk of incomplete recovery 6 months after discontinuation of TDF therapy. Conclusions. This study shows that a decline in the eGFR during TDF therapy was not fully reversible in one third of patients and suggests that prolonged TDF exposure at a low eGFR should be avoided.</description><identifier>ISSN: 0022-1899</identifier><identifier>EISSN: 1537-6613</identifier><identifier>DOI: 10.1093/infdis/jiu107</identifier><identifier>PMID: 24585896</identifier><identifier>CODEN: JIDIAQ</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Adenine - adverse effects ; Adenine - analogs &amp; derivatives ; Adenine - therapeutic use ; Adult ; AIDS ; Anti-HIV Agents - adverse effects ; Anti-HIV Agents - therapeutic use ; Antiretrovirals ; Biological and medical sciences ; Carts ; Cohort Studies ; Drug Administration Schedule ; Female ; Fundamental and applied biological sciences. Psychology ; Funding ; Glomerular filtration rate ; Glomerular Filtration Rate - drug effects ; Health care industry ; HIV ; HIV Infections - drug therapy ; HIV/AIDS ; Humans ; Infectious diseases ; Kidney Diseases - chemically induced ; Major and Brief Reports ; Male ; Medical research ; Medical sciences ; Microbiology ; Middle Aged ; Organophosphonates - adverse effects ; Organophosphonates - therapeutic use ; Proportional Hazards Models ; Renal function ; Tenofovir ; Viral Load</subject><ispartof>The Journal of infectious diseases, 2014-08, Vol.210 (3), p.363-373</ispartof><rights>Copyright © 2014 Oxford University Press on behalf of the Infectious Diseases Society of America</rights><rights>2015 INIST-CNRS</rights><rights>The Author 2014. Published by Oxford University Press on behalf of the Infectious Diseases Society of America.</rights><rights>The Author 2014. 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Tenofovir disoproxil fumarate (TDF) has been linked to renal impairment, but the extent to which this impairment is reversible is unclear. We aimed to investigate the reversibility of renal decline during TDF therapy. Methods. Cox proportional hazards models assessed factors associated with discontinuing TDF in those with an exposure duration of &gt;6 months. In those who discontinued TDF therapy, linear piecewise regression models estimated glomerular filtration rate (eGFR) slopes before initiation of, during, and after discontinuation of TDF therapy. Factors associated with not achieving eGFR recovery 6 months after discontinuing TDF were assessed using multivariable logistic regression. Results. We observed declines in the eGFR during TDF exposure (mean slopes, -15.7 mL/minute/1.73 m²/year [95% confidence interval {CI}, -20.5 to -10.9] during the first 3 months and -3.1 mL/minute/1.73 m²/year [95% CI, -4.6 to -1.7] thereafter) and evidence of eGFR increases following discontinuation of TDF therapy (mean slopes, 12.5 mL/minute/1.73 m²/year [95% CI, 8.9-16.1] during the first 3 months and 0.8 mL/minute/1.73 m²/year [95% CI, .1-1.5] thereafter). Following TDF discontinuation, 38.6% of patients with a decline in the eGFR did not experience recovery. A higher eGFR at baseline, a lower eGFR after discontinuation of TDF therapy, and more-prolonged exposure to TDF were associated with an increased risk of incomplete recovery 6 months after discontinuation of TDF therapy. Conclusions. This study shows that a decline in the eGFR during TDF therapy was not fully reversible in one third of patients and suggests that prolonged TDF exposure at a low eGFR should be avoided.</description><subject>Adenine - adverse effects</subject><subject>Adenine - analogs &amp; derivatives</subject><subject>Adenine - therapeutic use</subject><subject>Adult</subject><subject>AIDS</subject><subject>Anti-HIV Agents - adverse effects</subject><subject>Anti-HIV Agents - therapeutic use</subject><subject>Antiretrovirals</subject><subject>Biological and medical sciences</subject><subject>Carts</subject><subject>Cohort Studies</subject><subject>Drug Administration Schedule</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Funding</subject><subject>Glomerular filtration rate</subject><subject>Glomerular Filtration Rate - drug effects</subject><subject>Health care industry</subject><subject>HIV</subject><subject>HIV Infections - drug therapy</subject><subject>HIV/AIDS</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Kidney Diseases - chemically induced</subject><subject>Major and Brief Reports</subject><subject>Male</subject><subject>Medical research</subject><subject>Medical sciences</subject><subject>Microbiology</subject><subject>Middle Aged</subject><subject>Organophosphonates - adverse effects</subject><subject>Organophosphonates - therapeutic use</subject><subject>Proportional Hazards Models</subject><subject>Renal function</subject><subject>Tenofovir</subject><subject>Viral Load</subject><issn>0022-1899</issn><issn>1537-6613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkc1v1DAQxS0EosvCkSPIF46h49iJnQsSandLpUpIVTlHjndcvHLsyE623f-erFJWcJrD-82bj0fIRwZfGTT80gW7c_ly7yYG8hVZsYrLoq4Zf01WAGVZMNU0F-RdznsAELyWb8lFKSpVqaZekeNtMLEfPI5I7_GAKbvOeTceabR0k0fX6xF39MbHHtPkdaJb58ekRxcDvZ81eo3Gu4B0G72PTy480gcM0caDS_Ta5Tik-Ow83U69Tid-8zzEPCV8T95Y7TN-eKlr8mu7ebj6Udz9vLm9-n5XmAqqsTCAAkFppbUqObONlUZ09U6yWphGl1I1ViN2YDqU1nBoBNpOWzkXAZrzNfm2-A5T1-POYJjX9-2Q5tPSsY3atf8rwf1uH-OhFdCwap65JsViYFLMOaE99zJoTxm0SwbtksHMf_534Jn--_QZ-PIC6Gy0t0kHM7efOVUzoaqT0aeF2-cxprMuuARVAeN_AOzHoTs</recordid><startdate>20140801</startdate><enddate>20140801</enddate><creator>Jose, Sophie</creator><creator>Hamzah, Lisa</creator><creator>Campbell, Lucy J.</creator><creator>Hill, Teresa</creator><creator>Fisher, Martin</creator><creator>Leen, Clifford</creator><creator>Gilson, Richard</creator><creator>Walsh, John</creator><creator>Nelson, Mark</creator><creator>Hay, Phillip</creator><creator>Johnson, Margaret</creator><creator>Chadwick, David</creator><creator>Nitsch, Dorothea</creator><creator>Jones, Rachael</creator><creator>Sabin, Caroline A.</creator><creator>Post, Frank A.</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>5PM</scope></search><sort><creationdate>20140801</creationdate><title>Incomplete Reversibility of Estimated Glomerular Filtration Rate Decline Following Tenofovir Disoproxil Fumarate Exposure</title><author>Jose, Sophie ; Hamzah, Lisa ; Campbell, Lucy J. ; Hill, Teresa ; Fisher, Martin ; Leen, Clifford ; Gilson, Richard ; Walsh, John ; Nelson, Mark ; Hay, Phillip ; Johnson, Margaret ; Chadwick, David ; Nitsch, Dorothea ; Jones, Rachael ; Sabin, Caroline A. ; Post, Frank A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c505t-c0e4e08a8aa8231f9f7c4b6d7164c9a2789faeeb0cbe7fc3094efbaf74ef40a33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adenine - adverse effects</topic><topic>Adenine - analogs &amp; derivatives</topic><topic>Adenine - therapeutic use</topic><topic>Adult</topic><topic>AIDS</topic><topic>Anti-HIV Agents - adverse effects</topic><topic>Anti-HIV Agents - therapeutic use</topic><topic>Antiretrovirals</topic><topic>Biological and medical sciences</topic><topic>Carts</topic><topic>Cohort Studies</topic><topic>Drug Administration Schedule</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Funding</topic><topic>Glomerular filtration rate</topic><topic>Glomerular Filtration Rate - drug effects</topic><topic>Health care industry</topic><topic>HIV</topic><topic>HIV Infections - drug therapy</topic><topic>HIV/AIDS</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Kidney Diseases - chemically induced</topic><topic>Major and Brief Reports</topic><topic>Male</topic><topic>Medical research</topic><topic>Medical sciences</topic><topic>Microbiology</topic><topic>Middle Aged</topic><topic>Organophosphonates - adverse effects</topic><topic>Organophosphonates - therapeutic use</topic><topic>Proportional Hazards Models</topic><topic>Renal function</topic><topic>Tenofovir</topic><topic>Viral Load</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jose, Sophie</creatorcontrib><creatorcontrib>Hamzah, Lisa</creatorcontrib><creatorcontrib>Campbell, Lucy J.</creatorcontrib><creatorcontrib>Hill, Teresa</creatorcontrib><creatorcontrib>Fisher, Martin</creatorcontrib><creatorcontrib>Leen, Clifford</creatorcontrib><creatorcontrib>Gilson, Richard</creatorcontrib><creatorcontrib>Walsh, John</creatorcontrib><creatorcontrib>Nelson, Mark</creatorcontrib><creatorcontrib>Hay, Phillip</creatorcontrib><creatorcontrib>Johnson, Margaret</creatorcontrib><creatorcontrib>Chadwick, David</creatorcontrib><creatorcontrib>Nitsch, Dorothea</creatorcontrib><creatorcontrib>Jones, Rachael</creatorcontrib><creatorcontrib>Sabin, Caroline A.</creatorcontrib><creatorcontrib>Post, Frank A.</creatorcontrib><creatorcontrib>UK Collaborative HIV Cohort Study Steering Committee</creatorcontrib><creatorcontrib>for the UK Collaborative HIV Cohort Study Steering Committee</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>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jose, Sophie</au><au>Hamzah, Lisa</au><au>Campbell, Lucy J.</au><au>Hill, Teresa</au><au>Fisher, Martin</au><au>Leen, Clifford</au><au>Gilson, Richard</au><au>Walsh, John</au><au>Nelson, Mark</au><au>Hay, Phillip</au><au>Johnson, Margaret</au><au>Chadwick, David</au><au>Nitsch, Dorothea</au><au>Jones, Rachael</au><au>Sabin, Caroline A.</au><au>Post, Frank A.</au><aucorp>UK Collaborative HIV Cohort Study Steering Committee</aucorp><aucorp>for the UK Collaborative HIV Cohort Study Steering Committee</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Incomplete Reversibility of Estimated Glomerular Filtration Rate Decline Following Tenofovir Disoproxil Fumarate Exposure</atitle><jtitle>The Journal of infectious diseases</jtitle><addtitle>J Infect Dis</addtitle><date>2014-08-01</date><risdate>2014</risdate><volume>210</volume><issue>3</issue><spage>363</spage><epage>373</epage><pages>363-373</pages><issn>0022-1899</issn><eissn>1537-6613</eissn><coden>JIDIAQ</coden><abstract>Background. Tenofovir disoproxil fumarate (TDF) has been linked to renal impairment, but the extent to which this impairment is reversible is unclear. We aimed to investigate the reversibility of renal decline during TDF therapy. Methods. Cox proportional hazards models assessed factors associated with discontinuing TDF in those with an exposure duration of &gt;6 months. In those who discontinued TDF therapy, linear piecewise regression models estimated glomerular filtration rate (eGFR) slopes before initiation of, during, and after discontinuation of TDF therapy. Factors associated with not achieving eGFR recovery 6 months after discontinuing TDF were assessed using multivariable logistic regression. Results. We observed declines in the eGFR during TDF exposure (mean slopes, -15.7 mL/minute/1.73 m²/year [95% confidence interval {CI}, -20.5 to -10.9] during the first 3 months and -3.1 mL/minute/1.73 m²/year [95% CI, -4.6 to -1.7] thereafter) and evidence of eGFR increases following discontinuation of TDF therapy (mean slopes, 12.5 mL/minute/1.73 m²/year [95% CI, 8.9-16.1] during the first 3 months and 0.8 mL/minute/1.73 m²/year [95% CI, .1-1.5] thereafter). Following TDF discontinuation, 38.6% of patients with a decline in the eGFR did not experience recovery. A higher eGFR at baseline, a lower eGFR after discontinuation of TDF therapy, and more-prolonged exposure to TDF were associated with an increased risk of incomplete recovery 6 months after discontinuation of TDF therapy. Conclusions. This study shows that a decline in the eGFR during TDF therapy was not fully reversible in one third of patients and suggests that prolonged TDF exposure at a low eGFR should be avoided.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>24585896</pmid><doi>10.1093/infdis/jiu107</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
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subjects Adenine - adverse effects
Adenine - analogs & derivatives
Adenine - therapeutic use
Adult
AIDS
Anti-HIV Agents - adverse effects
Anti-HIV Agents - therapeutic use
Antiretrovirals
Biological and medical sciences
Carts
Cohort Studies
Drug Administration Schedule
Female
Fundamental and applied biological sciences. Psychology
Funding
Glomerular filtration rate
Glomerular Filtration Rate - drug effects
Health care industry
HIV
HIV Infections - drug therapy
HIV/AIDS
Humans
Infectious diseases
Kidney Diseases - chemically induced
Major and Brief Reports
Male
Medical research
Medical sciences
Microbiology
Middle Aged
Organophosphonates - adverse effects
Organophosphonates - therapeutic use
Proportional Hazards Models
Renal function
Tenofovir
Viral Load
title Incomplete Reversibility of Estimated Glomerular Filtration Rate Decline Following Tenofovir Disoproxil Fumarate Exposure
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