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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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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fullrecord | <record><control><sourceid>jstor_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4091582</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><jstor_id>43708501</jstor_id><sourcerecordid>43708501</sourcerecordid><originalsourceid>FETCH-LOGICAL-c505t-c0e4e08a8aa8231f9f7c4b6d7164c9a2789faeeb0cbe7fc3094efbaf74ef40a33</originalsourceid><addsrcrecordid>eNpVkc1v1DAQxS0EosvCkSPIF46h49iJnQsSandLpUpIVTlHjndcvHLsyE623f-erFJWcJrD-82bj0fIRwZfGTT80gW7c_ly7yYG8hVZsYrLoq4Zf01WAGVZMNU0F-RdznsAELyWb8lFKSpVqaZekeNtMLEfPI5I7_GAKbvOeTceabR0k0fX6xF39MbHHtPkdaJb58ekRxcDvZ81eo3Gu4B0G72PTy480gcM0caDS_Ta5Tik-Ow83U69Tid-8zzEPCV8T95Y7TN-eKlr8mu7ebj6Udz9vLm9-n5XmAqqsTCAAkFppbUqObONlUZ09U6yWphGl1I1ViN2YDqU1nBoBNpOWzkXAZrzNfm2-A5T1-POYJjX9-2Q5tPSsY3atf8rwf1uH-OhFdCwap65JsViYFLMOaE99zJoTxm0SwbtksHMf_534Jn--_QZ-PIC6Gy0t0kHM7efOVUzoaqT0aeF2-cxprMuuARVAeN_AOzHoTs</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Incomplete Reversibility of Estimated Glomerular Filtration Rate Decline Following Tenofovir Disoproxil Fumarate Exposure</title><source>Jstor Complete Legacy</source><source>MEDLINE</source><source>Oxford Journals - Connect here FIRST to enable access</source><source>Alma/SFX Local Collection</source><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.</creator><creatorcontrib>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. ; UK Collaborative HIV Cohort Study Steering Committee ; for the UK Collaborative HIV Cohort Study Steering Committee</creatorcontrib><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.</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 & 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. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c505t-c0e4e08a8aa8231f9f7c4b6d7164c9a2789faeeb0cbe7fc3094efbaf74ef40a33</citedby><cites>FETCH-LOGICAL-c505t-c0e4e08a8aa8231f9f7c4b6d7164c9a2789faeeb0cbe7fc3094efbaf74ef40a33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/43708501$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/43708501$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,776,780,799,881,27901,27902,57992,58225</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28614857$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24585896$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><title>Incomplete Reversibility of Estimated Glomerular Filtration Rate Decline Following Tenofovir Disoproxil Fumarate Exposure</title><title>The Journal of infectious diseases</title><addtitle>J Infect Dis</addtitle><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.</description><subject>Adenine - adverse effects</subject><subject>Adenine - analogs & 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 & 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 >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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