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Impact of early versus deferred antiretroviral therapy on estimated glomerular filtration rate in HIV-positive individuals in the START trial.

Identifieur interne : 004339 ( Ncbi/Merge ); précédent : 004338; suivant : 004340

Impact of early versus deferred antiretroviral therapy on estimated glomerular filtration rate in HIV-positive individuals in the START trial.

Auteurs : Amit C. Achhra [États-Unis] ; Amanda Mocroft [Royaume-Uni] ; Michael Ross [États-Unis] ; Lene Ryom-Nielson [Danemark] ; Anchalee Avihingsanon [Thaïlande] ; Elzbieta Bakowska [Pologne] ; Waldo Belloso [Argentine] ; Amanda Clarke [Royaume-Uni] ; Hansjakob Furrer [Suisse] ; Gregory M. Lucas [États-Unis] ; Matti Ristola [Finlande] ; Mohammed Rassool [Afrique du Sud] ; Jonathan Ross [Royaume-Uni] ; Charurut Somboonwit [États-Unis] ; Shweta Sharma [États-Unis] ; Christina Wyatt [Royaume-Uni]

Source :

RBID : pubmed:28668686

Abstract

The impact of early ART initiation (versus deferring) on kidney function has not been studied. START was a randomised comparison of immediate versus deferred ART initiation among HIV-positive persons with CD4(+) (cells/mm(3)) counts >500. Serum creatinine and urine dipstick protein were measured at Months 0, 1, 4, 8 and 12, and annually thereafter. The two arms were compared for changes in eGFR (mL/min/1.73 m(2), calculated by CKD-EPI equation), over time using longitudinal mixed models. Of 4685 START participants, 4629 (2294 in immediate and 2335 deferred arm) were included. Median baseline CD4(+) and eGFR were 651 and 111.5, respectively. ART was initiated in 2271 participants (99.0%) in the immediate and 1127 (48.3%) in the deferred arm, accounting for >94% and >19% of follow-up time, respectively. Overall, 89% started ART using a tenofovir-based regimen. Over 2.1 years median follow-up, mean eGFR was 0.56 (95% CI 0.003-1.11) higher in the immediate versus deferred arm, which was more prominent after adjustment for current tenofovir or bPI use (1.85, 95% CI 1.21-2.50) and in Black participants (30.1% overall) (3.90, 95% CI 2.84-4.97) versus non-Blacks (1.05, 95% CI 0.33-1.77) (P < 0.001 for interaction). Relative risk for proteinuria in the immediate versus deferred arm was 0.74 (95% CI 0.55-1.00) (P = 0.049). In the short-term, immediate ART initiation was associated with a modestly higher eGFR and lower proteinuria risk versus deferring ART (more pronounced in Black participants). Whether this early benefit translates into a lower risk of CKD requires further follow-up.

DOI: 10.1016/j.ijantimicag.2017.04.021
PubMed: 28668686

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Le document en format XML

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<name sortKey="Wyatt, Christina" sort="Wyatt, Christina" uniqKey="Wyatt C" first="Christina" last="Wyatt">Christina Wyatt</name>
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<name sortKey="Clarke, Amanda" sort="Clarke, Amanda" uniqKey="Clarke A" first="Amanda" last="Clarke">Amanda Clarke</name>
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<nlm:affiliation>Department of Infectious Diseases, Bern University Hospital, University of Bern, Bern, Switzerland.</nlm:affiliation>
<country xml:lang="fr">Suisse</country>
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<nlm:affiliation>Division of Infectious Diseases, Helsinki University Hospital, Helsinki, Finland.</nlm:affiliation>
<country xml:lang="fr">Finlande</country>
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<name sortKey="Rassool, Mohammed" sort="Rassool, Mohammed" uniqKey="Rassool M" first="Mohammed" last="Rassool">Mohammed Rassool</name>
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<nlm:affiliation>Cardiovascular Pathophysiology and Genomics Research Unit, University of the Witwatersrand, Johannesburg, South Africa.</nlm:affiliation>
<country xml:lang="fr">Afrique du Sud</country>
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<orgName type="university">Université du Witwatersrand</orgName>
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<name sortKey="Ross, Jonathan" sort="Ross, Jonathan" uniqKey="Ross J" first="Jonathan" last="Ross">Jonathan Ross</name>
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<wicri:regionArea>University Hospital Birmingham NHS Foundation Trust, Birmingham</wicri:regionArea>
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<settlement type="city">Birmingham</settlement>
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<name sortKey="Somboonwit, Charurut" sort="Somboonwit, Charurut" uniqKey="Somboonwit C" first="Charurut" last="Somboonwit">Charurut Somboonwit</name>
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<wicri:regionArea>Moroni College of Medicine, University of South Florida, Tampa, FL</wicri:regionArea>
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<region type="state">Floride</region>
<settlement type="city">Tampa</settlement>
</placeName>
<orgName type="university">Université de Floride du Sud</orgName>
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<name sortKey="Sharma, Shweta" sort="Sharma, Shweta" uniqKey="Sharma S" first="Shweta" last="Sharma">Shweta Sharma</name>
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<region type="state">Minnesota</region>
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<name sortKey="Wyatt, Christina" sort="Wyatt, Christina" uniqKey="Wyatt C" first="Christina" last="Wyatt">Christina Wyatt</name>
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<title level="j">International journal of antimicrobial agents</title>
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<div type="abstract" xml:lang="en">The impact of early ART initiation (versus deferring) on kidney function has not been studied. START was a randomised comparison of immediate versus deferred ART initiation among HIV-positive persons with CD4(+) (cells/mm(3)) counts >500. Serum creatinine and urine dipstick protein were measured at Months 0, 1, 4, 8 and 12, and annually thereafter. The two arms were compared for changes in eGFR (mL/min/1.73 m(2), calculated by CKD-EPI equation), over time using longitudinal mixed models. Of 4685 START participants, 4629 (2294 in immediate and 2335 deferred arm) were included. Median baseline CD4(+) and eGFR were 651 and 111.5, respectively. ART was initiated in 2271 participants (99.0%) in the immediate and 1127 (48.3%) in the deferred arm, accounting for >94% and >19% of follow-up time, respectively. Overall, 89% started ART using a tenofovir-based regimen. Over 2.1 years median follow-up, mean eGFR was 0.56 (95% CI 0.003-1.11) higher in the immediate versus deferred arm, which was more prominent after adjustment for current tenofovir or bPI use (1.85, 95% CI 1.21-2.50) and in Black participants (30.1% overall) (3.90, 95% CI 2.84-4.97) versus non-Blacks (1.05, 95% CI 0.33-1.77) (P < 0.001 for interaction). Relative risk for proteinuria in the immediate versus deferred arm was 0.74 (95% CI 0.55-1.00) (P = 0.049). In the short-term, immediate ART initiation was associated with a modestly higher eGFR and lower proteinuria risk versus deferring ART (more pronounced in Black participants). Whether this early benefit translates into a lower risk of CKD requires further follow-up.</div>
</front>
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<Year>2017</Year>
<Month>09</Month>
<Day>05</Day>
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<Volume>50</Volume>
<Issue>3</Issue>
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<Year>2017</Year>
<Month>Sep</Month>
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<Title>International journal of antimicrobial agents</Title>
<ISOAbbreviation>Int. J. Antimicrob. Agents</ISOAbbreviation>
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<ArticleTitle>Impact of early versus deferred antiretroviral therapy on estimated glomerular filtration rate in HIV-positive individuals in the START trial.</ArticleTitle>
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<AbstractText>The impact of early ART initiation (versus deferring) on kidney function has not been studied. START was a randomised comparison of immediate versus deferred ART initiation among HIV-positive persons with CD4(+) (cells/mm(3)) counts >500. Serum creatinine and urine dipstick protein were measured at Months 0, 1, 4, 8 and 12, and annually thereafter. The two arms were compared for changes in eGFR (mL/min/1.73 m(2), calculated by CKD-EPI equation), over time using longitudinal mixed models. Of 4685 START participants, 4629 (2294 in immediate and 2335 deferred arm) were included. Median baseline CD4(+) and eGFR were 651 and 111.5, respectively. ART was initiated in 2271 participants (99.0%) in the immediate and 1127 (48.3%) in the deferred arm, accounting for >94% and >19% of follow-up time, respectively. Overall, 89% started ART using a tenofovir-based regimen. Over 2.1 years median follow-up, mean eGFR was 0.56 (95% CI 0.003-1.11) higher in the immediate versus deferred arm, which was more prominent after adjustment for current tenofovir or bPI use (1.85, 95% CI 1.21-2.50) and in Black participants (30.1% overall) (3.90, 95% CI 2.84-4.97) versus non-Blacks (1.05, 95% CI 0.33-1.77) (P < 0.001 for interaction). Relative risk for proteinuria in the immediate versus deferred arm was 0.74 (95% CI 0.55-1.00) (P = 0.049). In the short-term, immediate ART initiation was associated with a modestly higher eGFR and lower proteinuria risk versus deferring ART (more pronounced in Black participants). Whether this early benefit translates into a lower risk of CKD requires further follow-up.</AbstractText>
<CopyrightInformation>Copyright © 2017 Elsevier B.V. and International Society of Chemotherapy. All rights reserved.</CopyrightInformation>
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<ForeName>Amit C</ForeName>
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<ForeName>Waldo</ForeName>
<Initials>W</Initials>
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<ForeName>Gregory M</ForeName>
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<ForeName>Matti</ForeName>
<Initials>M</Initials>
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<Initials>M</Initials>
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<Affiliation>Cardiovascular Pathophysiology and Genomics Research Unit, University of the Witwatersrand, Johannesburg, South Africa.</Affiliation>
</AffiliationInfo>
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<LastName>Ross</LastName>
<ForeName>Jonathan</ForeName>
<Initials>J</Initials>
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</AffiliationInfo>
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<LastName>Somboonwit</LastName>
<ForeName>Charurut</ForeName>
<Initials>C</Initials>
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<Affiliation>Moroni College of Medicine, University of South Florida, Tampa, FL, USA.</Affiliation>
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<ForeName>Shweta</ForeName>
<Initials>S</Initials>
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</AffiliationInfo>
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<ForeName>Christina</ForeName>
<Initials>C</Initials>
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<Language>eng</Language>
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<Country>United States</Country>
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<Keyword MajorTopicYN="N">HAART</Keyword>
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