Loading…

Blood Telomere Length Changes After Ritonavir-Boosted Darunavir Combined With Raltegravir or Tenofovir-Emtricitabine in Antiretroviral-Naive Adults Infected With HIV-1: J Infect Dis

Background. Tenofovir is a potent inhibitor of human telomerase. The clinical relevance of this inhibition is unknown. Methods. NEAT001/ANRS143 is a randomized trial that showed noninferiority over 96 weeks of ritonavir-boosted darunavir plus raltegravir versus tenofovir disoproxil fumarate/emtricit...

Full description

Saved in:
Bibliographic Details
Published in:The Journal of infectious diseases 2018, Vol.218 (10), p.1523-1530
Main Authors: Stella-Ascariz, N., Montejano, R., Rodriguez-Centeno, J., Alejos, B., Schwimmer, Christine, Bernardino, J. I., Rodes, B., Allavena, C., Hoffmann, C., Gisslen, M., de Miguel, R., Esteban-Cantos, A., Wallet, Cedrick, Raffi, F., Arribas, J. R.
Format: Article
Language:English
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page 1530
container_issue 10
container_start_page 1523
container_title The Journal of infectious diseases
container_volume 218
creator Stella-Ascariz, N.
Montejano, R.
Rodriguez-Centeno, J.
Alejos, B.
Schwimmer, Christine
Bernardino, J. I.
Rodes, B.
Allavena, C.
Hoffmann, C.
Gisslen, M.
de Miguel, R.
Esteban-Cantos, A.
Wallet, Cedrick
Raffi, F.
Arribas, J. R.
description Background. Tenofovir is a potent inhibitor of human telomerase. The clinical relevance of this inhibition is unknown. Methods. NEAT001/ANRS143 is a randomized trial that showed noninferiority over 96 weeks of ritonavir-boosted darunavir plus raltegravir versus tenofovir disoproxil fumarate/emtricitabine in 805 antiretroviral antiretrovrial-naive HIV-infected adults. We compared changes in whole-blood telomere length measured with quantitative polymerase chain reaction in 201 randomly selected participants (104 raltegravir and 97 tenofovir disoproxil fumarate/emtricitabine). We performed multivariable estimative and predictive linear regression. Results. At week 96, participants receiving tenofovir disoproxil fumarate/emtricitabine had a statistically significant higher gain in telomere length than participants receiving raltegravir. Difference in mean telomere length change between groups (tenofovir disoproxil fumarate/emtricitabine minus raltegravir) from baseline to week 96 adjusted by baseline telomere length was 0.031 (P = .009). This difference was not significantly confounded by age, gender, known duration of HIV infection, CD4 (baseline/nadir), CD8 cells, CD4/CD8 ratio, HIV viral load (baseline/week 96), tobacco and alcohol consumption, statins, or hepatitis C. Conclusion. Antiretroviral-naive HIV-infected adults receiving ritonavir-boosted darunavir and tenofovir disoproxil fumarate/emtricitabine had a significant higher gain in blood telomere length than those receiving ritonavir-boosted darunavir and raltegravir, suggesting a better initial recovery from HIV-associated immunosenescence.
doi_str_mv 10.1093/infdis/jiy399
format article
fullrecord <record><control><sourceid>hal</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_03193819v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>oai_HAL_hal_03193819v1</sourcerecordid><originalsourceid>FETCH-hal_primary_oai_HAL_hal_03193819v13</originalsourceid><addsrcrecordid>eNqVjL1OwzAUhS0EEuFnZPfKYGrXkNZjGopSqWKoKhgj09wkt3JsZLuR-kS8ZpMKHoDpSN_5ziHkQfAnwZWcoK0rDJM9HqVSFyQRL3LG0lTIS5JwPp0yMVfqmtyEsOecP8t0lpCfhXGuolswrgMPdA22iS3NW20bCDSrI3i6weis7tGzhXMhQkVftT-cCc1d94V2QJ847DbaRGj8uXF-uLWuduNw2UWPO4x6lClamtmIHqIfW23Yu8YeaFYdTAx0ZWvYxb_PYvXBxB25qrUJcP-bt-TxbbnNC9ZqU3577LQ_lk5jWWTrcmRcCiXnQvVC_sc9AWDxaiI</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Blood Telomere Length Changes After Ritonavir-Boosted Darunavir Combined With Raltegravir or Tenofovir-Emtricitabine in Antiretroviral-Naive Adults Infected With HIV-1: J Infect Dis</title><source>Oxford Journals Online</source><source>JSTOR Archival Journals</source><creator>Stella-Ascariz, N. ; Montejano, R. ; Rodriguez-Centeno, J. ; Alejos, B. ; Schwimmer, Christine ; Bernardino, J. I. ; Rodes, B. ; Allavena, C. ; Hoffmann, C. ; Gisslen, M. ; de Miguel, R. ; Esteban-Cantos, A. ; Wallet, Cedrick ; Raffi, F. ; Arribas, J. R.</creator><creatorcontrib>Stella-Ascariz, N. ; Montejano, R. ; Rodriguez-Centeno, J. ; Alejos, B. ; Schwimmer, Christine ; Bernardino, J. I. ; Rodes, B. ; Allavena, C. ; Hoffmann, C. ; Gisslen, M. ; de Miguel, R. ; Esteban-Cantos, A. ; Wallet, Cedrick ; Raffi, F. ; Arribas, J. R.</creatorcontrib><description>Background. Tenofovir is a potent inhibitor of human telomerase. The clinical relevance of this inhibition is unknown. Methods. NEAT001/ANRS143 is a randomized trial that showed noninferiority over 96 weeks of ritonavir-boosted darunavir plus raltegravir versus tenofovir disoproxil fumarate/emtricitabine in 805 antiretroviral antiretrovrial-naive HIV-infected adults. We compared changes in whole-blood telomere length measured with quantitative polymerase chain reaction in 201 randomly selected participants (104 raltegravir and 97 tenofovir disoproxil fumarate/emtricitabine). We performed multivariable estimative and predictive linear regression. Results. At week 96, participants receiving tenofovir disoproxil fumarate/emtricitabine had a statistically significant higher gain in telomere length than participants receiving raltegravir. Difference in mean telomere length change between groups (tenofovir disoproxil fumarate/emtricitabine minus raltegravir) from baseline to week 96 adjusted by baseline telomere length was 0.031 (P = .009). This difference was not significantly confounded by age, gender, known duration of HIV infection, CD4 (baseline/nadir), CD8 cells, CD4/CD8 ratio, HIV viral load (baseline/week 96), tobacco and alcohol consumption, statins, or hepatitis C. Conclusion. Antiretroviral-naive HIV-infected adults receiving ritonavir-boosted darunavir and tenofovir disoproxil fumarate/emtricitabine had a significant higher gain in blood telomere length than those receiving ritonavir-boosted darunavir and raltegravir, suggesting a better initial recovery from HIV-associated immunosenescence.</description><identifier>ISSN: 0022-1899</identifier><identifier>EISSN: 1537-6613</identifier><identifier>DOI: 10.1093/infdis/jiy399</identifier><language>eng</language><publisher>Oxford University Press</publisher><subject>Life Sciences ; Santé publique et épidémiologie</subject><ispartof>The Journal of infectious diseases, 2018, Vol.218 (10), p.1523-1530</ispartof><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,777,781,882,4010,27904,27905,27906</link.rule.ids><backlink>$$Uhttps://hal.science/hal-03193819$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Stella-Ascariz, N.</creatorcontrib><creatorcontrib>Montejano, R.</creatorcontrib><creatorcontrib>Rodriguez-Centeno, J.</creatorcontrib><creatorcontrib>Alejos, B.</creatorcontrib><creatorcontrib>Schwimmer, Christine</creatorcontrib><creatorcontrib>Bernardino, J. I.</creatorcontrib><creatorcontrib>Rodes, B.</creatorcontrib><creatorcontrib>Allavena, C.</creatorcontrib><creatorcontrib>Hoffmann, C.</creatorcontrib><creatorcontrib>Gisslen, M.</creatorcontrib><creatorcontrib>de Miguel, R.</creatorcontrib><creatorcontrib>Esteban-Cantos, A.</creatorcontrib><creatorcontrib>Wallet, Cedrick</creatorcontrib><creatorcontrib>Raffi, F.</creatorcontrib><creatorcontrib>Arribas, J. R.</creatorcontrib><title>Blood Telomere Length Changes After Ritonavir-Boosted Darunavir Combined With Raltegravir or Tenofovir-Emtricitabine in Antiretroviral-Naive Adults Infected With HIV-1: J Infect Dis</title><title>The Journal of infectious diseases</title><description>Background. Tenofovir is a potent inhibitor of human telomerase. The clinical relevance of this inhibition is unknown. Methods. NEAT001/ANRS143 is a randomized trial that showed noninferiority over 96 weeks of ritonavir-boosted darunavir plus raltegravir versus tenofovir disoproxil fumarate/emtricitabine in 805 antiretroviral antiretrovrial-naive HIV-infected adults. We compared changes in whole-blood telomere length measured with quantitative polymerase chain reaction in 201 randomly selected participants (104 raltegravir and 97 tenofovir disoproxil fumarate/emtricitabine). We performed multivariable estimative and predictive linear regression. Results. At week 96, participants receiving tenofovir disoproxil fumarate/emtricitabine had a statistically significant higher gain in telomere length than participants receiving raltegravir. Difference in mean telomere length change between groups (tenofovir disoproxil fumarate/emtricitabine minus raltegravir) from baseline to week 96 adjusted by baseline telomere length was 0.031 (P = .009). This difference was not significantly confounded by age, gender, known duration of HIV infection, CD4 (baseline/nadir), CD8 cells, CD4/CD8 ratio, HIV viral load (baseline/week 96), tobacco and alcohol consumption, statins, or hepatitis C. Conclusion. Antiretroviral-naive HIV-infected adults receiving ritonavir-boosted darunavir and tenofovir disoproxil fumarate/emtricitabine had a significant higher gain in blood telomere length than those receiving ritonavir-boosted darunavir and raltegravir, suggesting a better initial recovery from HIV-associated immunosenescence.</description><subject>Life Sciences</subject><subject>Santé publique et épidémiologie</subject><issn>0022-1899</issn><issn>1537-6613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqVjL1OwzAUhS0EEuFnZPfKYGrXkNZjGopSqWKoKhgj09wkt3JsZLuR-kS8ZpMKHoDpSN_5ziHkQfAnwZWcoK0rDJM9HqVSFyQRL3LG0lTIS5JwPp0yMVfqmtyEsOecP8t0lpCfhXGuolswrgMPdA22iS3NW20bCDSrI3i6weis7tGzhXMhQkVftT-cCc1d94V2QJ847DbaRGj8uXF-uLWuduNw2UWPO4x6lClamtmIHqIfW23Yu8YeaFYdTAx0ZWvYxb_PYvXBxB25qrUJcP-bt-TxbbnNC9ZqU3577LQ_lk5jWWTrcmRcCiXnQvVC_sc9AWDxaiI</recordid><startdate>2018</startdate><enddate>2018</enddate><creator>Stella-Ascariz, N.</creator><creator>Montejano, R.</creator><creator>Rodriguez-Centeno, J.</creator><creator>Alejos, B.</creator><creator>Schwimmer, Christine</creator><creator>Bernardino, J. I.</creator><creator>Rodes, B.</creator><creator>Allavena, C.</creator><creator>Hoffmann, C.</creator><creator>Gisslen, M.</creator><creator>de Miguel, R.</creator><creator>Esteban-Cantos, A.</creator><creator>Wallet, Cedrick</creator><creator>Raffi, F.</creator><creator>Arribas, J. R.</creator><general>Oxford University Press</general><scope>1XC</scope></search><sort><creationdate>2018</creationdate><title>Blood Telomere Length Changes After Ritonavir-Boosted Darunavir Combined With Raltegravir or Tenofovir-Emtricitabine in Antiretroviral-Naive Adults Infected With HIV-1</title><author>Stella-Ascariz, N. ; Montejano, R. ; Rodriguez-Centeno, J. ; Alejos, B. ; Schwimmer, Christine ; Bernardino, J. I. ; Rodes, B. ; Allavena, C. ; Hoffmann, C. ; Gisslen, M. ; de Miguel, R. ; Esteban-Cantos, A. ; Wallet, Cedrick ; Raffi, F. ; Arribas, J. R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-hal_primary_oai_HAL_hal_03193819v13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Life Sciences</topic><topic>Santé publique et épidémiologie</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stella-Ascariz, N.</creatorcontrib><creatorcontrib>Montejano, R.</creatorcontrib><creatorcontrib>Rodriguez-Centeno, J.</creatorcontrib><creatorcontrib>Alejos, B.</creatorcontrib><creatorcontrib>Schwimmer, Christine</creatorcontrib><creatorcontrib>Bernardino, J. I.</creatorcontrib><creatorcontrib>Rodes, B.</creatorcontrib><creatorcontrib>Allavena, C.</creatorcontrib><creatorcontrib>Hoffmann, C.</creatorcontrib><creatorcontrib>Gisslen, M.</creatorcontrib><creatorcontrib>de Miguel, R.</creatorcontrib><creatorcontrib>Esteban-Cantos, A.</creatorcontrib><creatorcontrib>Wallet, Cedrick</creatorcontrib><creatorcontrib>Raffi, F.</creatorcontrib><creatorcontrib>Arribas, J. R.</creatorcontrib><collection>Hyper Article en Ligne (HAL)</collection><jtitle>The Journal of infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stella-Ascariz, N.</au><au>Montejano, R.</au><au>Rodriguez-Centeno, J.</au><au>Alejos, B.</au><au>Schwimmer, Christine</au><au>Bernardino, J. I.</au><au>Rodes, B.</au><au>Allavena, C.</au><au>Hoffmann, C.</au><au>Gisslen, M.</au><au>de Miguel, R.</au><au>Esteban-Cantos, A.</au><au>Wallet, Cedrick</au><au>Raffi, F.</au><au>Arribas, J. R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Blood Telomere Length Changes After Ritonavir-Boosted Darunavir Combined With Raltegravir or Tenofovir-Emtricitabine in Antiretroviral-Naive Adults Infected With HIV-1: J Infect Dis</atitle><jtitle>The Journal of infectious diseases</jtitle><date>2018</date><risdate>2018</risdate><volume>218</volume><issue>10</issue><spage>1523</spage><epage>1530</epage><pages>1523-1530</pages><issn>0022-1899</issn><eissn>1537-6613</eissn><abstract>Background. Tenofovir is a potent inhibitor of human telomerase. The clinical relevance of this inhibition is unknown. Methods. NEAT001/ANRS143 is a randomized trial that showed noninferiority over 96 weeks of ritonavir-boosted darunavir plus raltegravir versus tenofovir disoproxil fumarate/emtricitabine in 805 antiretroviral antiretrovrial-naive HIV-infected adults. We compared changes in whole-blood telomere length measured with quantitative polymerase chain reaction in 201 randomly selected participants (104 raltegravir and 97 tenofovir disoproxil fumarate/emtricitabine). We performed multivariable estimative and predictive linear regression. Results. At week 96, participants receiving tenofovir disoproxil fumarate/emtricitabine had a statistically significant higher gain in telomere length than participants receiving raltegravir. Difference in mean telomere length change between groups (tenofovir disoproxil fumarate/emtricitabine minus raltegravir) from baseline to week 96 adjusted by baseline telomere length was 0.031 (P = .009). This difference was not significantly confounded by age, gender, known duration of HIV infection, CD4 (baseline/nadir), CD8 cells, CD4/CD8 ratio, HIV viral load (baseline/week 96), tobacco and alcohol consumption, statins, or hepatitis C. Conclusion. Antiretroviral-naive HIV-infected adults receiving ritonavir-boosted darunavir and tenofovir disoproxil fumarate/emtricitabine had a significant higher gain in blood telomere length than those receiving ritonavir-boosted darunavir and raltegravir, suggesting a better initial recovery from HIV-associated immunosenescence.</abstract><pub>Oxford University Press</pub><doi>10.1093/infdis/jiy399</doi></addata></record>
fulltext fulltext
identifier ISSN: 0022-1899
ispartof The Journal of infectious diseases, 2018, Vol.218 (10), p.1523-1530
issn 0022-1899
1537-6613
language eng
recordid cdi_hal_primary_oai_HAL_hal_03193819v1
source Oxford Journals Online; JSTOR Archival Journals
subjects Life Sciences
Santé publique et épidémiologie
title Blood Telomere Length Changes After Ritonavir-Boosted Darunavir Combined With Raltegravir or Tenofovir-Emtricitabine in Antiretroviral-Naive Adults Infected With HIV-1: J Infect Dis
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-19T22%3A40%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-hal&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Blood%20Telomere%20Length%20Changes%20After%20Ritonavir-Boosted%20Darunavir%20Combined%20With%20Raltegravir%20or%20Tenofovir-Emtricitabine%20in%20Antiretroviral-Naive%20Adults%20Infected%20With%20HIV-1:%20J%20Infect%20Dis&rft.jtitle=The%20Journal%20of%20infectious%20diseases&rft.au=Stella-Ascariz,%20N.&rft.date=2018&rft.volume=218&rft.issue=10&rft.spage=1523&rft.epage=1530&rft.pages=1523-1530&rft.issn=0022-1899&rft.eissn=1537-6613&rft_id=info:doi/10.1093/infdis/jiy399&rft_dat=%3Chal%3Eoai_HAL_hal_03193819v1%3C/hal%3E%3Cgrp_id%3Ecdi_FETCH-hal_primary_oai_HAL_hal_03193819v13%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true