TY - JOUR
T1 - Incidence of dyslipidemia in people with HIV who are treated with integrase inhibitors versus other antiretroviral agents
AU - Byonanebye, Dathan M.
AU - Polizzotto, Mark N.
AU - Begovac, Josip
AU - Grabmeier-Pfistershammer, Katharina
AU - Abela, Irene
AU - Castagna, Antonella
AU - de Wit, Stéphane
AU - Mussini, Cristina
AU - Vehreschild, Jörg J.
AU - d'Arminio Monforte, Antonella
AU - Wit, Ferdinand W.N.M.
AU - Pradier, Christian
AU - Chkhartishvili, Nikoloz
AU - Sönnerborg, Anders
AU - Hoy, Jennifer
AU - Lundgren, Jens
AU - Neesgaard, Bastian
AU - Bansi-Matharu, Loveleen
AU - Greenberg, Lauren
AU - Llibre, Josep M.
AU - Vannappagari, Vani
AU - Gallant, Joel
AU - Necsoi, Coca
AU - Cichon, Piotr
AU - Reiss, Peter
AU - Aho, Inka
AU - Tsertsvadze, Tengiz
AU - Mennozzi, Marianna
AU - Rauch, Andri
AU - Muccini, Camilla
AU - Law, Matthew
AU - Mocroft, Amanda
AU - Ryom, Lene
AU - Petoumenos, Kathy
AU - Hillebregt, M.
AU - Rose, N.
AU - Zangerle, R.
AU - Appoyer, H.
AU - Delforge, M.
AU - Wandeler, Gilles
AU - Stephan, C.
AU - Bucht, M.
AU - Chokoshvili, O.
AU - Rodano, A.
AU - Tavelli, A.
AU - Fanti, I.
AU - Borghi, V.
AU - Fontas, E.
AU - Dollet, K.
AU - Caissotti, C.
AU - Casabona, J.
AU - Miro, J. M.
AU - Smith, C.
AU - Lampe, F.
AU - Johnson, M.
AU - Burns, F.
AU - Chaloner, C.
AU - Lazzarin, A.
AU - Poli, A.
AU - Falconer, K.
AU - Svedhem, V.
AU - Günthard, H.
AU - Ledergerber, B.
AU - Bucher, H.
AU - Scherrer, A.
AU - Wasmuth, J. C.
AU - Rockstroh, J.
AU - Fätkenheuer, G.
AU - Stecher, M.
AU - Schulze, N.
AU - Franke, B.
AU - Rooney, J.
AU - Rogatto, F.
AU - Garges, H.
AU - Kowalska, J.
AU - Raben, D.
AU - Peters, L.
AU - Anne, A. Volny
AU - Dedes, N.
AU - Williams, E. Dixon
AU - Bruguera, A.
AU - Haubrich, R.
AU - Svedhem-Johansson, V.
AU - Bloch, M.
AU - Braun, D.
AU - Calmy, A.
AU - Schüttfort, G.
AU - Youle, M.
AU - Zona, S.
AU - Antinori, A.
AU - Bolokadze, N.
AU - Schwarze-Zander, C.
AU - Duvivier, C.
AU - Dragovic, G.
AU - Radoi, R.
AU - Oprea, C.
AU - Vasylyev, M.
AU - Matulionyte, R.
AU - Mulabdic, V.
AU - Marchetti, G.
AU - Kuzovatova, E.
AU - Coppola, N.
AU - Martini, S.
AU - Harxhi, A.
AU - Wæhre, T.
AU - Pharris, A.
AU - Vassilenko, A.
AU - Bogner, J.
AU - Maagaard, A.
AU - Jablonowska, E.
AU - Elbirt, D.
AU - Marrone, G.
AU - Leen, C.
AU - Wyen, C.
AU - Kundro, M.
AU - Gallant, J.
AU - Thorpe, D.
AU - Volny-Anne, A.
AU - Mendao, L.
AU - Larsen, J. F.
AU - Jakobsen, M. L.
AU - Bruun, T.
AU - Bojesen, A.
AU - Hansen, E. V.
AU - Elsing, T. W.
AU - Kristensen, D.
AU - Thomsen, S.
AU - Weide, T.
AU - Pelchen-Matthews, A.
AU - The RESPOND Study Group
N1 - Funding Information:
RESPOND is externally funded by Gilead Sciences and ViiV Healthcare LLC. Funding companies had no direct involvement in the conduct of scientific projects. Additional support has been provided by participating cohorts contributing data in-kind and/or statistical support: Austrian HIV Cohort Study (AHIVCOS), The Australian HIV Observational Database (AHOD), Brussels Saint Pierre cohort, University Hospital Cologne, The EuroSIDA cohort, Frankfurt HIV Cohort Study, Georgian National AIDS Health Information System (AIDS HIS), Modena HIV Cohort, San Raffaele Scientific Institute, Swiss HIV Cohort Study (SHCS), Royal Free HIV Cohort Study.
Funding Information:
S.D.W.’s affiliated institution received grants from Gilead, Janssen, MSD and ViiV. J.M.L. has received payments for advisory boards, consultancy, payment for lectures including service on speakers’ bureaus from ViiV Healthcare, Gilead Sciences, and Janssen-Cilag, all of them out of the present study. J.B. has received payments for advisory boards, consultancy, payment for lectures from ViiV Healthcare, Gilead Sciences, and MSD, all of them out of the present study. V.V. is a salaried employee of ViiV Healthcare and receives GlaxoSmithKline stock as part of her compensation. J.G. is an employee of Gilead Sciences. A.R. reports fees for sitting on advisory boards from Merck Sharp & Dohme and Gilead Sciences; travel grants from Gilead Sciences, Pfizer, and AbbVie; and a research grant from Gilead Sciences, outside of the submitted work. All fees were paid to A.R.’s institution and not directly to A.R. There are no conflicts of interest.
Publisher Copyright:
Copyright © 2021 Wolters Kluwer Health, Inc. All rights reserved.
PY - 2021/5/1
Y1 - 2021/5/1
N2 - Objective: To compare the incidence of dyslipidemia in people with HIV receiving integrase inhibitors (INSTI) versus boosted protease inhibitors (PI/b) and nonnucleoside reverse transcriptase inhibitors (NNRTI) within RESPOND consortium of prospective cohorts. Methods: Participants were eligible if they were at least 18 years, without dyslipidemia and initiated or switched to a three-drug antiretroviral therapy (ART)-regimen consisting of either INSTI, NNRTI, or PI/b for the first time, between 1 January 2012 and 31 December 2018. Dyslipidemia was defined as random total cholesterol more than 240 mg/dl, HDL less than 35 mg/dl, triglyceride more than 200 mg/dl, or initiation of lipid-lowering therapy. Poisson regression was used to determine the adjusted incidence rate ratios. Follow-up was censored after 3 years or upon ART-regimen discontinuation or last lipid measurement or 31 December 2019, whichever occurred first. Results: Overall, 4577 people with HIV were eligible (INSTI = 66.9%, PI/b = 12.5%, and NNRTI = 20.6%), 1938 (42.3%) of whom were ART-naive. During 1.7 (interquartile range, 0.6 - 3.0) median years of follow-up, 1460 participants developed dyslipidemia [incidence rate: 191.6 per 1000 person-years, 95% confidence interval (CI) 182.0 - 201.7]. Participants taking INSTI had a lower incidence of dyslipidemia compared with those on PI/b (adjusted incidence rate ratio 0.71; CI 0.59 - 0.85), but higher rate compared with those on NNRTI (1.35; CI 1.15 - 1.58). Compared with dolutegravir, the incidence of dyslipidemia was higher with elvitegravir/cobicistat (1.20; CI 1.00 - 1.43) and raltegravir (1.24; CI 1.02 - 1.51), but lower with rilpivirine (0.77; CI 0.63 - 0.94). Conclusion: In this large consortium of heterogeneous cohorts, dyslipidemia was less common with INSTI than with PI/b. Compared with dolutegravir, dyslipidemia was more common with elvitegravir/cobicistat and raltegravir, but less common with rilpivirine.
AB - Objective: To compare the incidence of dyslipidemia in people with HIV receiving integrase inhibitors (INSTI) versus boosted protease inhibitors (PI/b) and nonnucleoside reverse transcriptase inhibitors (NNRTI) within RESPOND consortium of prospective cohorts. Methods: Participants were eligible if they were at least 18 years, without dyslipidemia and initiated or switched to a three-drug antiretroviral therapy (ART)-regimen consisting of either INSTI, NNRTI, or PI/b for the first time, between 1 January 2012 and 31 December 2018. Dyslipidemia was defined as random total cholesterol more than 240 mg/dl, HDL less than 35 mg/dl, triglyceride more than 200 mg/dl, or initiation of lipid-lowering therapy. Poisson regression was used to determine the adjusted incidence rate ratios. Follow-up was censored after 3 years or upon ART-regimen discontinuation or last lipid measurement or 31 December 2019, whichever occurred first. Results: Overall, 4577 people with HIV were eligible (INSTI = 66.9%, PI/b = 12.5%, and NNRTI = 20.6%), 1938 (42.3%) of whom were ART-naive. During 1.7 (interquartile range, 0.6 - 3.0) median years of follow-up, 1460 participants developed dyslipidemia [incidence rate: 191.6 per 1000 person-years, 95% confidence interval (CI) 182.0 - 201.7]. Participants taking INSTI had a lower incidence of dyslipidemia compared with those on PI/b (adjusted incidence rate ratio 0.71; CI 0.59 - 0.85), but higher rate compared with those on NNRTI (1.35; CI 1.15 - 1.58). Compared with dolutegravir, the incidence of dyslipidemia was higher with elvitegravir/cobicistat (1.20; CI 1.00 - 1.43) and raltegravir (1.24; CI 1.02 - 1.51), but lower with rilpivirine (0.77; CI 0.63 - 0.94). Conclusion: In this large consortium of heterogeneous cohorts, dyslipidemia was less common with INSTI than with PI/b. Compared with dolutegravir, dyslipidemia was more common with elvitegravir/cobicistat and raltegravir, but less common with rilpivirine.
UR - http://www.scopus.com/inward/record.url?scp=85104047208&partnerID=8YFLogxK
U2 - 10.1097/QAD.0000000000002811
DO - 10.1097/QAD.0000000000002811
M3 - Article
C2 - 33443370
AN - SCOPUS:85104047208
SN - 0269-9370
VL - 35
SP - 869
EP - 882
JO - AIDS
JF - AIDS
IS - 6
ER -