Incidence and risk factors for liver enzyme elevation among naive HIV-1-infected patients receiving ART in the ICONA cohort.
Adult
Anti-HIV Agents
/ adverse effects
Coinfection
/ drug therapy
Female
HIV Infections
/ complications
HIV Integrase Inhibitors
/ adverse effects
HIV Protease Inhibitors
/ adverse effects
HIV-1
/ drug effects
Hepatitis B Surface Antigens
/ blood
Hepatitis C
/ drug therapy
Humans
Incidence
Liver Diseases
/ enzymology
Male
Middle Aged
Prospective Studies
Regression Analysis
Reverse Transcriptase Inhibitors
/ adverse effects
Risk Factors
Journal
The Journal of antimicrobial chemotherapy
ISSN: 1460-2091
Titre abrégé: J Antimicrob Chemother
Pays: England
ID NLM: 7513617
Informations de publication
Date de publication:
01 11 2019
01 11 2019
Historique:
received:
22
12
2018
revised:
17
05
2019
accepted:
16
07
2019
pubmed:
11
9
2019
medline:
17
9
2020
entrez:
11
9
2019
Statut:
ppublish
Résumé
To evaluate the incidence and risk factors for liver enzyme elevations (LEE) in patients initiating first-line ART in the ICONA prospective observational cohort, between June 2009 and December 2017. In total, 6575 ART-naive patients were selected, initiating two NRTIs with the third drug being a boosted PI (n=2436; 37.0%), an NNRTI (n=2384; 36.3%) or an integrase strand transfer inhibitor (INSTI) (n=1755; 26.7%). HBV surface antigen and HCV RNA were detected in 3.9% and 5.8% of the study population. Inverse probability weighted Cox regression analysis was used to calculate the HRs, according to first-line regimen, for LEE, defined as ALT or AST increases of ≥2.5× upper limit of normal (ULN) for patients with normal baseline values or ≥2.5× baseline for patients with higher baseline values. One hundred and eighty-three LEE occurred over 20722 patient-years of follow-up. After adjusting for the main confounders, the risk of LEE halved with INSTIs compared with NNRTIs (HR 0.46, 95% CI 0.25-0.86), with a significant reduction in the raltegravir group (HR 0.11, 95% CI 0.02-0.84 using the NNRTI class as reference). HRs for LEE were significantly higher in subjects with HBV or HCV coinfection, in patients with poorly controlled HIV infection and in those who acquired HIV through homosexual transmission. In our study, INSTI use almost halved the risk of LEE compared with other regimens. This finding could be particularly important for choosing ART in patients with risk factors for liver toxicity such as HCV and HBV coinfections.
Identifiants
pubmed: 31504633
pii: 5555519
doi: 10.1093/jac/dkz353
doi:
Substances chimiques
Anti-HIV Agents
0
HIV Integrase Inhibitors
0
HIV Protease Inhibitors
0
Hepatitis B Surface Antigens
0
Reverse Transcriptase Inhibitors
0
Types de publication
Journal Article
Observational Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
3295-3304Investigateurs
A d'Arminio Monforte
(A)
A Antinori
(A)
M Andreoni
(M)
A Castagna
(A)
F Castelli
(F)
R Cauda
(R)
G Di Perri
(G)
M Galli
(M)
R Iardino
(R)
G Ippolito
(G)
A Lazzarin
(A)
G C Marchetti
(GC)
G Rezza
(G)
F von Schloesser
(F)
P Viale
(P)
A d'Arminio Monforte
(A)
A Antinori
(A)
A Castagna
(A)
F Ceccherini-Silberstein
(F)
A Cozzi-Lepri
(A)
E Girardi
(E)
S Lo Caputo
(S)
C Mussini
(C)
M Puoti
(M)
C F Perno
(CF)
A Antinori
(A)
F Bai
(F)
C Balotta
(C)
A Bandera
(A)
S Bonora
(S)
M Borderi
(M)
A Calcagno
(A)
A Capetti
(A)
M R Capobianchi
(MR)
A Castagna
(A)
F Ceccherini-Silberstein
(F)
S Cicalini
(S)
A Cingolani
(A)
P Cinque
(P)
A Cozzi-Lepri
(A)
A d'Arminio Monforte
(A)
A De Luca
(A)
A Di Biagio
(A)
E Girardi
(E)
N Gianotti
(N)
A Gori
(A)
G Guaraldi
(G)
G Lapadula
(G)
M Lichtner
(M)
S Lo Caputo
(S)
G Madeddu
(G)
F Maggiolo
(F)
G Marchetti
(G)
L Monno
(L)
C Mussini
(C)
S Nozza
(S)
C F Perno
(CF)
C Pinnetti
(C)
M Puoti
(M)
E Quiros Roldan
(E)
R Rossotti
(R)
S Rusconi
(S)
M M Santoro
(MM)
A Saracino
(A)
L Sarmati
(L)
A Cozzi-Lepri
(A)
I Fanti
(I)
L Galli
(L)
P Lorenzini
(P)
A Rodano'
(A)
M Macchia
(M)
A Tavelli
(A)
F Carletti
(F)
S Carrara
(S)
A Di Caro
(A)
S Graziano
(S)
F Petroni
(F)
G Prota
(G)
S Truffa
(S)
A Giacometti
(A)
A Costantini
(A)
V Barocci
(V)
G Angarano
(G)
L Monno
(L)
E Milano
(E)
F Maggiolo
(F)
C Suardi
(C)
P Viale
(P)
V Donati
(V)
G Verucchi
(G)
F Castelnuovo
(F)
C Minardi
(C)
E Quiros Roldan
(E)
B Menzaghi
(B)
C Abeli
(C)
B Cacopardo
(B)
B Celesia
(B)
J Vecchiet
(J)
K Falasca
(K)
A Pan
(A)
S Lorenzotti
(S)
L Sighinolfi
(L)
D Segala
(D)
P Blanc
(P)
F Vichi
(F)
G Cassola
(G)
C Viscoli
(C)
A Alessandrini
(A)
N Bobbio
(N)
G Mazzarello
(G)
M Lichtner
(M)
S Vita
(S)
P Bonfanti
(P)
C Molteni
(C)
A Chiodera
(A)
P Milini
(P)
G Nunnari
(G)
G Pellicanò
(G)
A d'Arminio Monforte
(A)
M Galli
(M)
A Lazzarin
(A)
G Rizzardini
(G)
M Puoti
(M)
A Castagna
(A)
E S Cannizzo
(ES)
M C Moioli
(MC)
R Piolini
(R)
D Bernacchia
(D)
S Salpietro
(S)
C Tincati
(C)
C Mussini
(C)
C Puzzolante
(C)
C Migliorino
(C)
G Lapadula
(G)
V Sangiovanni
(V)
G Borgia
(G)
V Esposito
(V)
F Di Martino
(F)
I Gentile
(I)
V Rizzo
(V)
A M Cattelan
(AM)
S Marinello
(S)
A Cascio
(A)
M Trizzino
(M)
F Baldelli
(F)
E Schiaroli
(E)
G Parruti
(G)
F Sozio
(F)
G Magnani
(G)
M A Ursitti
(MA)
M Andreoni
(M)
A Antinori
(A)
R Cauda
(R)
A Cristaudo
(A)
V Vullo
(V)
R Acinapura
(R)
D Moschese
(D)
M Capozzi
(M)
A Mondi
(A)
A Cingolani
(A)
M Rivano Capparuccia
(MR)
G Iaiani
(G)
A Latini
(A)
R Gagliardini
(R)
M M Plazzi
(MM)
S Savinelli
(S)
A Vergori
(A)
M Cecchetto
(M)
F Viviani
(F)
G Madeddu
(G)
A De Vito
(A)
B Rossetti
(B)
F Montagnani
(F)
A Franco
(A)
R Fontana Del Vecchio
(R)
D Francisci
(D)
C Di Giuli
(C)
P Caramello
(P)
G Di Perri
(G)
S Bonora
(S)
G C Orofino
(GC)
M Sciandra
(M)
M Bassetti
(M)
A Londero
(A)
G Pellizzer
(G)
V Manfrin
(V)
G Starnini
(G)
A Ialungo
(A)
Informations de copyright
© The Author(s) 2019. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For permissions, please email: journals.permissions@oup.com.