Early Antiretroviral Therapy Not Associated With Higher Cryptococcal Meningitis Mortality in People With Human Immunodeficiency Virus in High-Income Countries: An International Collaborative Cohort Study.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
05 07 2023
Historique:
received: 17 06 2022
medline: 6 7 2023
pubmed: 9 3 2023
entrez: 8 3 2023
Statut: ppublish

Résumé

Randomized controlled trials (RCTs) from low- and middle-income settings suggested that early initiation of antiretroviral therapy (ART) leads to higher mortality rates among people with HIV (PWH) who present with cryptococcal meningitis (CM). There is limited information about the impact of ART timing on mortality rates in similar people in high-income settings. Data on ART-naive PWH with CM diagnosed from 1994 to 2012 from Europe/North America were pooled from the COHERE, NA-ACCORD, and CNICS HIV cohort collaborations. Follow-up was considered to span from the date of CM diagnosis to earliest of the following: death, last follow-up, or 6 months. We used marginal structural models to mimic an RCT comparing the effects of early (within 14 days of CM) and late (14-56 days after CM) ART on all-cause mortality, adjusting for potential confounders. Of 190 participants identified, 33 (17%) died within 6 months. At CM diagnosis, their median age (interquartile range) was 38 (33-44) years; the median CD4+ T-cell count, 19/μL (10-56/μL); and median HIV viral load, 5.3 (4.9-5.6) log10 copies/mL. Most participants (n = 157 [83%]) were male, and 145 (76%) started ART. Mimicking an RCT, with 190 people in each group, there were 13 deaths among participants with an early ART regimen and 20 deaths among those with a late ART regimen. The crude and adjusted hazard ratios comparing late with early ART were 1.28 (95% confidence interval, .64-2.56) and 1.40 (.66-2.95), respectively. We found little evidence that early ART was associated with higher mortality rates among PWH presenting with CM in high-income settings, although confidence intervals were wide.

Sections du résumé

BACKGROUND
Randomized controlled trials (RCTs) from low- and middle-income settings suggested that early initiation of antiretroviral therapy (ART) leads to higher mortality rates among people with HIV (PWH) who present with cryptococcal meningitis (CM). There is limited information about the impact of ART timing on mortality rates in similar people in high-income settings.
METHODS
Data on ART-naive PWH with CM diagnosed from 1994 to 2012 from Europe/North America were pooled from the COHERE, NA-ACCORD, and CNICS HIV cohort collaborations. Follow-up was considered to span from the date of CM diagnosis to earliest of the following: death, last follow-up, or 6 months. We used marginal structural models to mimic an RCT comparing the effects of early (within 14 days of CM) and late (14-56 days after CM) ART on all-cause mortality, adjusting for potential confounders.
RESULTS
Of 190 participants identified, 33 (17%) died within 6 months. At CM diagnosis, their median age (interquartile range) was 38 (33-44) years; the median CD4+ T-cell count, 19/μL (10-56/μL); and median HIV viral load, 5.3 (4.9-5.6) log10 copies/mL. Most participants (n = 157 [83%]) were male, and 145 (76%) started ART. Mimicking an RCT, with 190 people in each group, there were 13 deaths among participants with an early ART regimen and 20 deaths among those with a late ART regimen. The crude and adjusted hazard ratios comparing late with early ART were 1.28 (95% confidence interval, .64-2.56) and 1.40 (.66-2.95), respectively.
CONCLUSIONS
We found little evidence that early ART was associated with higher mortality rates among PWH presenting with CM in high-income settings, although confidence intervals were wide.

Identifiants

pubmed: 36883578
pii: 7072297
doi: 10.1093/cid/ciad122
pmc: PMC10320049
doi:

Substances chimiques

Anti-Retroviral Agents 0

Types de publication

Journal Article Research Support, U.S. Gov't, P.H.S. Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, N.I.H., Intramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

64-73

Subventions

Organisme : Medical Research Council
Pays : United Kingdom
Organisme : Department of Health
ID : NF-SI-0611-10168
Pays : United Kingdom
Organisme : NIAAA NIH HHS
ID : U01 AA026209
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Organisme : NIAID NIH HHS
ID : R24 AI067039
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Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

Déclaration de conflit d'intérêts

Potential conflicts of interest. J. M. M. has received consulting honoraria and/or research grants from AbbVie, Angelini, Contrafect, Cubist, Genentech, Gilead Sciences, Jansen, Medtronic, MSD, Novartis, Pfizer, and ViiV Healthcare, outside the submitted work, as well as consulting fees from Lysovant. L. E. C. has stock or stock options and is an employee of AbbVie. C. Sabin reports payment or honoraria for lectures, presentations, speakers, bureaus, manuscript writing, or educational events from Gilead Sciences and ViiV Healthcare (payments to the author for preparation of educational materials); participation on a data and safety monitoring board (DSMB) or advisory board for Gilead Sciences and ViiV Healthcare (paid to the author); and service as vice chair of the British HIV Association. H. S. reports consulting fees from ViiV and MSD and payment or honoraria for lectures, presentations, speakers, bureaus, manuscript writing or educational events from MSD, ViiV, and Gilead. P. R., through his institution, has received independent scientific grant support from Gilead Sciences, Janssen Pharmaceuticals, Merck, and ViiV Healthcare and has served on scientific advisory boards for Gilead Sciences, ViiV Healthcare, and Merck, honoraria for which were all paid to his institution (all support outside the submitted work). V. B. reports support for attending meetings and/or travel from Gilead and Janssen and has stock or stock options in DWS Biotech LC Fond (private self-investment; no payments to author or institution received from any third party). F. V. received research or teaching grants from Gilead Sciences, ViiV Healthcare, and MSD, unrelated to the submitted work. N. O. reports grants or contracts from Simonsens Fond (paid to the institution). A. M. reports travel support, lecture fees, honorarium and consultancy fees from ViiV, Gilead, Eiland, and Bonnin, all outside the submitted work. L. W. reports grants or contracts from ANRS MIE. R. T. reports a research grant from Gilead Science; payment or honoraria for lectures, presentations, speakers, bureaus, manuscript writing, or educational events from Gilead Science (payment for lectures), Janssen (payment for lectures), and ViiV Healthcare (payment for lectures); support for travel from Gilead Science and Janssen; and participation on an advisory board for Gilead Science. A. D. M. reports consulting fees from ViiV, Gilead, and Janssen (paid to the author); payment or honoraria for lectures, presentations, speakers, bureaus, manuscript writing or educational events from Gilead and ViiV (paid to the author); and participation on a DSMB or advisory board for Janssen, Gilead, and ViiV (payment to the author). C. M. reports research grant from Gilead; payment or honoraria for lectures, presentations, speakers, bureaus, manuscript writing, or educational events from ViiV and Gilead; and participation on a DSMB or advisory board for Corimuno, Gilead, ViiV, Janssen, and MSD. H. F.’s institution received educational grants from AbbVie, ViiV, Gilead, MSD, Sandoz, and Pfizer, all outside the submitted work. M. S. S. reports research grants from Gilead Sciences and ViiV Healthcare (paid to the institution); payment or honoraria for lectures, presentations, speakers, bureaus, manuscript writing; or educational events from IAS-USA (not-for-profit organization); serving on the DSMB for the I-Spy COVID trial; and serving as board chair for IAS-USA. H. M. C. reports grants or contracts from the National Institutes of Health (NIH), the Agency for Healthcare Research and Quality, and ViiV (paid to institution); consulting fees from ViiV (pending); and participation on the Office of AIDS Research Scientific Advisory Board. J. J. E. reports grants or contracts from ViiV Healthcare, Gilead Sciences, and Janssen; consulting fees from Merck, ViiV Healthcare, Gilead Science, and Janssen; and leadership or fiduciary roles in other boards, societies, committees, or advocacy groups for the IAS-USA antiretroviral therapy guidelines committee. K. N. A. reports grants or contracts from the NIH (paid to institution), royalties or licenses from Coursera, consulting fees from the NIH (for the All of US Study), and payment or honoraria for lectures, presentations, speakers, bureaus, manuscript writing, or educational events for DC HIV Cohort (author served on the DC HIV Cohort’s external advisory board). M. J. G. reports consulting fees from Merck, Gilead, and ViiV (with occasional honoraria for ad hoc membership on human immunodeficiency virus advisory boards). H. C. B., in the 36 months before the submission of the current manuscript, has received grants, support for traveling, consultancy fees, and honoraria from Gilead, BMS, ViiV Healthcare, Roche, and Pfizer, unrelated to the current work. He served as the president of the Association Contre le HIV et Autres Infections Transmissibles until June 2022; in this function he received support for the Swiss HIV Cohort Study from ViiV Healthcare, Gilead, BMS, and MSD. All other authors report no potential conflicts. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.

Références

N Engl J Med. 1997 Jul 3;337(1):15-21
pubmed: 9203426
AIDS. 2013 Aug 24;27(13):2089-99
pubmed: 23525034
BMJ. 2018 Feb 1;360:k182
pubmed: 29419381
MMWR Recomm Rep. 1992 Dec 18;41(RR-17):1-19
pubmed: 1361652
Nat Commun. 2019 May 2;10(1):2035
pubmed: 31048698
Clin Infect Dis. 2011 Jun;52(11):1374-83
pubmed: 21596680
PLoS One. 2009;4(5):e5575
pubmed: 19440326
Eur J Clin Microbiol Infect Dis. 2018 Jul;37(7):1231-1240
pubmed: 29218468
PLoS One. 2010 Jul 01;5(7):e11416
pubmed: 20617176
Int J Infect Dis. 2017 Oct;63:57-63
pubmed: 28807740
Lancet Infect Dis. 2017 Aug;17(8):873-881
pubmed: 28483415
Int J Biostat. 2010;6(2):Article 18
pubmed: 21972433
Clin Infect Dis. 2010 Jun 1;50(11):1532-8
pubmed: 20415574
Med Mycol. 2021 Jul 06;59(7):712-719
pubmed: 33399865
N Engl J Med. 2014 Jun 26;370(26):2487-98
pubmed: 24963568
J Infect Dis. 2019 Feb 23;219(6):877-883
pubmed: 30325463
Lancet Infect Dis. 2019 Apr;19(4):e143-e147
pubmed: 30344084
Cochrane Database Syst Rev. 2018 Jul 24;7:CD009012
pubmed: 30039850
Clin Infect Dis. 2014 Dec 1;59(11):1607-14
pubmed: 25057102
Clin Infect Dis. 2000 Apr;30(4):710-8
pubmed: 10770733
Int J Epidemiol. 2007 Apr;36(2):294-301
pubmed: 17213214
Int J Epidemiol. 2017 Jun 1;46(3):797-797n
pubmed: 27864413
Stat Med. 2014 Sep 20;33(21):3725-37
pubmed: 24782349
Clin Infect Dis. 2013 Apr;56(8):1165-73
pubmed: 23362285
N Engl J Med. 2018 Mar 15;378(11):1004-1017
pubmed: 29539274
Antimicrob Agents Chemother. 2015 Dec;59(12):7197-204
pubmed: 26324276
N Engl J Med. 2013 Apr 4;368(14):1291-1302
pubmed: 23550668
Can J Microbiol. 2012 Jul;58(7):932-6
pubmed: 22716223
Front Med (Lausanne). 2021 Nov 19;8:779181
pubmed: 34869498
Int J Epidemiol. 2008 Oct;37(5):948-55
pubmed: 18263650

Auteurs

Suzanne M Ingle (SM)

Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.

Jose M Miro (JM)

Infectious Diseases Service Hospital Clinic-IDIBAPS, University of Barcelona, Barcelona, Spain.
CIBERINFEC, Instituto de Salud Carlos III, Madrid, Spain.

Margaret T May (MT)

Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.

Lauren E Cain (LE)

Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.
Global Epidemiology, AbbVie, Chicago, Illinois, USA.

Christine Schwimmer (C)

University of Bordeaux, INSERM, Institut Bergonié, CHU de Bordeaux, CIC-EC 1401, Bordeaux, France.

Robert Zangerle (R)

Department of Dermatology, Venereology, and Allergy, Medical University Innsbruck, Innsbruck, Austria.

Helen Sambatakou (H)

2nd Department of Internal Medicine, HIV Unit, Medical School, Hippokration General Hospital, National and Kapodistrian University of Athens, Athens, Greece.

Charles Cazanave (C)

Infectious and Tropical Diseases Department, CHU de Bordeaux, Bordeaux, France.

Peter Reiss (P)

Stichting HIV Monitoring, Amsterdam, The Netherlands.

Vanessa Brandes (V)

Department I of Internal Medicine, Division of Infectious Diseases, University of Cologne, Cologne, Germany.

Heiner C Bucher (HC)

Basel Institute for Clinical Epidemiology & Biostatistics, Division of Infectious Diseases & Hospital Hygiene, University Hospital Basel, Basel, Switzerland.

Caroline Sabin (C)

Centre for Clinical Research, Epidemiology, Modelling and Evaluation, Institute for Global Health, University College London, London, United Kingdom.

Francesc Vidal (F)

Infectious Diseases Unit, Hospital Universitari de Tarragona Joan XXIII, IISPV, Universitat Rovira i Virgili, Tarragona, Spain.
CIBER Enfermedades Infecciosas, Instituto de Salud Carlos III, Madrid, Spain.

Niels Obel (N)

Department of Infectious Diseases, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.

Amanda Mocroft (A)

Centre of Excellence for Health, Immunity and Infections (CHIP) and PERSIMUNE, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

Linda Wittkop (L)

ISPED, INSERM, Bordeaux Population Health Research Center, University of Bordeaux, Bordeaux, France.

Antonella d'Arminio Monforte (A)

Clinic of Infectious and Tropical Diseases, Department of Health Sciences, University of Milan, San Paolo Hospital, Milan, Italy.

Carlo Torti (C)

Department of Surgical and Medical Sciences, University "Magna Graecia,", Catanzaro, Italy.

Cristina Mussini (C)

Infectious Diseases Unit, University of Modena and Reggio Emilia, Modena, Italy.

Hansjakob Furrer (H)

Department of Infectious Diseases, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Deborah Konopnicki (D)

Infectious Diseases Department, Saint-Pierre University Hospital, Université Libre de Bruxelles, Brussels, Belgium.

Ramon Teira (R)

Service of Internal Medicine, Hospital Universitario de Sierrallana, Torrelavega, Spain.

Michael S Saag (MS)

Center for AIDS Research, University of Alabama at Birmingham, Birmingham, Alabama, USA.

Heidi M Crane (HM)

Division of Infectious Diseases, Department of Medicine, University of Washington, Seattle, Washington, USA.

Richard D Moore (RD)

School of Medicine, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.

Jeffrey M Jacobson (JM)

Case Western Reserve University, Cleveland, Ohio, USA.

W Chris Mathews (WC)

Department of Medicine, University of California San Diego, San Diego, California, USA.

Elvin Geng (E)

Division of Infectious Diseases, Department of Medicine and the Center for Dissemination and Implementation, Institute for Public Health, Washington University in St Louis, St Louis, Missouri, USA.

Joseph J Eron (JJ)

Department of Medicine, UNC School of Medicine, Chapel Hill, North Carolina, USA.

Keri N Althoff (KN)

Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.

Abigail Kroch (A)

University of Toronto, Toronto, Ontario, Canada.

Raynell Lang (R)

Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.

M John Gill (MJ)

Department of Medicine, University of Calgary, Southern Alberta HIV Clinic, Calgary, Alberta, Canada.

Jonathan A C Sterne (JAC)

Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.

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