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Author Notes:

Correspondence: M. T. May, School of Social and Community Medicine, University of Bristol, Bristol BS8 2PS, UK (m.t.may@bristol.ac.uk).

See Publication for full list of authors.

We thank all patients, doctors, and study nurses associated with the participating cohort studies.

M. T. M. and J. A. C. S. report grants from the UK MRC and the UK National Institute for Health Research, during the conduct of the study.

P. R. reports grants from Gilead Sciences, ViiV Healthcare, Janssen Pharmaceutica, Bristol-Myers Squibb, and Merck; and honoraria paid to institution from Gilead Sciences for Scientific Advisory Board participation, from Janssen Pharmaceutica for Data Safety Monitoring Board participation, and from ViiV healthcare for chairing scientific symposium.

F. B. reports grants from Gilead; personal fees from Gilead, ViiV Healthcare, Janssen, BMS, and Pierre Fabre Dermatology; and nonfinancial support from Gilead, ViiV Healthcare, Janssen, and BMS.

M. J. G. reports personal fees from the ad hoc HIV advisory boards to Merck, Gilead, and ViiV Healthcare.

J.-J. V. reports grants from Astellas, Basilea, Merck/MSD, Gilead, and Pfizer; personal fees from Basilea, Merck/MSD, Gilead, and Pfizer; and nonfinancial support from Astellas, Merck/MSD, and Gilead.

M. C. reports grants from Gilead and ViiV.

G. A. B. reports grants from Bristol-Myers Squibb, and research support to institution from Amgen and consultant fee from Definitcare, LLC.

H. M. C. reports grants from NIH and Patient-Centered Outcomes Research Institute.

T. R. S. reports grants from Wellcome Trust.

J. M. M. reports research and academic grants, personal fees, and fees for lectures from AbbVie, BMS, Gilead, Merck, Novartis, Pfizer, and ViiV Healthcare.

All other authors report no potential conflicts.

Subjects:

Research Funding:

This work is jointly funded by the UK Medical Research Council (MRC) (grant number MR/J002380/1) and the UK Department for International Development (DFID) under the MRC/DFID Concordat agreement and is also part of the EDCTP2 program supported by the European Union.

J. A. C. S. is funded by a National Institute for Health Research Senior Investigator award (NF-SI-0611-10168).

Sources of funding of individual cohorts include the Agence Nationale de Recherche sur le SIDA et les hépatites virales; the Institut National de la Santé et de la Recherche Médicale; the French, Italian, and Spanish Ministries of Health; the Swiss National Science Foundation (grant 33CS30_134277); the Ministry of Science and Innovation and the Spanish Network for AIDS Research (ISCIII-RETIC RD06/006); the Stichting HIV Monitoring; the European Commission (EuroCoord grant 260694); the British Columbia and Alberta governments, the National Institutes of Health (NIH) (UW Center for AIDS Research [CFAR], NIH grant P30 AI027757); University of Alabama at Birmingham CFAR (NIH grant P30-AI027767); the Vanderbilt-Meharry CFAR (NIH grant P30 AI54999); the National Institute on Alcohol Abuse and Alcoholism (U10-AA13566;, U24-AA020794); the US Department of Veterans Affairs; the Michael Smith Foundation for Health Research; the Canadian Institutes of Health Research; the Veterans Health Administration Office of Research and Development; and unrestricted grants from Abbott, Gilead, Tibotec-Upjohn, ViiV Healthcare, MSD, GlaxoSmithKline, Pfizer, Bristol-Myers Squibb, Roche, and Boehringer-Ingelheim.

COHERE receives funding from the European Union Seventh Framework Programme (FP7/2007–2013) under EuroCoord grant agreement number 260694.

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Immunology
  • Infectious Diseases
  • Microbiology
  • HIV
  • CD4 count
  • antiretroviral therapy
  • mortality
  • cohort collaboration
  • T-CELL RECOVERY
  • HIV-1-INFECTED PATIENTS
  • SURVIVAL
  • INITIATION
  • PROGNOSIS
  • INTENSIFICATION
  • MARAVIROC
  • PREDICT
  • RISK
  • TIME

Mortality According to CD4 Count at Start of Combination Antiretroviral Therapy Among HIV-infected Patients Followed for up to 15 Years After Start of Treatment: Collaborative Cohort Study

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Journal Title:

Clinical Infectious Diseases

Volume:

Volume 62, Number 12

Publisher:

, Pages 1571-1577

Type of Work:

Article | Final Publisher PDF

Abstract:

Background. CD4 count at start of combination antiretroviral therapy (ART) is strongly associated with short-term survival, but its association with longer-term survival is less well characterized. Methods. We estimated mortality rates (MRs) by time since start of ART (<0.5, 0.5-0.9, 1-2.9, 3-4.9, 5-9.9, and ≥10 years) among patients from 18 European and North American cohorts who started ART during 1996-2001. Piecewise exponential models stratified by cohort were used to estimate crude and adjusted (for sex, age, transmission risk, period of starting ART [1996-1997, 1998-1999, 2000-2001], and AIDS and human immunodeficiency virus type 1 RNA at baseline) mortality rate ratios (MRRs) by CD4 count at start of ART (0-49, 50-99, 100-199, 200-349, 350-499, ≥500 cells/μL) overall and separately according to time since start of ART. Results. A total of 6344 of 37 496 patients died during 359 219 years of follow-up. The MR per 1000 person-years was 32.8 (95% confidence interval [CI], 30.2-35.5) during the first 6 months, declining to 16.0 (95% CI, 15.4-16.8) during 5-9.9 years and 14.2 (95% CI, 13.3-15.1) after 10 years' duration of ART. During the first year of ART, there was a strong inverse association of CD4 count at start of ART with mortality. This diminished over the next 4 years. The adjusted MRR per CD4 group was 0.97 (95% CI,. 94-1.00; P =. 054) and 1.02 (95% CI,. 98-1.07; P =. 32) among patients followed for 5-9.9 and ≥10 years, respectively. Conclusions. After surviving 5 years of ART, the mortality of patients who started ART with low baseline CD4 count converged with mortality of patients with intermediate and high baseline CD4 counts.

Copyright information:

© 2016 The Author. Published by Oxford University Press for the Infectious Diseases Society of America.

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/).
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