TY - JOUR
T1 - Trends in underlying causes of death in people with HIV from 1999 to 2011 (D:A:D): A multicohort collaboration
T2 - The Lancet
AU - Smith, C.J.
AU - Ryom, L.
AU - Weber, R.
AU - Morlat, P.
AU - Pradier, C.
AU - Reiss, P.
AU - Kowalska, J.D.
AU - De Wit, S.
AU - Law, M.
AU - Sadr, W.
AU - Kirk, O.
AU - Friis-Moller, N.
AU - D'Arminio Monforte, A.
AU - Phillips, A.N.
AU - Sabin, C.A.
AU - Lundgren, J.D.
AU - Torres, Ferran
N1 - Cited By :572
Export Date: 17 February 2022
CODEN: LANCA
Correspondence Address: Smith, C.J.; Research Department of Infection and Population Health, Rowland Hill Street, London NW3 2PF, United Kingdom; email: c.smith@ucl.ac.uk
Funding details: U.S. Food and Drug Administration, FDA
Funding details: Abbott Laboratories
Funding details: Bristol-Myers Squibb, BMS
Funding details: Pfizer
Funding details: GlaxoSmithKline, GSK
Funding details: Merck
Funding details: Roche
Funding details: Gilead Sciences
Funding details: AbbVie
Funding details: F. Hoffmann-La Roche
Funding details: Boehringer Ingelheim
Funding details: Janssen Pharmaceuticals
Funding details: Merck Sharp and Dohme, MSD
Funding details: ViiV Healthcare
Funding details: Gilead UK and Ireland Corporate Contributions
Funding details: Medical Research Council, MRC, G0701639
Funding details: European Commission, EC
Funding text 1: CJS reports personal fees from Gilead Sciences Ltd, Bristol-Myers Squibb, Janssen, and ViiV Healthcare. ANP reports personal fees from Gilead, grants from BMS, personal fees from GSK Vaccines, and personal fees from Abbvie. NFM reports personal fees from BMS, Pfizer, and Viiv Healthcare. CAS reports personal fees from Gilead Sciences, Bristol-Myers Squibb, Janssen-Cilag, Abbott Pharmaceuticals, and Viiv Healthcare. ML reports grants from Boehringer Ingelhiem, Bristol-Myers Squibb, Gilead, GlaxoSmithKline, Janssen-Cilag Pty Ltd, Merck Sharp and Dohme, Pfizer, and Roche. PM reports personal fees and non-financial support from Gilead Sciences Ltd, BMS, and ViiV Healthcare; personal fees from Abbott; and non-financial support from Janssen. PR reports grants and other from Gilead Sciences and Janssen Pharmaceutica, and grants from ViiV Healthcare, Merck & Co, and Bristol-Myers Squibb. SdW, CP, LRN, WES, RW, JKO, JDL, OK, and AdAM declare no competing interests.
Funding text 2: The D:A:D Study is funded by a grant from Highly Active Antiretroviral Therapy Oversight Committee (HAART-OC), a collaborative committee with representation from academic institutions, the European Agency for the Evaluation of Medicinal Products, the US Food and Drug Administration, the patient community, and all pharmaceutical companies with licensed anti-HIV drugs in the European Union: Abbott Laboratories, Boehringer Ingelheim Pharmaceuticals Inc, Bristol-Myers Squibb, Gilead Sciences Inc, Viiv Healthcare, Merck & Co Inc, Pfizer Inc, F Hoffman-La Roche Ltd, and Janssen Pharmaceuticals.
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Abstract THAB0303; Worm, S.W., Bower, M., Reiss, P., Non-AIDS defining malignancies (NADM) and immunosuppression: The D:A:D study 19th Conference on Retroviruses and Opportunistic Infections (CROI), , Seattle, Washington, USA; March 3-6, 2012. Abstract 130; Worm, S.W., Bower, M., Reiss, P., Non-AIDs defining cancers in the D:A:D study-time trends and predictors of survival: A cohort study (2013) BMC Infect Dis, 13, p. 471. , for the D:A:D Study Group; Bruyand, M., Ryom, L., Shepherd, L., Cancer Risk and Use of Protease Inhibitor-or NNRTI-based cART: The D:A:D Study 20th Conference on Retroviruses and Opportunistic Infections (CROI), , Georgia, Atlanta, USA; March 3-6, 2013. Abstract 742b; Conigliaro, J., Gordon, A.J., McGinnis, K.A., Rabeneck, L., Justice, A.C., How harmful is hazardous alcohol use and abuse in HIV infection: Do health care providers know who is at risk? 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Abstract 748; Worm, S.W., Sabin, C., Weber, R., Risk of myocardial infarction in patients with HIV infection exposed to specific individual antiretroviral drugs from the 3 major drug classes: The data collection on adverse events of anti-HIV drugs (D:A:D) study (2010) J Infect Dis, 201, pp. 318-330; Kovari, H., Sabin, C.A., Ledergerber, B., Antiretroviral drug-related liver mortality among HIV-positive persons in the absence of HBV or HCV co-infection. 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PY - 2014/7
Y1 - 2014/7
N2 - Background With the advent of effective antiretroviral treatment, the life expectancy for people with HIV is now approaching that seen in the general population. Consequently, the relative importance of other traditionally non-AIDS-related morbidities has increased. We investigated trends over time in all-cause mortality and for specific causes of death in people with HIV from 1999 to 2011. Methods Individuals from the Data collection on Adverse events of anti-HIV Drugs (D:A:D) study were followed up from March, 1999, until death, loss to follow-up, or Feb 1, 2011, whichever occurred first. The D:A:D study is a collaboration of 11 cohort studies following HIV-1-positive individuals receiving care at 212 clinics in Europe, USA, and Australia. All fatal events were centrally validated at the D:A:D coordinating centre using coding causes of death in HIV (CoDe) methodology. We calculated relative rates using Poisson regression. Findings 3909 of the 49 731 D:A:D study participants died during the 308 719 person-years of follow-up (crude incidence mortality rate, 12.7 per 1000 person-years [95% CI 12.3-13.1]). Leading underlying causes were: AIDS-related (1123 [29%] deaths), non-AIDS-defining cancers (590 [15%] deaths), liver disease (515 [13%] deaths), and cardiovascular disease (436 [11%] deaths). Rates of all-cause death per 1000 person-years decreased from 17.5 in 1999-2000 to 9.1 in 2009-11; we saw similar decreases in death rates per 1000 person-years over the same period for AIDS-related deaths (5.9 to 2.0), deaths from liver disease (2.7 to 0.9), and cardiovascular disease deaths (1.8 to 0.9). However, non-AIDS cancers increased slightly from 1.6 per 1000 person-years in 1999-2000 to 2.1 in 2009-11 (p=0.58). After adjustment for factors that changed over time, including CD4 cell count, we detected no decreases in AIDS-related death rates (relative rate for 2009-11 vs 1999-2000: 0.92 [0.70-1.22]). However, all-cause (0.72 [0.61-0.83]), liver disease (0.48 [0.32-0.74]), and cardiovascular disease (0.33 [0.20-0.53) death rates still decreased over time. The percentage of all deaths that were AIDS-related (87/256 [34%] in 1999-2000 and 141/627 [22%] in 2009-11) and liver-related (40/256 [16%] in 1999-2000 and 64/627 [10%] in 2009-11) decreased over time, whereas non-AIDS cancers increased (24/256 [9%] in 1999-2000 to 142/627 [23%] in 2009-11). Interpretation Recent reductions in rates of AIDS-related deaths are linked with continued improvement in CD4 cell count. We hypothesise that the substantially reduced rates of liver disease and cardiovascular disease deaths over time could be explained by improved use of non-HIV-specific preventive interventions. Non-AIDS cancer is now the leading non-AIDS cause and without any evidence of improvement. Funding Oversight Committee for the Evaluation of Metabolic Complications of HAART, with representatives from academia, patient community, US Food and Drug Administration, European Medicines Agency and consortium of AbbVie, Boehringer Ingelheim, Bristol-Myers Squibb, Gilead Sciences, ViiV Healthcare, Merck, Pfizer, F Hoffmann-La Roche, and Janssen Pharmaceuticals.
AB - Background With the advent of effective antiretroviral treatment, the life expectancy for people with HIV is now approaching that seen in the general population. Consequently, the relative importance of other traditionally non-AIDS-related morbidities has increased. We investigated trends over time in all-cause mortality and for specific causes of death in people with HIV from 1999 to 2011. Methods Individuals from the Data collection on Adverse events of anti-HIV Drugs (D:A:D) study were followed up from March, 1999, until death, loss to follow-up, or Feb 1, 2011, whichever occurred first. The D:A:D study is a collaboration of 11 cohort studies following HIV-1-positive individuals receiving care at 212 clinics in Europe, USA, and Australia. All fatal events were centrally validated at the D:A:D coordinating centre using coding causes of death in HIV (CoDe) methodology. We calculated relative rates using Poisson regression. Findings 3909 of the 49 731 D:A:D study participants died during the 308 719 person-years of follow-up (crude incidence mortality rate, 12.7 per 1000 person-years [95% CI 12.3-13.1]). Leading underlying causes were: AIDS-related (1123 [29%] deaths), non-AIDS-defining cancers (590 [15%] deaths), liver disease (515 [13%] deaths), and cardiovascular disease (436 [11%] deaths). Rates of all-cause death per 1000 person-years decreased from 17.5 in 1999-2000 to 9.1 in 2009-11; we saw similar decreases in death rates per 1000 person-years over the same period for AIDS-related deaths (5.9 to 2.0), deaths from liver disease (2.7 to 0.9), and cardiovascular disease deaths (1.8 to 0.9). However, non-AIDS cancers increased slightly from 1.6 per 1000 person-years in 1999-2000 to 2.1 in 2009-11 (p=0.58). After adjustment for factors that changed over time, including CD4 cell count, we detected no decreases in AIDS-related death rates (relative rate for 2009-11 vs 1999-2000: 0.92 [0.70-1.22]). However, all-cause (0.72 [0.61-0.83]), liver disease (0.48 [0.32-0.74]), and cardiovascular disease (0.33 [0.20-0.53) death rates still decreased over time. The percentage of all deaths that were AIDS-related (87/256 [34%] in 1999-2000 and 141/627 [22%] in 2009-11) and liver-related (40/256 [16%] in 1999-2000 and 64/627 [10%] in 2009-11) decreased over time, whereas non-AIDS cancers increased (24/256 [9%] in 1999-2000 to 142/627 [23%] in 2009-11). Interpretation Recent reductions in rates of AIDS-related deaths are linked with continued improvement in CD4 cell count. We hypothesise that the substantially reduced rates of liver disease and cardiovascular disease deaths over time could be explained by improved use of non-HIV-specific preventive interventions. Non-AIDS cancer is now the leading non-AIDS cause and without any evidence of improvement. Funding Oversight Committee for the Evaluation of Metabolic Complications of HAART, with representatives from academia, patient community, US Food and Drug Administration, European Medicines Agency and consortium of AbbVie, Boehringer Ingelheim, Bristol-Myers Squibb, Gilead Sciences, ViiV Healthcare, Merck, Pfizer, F Hoffmann-La Roche, and Janssen Pharmaceuticals.
KW - anti human immunodeficiency virus agent
KW - acquired immune deficiency syndrome
KW - adult
KW - article
KW - Australia
KW - cardiovascular disease
KW - cause of death
KW - CD4 lymphocyte count
KW - Europe
KW - female
KW - follow up
KW - human
KW - Human immunodeficiency virus infection
KW - liver disease
KW - major clinical study
KW - male
KW - middle aged
KW - mortality
KW - priority journal
KW - trend study
KW - United States
KW - Article
KW - cohort analysis
KW - Human immunodeficiency virus
KW - Human immunodeficiency virus 1
KW - intervention study
KW - morbidity
KW - neoplasm
KW - validation study
KW - Acquired Immunodeficiency Syndrome
KW - Adult
KW - Cause of Death
KW - Female
KW - HIV Infections
KW - Humans
KW - Male
KW - Middle Aged
KW - Poisson Distribution
KW - Risk Factors
UR - http://linkinghub.elsevier.com/retrieve/pii/S0140673614606048
U2 - 10.1016/S0140-6736(14)60604-8
DO - 10.1016/S0140-6736(14)60604-8
M3 - Article
C2 - 25042234
VL - 384
SP - 241
EP - 248
IS - 9939
ER -