TY - JOUR
T1 - Global, regional, and national incidence, prevalence, and mortality of HIV, 1980-2017, and forecasts to 2030, for 195 countries and territories
T2 - A systematic analysis for the Global Burden of Diseases, Injuries, and Risk Factors Study 2017
AU - GBD 2017 HIV collaborators
AU - Frank, Tahvi D.
AU - Carter, Austin
AU - Jahagirdar, Deepa
AU - Biehl, Molly H.
AU - Douwes-Schultz, Dirk
AU - Larson, Samantha Leigh
AU - Arora, Megha
AU - Dwyer-Lindgren, Laura
AU - Steuben, Krista M.
AU - Abbastabar, Hedayat
AU - Abu-Raddad, Laith Jamal
AU - Abyu, Direslgne Misker
AU - Adabi, Maryam
AU - Adebayo, Oladimeji M.
AU - Adekanmbi, Victor
AU - Adetokunboh, Olatunji O.
AU - Ahmadi, Alireza
AU - Ahmadi, Keivan
AU - Ahmadian, Elham
AU - Ahmadpour, Ehsan
AU - Ahmed, Muktar Beshir
AU - Akal, Chalachew Genet
AU - Alahdab, Fares
AU - Alam, Noore
AU - Albertson, Samuel B.
AU - Alemnew, Birhan Tamene T.
AU - Alene, Kefyalew Addis
AU - Alipour, Vahid
AU - Alvis-Guzman, Nelson
AU - Amini, Saeed
AU - Anbari, Zohreh
AU - Anber, Nahla Hamed
AU - Anjomshoa, Mina
AU - Antonio, Carl Abelardo T.
AU - Arabloo, Jalal
AU - Aremu, Olatunde
AU - Areri, Habtamu Abera
AU - Asfaw, Ephrem Tsegay
AU - Ashagre, Alebachew Fasil
AU - Asmelash, Daniel
AU - Asrat, Anemaw A.
AU - Avokpaho, Euripide F.G.A.
AU - Awasthi, Ashish
AU - Awoke, Nefsu
AU - Ayanore, Martin Amogre
AU - Azari, Samad
AU - Badawi, Alaa
AU - Bagherzadeh, Mojtaba
AU - Banach, Maciej
AU - Unnikrishnan, Bhaskaran
AU - P C, Jagadish
N1 - Funding Information:
Research reported in this publication was supported by the Bill & Melinda Gates Foundation, the National Institute on Aging (NIA) of the NIH (award P30AG047845), and the National Institute of Mental Health of the NIH (award R01MH110163). The content is solely the responsibility of the authors and does not necessarily represent the official views of the Bill & Melinda Gates Foundation or the NIH. We thank Jeffery W Eaton from Imperial College London for the thoughtful feedback on an earlier version of this report. L J Abu-Raddad acknowledges the support of the Qatar National Research Fund (NPRP 9-040-3-008) who provided the main funding for generating the data provided to the GBD and Institute for Health Metrics and Evaluation effort. A Awasthi acknowledges funding support from the Department of Science and Technology, Government of India through the INSPIRE Faculty scheme. T B?rnighausen acknowledges support by the Alexander von Humboldt Foundation through the Alexander von Humboldt Professor award, funded by the Federal Ministry of Education and Research; the Wellcome Trust; and from National Institute of Child Health and Human Development (NICHD) of NIH (R01-HD084233), NIA of NIH (P01-AG041710), National Institute of Allergy and Infectious Diseases (NIAID) of NIH (R01-AI124389 and R01-AI112339), and Fogarty International Center (FIC) of NIH (D43-TW009775). A Badawi acknowledges the support of the Public Health Agency of Canada. A Barac acknowledges support for research from the Project of Ministry of Education, Science and Technology of the Republic of Serbia (No. III45005). M S Bin Sayeed acknowledges support from the Australian Government Research and Training Scholarship for PhD degree at the Australian National University, Australia. F Carvalho acknowledges UID/MULTI/04378/2019 and UID/QUI/50006/2019 support with funding from Funda??o para a Ci?ncia e a Tecnologia, Minist?rio da Ci?ncia, Tecnologia e Ensino Superior through national funds. J W De Neve acknowledges support by the Alexander von Humboldt Foundation. L Degenhardt acknowledges support by Australian National Health and Medical Research Council Fellowships (1135991, 1041742) and is supported by National Institute on Drug Abuse of NIH grants (R01DA1104470). D Demissie acknowledges support from the Bill & Melinda Gates Foundation. K Deribe acknowledges support from the Wellcome Trust (grant number 201900) as part of his International Intermediate Fellowship. A P Kengne acknowledges support from the South African Medical Research Council. Y J Kim acknowledges support from the Office of Research and Innovation, Xiamen University Malaysia. M Kumar acknowledges support from the FIC of the NIH (K43TW010716). O Oladimeji acknowledges support from the Human Sciences Research Council, South Africa, FIC of the NIH, and the University of Namibia. A M Samy acknowledges support from a fellowship from the Egyptian Fulbright Mission Program. A E Schutte acknowledges financial support from the South African Medical Research Council and National Research Foundation SARChI Research Programme. K Shibuya acknowledges support and grants from Japan Ministry of Health, Labour and Welfare, and grants from King's College London during the conduct of the study. N Taveira acknowledges partial funding by Funda??o para a Ci?ncia e Tecnologia, Portugal, and Aga Khan Development Network - Portugal Collaborative Research Network in Portuguese speaking countries in Africa (project 332821690) and by the European and Developing Countries Clinical Trials Partnership (project RIA2016MC-1615). S Topp acknowledges support by Rising Star Early Career Researcher Award from James Cook University, QLD, Australia and a National Health and Medical Research Council Hot North Career Development Fellowship. M Yotebieng acknowledges partial support from the NIAID of NIH (U01AI096299) and NICHD of the NIH (R01H087993).
Funding Information:
Research reported in this publication was supported by the Bill & Melinda Gates Foundation , the National Institute on Aging (NIA) of the NIH ( award P30AG047845 ), and the National Institute of Mental Health of the NIH ( award R01MH110163 ). The content is solely the responsibility of the authors and does not necessarily represent the official views of the Bill & Melinda Gates Foundation or the NIH. We thank Jeffery W Eaton from Imperial College London for the thoughtful feedback on an earlier version of this report. L J Abu-Raddad acknowledges the support of the Qatar National Research Fund ( NPRP 9-040-3-008 ) who provided the main funding for generating the data provided to the GBD and Institute for Health Metrics and Evaluation effort. A Awasthi acknowledges funding support from the Department of Science and Technology, Government of India through the INSPIRE Faculty scheme. T Bärnighausen acknowledges support by the Alexander von Humboldt Foundation through the Alexander von Humboldt Professor award, funded by the Federal Ministry of Education and Research; the Wellcome Trust; and from National Institute of Child Health and Human Development (NICHD) of NIH ( R01-HD084233 ), NIA of NIH ( P01-AG041710 ), National Institute of Allergy and Infectious Diseases (NIAID) of NIH ( R01-AI124389 and R01-AI112339 ), and Fogarty International Center (FIC) of NIH ( D43-TW009775 ). A Badawi acknowledges the support of the Public Health Agency of Canada. A Barac acknowledges support for research from the Project of Ministry of Education, Science and Technology of the Republic of Serbia ( No. III45005 ). M S Bin Sayeed acknowledges support from the Australian Government Research and Training Scholarship for PhD degree at the Australian National University, Australia. F Carvalho acknowledges UID/MULTI/04378/2019 and UID/QUI/50006/2019 support with funding from Fundação para a Ciência e a Tecnologia, Ministério da Ciência, Tecnologia e Ensino Superior through national funds. J W De Neve acknowledges support by the Alexander von Humboldt Foundation. L Degenhardt acknowledges support by Australian National Health and Medical Research Council Fellowships ( 1135991 , 1041742 ) and is supported by National Institute on Drug Abuse of NIH grants ( R01DA1104470 ). D Demissie acknowledges support from the Bill & Melinda Gates Foundation. K Deribe acknowledges support from the Wellcome Trust ( grant number 201900 ) as part of his International Intermediate Fellowship. A P Kengne acknowledges support from the South African Medical Research Council. Y J Kim acknowledges support from the Office of Research and Innovation, Xiamen University Malaysia. M Kumar acknowledges support from the FIC of the NIH ( K43TW010716 ). O Oladimeji acknowledges support from the Human Sciences Research Council, South Africa, FIC of the NIH, and the University of Namibia. A M Samy acknowledges support from a fellowship from the Egyptian Fulbright Mission Program. A E Schutte acknowledges financial support from the South African Medical Research Council and National Research Foundation SARChI Research Programme. K Shibuya acknowledges support and grants from Japan Ministry of Health, Labour and Welfare, and grants from King's College London during the conduct of the study. N Taveira acknowledges partial funding by Fundação para a Ciência e Tecnologia, Portugal, and Aga Khan Development Network - Portugal Collaborative Research Network in Portuguese speaking countries in Africa (project 332821690) and by the European and Developing Countries Clinical Trials Partnership ( project RIA2016MC-1615 ). S Topp acknowledges support by Rising Star Early Career Researcher Award from James Cook University, QLD, Australia and a National Health and Medical Research Council Hot North Career Development Fellowship. M Yotebieng acknowledges partial support from the NIAID of NIH ( U01AI096299 ) and NICHD of the NIH ( R01H087993 ).
Publisher Copyright:
© 2019 The Author(s).
PY - 2019/12
Y1 - 2019/12
N2 - Background Understanding the patterns of HIV/AIDS epidemics is crucial to tracking and monitoring the progress of prevention and control efforts in countries. We provide a comprehensive assessment of the levels and trends of HIV/AIDS incidence, prevalence, mortality, and coverage of antiretroviral therapy (ART) for 1980-2017 and forecast these estimates to 2030 for 195 countries and territories. Methods We determined a modelling strategy for each country on the basis of the availability and quality of data. For countries and territories with data from population-based seroprevalence surveys or antenatal care clinics, we estimated prevalence and incidence using an open-source version of the Estimation and Projection Package - a natural history model originally developed by the UNAIDS Reference Group on Estimates, Modelling, and Projections. For countries with cause-specific vital registration data, we corrected data for garbage coding (ie, deaths coded to an intermediate, immediate, or poorly defined cause) and HIV misclassification. We developed a process of cohort incidence bias adjustment to use information on survival and deaths recorded in vital registration to back-calculate HIV incidence. For countries without any representative data on HIV, we produced incidence estimates by pulling information from observed bias in the geographical region. We used a re-coded version of the Spectrum model (a cohort component model that uses rates of disease progression and HIV mortality on and off ART) to produce agesex- specific incidence, prevalence, and mortality, and treatment coverage results for all countries, and forecast these measures to 2030 using Spectrum with inputs that were extended on the basis of past trends in treatment scale-up and new infections. Findings Global HIV mortality peaked in 2006 with 1·95 million deaths (95% uncertainty interval 1·87-2·04) and has since decreased to 0·95 million deaths (0·91-1·01) in 2017. New cases of HIV globally peaked in 1999 (3·16 million, 2·79-3·67) and since then have gradually decreased to 1·94 million (1·63-2·29) in 2017. These trends, along with ART scale-up, have globally resulted in increased prevalence, with 36·8 million (34·8-39·2) people living with HIV in 2017. Prevalence of HIV was highest in southern sub-Saharan Africa in 2017, and countries in the region had ART coverage ranging from 65·7% in Lesotho to 85·7% in eSwatini. Our forecasts showed that 54 countries will meet the UNAIDS target of 81% ART coverage by 2020 and 12 countries are on track to meet 90% ART coverage by 2030. Forecasted results estimate that few countries will meet the UNAIDS 2020 and 2030 mortality and incidence targets. Interpretation Despite progress in reducing HIV-related mortality over the past decade, slow decreases in incidence, combined with the current context of stagnated funding for related interventions, mean that many countries are not on track to reach the 2020 and 2030 global targets for reduction in incidence and mortality. With a growing population of people living with HIV, it will continue to be a major threat to public health for years to come. The pace of progress needs to be hastened by continuing to expand access to ART and increasing investments in proven HIV prevention initiatives that can be scaled up to have population-level impact.
AB - Background Understanding the patterns of HIV/AIDS epidemics is crucial to tracking and monitoring the progress of prevention and control efforts in countries. We provide a comprehensive assessment of the levels and trends of HIV/AIDS incidence, prevalence, mortality, and coverage of antiretroviral therapy (ART) for 1980-2017 and forecast these estimates to 2030 for 195 countries and territories. Methods We determined a modelling strategy for each country on the basis of the availability and quality of data. For countries and territories with data from population-based seroprevalence surveys or antenatal care clinics, we estimated prevalence and incidence using an open-source version of the Estimation and Projection Package - a natural history model originally developed by the UNAIDS Reference Group on Estimates, Modelling, and Projections. For countries with cause-specific vital registration data, we corrected data for garbage coding (ie, deaths coded to an intermediate, immediate, or poorly defined cause) and HIV misclassification. We developed a process of cohort incidence bias adjustment to use information on survival and deaths recorded in vital registration to back-calculate HIV incidence. For countries without any representative data on HIV, we produced incidence estimates by pulling information from observed bias in the geographical region. We used a re-coded version of the Spectrum model (a cohort component model that uses rates of disease progression and HIV mortality on and off ART) to produce agesex- specific incidence, prevalence, and mortality, and treatment coverage results for all countries, and forecast these measures to 2030 using Spectrum with inputs that were extended on the basis of past trends in treatment scale-up and new infections. Findings Global HIV mortality peaked in 2006 with 1·95 million deaths (95% uncertainty interval 1·87-2·04) and has since decreased to 0·95 million deaths (0·91-1·01) in 2017. New cases of HIV globally peaked in 1999 (3·16 million, 2·79-3·67) and since then have gradually decreased to 1·94 million (1·63-2·29) in 2017. These trends, along with ART scale-up, have globally resulted in increased prevalence, with 36·8 million (34·8-39·2) people living with HIV in 2017. Prevalence of HIV was highest in southern sub-Saharan Africa in 2017, and countries in the region had ART coverage ranging from 65·7% in Lesotho to 85·7% in eSwatini. Our forecasts showed that 54 countries will meet the UNAIDS target of 81% ART coverage by 2020 and 12 countries are on track to meet 90% ART coverage by 2030. Forecasted results estimate that few countries will meet the UNAIDS 2020 and 2030 mortality and incidence targets. Interpretation Despite progress in reducing HIV-related mortality over the past decade, slow decreases in incidence, combined with the current context of stagnated funding for related interventions, mean that many countries are not on track to reach the 2020 and 2030 global targets for reduction in incidence and mortality. With a growing population of people living with HIV, it will continue to be a major threat to public health for years to come. The pace of progress needs to be hastened by continuing to expand access to ART and increasing investments in proven HIV prevention initiatives that can be scaled up to have population-level impact.
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UR - http://www.scopus.com/inward/citedby.url?scp=85075667976&partnerID=8YFLogxK
U2 - 10.1016/S2352-3018(19)30196-1
DO - 10.1016/S2352-3018(19)30196-1
M3 - Article
C2 - 31439534
AN - SCOPUS:85075667976
SN - 2352-3018
VL - 6
SP - e831-e859
JO - The Lancet HIV
JF - The Lancet HIV
IS - 12
ER -