Burden of 375 diseases and injuries, risk-attributable burden of 88 risk factors, and healthy life expectancy in 204 countries and territories, including 660 subnational locations, 1990–2023: a systematic analysis for the Global Burden of Disease Study 2023

dc.contributor.authorHay, Simon I.en
dc.contributor.authorOng, Kanyin Lianeen
dc.contributor.authorSantomauro, Damian F.en
dc.contributor.authorBhoomadevi, A.en
dc.contributor.authorAalipour, Mohammad Aminen
dc.contributor.authorAalruz, Hasanen
dc.contributor.authorAbabneh, Hazim S.en
dc.contributor.authorAbaraogu, Ukachukwu O.en
dc.contributor.authorAbate, Biruk Beletewen
dc.contributor.authorAbbafati, Cristianaen
dc.contributor.authorAbbas, Nasiren
dc.contributor.authorAbbasifard, Mitraen
dc.contributor.authorAbbasi-Kangevari, Mohsenen
dc.contributor.authorAbd ElHafeez, Samaren
dc.contributor.authorAbdalla, Ashraf Nabielen
dc.contributor.authorAbdalla, Mohammed Altiganien
dc.contributor.authorAbdallah, Emad M.en
dc.contributor.authorAbdeeq, Barkhad Adenen
dc.contributor.authorAbdel Razeq, Nadin M.I.en
dc.contributor.authorAbdelgalil, Ahmed Abdelrahmanen
dc.contributor.authorAbdel-Hameed, Redaen
dc.contributor.authorAbdelmasseh, Michaelen
dc.contributor.authorAbdelnabi, Mahmouden
dc.contributor.authorAbdel-Rahman, Wael M.en
dc.contributor.authorAbd-Elsalam, Sheriefen
dc.contributor.authorAbdi, Sepidehen
dc.contributor.authorAbdollahi, Mohammaden
dc.contributor.authorAbdoun, Meriemen
dc.contributor.authorAbdous, Armanen
dc.contributor.authorAbdul Aziz, Jeza Muhamaden
dc.contributor.authorAbdulah, Deldar Moraden
dc.contributor.authorAbdulkader, Rizwan Suliankatchien
dc.contributor.authorAbdullahi, Adamen
dc.contributor.authorAbdullahi, Auwalen
dc.contributor.authorAbdul-Rahman, Toufiken
dc.contributor.authorAbdykerimova, Kulmiraen
dc.contributor.authorAbebe Getahun, Habtamuen
dc.contributor.authorAbedi, Aidinen
dc.contributor.authorAbedi, Armitaen
dc.contributor.authorAbejew, Asrat Agaluen
dc.contributor.authorAbeldaño Zuñiga, Roberto Arielen
dc.contributor.authorAbhilash, E. S.en
dc.contributor.authorAdhikary, Ripon Kumaren
dc.contributor.authorAhmad, Danishen
dc.contributor.authorAhmed, Olien
dc.contributor.authorAsgary, Saeeden
dc.contributor.authorBagheri, Nasseren
dc.contributor.authorBurns, Richard A.en
dc.contributor.authorKamal, Md Moustafaen
dc.contributor.authorKinfu, Yohannesen
dc.date.accessioned2026-02-01T12:40:38Z
dc.date.available2026-02-01T12:40:38Z
dc.date.issued2025-10-12en
dc.description.abstractBackground For more than three decades, the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) has provided a framework to quantify health loss due to diseases, injuries, and associated risk factors. This paper presents GBD 2023 findings on disease and injury burden and risk-attributable health loss, offering a global audit of the state of world health to inform public health priorities. This work captures the evolving landscape of health metrics across age groups, sexes, and locations, while reflecting on the remaining post-COVID-19 challenges to achieving our collective global health ambitions.  Methods The GBD 2023 combined analysis estimated years lived with disability (YLDs), years of life lost (YLLs), and disability-adjusted life-years (DALYs) for 375 diseases and injuries, and risk-attributable burden associated with 88 modifiable risk factors. Of the more than 310 000 total data sources used for all GBD 2023 (about 30% of which were new to this estimation round), more than 120 000 sources were used for estimation of disease and injury burden and 59 000 for risk factor estimation, and included vital registration systems, surveys, disease registries, and published scientific literature. Data were analysed using previously established modelling approaches, such as disease modelling meta-regression version 2.1 (DisMod-MR 2.1) and comparative risk assessment methods. Diseases and injuries were categorised into four levels on the basis of the established GBD cause hierarchy, as were risk factors using the GBD risk hierarchy. Estimates stratified by age, sex, location, and year from 1990 to 2023 were focused on disease-specific time trends over the 2010–23 period and presented as counts (to three significant figures) and age-standardised rates per 100 000 person-years (to one decimal place). For each measure, 95% uncertainty intervals [UIs] were calculated with the 2·5th and 97·5th percentile ordered values from a 250-draw distribution.  Findings Total numbers of global DALYs grew 6·1% (95% UI 4·0–8·1), from 2·64 billion (2·46–2·86) in 2010 to 2·80 billion (2·57–3·08) in 2023, but age-standardised DALY rates, which account for population growth and ageing, decreased by 12·6% (11·0–14·1), revealing large long-term health improvements. Non-communicable diseases (NCDs) contributed 1·45 billion (1·31–1·61) global DALYs in 2010, increasing to 1·80 billion (1·63–2·03) in 2023, alongside a concurrent 4·1% (1·9–6·3) reduction in age-standardised rates. Based on DALY counts, the leading level 3 NCDs in 2023 were ischaemic heart disease (193 million [176–209] DALYs), stroke (157 million [141–172]), and diabetes (90·2 million [75·2–107]), with the largest increases in age-standardised rates since 2010 occurring for anxiety disorders (62·8% [34·0–107·5]), depressive disorders (26·3% [11·6–42·9]), and diabetes (14·9% [7·5–25·6]). Remarkable health gains were made for communicable, maternal, neonatal, and nutritional (CMNN) diseases, with DALYs falling from 874 million (837–917) in 2010 to 681 million (642–736) in 2023, and a 25·8% (22·6–28·7) reduction in age-standardised DALY rates. During the COVID-19 pandemic, DALYs due to CMNN diseases rose but returned to pre-pandemic levels by 2023. From 2010 to 2023, decreases in age-standardised rates for CMNN diseases were led by rate decreases of 49·1% (32·7–61·0) for diarrhoeal diseases, 42·9% (38·0–48·0) for HIV/AIDS, and 42·2% (23·6–56·6) for tuberculosis. Neonatal disorders and lower respiratory infections remained the leading level 3 CMNN causes globally in 2023, although both showed notable rate decreases from 2010, declining by 16·5% (10·6–22·0) and 24·8% (7·4–36·7), respectively. Injury-related age-standardised DALY rates decreased by 15·6% (10·7–19·8) over the same period. Differences in burden due to NCDs, CMNN diseases, and injuries persisted across age, sex, time, and location. Based on our risk analysis, nearly 50% (1·27 billion [1·18–1·38]) of the roughly 2·80 billion total global DALYs in 2023 were attributable to the 88 risk factors analysed in GBD. Globally, the five level 3 risk factors contributing the highest proportion of risk-attributable DALYs were high systolic blood pressure (SBP), particulate matter pollution, high fasting plasma glucose (FPG), smoking, and low birthweight and short gestation—with high SBP accounting for 8·4% (6·9–10·0) of total DALYs. Of the three overarching level 1 GBD risk factor categories—behavioural, metabolic, and environmental and occupational—risk-attributable DALYs rose between 2010 and 2023 only for metabolic risks, increasing by 30·7% (24·8–37·3); however, age-standardised DALY rates attributable to metabolic risks decreased by 6·7% (2·0–11·0) over the same period. For all but three of the 25 leading level 3 risk factors, age-standardised rates dropped between 2010 and 2023—eg, declining by 54·4% (38·7–65·3) for unsafe sanitation, 50·5% (33·3–63·1) for unsafe water source, and 45·2% (25·6–72·0) for no access to handwashing facility, and by 44·9% (37·3–53·5) for child growth failure. The three leading level 3 risk factors for which age-standardised attributable DALY rates rose were high BMI (10·5% [0·1 to 20·9]), drug use (8·4% [2·6 to 15·3]), and high FPG (6·2% [–2·7 to 15·6]; non-significant).  Interpretation Our findings underscore the complex and dynamic nature of global health challenges. Since 2010, there have been large decreases in burden due to CMNN diseases and many environmental and behavioural risk factors, juxtaposed with sizeable increases in DALYs attributable to metabolic risk factors and NCDs in growing and ageing populations. This long-observed consequence of the global epidemiological transition was only temporarily interrupted by the COVID-19 pandemic. The substantially decreasing CMNN disease burden, despite the 2008 global financial crisis and pandemic-related disruptions, is one of the greatest collective public health successes known. However, these achievements are at risk of being reversed due to major cuts to development assistance for health globally, the effects of which will hit low-income countries with high burden the hardest. Without sustained investment in evidence-based interventions and policies, progress could stall or reverse, leading to widespread human costs and geopolitical instability. Moreover, the rising NCD burden necessitates intensified efforts to mitigate exposure to leading risk factors—eg, air pollution, smoking, and metabolic risks, such as high SBP, BMI, and FPG—including policies that promote food security, healthier diets, physical activity, and equitable and expanded access to potential treatments, such as GLP-1 receptor agonists. Decisive, coordinated action is needed to address long-standing yet growing health challenges, including depressive and anxiety disorders. Yet this can be only part of the solution. Our response to the NCD syndemic—the complex interaction of multiple health risks, social determinants, and systemic challenges—will define the future landscape of global health. To ensure human wellbeing, economic stability, and social equity, global action to sustain and advance health gains must prioritise reducing disparities by addressing socioeconomic and demographic determinants, ensuring equitable health-care access, tackling malnutrition, strengthening health systems, and improving vaccination coverage. We live in times of great opportunity.  Funding Gates Foundation and Bloomberg Philanthropies.en
dc.description.sponsorshipResearch reported in this publication was supported by the Gates Foundation (OPP1152504); Queensland Department of Health, Australia; UK Department of Health and Social Care; the Norwegian Institute of Public Health; St Jude Children's Research Hospital; the New Zealand Ministry of Health; and Bloomberg Philanthropies. The content is solely the responsibility of the authors and does not necessarily represent the official views of the funders. This study has been realized using the data collected by the Swiss Household Panel (SHP), which is based at the Swiss Centre of Expertise in the Social Sciences FORS. The project is financed by the Swiss National Science Foundation. The HRS (Health and Retirement Study) is sponsored by the National Institute on Aging (grant number NIA U01AG009740) and is conducted by the University of Michigan. The data reported here have been supplied by the United States Renal Data System (USRDS). The interpretation and reporting of these data are the responsibility of the author(s) and in no way should be seen as an official policy or interpretation of the US government.en
dc.description.statusPeer-revieweden
dc.format.extent50en
dc.identifier.issn0140-6736en
dc.identifier.otherPubMed:41092926en
dc.identifier.otherORCID:/0000-0002-7750-4341/work/203697581en
dc.identifier.otherORCID:/0000-0002-5441-6146/work/203697920en
dc.identifier.otherORCID:/0000-0001-7891-3756/work/203697992en
dc.identifier.scopus105019277501en
dc.identifier.urihttps://hdl.handle.net/1885/733805163
dc.language.isoenen
dc.provenanceThis is an Open Access article under the CC BY 4.0 license.en
dc.rightsPublisher Copyright: © 2025 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license.en
dc.sourceThe Lancet en
dc.titleBurden of 375 diseases and injuries, risk-attributable burden of 88 risk factors, and healthy life expectancy in 204 countries and territories, including 660 subnational locations, 1990–2023: a systematic analysis for the Global Burden of Disease Study 2023en
dc.typeJournal articleen
dspace.entity.typePublicationen
local.bibliographicCitation.lastpage1922en
local.bibliographicCitation.startpage1873en
local.contributor.affiliationHay, Simon I.; University of Washingtonen
local.contributor.affiliationOng, Kanyin Liane; University of Washingtonen
local.contributor.affiliationSantomauro, Damian F.; University of Washingtonen
local.contributor.affiliationBhoomadevi, A.; Amity University, Noidaen
local.contributor.affiliationAalipour, Mohammad Amin; Shahid Beheshti University of Medical Sciencesen
local.contributor.affiliationAalruz, Hasan; Al-Zaytoonah University of Jordanen
local.contributor.affiliationAbabneh, Hazim S.; Massachusetts General Hospitalen
local.contributor.affiliationAbaraogu, Ukachukwu O.; University of the West of Scotlanden
local.contributor.affiliationAbate, Biruk Beletew; Curtin Universityen
local.contributor.affiliationAbbafati, Cristiana; University of Rome La Sapienzaen
local.contributor.affiliationAbbas, Nasir; Chinese Academy of Sciencesen
local.contributor.affiliationAbbasifard, Mitra; Rafsanjan University of Medical Sciencesen
local.contributor.affiliationAbbasi-Kangevari, Mohsen; Shahid Beheshti University of Medical Sciencesen
local.contributor.affiliationAbd ElHafeez, Samar; Alexandria Universityen
local.contributor.affiliationAbdalla, Ashraf Nabiel; Umm Al-Qura Universityen
local.contributor.affiliationAbdalla, Mohammed Altigani; Hull York Medical Schoolen
local.contributor.affiliationAbdallah, Emad M.; Qassim Universityen
local.contributor.affiliationAbdeeq, Barkhad Aden; Save the Childrenen
local.contributor.affiliationAbdel Razeq, Nadin M.I.; University of Jordanen
local.contributor.affiliationAbdelgalil, Ahmed Abdelrahman; King Saud Universityen
local.contributor.affiliationAbdel-Hameed, Reda; University of Hailen
local.contributor.affiliationAbdelmasseh, Michael; Marshall Universityen
local.contributor.affiliationAbdelnabi, Mahmoud; Mayo Clinic Scottsdale, AZen
local.contributor.affiliationAbdel-Rahman, Wael M.; University of Sharjahen
local.contributor.affiliationAbd-Elsalam, Sherief; Tanta Universityen
local.contributor.affiliationAbdi, Sepideh; Stanford Universityen
local.contributor.affiliationAbdollahi, Mohammad; Tehran University of Medical Sciencesen
local.contributor.affiliationAbdoun, Meriem; Ferhat Abbas Sétif University 1en
local.contributor.affiliationAbdous, Arman; Islamic Azad Universityen
local.contributor.affiliationAbdul Aziz, Jeza Muhamad; Komar University of Science and Technologyen
local.contributor.affiliationAbdulah, Deldar Morad; University of Dohuken
local.contributor.affiliationAbdulkader, Rizwan Suliankatchi; Indian Council of Medical Researchen
local.contributor.affiliationAbdullahi, Adam; Harvard Universityen
local.contributor.affiliationAbdullahi, Auwal; Bayero Universityen
local.contributor.affiliationAbdul-Rahman, Toufik; Toufik's World Medical Associationen
local.contributor.affiliationAbdykerimova, Kulmira; Kazakh National Medical Universityen
local.contributor.affiliationAbebe Getahun, Habtamu; Gondar Universityen
local.contributor.affiliationAbedi, Aidin; University of Southern Californiaen
local.contributor.affiliationAbedi, Armita; Zanjan University of Medical Sciencesen
local.contributor.affiliationAbejew, Asrat Agalu; Bahar Dar Universityen
local.contributor.affiliationAbeldaño Zuñiga, Roberto Ariel; University of Sierra Suren
local.contributor.affiliationAbhilash, E. S.; University of Calicuten
local.contributor.affiliationAdhikary, Ripon Kumar; The Australian National Universityen
local.contributor.affiliationAhmad, Danish; School of Medicine and Psychology, ANU College of Science and Medicine, The Australian National Universityen
local.contributor.affiliationAhmed, Oli; University of Chittagongen
local.contributor.affiliationAsgary, Saeed; Shahid Beheshti University of Medical Sciencesen
local.contributor.affiliationBagheri, Nasser; University of Canberraen
local.contributor.affiliationBurns, Richard A.; National Centre for Epidemiology and Population Health, ANU College of Law, Governance and Policy, The Australian National Universityen
local.contributor.affiliationKamal, Md Moustafa; The University of Sydneyen
local.contributor.affiliationKinfu, Yohannes; The Pacific Communityen
local.identifier.citationvolume406en
local.identifier.doi10.1016/S0140-6736(25)01637-Xen
local.identifier.pure93af182a-8a08-4349-9055-af741f357dceen
local.identifier.urlhttps://www.scopus.com/pages/publications/105019277501en
local.type.statusPublisheden

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