Nasir Abbas

56940204900

Publications - 7

Global, Regional, and National Burden of Cardiovascular Diseases and Risk Factors in 204 Countries and Territories, 1990-2023

Nermeen Abu-Elala Rana Kamal Abu Farha Madineh Abbasi Abdallah H.A. Abd Al Magied Kamoru Ademola Adedokun Nurudeen A. Adegoke Eman Abu-Gharbieh Lisa C. Adams Mesfin Abebe Armita Abedi Mohammad Amin Aalipour A. Bhoomadevi Bedru J. Abafita Ukachukwu O. Abaraogu Dariush Abtahi Ripon Kumar Adhikary Mohd Adnan Hasan Aalruz E. S. Abhilash Hana J. Abukhadijah Muhammad Sohail Afzal Nasir Abbas Bedru J. Abafita Tanin Adl Parvar César Agostinis Sobrinho Saira Afzal Samar Abd Elhafeez Navidha Aggarwal Olorunsola Israel Adeyomoye Nermeen Abu-Elala Prof Bhoomadevi A Benjamin A. Stark Nicole K. DeCleene Prerna Agarwal Emily C. Desai Johnathan M. Hsu Catherine O. Johnson Laura Lara-Castor Suneth Buddhika Agampodi Sepehr Aghajanian Prof Ahmed Abdelalim Salahdein Aburuz Omar M. Abdelfattah Prof Reda Abdel-Hameed Prof Wael M Abdel-Rahman Mahmoud Abdelnabi Lucas Guimarães Abreu Prof Olumide Abiodun Rui Adão Mujahid Abdullah Apurba Acharya Aminu Kende Kende Abubakar Ibrahim Jatau Abubakar Swetha Acharya Charles Oluwaseun Adetunji Rishan Adha Wirawan Adikusuma Lawan Hassan Adamu Qorinah Estiningtyas Sakilah Adnani Gina Agarwal Ahmed M. Afifi Fatemeh Afrashteh Hedayat Abbastabar Samar Abd ElHafeez Asrat Agalu Abejew Kulmira Abdykerimova Aidin Abedi Olugbenga Olusola Abiodun Shady Abohashem Rahim Abo Kasem Nagah M. Abourashed Dmitry Abramov Anirudh Balakrishna Acharya Meshack Achore Ousman Adal Habeeb Abiodun Afolabi Hasan Aalruz Arman Abdous Auwal Abdullahi Isaac Yeboah Addo David Adedia Hassan Abolhassani Richard Gyan Aboagye Ulric Sena Abonie Abdullahi Tunde Aborode Parsa Abdi Wakgari Mosisa Abdisa Victor Adekanmbi Kate E. LeGrand Mohammad Abavisani Oladimeji Muritala Adebayo Oyelola A. Adegboye Daba Abdissa Mohammadreza Abbasian Arya Afrooghe Dhiraj Motilal Agarwal Temesgen Anjulo Ageru Dina Abushanab Tajudeen Adesanmi Adebisi Oluwatobi E. Adegbile Olumide Thomas Adeleke David Adzrago Leticia Akua Adzigbli Nasir Abbas Prince Owusu Adoma Kishor Adhikari Salahdein Aburuz

Publication Name: Journal of the American College of Cardiology

Publication Date: 2025-12-02

Volume: 86

Issue: 22

Page Range: 2167-2243

Description:

Background: Cardiovascular diseases (CVDs) are the leading cause of mortality and are among the foremost causes of disability globally. CVD burden has continued to increase in most countries since 1990, with trends driven by changing exposures to harmful risk factors, population growth, and population aging. Objectives: We report estimates of global, national, and subnational CVD burden, including 18 subdiseases and 12 associated modifiable risk factors. We analyzed change in CVD burden from 1990 to 2023 and identified drivers of change including population growth, population aging, and risk factor exposure. Methods: The Global Burden of Disease (GBD) 2023 study, a multinational collaborative research study, quantified burden due to 375 diseases including CVD burden and identified drivers of change from 1990 to 2023 using all available data and statistical models. GBD 2023 estimated the population-level burden of diseases in 204 countries and territories from 1990 to 2023. Results: CVDs were the leading cause of disability-adjusted life years (DALYs) and deaths estimated in the GBD. As of 2023, there were 437 million (95% UI: 401 to 465 million) CVD DALYs globally, a 1.4-fold increase from the number in 1990 of 320 million (292 to 344 million). Ischemic heart disease, intracerebral hemorrhage, ischemic stroke, and hypertensive heart disease were the leading cardiovascular causes of DALYs in 2023 globally. As of 2023, age-standardized CVD DALY rates were highest in low and low-middle Socio-demographic Index (SDI) settings and lowest in high SDI settings. The number of CVD deaths increased globally from 13.1 million (95% UI: 12.2 to 14.0 million) in 1990 to 19.2 million (95% UI: 17.4 to 20.4 million) in 2023. The number of prevalent cases of CVD more than doubled since 1990, with 311 million (95% UI: 294 to 333 million) prevalent cases of CVD in 1990 and 626 million (95% UI: 591 to 672 million) prevalent cases in 2023 globally. A total of 79.6% (95% UI: 75.7% to 82.5%) of CVD burden is attributable to modifiable risk factors 347 million [95% UI: 318 to 373 million] DALYs in 2023). Globally, high systolic blood pressure, dietary risks, high low-density lipoprotein cholesterol, and air pollution were the modifiable risks responsible for most attributable CVD burden in 2023. Since 1990, changes in exposure to modifiable risk factors have had mixed effects on CVD burden, with increases in high body mass index, high fasting plasma glucose, and low physical activity leading to higher burden, while reductions in tobacco usage have mitigated some of these increases. Population growth and population aging were the main drivers of the increasing burden since 1990, adding 128 million (95% UI: 115 to 139 million) and 139 million (95% UI: 126 to 151 million) CVD DALYs to the increase in CVD burden since 1990. Conclusions: CVD remains the leading cause of disease burden and death worldwide with the greatest burden in low, low-middle, and middle SDI regions. Large variation exists in CVD burden even for countries at similar levels of development, a gap explained substantially by known, modifiable risk factors that are inadequately controlled. The decades-long increase in CVD burden was the result of population growth, population aging, and increased exposure to a subset of risk factors led by metabolic risks. Countries will need to adopt effective health system and public health strategies if they are to progress in achieving global goals to reduce the burden of CVD.

Open Access: Yes

DOI: 10.1016/j.jacc.2025.08.015

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

Jeza Muhamad Abdul Aziz Shehab Uddin Al Abid Niveen M.E. Abu-Rmeileh Rana Kamal Abu Farha Cristiana Abbafati Barkhad Aden Abdeeq Mohammed Altigani Abdalla Nadin M.I. Abdel Razeq Ahmed Abdelrahman Abdelgalil Wael M. Abdel-Rahman Reda Abdel-Hameed Aminu Kende Abubakar Michael Abdelmasseh Kamoru Ademola Adedokun Nurudeen A. Adegoke Isaac Ayodeji Adesina Ashraf Nabiel Abdalla Raghu Ram Achar Habtamu Abebe Getahun Eman Abu-Gharbieh Lisa C. Adams Armita Abedi Usha Adiga Mitra Abbasifard Mohammad Amin Aalipour A. Bhoomadevi Hazim S. Ababneh Ukachukwu O. Abaraogu Dariush Abtahi Rizwan Suliankatchi Abdulkader Ripon Kumar Adhikary Mohd Adnan Simon I. Hay Kanyin Liane Ong Damian F. Santomauro Biruk Beletew Abate Hasan Aalruz Mohsen Abbasi-Kangevari Sepideh Abdi Roberto Ariel Abeldaño Zuñiga Mohammad Abdollahi E. S. Abhilash Alemwork Abie Hana J. Abukhadijah Nasir Abbas Ilana N. Ackerman Mesafint Molla Adane Zenaw Debasu Addisu Rufus Adesoji Adedoyin Emad M. Abdallah Samar Abd Elhafeez Olorunsola Israel Adeyomoye Meriem Abdoun Salahdein Aburuz Mahmoud Abdelnabi Lucas Guimarães Abreu Apurba Acharya Lawan Hassan Adamu Oluwafemi Atanda Adeagbo Qorinah Estiningtyas Sakilah Adnani Sherief Abd-Elsalam Adam Abdullahi Deldar Morad Abdulah Toufik Abdul-Rahman Asrat Agalu Abejew Fuad Hamdi A. Abuadas Kulmira Abdykerimova Aidin Abedi Olugbenga Olusola Abiodun Shady Abohashem Nagah M. Abourashed Mohamed Abouzid Dmitry Abramov Roberto Ariel Abeldaño Zuñiga Juan Manuel Acuna Anirudh Balakrishna Acharya Ousman Adal Hasan Aalruz Arman Abdous Auwal Abdullahi Bilyaminu Abubakar Isaac Yeboah Addo Sawsan Abuhammad David Adedia Syed Hani Abidi Olumide Abiodun Hassan Abolhassani Richard Gyan Aboagye Ulric Sena Abonie Habeeb Omoponle Adewuyi Oyelola A. Adegboye Isaac Akinkunmi Adedeji Ahmad Y. Abuhelwa Dina Abushanab Tajudeen Adesanmi Adebisi Oluwatobi E. Adegbile Olumide Thomas Adeleke Miracle Ayomikun Adesina Temitayo Esther Adeyeoluwa Leticia Akua Adzigbli Nasir Abbas Prince Owusu Adoma Kishor Adhikari Salahdein Aburuz Rizwan Suliankatchi Abdulkader

Publication Name: Lancet

Publication Date: 2025-10-18

Volume: 406

Issue: 10513

Page Range: 1873-1922

Description:

Background 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.

Open Access: Yes

DOI: 10.1016/S0140-6736(25)01637-X

Global, regional, and national burden of breast cancer among females, 1990–2023, with forecasts to 2050: a systematic analysis for the Global Burden of Disease Study 2023

Usha Adiga Meriem Abdoun Eman Abu-Gharbieh Anisuddin Ahmed Siddig Ibrahim Abdelwahab Roland Eghoghosoa Akhigbe Marjan Ajami Mohd Adnan Victor Adekanmbi Mehrandokht Abedini Reda Abdel-Hameed Samar Abd Elhafeez Rabail Alam Muhammad Sohail Afzal Jonathan M. Kocarnik Auwal Abdullahi Ukachukwu O. Abaraogu Khurshid Ahmad Rana Kamal Abu Farha Isaac Yeboah Addo Bilyaminu Abubakar Juan Manuel Acuna Nasir Abbas Hanadi Al Hamad César Agostinis Sobrinho Habeeb Omoponle Adewuyi Swetha Acharya Williams Agyemang-Duah Lisa C. Adams Fuad Hamdi A. Abuadas Dagninet Derebe Abie Ali Ahmadi Yazan Al Thaher Bright Opoku Ahinkorah Natalie Pritchett Nurudeen A. Adegoke Ayman Ahmed Deldar Morad Abdulah Kedir Hussein Abegaz Syed Mahfuz Al Hasan Mohammad Al Qadire Danish Ahmad Mohammed Albashtawy Feleke Doyore Agide Babatope Oluwadamilare Adebiyi Armita Abedi Dina Abushanab David Adedia Muktar Beshir Ahmed Kamoru Ademola Adedokun A. Bhoomadevi Muayyad M. Ahmad Aqeel Ahmad Qorinah Estiningtyas Sakilah Adnani Miracle Ayomikun Adesina Domenico Albano Ulric Sena Abonie Mai Abdel Haleem Abusalah Hasan Aalruz Kayleigh Bhangdia Temitayo Esther Adeyeoluwa Gasha Salih Ahmed Aanuoluwapo Adeyimika Afolabi Louise Penberthy Richard Gyan Aboagye Mesfin Abebe Mahnaz Ahmadi Hazim S. Ababneh Zhanar Abu Toufik Abdul-Rahman Naveed Ahmed Hana J. Abukhadijah Leticia Akua Adzigbli Alistair Acheson Alemwork Abie Mehrunnisha Sharif Ahmed Hassan Abolhassani Arash Abdollahi Dolapo Emmanuel Ajala Saheed Ayodeji Adekola Aminu Kende Abubakar Abebaw Alamrew Lee Deitesfeld Austin J. Ahlstrom Meqdad Saleh Ahmed None Abdullah Mohammed Mehdi Abrar Mohammad Ahmmad Mahmoud Al Zoubi Kulmira Abdykerimova Andrew Crist Miranda L. May Aram Mahmood Ahmed Sepideh Abdi Hasan Aalruz Syed Anees Ahmed Haroon Ahmed Zhanar Abu MD Faisal Ahmed Bhoomadevi A Salah Al Awaidy Wael M. Abdel-Rahman Olumide Abiodun Muhammad Nadeem Akhtar

Publication Name: Lancet Oncology

Publication Date: 2026-03-01

Volume: 27

Issue: 3

Page Range: 302-326

Description:

Background Breast cancer is a leading cause of mortality and morbidity among females worldwide. As part of the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2023, we provided an updated comprehensive assessment of the epidemiological trends, disease burden, and risk factors associated with breast cancer globally, regionally, and nationally from 1990 to 2023. Methods Breast cancer incidence, mortality, prevalence, years lived with disability (YLDs), years of life lost (YLLs), and disability-adjusted life-years (DALYs) were estimated by age and sex for 204 countries and territories from 1990 to 2023. Mortality estimates were generated using GBD Cause of Death Ensemble models, leveraging data from population-based cancer registration systems, vital registration systems, and verbal autopsies. Mortality-to-incidence ratios were calculated to derive both mortality and incidence estimates. Prevalence was calculated by combining incidence and modelled survival estimates. YLLs were established by multiplying age-specific deaths with the GBD standard life expectancy at the age of death. YLDs were estimated by applying disability weights to prevalence estimates. The sum of YLLs and YLDs equalled the number of DALYs. Breast cancer burden attributable to seven risk factors was examined through the comparative risk assessment framework. The GBD forecasting framework was used to forecast breast cancer incidence and mortality from 2024 to 2050. Age-standardised rates were calculated for each metric using the GBD 2023 world standard population. Findings In 2023, there were an estimated 2·30 million (95% uncertainty interval [UI] 2·01 to 2·61) breast cancer incident cases, 764 000 deaths (672 000 to 854 000), and 24·1 million (21·3 to 27·5) DALYs among females globally. In the World Bank low-income group, where a low age-standardised incidence rate (ASIR) was estimated (44·2 per 100 000 person-years [31·2 to 58·4]), the age-standardised mortality rate (ASMR) was the highest (24·1 per 100 000 [16·8 to 31·9]). The highest ASIR was in the high-income group (75·7 per 100 000 [67·1 to 84·0]), and the lowest ASMR was in the upper-middle-income group (11·2 per 100 000 [10·2 to 12·3]). Between 1990 and 2023, the ASIR in the low-income group increased by 147·2% (38·1 to 271·7), compared with a 1·2% (–11·5 to 17·2) change in the high-income group. The ASMR decreased in the high-income group, changing by –29·9% (–33·6 to –25·9), but increased by 99·3% (12·5 to 202·9) in the low-income group. The increase in age-standardised DALY rates followed that of ASMRs. Risk factors such as dietary risks, tobacco use, and high fasting plasma glucose contributed to 28·3% (16·6 to 38·9) of breast cancer DALYs in 2023. The risk factors with a decrease in attributable DALYs between 1990 and 2023 were high alcohol use and tobacco. By 2050, the global incident cases of breast cancer among females were forecast to reach 3·56 million (2·29 to 4·83), with 1·37 million (0·841 to 2·02) deaths. Interpretation The stable incidence and declining mortality rates of female breast cancer in high-income nations reflect success in screening, diagnosis, and treatment. In contrast, the concurrent rise in incidence and mortality in other regions signals health system deficits. Without effective interventions, many countries will fall short of the WHO Global Breast Cancer Initiative's ambitious target of achieving an annual reduction of 2·5% in age-standardised mortality rates by 2040. The mounting breast cancer burden, disproportionately affecting some of the world's most vulnerable populations, will further exacerbate health inequalities across the globe without decisive immediate action. Funding Gates Foundation, St Jude Children's Research Hospital.

Open Access: Yes

DOI: 10.1016/S1470-2045(25)00730-2

Global, regional, and national sepsis incidence and mortality, 1990–2021: a systematic analysis

Usha Adiga Samah W. Al-Jabi Meriem Abdoun Quique Bassat Zulfiqar A. Bhutta Hany Aly Ashish Bhargava Hasan Yaser Alniss Razique Anwer Abdul Monim Batiha Asrat Agalu Abejew Samar Abd Elhafeez Mahwish Arooj Matteo Bauckneht Mohammad R. Alqudimat Alok Atreya Abdelazeem M. Algammal Saeid Anvari Auwal Abdullahi Tahira Ashraf Shereen M. Aleidi Mohammad R. Alosta Senthilkumar Balakrishnan Zarrin Basharat Montaha Al-Iede Nasir Abbas Syed Shujait Ali Williams Agyemang-Duah Sahel Majed Alrousan Lucien R. Swetschinski Sonu Bhaskar Anayochukwu Edward Anyasodor Lisa C. Adams Ahmad Naoras Bitar Madineh Abbasi Habib Benzian Intima Alrimawi Nicole Davis Weaver Mohammed Albashtawy Meshack Achore Domenico Azzolino Eve E. Wool Kamoru Ademola Adedokun Fahad A. Alhumaydhi Ahmad Alrawashdeh Aqeel Ahmad Simachew Animen Bante Nelson Alvis-Guzman Umar Muhammad Bello Rafat Ali Kevin S. Ikuta Qorinah Estiningtyas Sakilah Adnani Rajon Banik Amadou Barrow Mina Borran Wondu Feyisa Balcha Chieh Han Gasha Salih Ahmed Aanuoluwapo Adeyimika Afolabi Alaa Aboelnour Badran Anna Gershberg Hayoon Hamed Borhany Nikha Bhardwaj Ahmad Rajeh Al-Qudimat Najim Z. Alshahrani Fentahun Alemnew Mesfin Abebe Md Akib Al-Zubayer Ema Akter Ridwan Olamilekan Adesola Ali Azargoonjahromi Authia P. Gray Mahsa Ahadi Mohammed Usman Ali Zelalem Asmare Hana J. Abukhadijah Alemwork Abie Amani Alansari Asnake Gashaw Belayneh Yaser Mohammed Al-Worafi Filippos Anagnostakis Daniel T. Araki Hassan Abolhassani Sabah Al-Marwani Gokce Belge Bilgin Mohammad Mahdi Bastan Meqdad Saleh Ahmed Rebecca L. Hsu Abiye Assefa Berihun Erin Chung Hiba Jawdat Barqawi Julie Alaere Atta Nurila Aryntayeva Wakgari Mosisa Abdisa Qorinah Estiningtyas Sakilah Adnani Redeat Libanos Assefa Syed Anees Ahmed Haroon Ahmed Sadat Abdulla Aziz Avinash Aujayeb Tomislav Mestrovic

Publication Name: Lancet Global Health

Publication Date: 2025-12-01

Volume: 13

Issue: 12

Page Range: e2013-e2026

Description:

Background: The global burden of sepsis, a life-threatening dysregulated host response to infection leading to organ dysfunction, remains challenging to quantify. We aimed to comprehensively estimate the global, regional, and national burden of sepsis, including the impact of the COVID-19 pandemic and underlying causes of sepsis-related deaths with co-occurring infectious syndromes. Methods: We used multiple cause-of-death, hospital, minimally invasive tissue sampling, and linked death certificate and hospital record data representing 149 million deaths, covering 4290 location-years with mortality estimates from the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2021 to capture explicit and implicit sepsis cases and deaths. We estimated age-location-sex-specific fractions of sepsis-related deaths from 195 underlying causes of death and 22 infectious syndromes from 1990 to 2021 using binomial logistic regression models, and estimated sepsis-related deaths using GBD cause-specific mortality estimates. Using 250 million hospital admissions and 7·82 million deaths from hospital data, representing 1310 location-years, we modelled case fatality rates by use of binomial logistic regression, applied to sepsis death estimates to estimate sepsis incidence by age, location, and year. Findings: In 2021, we estimated 166 million (95% uncertainty interval 135–201) sepsis cases and 21·4 million (20·3–22·5) all-cause sepsis-related deaths globally, representing 31·5% of total global deaths. Sepsis-related deaths decreased between 1990 and 2019, followed by a surge in 2020 and 2021. As of 2021, individuals aged 15 years and older experienced increases across incidence (230%) and mortality (26·3%) since 1990. Those aged 70 years and older had the highest sepsis-related mortality in 2021 (9·28 million [8·74–9·86] deaths). Sepsis-related deaths from infectious underlying causes decreased from 11·8 million (11·1–12·5) in 1990 to 8·34 million (7·72–9·01) in 2019, then increased by 86·4% to 15·5 million (14·7–16·4) in 2021. Sepsis-related mortality due to non-infectious underlying causes of death increased from 4·69 million (4·35–5·05) in 1990 to 5·81 million (5·40–6·25) in 2021; the leading non-infectious underlying causes of death with sepsis were stroke, chronic obstructive pulmonary disease, and cirrhosis. In 2021, bloodstream infections inclusive of HIV and malaria (3·08 million [2·83–3·35]) and lower respiratory infections inclusive of COVID-19 (11·33 million [1·20–1·47]) were the most prominent infectious syndromes complicating sepsis-related deaths from non-infectious underlying causes, representing a consistent trend since 1990. Interpretation: The global burden of sepsis increased in 2020 and 2021, reversing progress from 1990. Sepsis incidence and mortality increased in people aged 15 years and older, especially those aged 70 years and older, and as a complication of non-infectious underlying causes of death such as stroke, primarily through bloodstream infections and lower respiratory infections. The global burden of sepsis is substantial, and sepsis is increasingly a complication of non-infectious causes of death. Funding: Gates Foundation, Wellcome Trust, and Department of Health and Social Care using UK aid funding managed by the Fleming Fund.

Open Access: Yes

DOI: 10.1016/S2214-109X(25)00356-0

Global burden of metabolic dysfunction-associated steatotic liver disease, 1990–2023, and projections to 2050: a systematic analysis for the Global Burden of Disease Study 2023

Jasvinder Singh Bhatti Usha Adiga Stephen E. Congly Neeraj Bhala Karolina Akinosoglou Saleh A. Alqahtani Seyyed Shamsadin Athari Juan Pablo Arab Aleksandr Y. Aravkin Bruce B. Duncan Archith Boloor Catalina Liliana Andrei Ahmed Abu-Zaid Fadwa Naji Alhalaiqa Oyewole Christopher Durojaiye Ferry Efendi Anis Ahmad Chaudhary Sushil Dohare Ajeet Singh Bhadoria Vijay Kumar Chattu Floriane Ausloos Muhammad Sohail Afzal Isaac Yeboah Addo Ashish D. Badiye Tahira Ashraf Yogesh Bahurupi Luis Antonio Diaz Nasir Abbas Anton A. Artamonov Hubert Amu Sheikh Mohammad Alif Charles Oluwaseun Adetunji Demelash Areda Wirawan Adikusuma Shady Abohashem Maha Moh'd Wahbi Atout Awais Altaf Deanna Anderlini Zahid A. Butt Walid A. Al-Zyoud Ismael Campos-Nonato Omid Dadras Foolad Eghbali Jalal Arabloo Narasimha M. Beeraka Nelson Alvis-Guzman Omar Ali Mohammed Al Zaabi Fariba Dorostkar Diana Fernanda Bejarano Ramirez Hasan Aalruz Amadou Barrow Isaac Sunday Chukwu Rajaa M. Al-Raddadi Robert Kokou Dowou Richard Gyan Aboagye Xiaochen Dai Arkadeep Dhali Najim Z. Alshahrani Menayit Tamrat Dresse Mohammed Ahmed Akkaif Patrick R. Ching Pankaj Bhardwaj Fatemeh Chichagi Shahkaar Aziz Bryan Chong Shewatatek Melaku Asefa Felix Busch Mainak Bardhan Ajay Nagesh Bhat Pojsakorn Danpanichkul Amani Alansari Joshua Chadwick Yaser Mohammed Al-Worafi Filippos Anagnostakis Behrad Eftekhari Soeun Kim Amol S. Dhane Khushboo Bisht Jiyeon Oh Mohammad Mahdi Bastan Melak Gedamu Beyene Ashel Chelsea Dsouza Sandip Chakraborty Abiye Assefa Berihun Abdel Rahman E’mar Mohammad Daud Ali Shahid Bashir Jae Il Shin Huyen Phuc Do Hasan Aalruz Syed Anees Ahmed Haroon Ahmed Abisola Esther Abdulmalik Omar Al Ta'ani Maha Moh'd Wahbi Atout Salah Al Awaidy Luis Alberto Cámera Giovanni Addolorato Márcia Carvalho Mohammad Khursheed Alam Yasser Bustanji Jaffar A. Al-Tawfiq

Publication Name: Lancet Gastroenterology and Hepatology

Publication Date: 2026-06-01

Volume: 11

Issue: 6

Page Range: 463-494

Description:

Background: Metabolic dysfunction-associated steatotic liver disease (MASLD), previously known as non-alcoholic fatty liver disease, is one of the most prevalent liver diseases globally, contributing to both economic and health-related challenges. We aimed to evaluate the global, regional, and national burden of MASLD from 1990 to 2023, quantify the contribution of identified modifiable risk factors, and project future prevalence up to the year 2050. Methods: Estimates of MASLD prevalence and disability-adjusted life-years (DALYs) were produced by age, sex, region, Socio-demographic Index (SDI), and Healthcare Access and Quality (HAQ) index across 204 countries and territories from 1990 to 2023 as part of the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2023. The MASLD burden attributable to three risk factors (smoking, high BMI, and high fasting plasma glucose) was assessed as part of the GBD comparative risk assessment. As a secondary analysis, we used these estimates to forecast MASLD prevalence up to 2050 using fasting plasma glucose and mean BMI as predictors. Furthermore, to examine the relative contributions of population ageing, population growth, and changes in MASLD prevalence rate to the forecasted changes in case counts from 2023 to 2050, we conducted a decomposition analysis. Findings: In 2023, approximately 1·3 billion (95% uncertainty interval [UI] 1·2 to 1·4) individuals were estimated to be living with MASLD (ie, 16·1% of the global population), with an age-standardised prevalence rate of 14 429·3 (95% UI 13 268·3 to 15 990·6) per 100 000 population, representing a percentage increase of 142·7% (95% UI 139·2 to 146·7) in crude numbers from 1990 (0·5 billion [0·5 to 0·6]) and of 28·6% (27·8 to 29·5) in the rate (11 217·2 [10 276·8 to 12 467·0] per 100 000 in 1990). An estimated 3·6 million (2·8 to 4·5) total DALYs were attributable to MASLD worldwide in 2023, corresponding to an age-standardised DALY rate of 39·6 (31·2 to 49·9) per 100 000 population. Despite a 116·3% (93·3 to 139·4) increase in crude DALYs (from 1·7 million [1·3 to 2·1] in 1990), its age-standardised estimate remained consistent (1·8% [–8·6 to 12·8]) from 1990 (38·9 [30·1 to 49·8] per 100 000) to 2023. There was substantial variation in age-standardised estimates across regions. North Africa and the Middle East had the highest prevalence rate (29 246·1 [26 848·3 to 32 048·7] per 100 000) and Andean Latin America showed the highest DALY rate (152·3 [114·1 to 194·7] per 100 000). By contrast, the high-income Asia Pacific region had the lowest prevalence rate (8653·5 [7923·7 to 9592·8] per 100 000) and east Asia had the lowest DALY rate (16·3 [13·5 to 19·9] per 100 000) among all GBD regions. North Africa and the Middle East showed disproportionately higher prevalence rates relative to other regions with similar SDIs. Lower SDIs and HAQs were associated with higher age-standardised DALY rates. The age-standardised prevalence rate was consistently higher in males (15 616·4 [14 349·2 to 17 263·3] per 100 000 people in 2023) than in females (13 245·2 [12 132·0 to 14 692·6] per 100 000 people), and peaked at age 80–84 years in both sexes. The number of MASLD prevalent cases was the highest in younger adults, peaking at age 35–39 years for males and age 55–59 years for females. Among the risk factors for MASLD, high fasting plasma glucose presented the largest contribution to the age-standardised DALY rate of total MASLD in 2023 (2·2 [95% UI 1·6 to 3·1] per 100 000 people), followed by high BMI (1·4 [0·6 to 2·4] per 100 000 people) and smoking (1·0 [0·3 to 1·8] per 100 000 people). Our forecasting model estimates that 1·8 billion (95% UI 1·6 to 2·0) individuals are likely to have MASLD by 2050, representing a 42·0% increase from 2023. The age-standardised prevalence rate is expected to increase to 15 774·9 (95% UI 14 613·9 to 17 336·2) per 100 000 people in 2050, representing an average annual percentage change of 0·3% (95% UI 0·3–0·3). According to our decomposition analysis, this change will be primarily due to population growth, particularly in sub-Saharan Africa and North Africa and Middle East, and less by population ageing or epidemiological change. Interpretation: With a global prevalence of 16·1% and approximately 1·3 billion people already living with MASLD in 2023, the condition has and will continue to have substantial health and economic impacts worldwide. An inverse association between the HAQ Index and age-standardised DALY rates suggests that countries with lower health-care access and quality might be less well positioned to manage the growing MASLD burden, underscoring the need for strengthened health-system capacity in these settings. Funding: Gates Foundation.

Open Access: Yes

DOI: 10.1016/S2468-1253(26)00011-7

The global, regional, and national burden of cancer, 1990–2023, with forecasts to 2050: a systematic analysis for the Global Burden of Disease Study 2023

Amani Alansari Ibukun Modupe Adesiyan Abdallah H.A. Abd Al Magied Mohammed Altigani Abdalla Arash Abdollahi Wael M. Abdel-Rahman Aminu Kende Abubakar Ahmed Abu-Zaid Kamoru Ademola Adedokun Nurudeen A. Adegoke Aanuoluwapo Adeyimika Afolabi Mohadese Ahmadzade Anisuddin Ahmed Fahmi Y. Al-Ashwal Dolapo Emmanuel Ajala Ashraf Nabiel Abdalla Raghu Ram Achar Eman Abu-Gharbieh Lisa C. Adams Muayyad M. Ahmad Maryam Abbasalipour bashash Mesfin Abebe Armita Abedi Sajjad Ahmad Syed Anees Ahmed Usha Adiga Faisal Ahmad Sajjad Ahmad A. Bhoomadevi Aqeel Ahmad Lisa M. Force Hasan Aalruz Kayleigh Bhangdia Jonathan M. Kocarnik Miranda L. May Feleke Doyore Agide Andrew Crist Williams Agyemang-Duah Roland Eghoghosoa Akhigbe Karolina Akinosoglou Omar Al Omari Alemwork Abie Hana J. Abukhadijah Muhammad Sohail Afzal Danish Ahmad Amir Mahmoud Ahmadzade Salah Al Awaidy Nasir Abbas Maryam Abbasalipour bashash Hanadi Al Hamad Syed Mahfuz Al Hasan Samar Abd Elhafeez Navidha Aggarwal Gasha Salih Ahmed Mehrunnisha Sharif Ahmed Meqdad Saleh Ahmed Muktar Beshir Ahmed Nesredin Ahmed Syed Anees Ahmed Marjan Ajami Mohammad Al Qadire Suneth Buddhika Agampodi Khurshid Ahmad César Agostinis Sobrinho Tauseef Ahmad Elham Ahmadi Ayman Ahmed Meriem Abdoun Salahdein Aburuz Yazan Al Thaher Zufishan Alam Lucas Guimarães Abreu Lawan Hassan Adamu Bhoomadevi A Louise Penberthy Natalie Pritchett Alistair Acheson Lee Deitesfeld Ahmed M. Afifi Bright Opoku Ahinkorah Fatemeh Afrashteh Qorinah Estiningtyas Sakilah Adnani Juan Manuel Acuna Hasan Aalruz Arman Abdous Auwal Abdullahi Bilyaminu Abubakar Isaac Yeboah Addo Syed Hani Abidi Olumide Abiodun Hassan Abolhassani Richard Gyan Aboagye Ulric Sena Abonie Habeeb Omoponle Adewuyi Parsa Abdi Wakgari Mosisa Abdisa Luai A. Ahmed Victor Adekanmbi Ibrar Ahmed Daba Abdissa Arya Afrooghe Omar Ali Mohammed Al Zaabi Khurshid Alam Leticia Akua Adzigbli Nasir Abbas Prince Owusu Adoma Khurshid Ahmad

Publication Name: Lancet

Publication Date: 2025-10-11

Volume: 406

Issue: 10512

Page Range: 1565-1586

Description:

Background: Cancer is a leading cause of death globally. Accurate cancer burden information is crucial for policy planning, but many countries do not have up-to-date cancer surveillance data. To inform global cancer-control efforts, we used the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2023 framework to generate and analyse estimates of cancer burden for 47 cancer types or groupings by age, sex, and 204 countries and territories from 1990 to 2023, cancer burden attributable to selected risk factors from 1990 to 2023, and forecasted cancer burden up to 2050. Methods: Cancer estimation in GBD 2023 used data from population-based cancer registration systems, vital registration systems, and verbal autopsies. Cancer mortality was estimated using ensemble models, with incidence informed by mortality estimates and mortality-to-incidence ratios (MIRs). Prevalence estimates were generated from modelled survival estimates, then multiplied by disability weights to estimate years lived with disability (YLDs). Years of life lost (YLLs) were estimated by multiplying age-specific cancer deaths by the GBD standard life expectancy at the age of death. Disability-adjusted life-years (DALYs) were calculated as the sum of YLLs and YLDs. We used the GBD 2023 comparative risk assessment framework to estimate cancer burden attributable to 44 behavioural, environmental and occupational, and metabolic risk factors. To forecast cancer burden from 2024 to 2050, we used the GBD 2023 forecasting framework, which included forecasts of relevant risk factor exposures and used Socio-demographic Index as a covariate for forecasting the proportion of each cancer not affected by these risk factors. Progress towards the UN Sustainable Development Goal (SDG) target 3.4 aim to reduce non-communicable disease mortality by a third between 2015 and 2030 was estimated for cancer. Findings: In 2023, excluding non-melanoma skin cancers, there were 18·5 million (95% uncertainty interval 16·4 to 20·7) incident cases of cancer and 10·4 million (9·65 to 10·9) deaths, contributing to 271 million (255 to 285) DALYs globally. Of these, 57·9% (56·1 to 59·8) of incident cases and 65·8% (64·3 to 67·6) of cancer deaths occurred in low-income to upper-middle-income countries based on World Bank income group classifications. Cancer was the second leading cause of deaths globally in 2023 after cardiovascular diseases. There were 4·33 million (3·85 to 4·78) risk-attributable cancer deaths globally in 2023, comprising 41·7% (37·8 to 45·4) of all cancer deaths. Risk-attributable cancer deaths increased by 72·3% (57·1 to 86·8) from 1990 to 2023, whereas overall global cancer deaths increased by 74·3% (62·2 to 86·2) over the same period. The reference forecasts (the most likely future) estimate that in 2050 there will be 30·5 million (22·9 to 38·9) cases and 18·6 million (15·6 to 21·5) deaths from cancer globally, 60·7% (41·9 to 80·6) and 74·5% (50·1 to 104·2) increases from 2024, respectively. These forecasted increases in deaths are greater in low-income and middle-income countries (90·6% [61·0 to 127·0]) compared with high-income countries (42·8% [28·3 to 58·6]). Most of these increases are likely due to demographic changes, as age-standardised death rates are forecast to change by –5·6% (–12·8 to 4·6) between 2024 and 2050 globally. Between 2015 and 2030, the probability of dying due to cancer between the ages of 30 years and 70 years was forecasted to have a relative decrease of 6·5% (3·2 to 10·3). Interpretation: Cancer is a major contributor to global disease burden, with increasing numbers of cases and deaths forecasted up to 2050 and a disproportionate growth in burden in countries with scarce resources. The decline in age-standardised mortality rates from cancer is encouraging but insufficient to meet the SDG target set for 2030. Effectively and sustainably addressing cancer burden globally will require comprehensive national and international efforts that consider health systems and context in the development and implementation of cancer-control strategies across the continuum of prevention, diagnosis, and treatment. Funding: Gates Foundation, St Jude Children's Research Hospital, and St Baldrick's Foundation.

Open Access: Yes

DOI: 10.1016/S0140-6736(25)01635-6

Global age-sex-specific all-cause mortality and life expectancy estimates for 204 countries and territories and 660 subnational locations, 1950–2023: a demographic analysis for the Global Burden of Disease Study 2023

Rana Kamal Abu Farha Cristiana Abbafati Faezeh Abbaspour Abdallah H.A. Abd Al Magied Mohammed Altigani Abdalla Nadin M.I. Abdel Razeq Arash Abdollahi Wael M. Abdel-Rahman Reda Abdel-Hameed Aminu Kende Abubakar Ahmed Abu-Zaid Kamoru Ademola Adedokun Nurudeen A. Adegoke Aanuoluwapo Adeyimika Afolabi Giuseppina Affinito Isaac Ayodeji Adesina Habtamu Abebe Getahun Eman Abu-Gharbieh Lisa C. Adams Armita Abedi Peng Zheng Usha Adiga Mitra Abbasifard Faisal Ahmad Austin E. Schumacher Mohammad Amin Aalipour A. Bhoomadevi Hazim S. Ababneh Ukachukwu O. Abaraogu Faezeh Abbaspour Ryan M. Barber Omar Ahmed Abdelwahab Dariush Abtahi Rizwan Suliankatchi Abdulkader Ripon Kumar Adhikary Mohd Adnan Abdullahi Salahudeen Abdulraheem Tanin Adl Parvar Mahdi Aghaalikhani Rabbiya Ahmad Feleke Doyore Agide Williams Agyemang-Duah Alemwork Abie Hana J. Abukhadijah Danish Ahmad Nasir Abbas Tanin Adl Parvar Rotimi Felix Afolabi Habtamu Abebe Getahun Rana Kamal Abu Farha Ahmed Abu Zaid César Agostinis Sobrinho Saira Afzal Gizachew Beykaso Agafari Emad M. Abdallah Samar Abd Elhafeez Navidha Aggarwal Tim Adair Mahdi Aghaalikhani César Agostinis Sobrinho Sepehr Aghajanian Rabbiya Ahmad Seyed Mohammad Kazem Aghamir Mary Dada Agoi Meriem Abdoun Salahdein Aburuz Anurag Agrawal Lucas Guimarães Abreu Bright Opoku Ahinkorah Qorinah Estiningtyas Sakilah Adnani Sherief Abd-Elsalam Samar Abd ElHafeez Deldar Morad Abdulah Asrat Agalu Abejew Fuad Hamdi A. Abuadas Parisa Abedi Olugbenga Olusola Abiodun Shady Abohashem Olatunji O. Adetokunboh Nagah M. Abourashed Mohamed Abouzid Dmitry Abramov Roberto Ariel Abeldaño Zuñiga Juan Manuel Acuna Anirudh Balakrishna Acharya Meshack Achore Hasan Aalruz Arman Abdous Auwal Abdullahi Bilyaminu Abubakar Sawsan Abuhammad David Adedia Syed Hani Abidi Olumide Abiodun Richard Gyan Aboagye Ulric Sena Abonie Parsa Abdi Oladimeji Muritala Adebayo Ahmad Y. Abuhelwa Dina Abushanab Tajudeen Adesanmi Adebisi Oluwatobi E. Adegbile Olumide Thomas Adeleke Miracle Ayomikun Adesina Mache Tsadik Adhana David Adzrago Temitayo Esther Adeyeoluwa Leticia Akua Adzigbli Nasir Abbas Kishor Adhikari Rizwan Suliankatchi Abdulkader

Publication Name: Lancet

Publication Date: 2025-10-18

Volume: 406

Issue: 10513

Page Range: 1731-1810

Description:

Comprehensive, comparable, and timely estimates of demographic metrics—including life expectancy and age-specific mortality—are essential for evaluating, understanding, and addressing trends in population health. The COVID-19 pandemic highlighted the importance of timely and all-cause mortality estimates for being able to respond to changing trends in health outcomes, showing a strong need for demographic analysis tools that can produce all-cause mortality estimates more rapidly with more readily available all-age vital registration (VR) data. The Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) is an ongoing research effort that quantifies human health by estimating a range of epidemiological quantities of interest across time, age, sex, location, cause, and risk. This study—part of the latest GBD release, GBD 2023—aims to provide new and updated estimates of all-cause mortality and life expectancy for 1950 to 2023 using a novel statistical model that accounts for complex correlation structures in demographic data across age and time. We used 24 025 data sources from VR, sample registration, surveys, censuses, and other sources to estimate all-cause mortality for males, females, and all sexes combined across 25 age groups in 204 countries and territories as well as 660 subnational units in 20 countries and territories, for the years 1950–2023. For the first time, we used complete birth history data for ages 5–14 years, age-specific sibling history data for ages 15–49 years, and age-specific mortality data from Health and Demographic Surveillance Systems. We developed a single statistical model that incorporates both parametric and non-parametric methods, referred to as OneMod, to produce estimates of all-cause mortality for each age-sex-location group. OneMod includes two main steps: a detailed regression analysis with a generalised linear modelling tool that accounts for age-specific covariate effects such as the Socio-demographic Index (SDI) and a population attributable fraction (PAF) for all risk factors combined; and a non-parametric analysis of residuals using a multivariate kernel regression model that smooths across age and time to adaptably follow trends in the data without overfitting. We calibrated asymptotic uncertainty estimates using Pearson residuals to produce 95% uncertainty intervals (UIs) and corresponding 1000 draws. Life expectancy was calculated from age-specific mortality rates with standard demographic methods. For each measure, 95% UIs were calculated with the 25th and 975th ordered values from a 1000-draw posterior distribution. In 2023, 60·1 million (95% UI 59·0–61·1) deaths occurred globally, of which 4·67 million (4·59–4·75) were in children younger than 5 years. Due to considerable population growth and ageing since 1950, the number of annual deaths globally increased by 35·2% (32·2–38·4) over the 1950–2023 study period, during which the global age-standardised all-cause mortality rate declined by 66·6% (65·8–67·3). Trends in age-specific mortality rates between 2011 and 2023 varied by age group and location, with the largest decline in under-5 mortality occurring in east Asia (67·7% decrease); the largest increases in mortality for those aged 5–14 years, 25–29 years, and 30–39 years occurring in high-income North America (11·5%, 31·7%, and 49·9%, respectively); and the largest increases in mortality for those aged 15–19 years and 20–24 years occurring in Eastern Europe (53·9% and 40·1%, respectively). We also identified higher than previously estimated mortality rates in sub-Saharan Africa for all sexes combined aged 5–14 years (87·3% higher in GBD 2023 than GBD 2021 on average across countries and territories over the 1950–2021 period) and for females aged 15–29 years (61·2% higher), as well as lower than previously estimated mortality rates in sub-Saharan Africa for all sexes combined aged 50 years and older (13·2% lower), reflecting advances in our modelling approach. Global life expectancy followed three distinct trends over the study period. First, between 1950 and 2019, there were considerable improvements, from 51·2 (50·6–51·7) years for females and 47·9 (47·4–48·4) years for males in 1950 to 76·3 (76·2–76·4) years for females and 71·4 (71·3–71·5) years for males in 2019. Second, this period was followed by a decrease in life expectancy during the COVID-19 pandemic, to 74·7 (74·6–74·8) years for females and 69·3 (69·2–69·4) years for males in 2021. Finally, the world experienced a period of post-pandemic recovery in 2022 and 2023, wherein life expectancy generally returned to pre-pandemic (2019) levels in 2023 (76·3 [76·0–76·6] years for females and 71·5 [71·2–71·8] years for males). 194 (95·1%) of 204 countries and territories experienced at least partial post-pandemic recovery in age-standardised mortality rates by 2023, with 61·8% (126 of 204) recovering to or falling below pre-pandemic levels. There were several mortality trajectories during and following the pandemic across countries and territories. Long-term mortality trends also varied considerably between age groups and locations, demonstrating the diverse landscape of health outcomes globally. This analysis identified several key differences in mortality trends from previous estimates, including higher rates of adolescent mortality, higher rates of young adult mortality in females, and lower rates of mortality in older age groups in much of sub-Saharan Africa. The findings also highlight stark differences across countries and territories in the timing and scale of changes in all-cause mortality trends during and following the COVID-19 pandemic (2020–23). Our estimates of evolving trends in mortality and life expectancy across locations, ages, sexes, and SDI levels in recent years as well as over the entire 1950–2023 study period provide crucial information for governments, policy makers, and the public to ensure that health-care systems, economies, and societies are prepared to address the world's health needs, particularly in populations with higher rates of mortality than previously known. The estimates from this study provide a robust framework for GBD and a valuable foundation for policy development, implementation, and evaluation around the world. Gates Foundation.

Open Access: Yes

DOI: 10.1016/S0140-6736(25)01330-3