Omar Ali Mohammed Al Zaabi
57211669993
Publications - 2
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
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