TY - JOUR
T1 - Global, regional, and national burden of tuberculosis and multidrug-resistant tuberculosis by HIV status, 1990–2023
T2 - a systematic analysis for the Global Burden of Disease Study 2023
AU - GBD 2023 TB HIV Collaborators
AU - Ledesma, Jorge R.
AU - Zhang, Meixin
AU - Liew, Mei Fong
AU - Dominguez, Regina Mae Villanueva
AU - Whikehart, Sophie Mei Lin
AU - Verma, Megan
AU - Ma, Jianing
AU - Movo, Amanda
AU - Chu, Huong Thi
AU - Ostroff, Samuel M.
AU - He, Jiawei
AU - Abdullah,
AU - A Eltaly, Hatem
AU - Abaraogu, Ukachukwu O.
AU - Abate, Belayneh Jejaw
AU - Abbas, Mazhar
AU - Abd ElHafeez, Samar
AU - Abdallah, Emad M.
AU - Abd-Elsalam, Sherief
AU - Abdelwahab, Siddig Ibrahim
AU - Abdisa, Wakgari Mosisa
AU - Abdolizadeh, Ali
AU - Abdou, Hassan A.
AU - Abdoun, Meriem
AU - Abdous, Arman
AU - Abdul Aziz, Jeza Muhamad
AU - Abdulah, Deldar Morad
AU - Abdulateef, Yasir M.
AU - Abdul-Ghani, Rashad
AU - Abdullahi, Auwal
AU - Abdulrahim, Abdulrakib
AU - Abukhadijah, Hana J.
AU - Afzal, Muhammad Sohail
AU - Ahmed, Khalid A.
AU - Ahmed, Mohamed Sherif Ali
AU - Alam, Mohammad Khursheed
AU - Ali, Mohammad Daud
AU - Ali, Mohammad Daud
AU - Ali, Mohammed Usman Usman
AU - Ali, Syed Shujait
AU - Hassan, Ibrahim Nagmeldin
AU - Islam, Md Shahinul
AU - Khan, Muhammad Umer
AU - Khan, Muhammad Umer
AU - Khan, Qamar Uz Zaman
AU - Khan, Wasif Ali
AU - Metwally, Mohamed M.M.
AU - Mohamed, Fatima Awad Elkarim Elfaki
AU - Rahman, Mohammad Hifz Ur
AU - Rahman, Mohammad Meshbahur
N1 - Publisher Copyright:
© 2026 Elsevier Ltd
PY - 2026
Y1 - 2026
N2 - Background: Tuberculosis (TB) is the leading global cause of death from a single infectious agent. Recent reductions in global health funding have threatened TB control, making comprehensive assessment of TB, HIV-related TB, and drug-resistant TB burdens before these disruptions essential for shaping effective responses. The WHO End TB Strategy sets targets of a 95% reduction in TB deaths and a 90% reduction in TB incidence between 2015 and 2035. Using results from the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2023, this study aims to assess the burden of TB and multidrug-resistant TB (MDR-TB) across 204 countries and territories, and to evaluate progress towards the WHO End TB incidence and mortality targets. Methods: We quantified TB mortality using the Cause of Death Ensemble modelling platform with global vital registration, surveillance, verbal autopsy, and minimally invasive tissue sampling data. For TB morbidity estimation, we simultaneously modelled incidence, prevalence, and mortality by age and sex using DisMod-MR 2.1. A population attributable fraction (PAF) approach was applied to stratify morbidity and mortality estimates by HIV and drug-resistance status. We also calculated disability-adjusted life-years (DALYs) as the sum of years of life lost and years lived with disability. For the risk factor analysis, a comparative risk assessment framework was used and PAFs were derived for alcohol use, smoking, and high fasting plasma glucose to determine the proportion of TB burden associated with these risk factors. Findings: In 2023, there were an estimated 9·11 million (95% uncertainty interval 8·04–10·3) incident cases of all-form TB, 1·22 million (0·98–1·49) deaths, and 54·6 million (43·8–65·5) DALYs globally. HIV-related TB comprised 781 000 (690 000–879 000) incident cases and 210 000 (142 000–279 000) deaths, contributing 11·0 million (7·56–14·3) DALYs. MDR-TB accounted for 466 000 (198 000–1 080 000) incident cases, 102 000 (31 700–238 000) deaths, and 3·96 million (1·31–9·01) DALYs. From 2015 to 2023, global all-form TB incidence rates declined by 19·2% (17·8–20·5) and deaths declined by 22·6% (4·7–35·7); declines were larger for drug-susceptible TB than for MDR-TB. Sub-Saharan Africa and south Asia had the highest mortality burdens in 2023; reductions in all-form TB incidence and mortality were uneven between 2000 and 2023, with limited progress in both measures in Latin America and the Caribbean. Removing smoking, alcohol use, and high fasting plasma glucose would reduce global TB deaths to 768 000 (592 000–970 000) and DALYs to 34·9 million (27·8–43·8) in 2023; MDR-TB deaths would decrease to 77 200 (23 400–183 000) and DALYs to 3·12 million (1·03–7·29). Interpretation: Global progress towards WHO End TB targets is disparate and fragile. Although many regions achieved meaningful gains, others have stagnated in recent years. The complexity of TB prevention is amplified by divergent MDR-TB trends, the persistent burden of HIV, and growing exposure to modifiable risk factors. Recent volatility in global health financing threatens to further destabilise this vulnerable epidemiological landscape; concerted action is urgently needed to temper disruptions and preserve progress. Funding: Gates Foundation.
AB - Background: Tuberculosis (TB) is the leading global cause of death from a single infectious agent. Recent reductions in global health funding have threatened TB control, making comprehensive assessment of TB, HIV-related TB, and drug-resistant TB burdens before these disruptions essential for shaping effective responses. The WHO End TB Strategy sets targets of a 95% reduction in TB deaths and a 90% reduction in TB incidence between 2015 and 2035. Using results from the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2023, this study aims to assess the burden of TB and multidrug-resistant TB (MDR-TB) across 204 countries and territories, and to evaluate progress towards the WHO End TB incidence and mortality targets. Methods: We quantified TB mortality using the Cause of Death Ensemble modelling platform with global vital registration, surveillance, verbal autopsy, and minimally invasive tissue sampling data. For TB morbidity estimation, we simultaneously modelled incidence, prevalence, and mortality by age and sex using DisMod-MR 2.1. A population attributable fraction (PAF) approach was applied to stratify morbidity and mortality estimates by HIV and drug-resistance status. We also calculated disability-adjusted life-years (DALYs) as the sum of years of life lost and years lived with disability. For the risk factor analysis, a comparative risk assessment framework was used and PAFs were derived for alcohol use, smoking, and high fasting plasma glucose to determine the proportion of TB burden associated with these risk factors. Findings: In 2023, there were an estimated 9·11 million (95% uncertainty interval 8·04–10·3) incident cases of all-form TB, 1·22 million (0·98–1·49) deaths, and 54·6 million (43·8–65·5) DALYs globally. HIV-related TB comprised 781 000 (690 000–879 000) incident cases and 210 000 (142 000–279 000) deaths, contributing 11·0 million (7·56–14·3) DALYs. MDR-TB accounted for 466 000 (198 000–1 080 000) incident cases, 102 000 (31 700–238 000) deaths, and 3·96 million (1·31–9·01) DALYs. From 2015 to 2023, global all-form TB incidence rates declined by 19·2% (17·8–20·5) and deaths declined by 22·6% (4·7–35·7); declines were larger for drug-susceptible TB than for MDR-TB. Sub-Saharan Africa and south Asia had the highest mortality burdens in 2023; reductions in all-form TB incidence and mortality were uneven between 2000 and 2023, with limited progress in both measures in Latin America and the Caribbean. Removing smoking, alcohol use, and high fasting plasma glucose would reduce global TB deaths to 768 000 (592 000–970 000) and DALYs to 34·9 million (27·8–43·8) in 2023; MDR-TB deaths would decrease to 77 200 (23 400–183 000) and DALYs to 3·12 million (1·03–7·29). Interpretation: Global progress towards WHO End TB targets is disparate and fragile. Although many regions achieved meaningful gains, others have stagnated in recent years. The complexity of TB prevention is amplified by divergent MDR-TB trends, the persistent burden of HIV, and growing exposure to modifiable risk factors. Recent volatility in global health financing threatens to further destabilise this vulnerable epidemiological landscape; concerted action is urgently needed to temper disruptions and preserve progress. Funding: Gates Foundation.
UR - https://www.scopus.com/pages/publications/105043890483
U2 - 10.1016/S1473-3099(26)00295-1
DO - 10.1016/S1473-3099(26)00295-1
M3 - Article
AN - SCOPUS:105043890483
SN - 1473-3099
JO - The Lancet Infectious Diseases
JF - The Lancet Infectious Diseases
ER -