TY - JOUR
T1 - Global, regional, and national prevalence of kidney failure with replacement therapy and associated aetiologies, 1990–2023
T2 - a systematic analysis for the Global Burden of Disease Study 2023
AU - GBD 2023 Kidney Failure with Replacement Therapy Collaborators
AU - Rafferty, Quinn
AU - Stafford, Lauryn K.
AU - Vos, Theo
AU - Thomé, Fernando Saldanha
AU - Aalruz, Hasan
AU - Abate, Yohannes Habtegiorgis
AU - Abbafati, Cristiana
AU - Abd ElHafeez, Samar
AU - Abedi, Armita
AU - Abiodun, Olugbenga Olusola
AU - Abreu, Lucas Guimarães
AU - Abu-Gharbieh, Eman
AU - Aburuz, Salahdein
AU - Abu-Zaid, Ahmed
AU - Adamu, Lawan Hassan
AU - Addo, Isaac Yeboah
AU - Adegboye, Oyelola A.
AU - Adepoju, Abiola Victor
AU - Adeyomoye, Olorunsola Israel
AU - Adnani, Qorinah Estiningtyas Sakilah
AU - Agarwal, Sanjay Kumar
AU - Aghamiri, Shahin
AU - Agrawaal, Krishna Kumar
AU - Ahinkorah, Bright Opoku
AU - Ahmad, Aqeel
AU - Ahmad, Muayyad M.
AU - Ahmad, Sajjad
AU - Ahmed, Ali
AU - Ahmed, Ayman
AU - Ahmed, Syed Anees
AU - Ajami, Marjan
AU - Akhlaghi, Shiva
AU - Akkala, Sreelatha
AU - Al-Aly, Ziyad
AU - Albashtawy, Mohammed
AU - Aldawsari, Khalifah A.
AU - Alemi, Hediyeh
AU - Al-Gheethi, Adel Ali Saeed
AU - Alhalaiqa, Fadwa Naji
AU - Ali, Endale Alemayehu
AU - Ali, Syed Shujait
AU - Almidani, Omar
AU - Al-Raddadi, Rajaa M.Mohammad
AU - Alvi, Farrukh Jawad
AU - Alvis-Guzman, Nelson
AU - Alvis-Zakzuk, Nelson J.
AU - Al-Worafi, Yaser Mohammed
AU - Aly, Safwat
AU - Alzoubi, Karem H.
AU - Amani, Reza
AU - Amu, Hubert
AU - Amusa, Ganiyu Adeniyi
AU - Andrei, Catalina Liliana
AU - Anil, Abhishek
AU - Ansar, Adnan
AU - Anyasodor, Anayochukwu Edward
AU - Arabloo, Jalal
AU - Arafa, Elshaimaa A.
AU - Arkew, Mesay
AU - Ärnlöv, Johan
AU - Ashraf, Tahira
AU - Athar, Mohammad
AU - Athari, Seyyed Shamsadin
AU - Atout, Maha Moh d.Wahbi
AU - Awotidebe, Adedapo Wasiu
AU - Aynalem, Zewdu Bishaw
AU - Azadnajafabad, Sina
AU - Azhdari Tehrani, Hamed
AU - Aziz, Shahkaar
AU - Babamohamadi, Hassan
AU - Badar, Muhammad
AU - Bagga, Arvind
AU - Bagherieh, Sara
AU - Baltatu, Ovidiu Constantin
AU - Barqawi, Hiba Jawdat
AU - Basu, Sanjay
AU - Basu, Saurav
AU - Batra, Kavita
AU - Bayleyegn, Nebiyou Simegnew
AU - Bedi, Neeraj
AU - Behnoush, Amir Hossein
AU - Bekele, Alehegn
AU - Belo, Luis
AU - Benfor, Bright
AU - Bensenor, Isabela M.
AU - Bermudez, Amiel Nazer C.
AU - Bhagavathula, Akshaya Srikanth
AU - Bhaskar, Sonu
AU - Bhatti, Gurjit Kaur
AU - Bhatti, Jasvinder Singh
AU - Bijani, Ali
AU - Bikbov, Boris
AU - Bilalaga, Mariah Malak
AU - Bitra, Veera R.
AU - Bora, Kaustubh
AU - Bustanji, Yasser
AU - Butt, Zahid A.
AU - Cámera, Luis Alberto
AU - Carrero, Juan Jesus
AU - Carvalho, Márcia
AU - Catalá-López, Ferrán
AU - Catapano, Alberico L.
AU - Cenderadewi, Muthia
AU - Chadwick, Joshua
AU - Chakraborty, Promit Ananyo
AU - Chandrasekar, Eeshwar K.
AU - Chattu, Vijay Kumar
AU - Chekol Abebe, Endeshaw
AU - Ching, Patrick R.
AU - Chowdhury, Enayet Karim
AU - Chowdhury, Rajiv
AU - Chu, Dinh Toi
AU - Chung, Sheng Chia
AU - Cirillo, Massimo
AU - Columbus, Alyssa
AU - Coresh, Josef
AU - Cruz-Martins, Natalia
AU - Dadras, Omid
AU - Dai, Xiaochen
AU - Dandona, Lalit
AU - Dandona, Rakhi
AU - Das, Saswati
AU - Dashtkoohi, Mohadese
AU - Davids, Mogamat Razeen
AU - Delgado-Enciso, Ivan
AU - Demessa, Berecha Hundessa
AU - Deng, Xinlei
AU - Desai, Hardik Dineshbhai
AU - Devanbu, Vinoth Gnana Chellaiyan
AU - Dewan, Syed Masudur Rahman
AU - Diaz, Daniel
AU - Digesa, Lankamo Ena
AU - Dixit, Abhinav
AU - Do, Thao Huynh Phuong
AU - do Prado, Camila Bruneli
AU - Doan, Khanh Duy
AU - Dokova, Klara Georgieva
AU - Dongarwar, Deepa
AU - Dowou, Robert Kokou
AU - Edinur, Hisham Atan
AU - Ekholuenetale, Michael
AU - Ekundayo, Temitope Cyrus
AU - Elhadi, Muhammed
AU - El-Huneidi, Waseem
AU - Elmonem, Mohamed A.
AU - Esezobor, Christopher Imokhuede
AU - Esposito, Francesco
AU - Etaee, Farshid
AU - Fagbamigbe, Adeniyi Francis
AU - Faiz, Razana
AU - Fallahzadeh, Aida
AU - Faraon, Emerito Jose A.Aquino
AU - Feizkhah, Alireza
AU - Fekadu, Ginenus
AU - Ferreira, Nuno
AU - Feyisa, Bikila Regassa
AU - Fischer, Florian
AU - Gaipov, Abduzhappar
AU - Gandhi, Aravind P.
AU - Gebregergis, Miglas Welay
AU - Gemmechu, Mathewos Mekonnen
AU - Ghafourifard, Mansour
AU - Ginawi, Ibrahim Abdelmageed
AU - Gindaba, Ebisa Zerihun
AU - Golechha, Mahaveer
AU - Goleij, Pouya
AU - Golinelli, Davide
AU - Guan, Shi Yang
AU - Gudeta, Mesay Dechasa
AU - Gupta, Anish Kumar
AU - Gupta, Rajat Das
AU - Gupta, Rajeev
AU - Gupta, Sapna
AU - Gupta, Veer Bala
AU - Gupta, Vivek Kumar
AU - Hadi, Najah R.
AU - Hagins, Hailey
AU - Haile, Teklehaimanot Gereziher
AU - Halim, Sobia Ahsan
AU - Halwani, Rabih
AU - Hamdy, Nadia M.
AU - Hamidi, Samer
AU - Hammoud, Ahmad
AU - Hareru, Habtamu Endashaw
AU - Hasan, S. M.Mahmudul
AU - Hasnain, Md Saquib
AU - Haubold, Johannes
AU - He, Jiawei
AU - Heydari, Keyvan
AU - Hiraike, Yuta
AU - Hoogar, Praveen
AU - Hosseinzadeh, Hassan
AU - Hosseinzadeh, Mehdi
AU - Hostiuc, Mihaela
AU - Huynh, Hong Han
AU - Ibitoye, Segun Emmanuel
AU - Ilic, Irena M.
AU - Islam, Md Rabiul
AU - Islam, Sheikh Mohammed Shariful
AU - Islampanah, Muhammad
N1 - Publisher Copyright:
© 2025 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license
PY - 2025/8
Y1 - 2025/8
N2 - Background: Kidney failure with replacement therapy (KFRT) such as dialysis or transplantation represents a severe stage of chronic kidney disease (CKD) and poses a major global health burden. Although many CKD cases are diagnosed in the earlier stages, the greatest risk occurs when CKD progresses to KFRT. Despite its considerable financial and imposing impact on public health, there is a notable gap in international policies addressing CKD and KFRT. To bridge this gap and help policy makers and health systems effectively tackle the public health challenge of KFRT, a better understanding of the disease burden is essential. Thus, this analysis aims to provide a detailed overview of the global prevalence of KFRT and its associated aetiologies with estimates from the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) from 1990 to 2023. Methods: This study defined KFRT as individuals on maintenance dialysis for 90 days or more or those who have undergone a kidney transplant, aligning with the Kidney Disease: Improving Global Outcomes (KDIGO) 2024 Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease. Renal registries served as the primary data sources. Prevalence and underlying aetiology estimates (type 1 diabetes, type 2 diabetes, hypertension, glomerulonephritis, and other causes) were generated with DisMod-MR 2.1, an epidemiological Bayesian mixed-effects meta-regression modelling tool. Both all-age and age-standardised estimates were reported and accompanied with 95% uncertainty intervals (UIs). Findings: In 2023, the number of global cases of KFRT was 4·59 million (95% UI 4·17–5·08) for both sexes and all ages, with an age-standardised prevalence of 50·7 (46·1–56·0) per 100 000 population. Over the past three decades, there has been a steady increase in KFRT prevalence globally. The highest prevalence was found in the GBD high-income regions, while the lowest was observed in sub-Saharan Africa. KFRT prevalence was generally higher in countries classified within the World Bank's high-income and upper-middle-income groups, while lower prevalence was more common in countries within the World Bank's low-income and lower-middle-income groups. Additionally, a pronounced sex disparity was identified, where male dialysis and transplant prevalence estimates were consistently higher than those for females in most countries. Type 2 diabetes and hypertension were among the leading associated aetiologies of KFRT globally. From 1990 to 2023, the all-age and age-standardised prevalence estimates across the ascribed aetiologies increased for KFRT, with the largest increases associated with type 2 diabetes and hypertension. Interpretation: KFRT affects approximately 5 million people globally, with high treatment and mortality costs. Our study unveiled considerable geographical variation in KFRT prevalence, which should be seen as indicators of health-care system opportunities. As the prevalence of the leading aetiologies of KFRT—type 2 diabetes and hypertension—continues to rise, there is a crucial need to prioritise the development and implementation of cost-effective strategies aimed at preventing CKD and its progression to KFRT, particularly in low-resource settings. These preventive efforts must happen in tandem with efforts to expand capacity for dialysis and transplant services. Funding: Gates Foundation.
AB - Background: Kidney failure with replacement therapy (KFRT) such as dialysis or transplantation represents a severe stage of chronic kidney disease (CKD) and poses a major global health burden. Although many CKD cases are diagnosed in the earlier stages, the greatest risk occurs when CKD progresses to KFRT. Despite its considerable financial and imposing impact on public health, there is a notable gap in international policies addressing CKD and KFRT. To bridge this gap and help policy makers and health systems effectively tackle the public health challenge of KFRT, a better understanding of the disease burden is essential. Thus, this analysis aims to provide a detailed overview of the global prevalence of KFRT and its associated aetiologies with estimates from the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) from 1990 to 2023. Methods: This study defined KFRT as individuals on maintenance dialysis for 90 days or more or those who have undergone a kidney transplant, aligning with the Kidney Disease: Improving Global Outcomes (KDIGO) 2024 Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease. Renal registries served as the primary data sources. Prevalence and underlying aetiology estimates (type 1 diabetes, type 2 diabetes, hypertension, glomerulonephritis, and other causes) were generated with DisMod-MR 2.1, an epidemiological Bayesian mixed-effects meta-regression modelling tool. Both all-age and age-standardised estimates were reported and accompanied with 95% uncertainty intervals (UIs). Findings: In 2023, the number of global cases of KFRT was 4·59 million (95% UI 4·17–5·08) for both sexes and all ages, with an age-standardised prevalence of 50·7 (46·1–56·0) per 100 000 population. Over the past three decades, there has been a steady increase in KFRT prevalence globally. The highest prevalence was found in the GBD high-income regions, while the lowest was observed in sub-Saharan Africa. KFRT prevalence was generally higher in countries classified within the World Bank's high-income and upper-middle-income groups, while lower prevalence was more common in countries within the World Bank's low-income and lower-middle-income groups. Additionally, a pronounced sex disparity was identified, where male dialysis and transplant prevalence estimates were consistently higher than those for females in most countries. Type 2 diabetes and hypertension were among the leading associated aetiologies of KFRT globally. From 1990 to 2023, the all-age and age-standardised prevalence estimates across the ascribed aetiologies increased for KFRT, with the largest increases associated with type 2 diabetes and hypertension. Interpretation: KFRT affects approximately 5 million people globally, with high treatment and mortality costs. Our study unveiled considerable geographical variation in KFRT prevalence, which should be seen as indicators of health-care system opportunities. As the prevalence of the leading aetiologies of KFRT—type 2 diabetes and hypertension—continues to rise, there is a crucial need to prioritise the development and implementation of cost-effective strategies aimed at preventing CKD and its progression to KFRT, particularly in low-resource settings. These preventive efforts must happen in tandem with efforts to expand capacity for dialysis and transplant services. Funding: Gates Foundation.
UR - https://www.scopus.com/pages/publications/105011185044
U2 - 10.1016/S2214-109X(25)00198-6
DO - 10.1016/S2214-109X(25)00198-6
M3 - Article
C2 - 40712611
AN - SCOPUS:105011185044
SN - 2572-116X
VL - 13
SP - e1378-e1395
JO - The Lancet Global Health
JF - The Lancet Global Health
IS - 8
ER -