TY - JOUR
T1 - Global, regional, and national burden of pulmonary arterial hypertension, 1990–2021
T2 - a systematic analysis for the Global Burden of Disease Study 2021
AU - GBD 2021 Pulmonary Arterial Hypertension Collaborators
AU - Leary, Peter J.
AU - Lindstrom, Megan
AU - Johnson, Catherine O.
AU - Emmons-Bell, Sophia
AU - Rich, Stuart
AU - Corris, Paul A.
AU - DuBrock, Hilary M.
AU - Ventetuolo, Corey E.
AU - Abate, Yohannes Habtegiorgis
AU - Abdelmasseh, Michael
AU - Aboagye, Richard Gyan
AU - Abualruz, Hasan
AU - Abu-Gharbieh, Eman
AU - Aburuz, Salahdein
AU - Adamu, Lawan Hassan
AU - Adão, Rui
AU - Addo, Isaac Yeboah
AU - Adedoyin, Rufus Adesoji
AU - Adetunji, Juliana Bunmi
AU - Adzigbli, Leticia Akua
AU - Ahinkorah, Bright Opoku
AU - Ahmad, Firdos
AU - Ahmadzade, Amir Mahmoud
AU - Ahmed, Ayman
AU - Ahmed, Haroon
AU - Ahmed, Syed Anees
AU - Akhlaghi, Shiva
AU - Akkaif, Mohammed Ahmed
AU - Al Awaidy, Salah
AU - Alalalmeh, Samer O.
AU - Albakri, Almaza
AU - Aldawsari, Khalifah A.
AU - Almahmeed, Wael
AU - Alshahrani, Najim Z.
AU - Altaf, Awais
AU - Aly, Hany
AU - Alzoubi, Karem H.
AU - Al-Zyoud, Walid Adnan
AU - Amani, Reza
AU - Amusa, Ganiyu Adeniyi
AU - Andrei, Catalina Liliana
AU - Anwar, Saleha
AU - Anyasodor, Anayochukwu Edward
AU - Aravkin, Aleksandr Y.
AU - Areda, Demelash
AU - Asmerom, Haftu Asmerom
AU - Aujayeb, Avinash
AU - Azzam, Ahmed Y.
AU - Babu, Abraham Samuel
AU - Bagherieh, Sara
AU - Baltatu, Ovidiu Constantin
AU - Barqawi, Hiba Jawdat
AU - Bastan, Mohammad-Mahdi
AU - Batra, Kavita
AU - Bayleyegn, Nebiyou Simegnew
AU - Behnoush, Amir Hossein
AU - Bhalla, Jaideep Singh
AU - Bhaskar, Sonu
AU - Bhat, Vivek
AU - Bitaraf, Saeid
AU - Bitra, Veera R.
AU - Boloor, Archith
AU - Braithwaite, Dejana
AU - Brauer, Michael
AU - Bulto, Lemma N.
AU - Bustanji, Yasser
AU - Chattu, Vijay Kumar
AU - Chi, Gerald
AU - Chichagi, Fatemeh
AU - Chong, Bryan
AU - Chowdhury, Rajiv
AU - Cindi, Zinhle
AU - Cruz-Martins, Natalia
AU - Dadana, Sriharsha
AU - Dadras, Omid
AU - Dahiru, Tukur
AU - Dai, Xiaochen
AU - Dashtkoohi, Mohadese
AU - DeAngelo, Sean
AU - Debopadhaya, Shayom
AU - Demessa, Berecha Hundessa
AU - Desai, Hardik Dineshbhai
AU - Dhulipala, Vishal R.
AU - Diaz, Michael J.
AU - Diress, Mengistie
AU - Do, Thanh Chi
AU - Do, Thao Huynh Phuong
AU - Doan, Khanh Duy
AU - dos Santos, Wendel Mombaque
AU - Doshi, Rajkumar Prakashbhai
AU - Dowou, Robert Kokou
AU - Dziedzic, Arkadiusz Marian
AU - Elhadi, Muhammed
AU - Etaee, Farshid
AU - Fabin, Natalia
AU - Fagbamigbe, Adeniyi Francis
AU - Faris, Pawan Sirwan
AU - Feyisa, Bikila Regassa
AU - Fortuna Rodrigues, Celia
AU - Gandhi, Aravind P.
AU - Ganiyani, Mohammad Arfat
AU - Gela, Yibeltal Yismaw
AU - Getie, Molla
AU - Ghaffari Jolfayi, Amir
AU - Ghasemzadeh, Afsaneh
AU - Goldust, Mohamad
AU - Golechha, Mahaveer
AU - Guan, Shi Yang
AU - Gudeta, Mesay Dechasa
AU - Gupta, Mohak
AU - Gupta, Rahul
AU - Hadei, Mostafa
AU - Hammoud, Ahmad
AU - Hasnain, Md Saquib
AU - Hassan Zadeh Tabatabaei, Mahgol Sadat
AU - Hay, Simon I.
AU - Hegazi, Omar E.
AU - Hemmati, Mehdi
AU - Hiraike, Yuta
AU - Hoan, Nguyen Quoc
AU - Hultström, Michael
AU - Huynh, Hong-Han
AU - Ibitoye, Segun Emmanuel
AU - Ilesanmi, Olayinka Stephen
AU - Ismail, Nahlah Elkudssiah
AU - Iwu, Chidozie Declan
AU - Jaggi, Khushleen
AU - Jain, Akhil
AU - Jakovljevic, Mihajlo
AU - Jee, Sun Ha
AU - Jeswani, Bijay Mukesh
AU - Jha, Anil K.
AU - Jokar, Mohammad
AU - Joseph, Nitin
AU - Jozwiak, Jacek Jerzy
AU - Kabir, Hannaneh
AU - Kahe, Farima
AU - Kamireddy, Arun
AU - Kanmanthareddy, Arun R.
AU - Karimi, Hanie
AU - Karimi Behnagh, Arman
AU - Kazemian, Sina
AU - Keshavarz, Pedram
AU - Khalaji, Amirmohammad
AU - Khan, Mohammad Jobair
AU - Khidri, Feriha Fatima
AU - Kim, Min Seo
AU - Kondlahalli, Shivakumar KM Marulasiddaiah
AU - Kothari, Nikhil
AU - Krishan, Kewal
AU - Kulimbet, Mukhtar
AU - Kumar, Ashish
AU - Latifinaibin, Kaveh
AU - Le, Thao Thi Thu
AU - Ledda, Caterina
AU - Lee, Seung Won
AU - Li, Ming-Chieh
AU - Lim, Stephen S.
AU - Liu, Shuke
AU - Mahmoudi, Elham
AU - Makram, Omar M.
AU - Malhotra, Kashish
AU - Malik, Ahmad Azam
AU - Malta, Deborah Carvalho
AU - Manla, Yosef
AU - Martorell, Miquel
AU - Mehrabani-Zeinabad, Kamran
AU - Merati, Mohsen
AU - Mestrovic, Tomislav
AU - Mirdamadi, Niloofar
AU - Misra, Arup Kumar
AU - Mokdad, Ali H.
AU - Moni, Mohammad Ali
AU - Moodi Ghalibaf, Amir Ali
AU - Moraga, Paula
AU - Morovatdar, Negar
AU - Motappa, Rohith
AU - Mousavi-Aghdas, Seyed Ali
AU - Mustafa, Ahmad
AU - Naik, Ganesh R.
AU - Najafi, Mohammad Sadeq
AU - Najdaghi, Soroush
AU - Nanavaty, Dhairya P.
AU - Narimani Davani, Delaram
AU - Natto, Zuhair S.
AU - Nauman, Javaid
AU - Nguyen, Dang H.
AU - Nguyen, Phat Tuan
AU - Niazi, Robina Khan
AU - Oancea, Bogdan
AU - Olanipekun, Titilope O.
AU - Oliveira, Gláucia Maria Moraes
AU - Omar, Hany A.
AU - P A, Mahesh Padukudru
AU - Pan, Feng
AU - Pandi-Perumal, Seithikurippu R.
AU - Pantazopoulos, Ioannis
AU - Parikh, Romil R.
AU - Petcu, Ionela Roxana
AU - Pham, Hoang Nhat
AU - Pham, Hoang Tran
AU - Philip, Anil K.
AU - Prates, Elton Junio Sady
AU - Puvvula, Jagadeesh
AU - Qian, Gangzhen
AU - Rafferty, Quinn
AU - Rahim, Fakher
AU - Rahimi, Mehran
AU - Rahman, Mosiur
AU - Rahman, Muhammad Aziz
AU - Rahmanian, Mohammad
AU - Rahmanian, Nazanin
AU - Rahmati, Masoud
AU - Rahmati, Rahem
AU - Ramadan, Mahmoud Mohammed
AU - Ramphul, Kamleshun
AU - Rana, Juwel
AU - Rao, Indu Ramachandra
AU - Rashedi, Sina
AU - Ravikumar, Nakul
AU - Rawaf, Salman
AU - Ray, Ayita
AU - Reddy, Murali Mohan Rama Krishna
AU - Redwan, Elrashdy Moustafa Mohamed
AU - Rezaei, Negar
AU - Roy, Priyanka
AU - Saad, Aly M.A.
AU - Saddik, Basema Ahmad
AU - Sadeghi, Masoumeh
AU - Saeb, Mohammad Reza
AU - Saheb Sharif-Askari, Fatemeh
AU - Saheb Sharif-Askari, Narjes
AU - Saleh, Mohamed A.
AU - Sani, Najib Yahaya
AU - Saraswati, Ushasi
AU - Saravanan, Aswini
AU - Saulam, Jennifer
AU - Schuermans, Art
AU - Schumacher, Austin E.
AU - Semagn, Birhan Ewunu
AU - Sethi, Yashendra
AU - Seylani, Allen
AU - Shafeghat, Melika
AU - Shahwan, Moyad Jamal
AU - Shamim, Muhammad Aaqib
AU - Shamsi, Anas
AU - Sharfaei, Sadaf
AU - Sharma, Kamal
AU - Sharma, Nitish
AU - Shorofi, Seyed Afshin
PY - 2025/1
Y1 - 2025/1
N2 - Background: Pulmonary arterial hypertension (PAH) is a vascular disease characterised by restricted flow and high pressure through the pulmonary arteries, leading to progressive right heart failure and death. This study reports the global burden of PAH, leveraging all available data and using methodology of the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) to understand the epidemiology of this under-researched and morbid disease. Methods: Prior to the current effort, the burden of PAH was included in GBD as a non-specific contributor to “other cardiovascular and circulatory disease” burden. In this study, PAH was distinguished as its own cause of death and disability in GBD, producing comparable and consistent estimates of PAH burden. We used epidemiological and vital registry data to estimate the non-fatal and fatal burden of PAH in 204 countries and territories from 1990 to 2021 using standard GBD modelling approaches. We specifically focused on PAH (group 1 pulmonary hypertension), and did not include pulmonary hypertension groups 2–5. Findings: In 2021, there were an estimated 192 000 (95% uncertainty interval [UI] 155 000–236 000) prevalent cases of PAH globally. Of these, 119 000 (95 900–146 000) were in females (62%) and 73 100 (58 900–89 600) in males (38%). The age-standardised prevalence was 2·28 cases per 100 000 population (95% UI 1·85–2·80). Prevalence increased with age such that the highest prevalence was among individuals aged 75–79 years. In 2021, there were 22 000 deaths (18 200–25 400) attributed to PAH globally, with an age-standardised mortality rate of 0·27 deaths from PAH per 100 000 population (0·23–0·32). The burden of disease appears to be improving over time (38·2% improvement in age-standardised years of life lost [YLLs] in 2021 relative to 1990). YLLs attributed to PAH were similar to estimates for conditions such as chronic myeloid leukaemia, multiple sclerosis, and Crohn's disease. Interpretation: PAH is a rare but fatal disease that accounts for a considerable health-associated burden worldwide. PAH is disproportionally diagnosed among females and older adults. Funding: Cardiovascular Medical Research and Education Fund and the Bill & Melinda Gates Foundation.
AB - Background: Pulmonary arterial hypertension (PAH) is a vascular disease characterised by restricted flow and high pressure through the pulmonary arteries, leading to progressive right heart failure and death. This study reports the global burden of PAH, leveraging all available data and using methodology of the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) to understand the epidemiology of this under-researched and morbid disease. Methods: Prior to the current effort, the burden of PAH was included in GBD as a non-specific contributor to “other cardiovascular and circulatory disease” burden. In this study, PAH was distinguished as its own cause of death and disability in GBD, producing comparable and consistent estimates of PAH burden. We used epidemiological and vital registry data to estimate the non-fatal and fatal burden of PAH in 204 countries and territories from 1990 to 2021 using standard GBD modelling approaches. We specifically focused on PAH (group 1 pulmonary hypertension), and did not include pulmonary hypertension groups 2–5. Findings: In 2021, there were an estimated 192 000 (95% uncertainty interval [UI] 155 000–236 000) prevalent cases of PAH globally. Of these, 119 000 (95 900–146 000) were in females (62%) and 73 100 (58 900–89 600) in males (38%). The age-standardised prevalence was 2·28 cases per 100 000 population (95% UI 1·85–2·80). Prevalence increased with age such that the highest prevalence was among individuals aged 75–79 years. In 2021, there were 22 000 deaths (18 200–25 400) attributed to PAH globally, with an age-standardised mortality rate of 0·27 deaths from PAH per 100 000 population (0·23–0·32). The burden of disease appears to be improving over time (38·2% improvement in age-standardised years of life lost [YLLs] in 2021 relative to 1990). YLLs attributed to PAH were similar to estimates for conditions such as chronic myeloid leukaemia, multiple sclerosis, and Crohn's disease. Interpretation: PAH is a rare but fatal disease that accounts for a considerable health-associated burden worldwide. PAH is disproportionally diagnosed among females and older adults. Funding: Cardiovascular Medical Research and Education Fund and the Bill & Melinda Gates Foundation.
KW - Global Burden of Disease Study 2021
KW - pulmonary arterial hypertension
KW - systematic analysis
UR - http://www.scopus.com/inward/record.url?scp=85209671750&partnerID=8YFLogxK
U2 - 10.1016/S2213-2600(24)00295-9
DO - 10.1016/S2213-2600(24)00295-9
M3 - Article
C2 - 39433052
AN - SCOPUS:85209671750
SN - 2213-2600
VL - 13
SP - 69
EP - 79
JO - The Lancet Respiratory Medicine
JF - The Lancet Respiratory Medicine
IS - 1
ER -