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 - Nauman, Javaid
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 - 2025/1
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.
UR - http://www.scopus.com/inward/record.url?scp=85209671750&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.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 -