Evidence map›Paper›PMID 39720660›Full record

ArticleFrontiers in medicine2024

Trends and levels of the global, regional, and national burden of pulmonary arterial hypertension from 1990 to 2021: findings from the global burden of disease study 2021.

Le Liu, Chen Li, Jing Cai, Renjing Kong, Yanjiao Wang, Yi Wang, Shuang Li, Junkun Zhan, Youshuo Liu

Abstract read
In one paragraph

Article in Frontiers in medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Pulmonary hypertension aetiologies in different parts of the world.International journal of cardiology. Congenital heart disease · 2025
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Le LiuDepartment of Geriatrics, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Chen LiDepartment of Geriatrics, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Jing CaiDepartment of Geriatrics, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Renjing KongDepartment of Geriatrics, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Yanjiao WangDepartment of Geriatrics, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Yi WangDepartment of Geriatrics, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Shuang LiDepartment of Geriatrics, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Junkun ZhanDepartment of Geriatrics, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Youshuo LiuDepartment of Geriatrics, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Pulmonary arterial hypertension (PAH) is a severe and progressive lung disease that significantly impairs patients' health and imposes heavy clinical and economic burdens. Currently, there is a lack of comprehensive epidemiological analysis on the global burden and trends of PAH. Methods: We estimated the prevalence, mortality, disability-adjusted life years (DALYs) of PAH from 1990 to 2021 using the results of the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD). The average annual percentage changes were used to estimate the trends of PAH across 21 regions and 204 countries and territories. Results: From 1990 to 2021, the number of prevalent cases and deaths associated with PAH worldwide increased by 81.5 and 48.4%. However, the age-standardized prevalence rate of PAH remained relatively stable, while the age-standardized mortality rate and DALYs declined. In 2021, the global age-standardized prevalence rate of PAH was 2.28 per 100,000, with 1.78 per 100,000 in males and 2.75 per 100,000 in females. The age-standardized mortality rate of PAH globally was 0.27 per 100,000, and the age-standardized DALYs was 8.24 per 100,000. Among the 21 regions, Western Europe had the highest age-standardized prevalence rate (3.56 per 100,000), while North Africa and the Middle East had the highest age-standardized mortality rate (0.44 per 100,000) and DALYs (14.81 per 100,000). Additionally, older individuals and females are at higher risk of PAH. The age-standardized mortality rate and DALYs associated with PAH increase with age, peaking in the 95+ age group. As the sociodemographic index increased, the age-standardized prevalence rates showed an upward trend, while both the age-standardized mortality rates and DALYs exhibited a downward trend. Conclusion: From 1990 to 2021, the overall trend of PAH burden presents regional and national variations and differs by age, sex, and sociodemographic index. These findings emphasize the importance of implementing targeted interventions to alleviate the burden of PAH.

Indexed as

disease burdenepidemiologyprevalencepulmonary arterial hypertensionsociodemographic index

Identifiers

PMID39720660
PMCPMC11666447

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.