Your new experience awaits. Try the new design now and help us make it even better

ORIGINAL RESEARCH article

Front. Med., 25 November 2025

Sec. Geriatric Medicine

Volume 12 - 2025 | https://doi.org/10.3389/fmed.2025.1595504

This article is part of the Research TopicAlleviating Age-Related Disease BurdenView all 4 articles

Global, regional, and national burden of pulmonary arterial hypertension in adults aged ≥60 years from 1990–2021: SDI-stratified trend analysis and projections to 2050

Guorui Xu&#x;Guorui Xu1Xiangyi Feng&#x;Xiangyi Feng1Nini Qu,
Nini Qu,2*
  • 1The First Clinical College of Liaoning University of Traditional Chinese Medicine, Shenyang, Liaoning, China
  • 2Department of Pulmonology, The First Affiliated Hospital of Liaoning University of Traditional Chinese Medicine, Shenyang, Liaoning, China

Background: Pulmonary arterial hypertension (PAH), a progressive and life-threatening condition, has significant implications for public health, particularly in the aging population. This study provides a comprehensive analysis of PAH in individuals aged 60 years and older from 1990 to 2021, utilizing data from the Global Burden of Disease (GBD) 2021 study, which encompasses 204 countries and territories.

Methods: We tracked PAH trends (1990–2021) with three metrics: the annual percentage change (APC) from joinpoint, the average APC (AAPC) across segments, and the estimated APC (EAPC) from the log-linear model. APC captures year-by-year shifts; AAPC summarises the whole period; EAPC gives a single long-term slope. Significance set at 95% CI excluding zero. For 2022–2050 we used the Bayesian age-period-cohort (BAPC) model, which extends these time-component ideas into future projections.

Results: Between 1990 and 2021, the number of new cases increased by 130%, deaths by 130%, and disability-adjusted life years (DALYs) increased by 100%. In 2021, there were 15,622 new cases, 15,443 deaths, and 248,064 DALYs globally. The incidence rate rose from 1.447 to 1.66 per 100,000 population. Looking ahead to 2050, we project the number of new cases to reach 31383 (95% CI: 17604.40, 45162.56), an incidence rate of 1.46 per 100,000, approximately 20,687 deaths, and 302,760 DALYs. In addition, Zambia recorded the highest incidence rate, while China had the largest total number of cases. The middle Sociodemographic Index (SDI) region bore the highest disease burden, highlighting disparities in the global distribution of PAH.

Conclusion: These findings underscore the escalating burden of PAH among the elderly and emphasize the urgent need for targeted public health strategies to address this growing challenge. Our study highlights the importance of continued surveillance and the development of interventions to mitigate the impact of PAH on aging populations worldwide.

1 Introduction

Pulmonary arterial hypertension (PAH) is a progressive disease characterized by increased pulmonary vascular resistance and altered right ventricular function and structure (1, 2). Patients with PAH typically experience shortness of breath, especially during activity, along with symptoms such as weakness, chest pain, swelling of the ankles or legs, and dizziness, which can eventually lead to death (36). Reportedly, approximately 1% of the global population suffers from PAH, which affects 10% of people over 65 years of age (7). Between 1990 and 2021, although the age-standardized incidence showed no significant change, the number of patients with PAH has increased by 81.5%, with a higher proportion in the elderly population (8). The Rotterdam Epidemiological Study of Hypertension reported higher incidence among elderly participants compared to younger patients (9). These findings indicate a growing disease burden of PAH in the elderly population, highlighting the need for greater attention to incidence and mortality trends among this demographic. However, comprehensive global studies focusing on the elderly remain limited, and systematic reports on incidence and mortality trends in elderly PAH patients are lacking.

The Global Burden of Disease (GBD) study, spearheaded by the Institute for Health Metrics and Evaluation (IHME) at the University of Washington, is widely recognized as one of the most comprehensive global epidemiological databases. It provides a robust framework for comparative assessments of morbidity and mortality across countries, regions, and globally, facilitating a nuanced understanding of disease distributions and trends (10, 11). Despite the significant advancements in our understanding of PAH distribution brought about by previous GBD studies, these investigations have predominantly focused on an overall perspective that encompasses all age groups (8). While these studies have documented global, regional, and national trends from 1990 to 2021, they are not without limitations. Specifically, data on the elderly population remain fragmented, and variations in methodology complicate cross-national comparisons and overall assessments. This fragmentation and methodological diversity hinder the development of a cohesive understanding of PAH’s impact on the elderly. Furthermore, existing research has insufficiently addressed the prediction of future disease burdens. This gap in predictive research introduces substantial uncertainty into addressing the healthcare demands arising from global population aging. As the global population continues to age, the need for accurate projections and targeted public health strategies becomes increasingly urgent.

This study aims to provide a comprehensive analysis of the epidemiological trends of PAH among adults aged 60 and older, utilizing data from the GBD database spanning from 1990 to 2021. The study will analyze global, regional, and national epidemiological data on PAH among adults aged 60 and older. Key disease burden indicators, including incidence rate, mortality rate, and disability-adjusted life years (DALYs), will be examined to identify detailed temporal and spatial trends. Additionally, building on established epidemiological data and trends, robust statistical projection models will be employed to forecast the incidence of PAH in this population through 2050. This study aims to support the development of targeted public health interventions and improve the management of PAH in aging populations globally.

2 Methods

2.1 Overview and methodological details

Data for this study were sourced from the GBD database, encompassing 204 countries and territories. In GBD 2021, PAH is classified under Group 1, characterized by pulmonary arterial remodelling, elevated pulmonary pressure, and eventual right ventricular dysfunction. Only records with ICD-10 codes 416 and I27.0 were included after chart review confirmed the diagnosis. Data coded I27.2 or in ICD-8, ICD-9-BTL, and ICD-10 tabular formats were excluded to ensure specificity, as they do not reliably distinguish PAH from other pulmonary disorders. In countries where the introduction of I27.0 caused abrupt changes in PAH mortality trends, pre-implementation years were omitted (11). This approach isolates PAH from other forms of pulmonary hypertension (PH) associated with left heart disease, lung diseases, hypoxia, pulmonary artery obstructions, and multifactorial mechanisms. The analysis covers multiple dimensions, including gender, age groups (60–64, 65–69, 70–74, 75–79, 80–84, 85–89, 90–94, and over 95 years), and location.

2.2 Sociodemographic Index

The Sociodemographic Index (SDI) is a composite indicator measuring a country or region’s socioeconomic development, incorporating factors such as economic level, education, health, social security, welfare, environment, and sustainability. The GBD database categorizes countries and regions into five SDI levels: low, low-middle, middle, high-middle, and high (12).

2.3 Statistical analysis

This study analyzed the incidence, mortality, and DALYs of PAH per 100,000 population, presenting estimates with 95% uncertainty intervals (UI) to quantify reliability. The 95% UI was calculated using the Bayesian hierarchical model employed by the GBD database, integrating uncertainties from multiple data sources (e.g., national registries, clinical studies, cohort studies) and estimating them via a Markov chain Monte Carlo (MCMC) approach, thereby reflecting estimation errors arising from data sources, diagnostic variations, model assumptions, and other factors.

To address potential data biases and varying age structures, we used the age-standardized rate (ASR) based on the GBD world standard population. Trends from 1990 to 2021 were assessed using multiple approaches: segmented regression (Joinpoint analysis) identified distinct temporal segments and calculated the annual percentage change (APC) with 95% confidence intervals (CI) for each segment; the average annual percentage change (AAPC) summarized the overall long-term trend; and a log-linear model estimated the average annual percentage change (EAPC) for sustained, long-term trends, providing a single summary slope for direct comparison of 1990–2021 trajectories across regions, countries, or diseases. For all measures (APC, AAPC, EAPC), trends were considered statistically significant if the 95% CI did not include zero (p < 0.05) (13). The association between PAH burden and the SDI was examined through curve fitting. In regional and national stratified analyses, the statistical significance of between-group differences was assessed by examining the overlap of UI, with non-overlapping UI suggesting significant differences.

To project the disease burden from 2022 to 2050, we employed the Bayesian age-period-cohort (BAPC) model. This model disentangles the independent effects of age, period, and cohort, making it suitable for long-term forecasting. The model was configured with second-order random walk priors for age, period, and cohort effects to ensure smoothness and identifiability (14, 15). The population aged 60 and above was divided into eight 5-year age groups: 60–64, 65–69, 70–74, 75–79, 80–84, 85–89, 90–94, and 95+.

The BAPC model was fitted using the integrated nested Laplace approximation (INLA) algorithm. Projections assume no major public health disruptions (e.g., pandemics, wars) and stable socioeconomic trends, indicating that current disease rates and population structures will persist into the future without significant external shocks.

The analyses, including the BAPC modelling, were conducted using R software (version 4.4.2) with packages such as BAPC and INLA. A two-tailed p-value of less than 0.05 was considered statistically significant.

2.4 Age-standardized rates

The proportion of people over 60 years of age based on the standard population is calculated and displayed in the “Age Distribution of Std Pop” column. These will be used as weights.

3 Results

3.1 Global burden of PAH in older adults (≥60 years)

3.1.1 Incidence

The global age-standardized incidence of PAH among adults aged ≥60 years increased from 1990 to 2021, with the steepest rise occurring between 1990 and 2000 (APC 34%, p < 0.05; Figure 1A) and a transient dip between 2015 and 2018. Globally, incident cases rose by 130%, while the EAPC was −0.01 (Table 1). The 75–79-year-old age group consistently had the highest incidence rates, and the 95+ year group had the lowest (Figures 2A, 3A). Incidence was higher in women across all age strata, with a 12% excess in the 95+ year-old group (Figure 2A).

Figure 1
Three line graphs labeled A, B, and C display trends over time with accompanying average percentage change (APC) values. Graph A shows incidence rates from 1990 to 2021 with periods of increase and decrease. Graph B presents death rates from 1990 to 2021, highlighting a significant rise followed by a pronounced decline after 2011. Graph C displays DALYs rates over the same period with notable fluctuations. Each graph is annotated with specific APC values for different time intervals.

Figure 1. Annual percent change (APC) in PAH incidence, mortality, and DALYs in older adults globally (DALYs) from 1990 to 2021. (A) Incidence. (B) Mortality. (C) DALYs rate.

Table 1
www.frontiersin.org

Table 1. Global and regional incidence of PAH in older adults from 1990–2021.

Figure 2
Three sets of graphs labeled A, B, and C show age-specific data trends across different age groups (60+ years) and genders over time. Each set includes line graphs by age group and gender, and bar graphs with 95% uncertainty intervals. Female data is shown in pink and male data in blue.

Figure 2. Trends in PAH incidence, mortality, and DALYs in older adults by age and sex, 1990–2021. (A) Incidence, cases and rates. (B) Mortality cases and rates. (C) Number of DALYs cases and rates.

Figure 3
Three sets of horizontal bar charts labeled A, B, and C display the age distribution of PAH burden across various regions for the years 1990 and 2021. Each chart compares age groups from 60 to 95+ years across global and regional categories. Different colors represent different age groups, showing changes in the proportion of PAH incidence, mortality, and DALYs attributed to older populations over time.

Figure 3. Age-specific percentages of PAH incidence, mortality, and DALYs in older age in 1990 and 2021. (A) incidence. (B) Death. (C) DALYs.

In 2021, at the national level, China had the highest number of PAH cases worldwide (4,129 cases; 95% UI: 2797.25, 5872.71), while Zambia had the highest incidence rate (2.89 per 100,000 people; 95% UI: 2.00, 4.07) (Figures 4A,B). From 1990 to 2021, Slovakia showed the largest increase in incidence (EAPC = 0.96; 95% CI: 0.74, 1.19), whereas Burkina Faso showed the largest decrease (EAPC = −1.99; 95% CI: −2.31, −1.67) (Table 1 and Figure 4C). The global incidence of PAH was 1.43 (95% UI: 0.97, 2.05) per 100,000 people in 2021, higher than the incidence reported in 75 of 204 countries and lower than in 129 countries.

Figure 4
Three world maps labeled A, B, and C, displaying data in varying color gradients. Each map has a corresponding legend indicating different ranges of values. Insets show detailed regions: Caribbean and Central America, Persian Gulf, Balkan Peninsula, Southeast Asia, West Africa, Eastern Mediterranean, and Northern Europe. Map A shows a broader range of darker colors, map B has lighter shades, and map C includes diverse color patterns. Each map provides a specific visual representation of the data for comparison across geographical areas.

Figure 4. Incidence of pulmonary hypertension in older adults in 204 countries and territories. (A) The number of incidence cases. (B) Incidence. (C) Estimates Annual percent change (EAPC) in incidence.

3.1.2 Mortality

Globally, mortality from PAH remained stable until 2006, then increased during 2006–2011 (APC 3.4%, p < 0.05; Figure 1B), before levelling off. Total deaths rose by 130% over the study period, with an EAPC of 0.03 (Table 2). The 95+ year age group accounted for the highest proportion of deaths in both 1990 and 2021, while the 60–64-year group contributed less than 2% (Figures 2B, 3B). Female mortality exceeded male mortality across all age strata, with an 87% excess in the 95+ year group (Figure 2B).

Table 2
www.frontiersin.org

Table 2. Global and regional deaths from PAH in older adults from 1990–2021.

In 2021, China had the highest number of PAH-related deaths among the regions considered (6223.37 cases; 95% UI: 4016.90, 7896.42), while the Democratic People’s Republic of Korea had the highest mortality rate (2.18 per 100,000 people; 95% UI: 1.19, 4.01) (Figures 5A,B). From 1990 to 2021, Latvia saw the largest increase in mortality (EAPC = 6.93; 95% CI: 4.63, 9.28), whereas Puerto Rico saw the largest decrease (EAPC = −6.45; 95% CI: −6.83, −6.06) (Figure 5C). The global mortality rate of PAH was 1.51 (95% UI: 1.15, 1.80) per 100,000 people in 2021, higher than the rate in 35 of 204 countries and lower than in 169 countries.

Figure 5
Map series showing global data categorized by regions: A, B, and C. Each map uses color gradients to depict different death rates, with insets highlighting areas like the Caribbean, Persian Gulf, Balkan Peninsula, Southeast Asia, West Africa, and Eastern Mediterranean. Color legends specify the data range for each map panel.

Figure 5. Mortality from pulmonary hypertension in older adults in 204 countries and territories. (A) Number of deaths. (B) Mortality. (C) Estimates annual percentage change (EAPC) in mortality.

3.1.3 DALYs

Globally, DALYs due to PAH remained stable until 2006, peaked in 2010, and rose most rapidly during 2006–2011 (APC 3.0%, p < 0.05; Figure 1C). DALYs increased by 100% over the study period, while the age-standardized rate showed an EAPC of −0.23 (Table 3). The 95+ year age group consistently had the highest DALY rates, and women experienced an 86% higher rate than men in the oldest stratum (Figure 2C).

Table 3
www.frontiersin.org

Table 3. Global and regional DALYs of PAH in older adults, 1990–2021.

In 2021, China had the highest number of DALYs for PAH globally (19,236; 95% UI: 12257.42, 24197.57), while Mongolia had the highest DALY rate (130.41 per 100,000 people; 95% UI: 70.47, 187.59) (Figures 6A,B). From 1990 to 2021, Georgia saw the greatest increase in DALYs (EAPC = 5.68; 95% CI: 4.81, 6.56), whereas Puerto Rico saw the greatest decrease (EAPC = −6.18; 95% CI: −6.57, −5.79) (Figure 6C). The global DALY rate of PAH was 23.54 (95% UI: 18.07, 27.89) per 100,000 people in 2021, higher than the rate in 40 of 204 countries and lower than in 166 countries.

Figure 6
Three world maps labeled A, B, and C show different data distributions. Map A displays red and blue shades indicating range values from 0 to over 44. Map B features color variations from dark blue to red, showing values from 1.17 to 131.72. Map C uses similar color ranges to represent values from -8.24 to 5.74. Insets focus on Caribbean and Central America, Persian Gulf, Balkan Peninsula, Southeast Asia, West Africa, Eastern Mediterranean, and Northern Europe in each map.

Figure 6. PAH DALYs in older adults in 204 countries and territories. (A) The number of DALYs. (B) DALYs rate. (C) Estimates annual percentage change (EAPC) in DALYs.

3.2 PAH in older people: regional trends by SDI

From 1990 to 2021, the incidence, mortality, and DALYs of PAH in individuals aged over 60 years across different SDI regions generally showed a declining trend, though with variations in the magnitude of change. In 2021, the middle-SDI region had the highest incidence rate (95% UI: 1.06, 2.26), while the high-SDI region had the lowest incidence rates in both 1990 (1.08, 95% UI: 0.72, 1.55) and 2021 (1.06, 95% UI: 0.71, 1.52).

For mortality, the middle-SDI region also had the highest death rate in 2021 (2.00; 95% UI: 1.25, 2.47), with the high-SDI region having the lowest death rates in both 1990 (1.24, 95% UI: 1.07–1.39) and 2021 (1.22, 95% UI: 1.02, 1.36).

Regarding DALYs, the middle-SDI region had the highest DALY rate in 2021 (30.13; 95% UI: 19.21, 37.14), whereas the high-SDI region had the lowest DALY rates in both 1990 (20.71; 95% UI: 18.45, 22.90) and 2021 (18.96; 95% UI: 16.45, 20.82).

However, the low-SDI region experienced the most significant decrease in incidence (EAPC = −0.31; 95% CI: −0.36, −0.27), while the high-SDI region showed the most substantial decline in the DALY rate (EAPC = −0.23; 95% CI: −0.42, −0.03) (Table 1 and Figures 7, 8).

Figure 7
Six line graphs illustrate trends from 1990 to 2021 by socioeconomic development index (SDI) categories: high, high-middle, middle, low, and low-middle. Top left shows increasing incidence numbers across categories. Top right depicts stable to slightly decreasing incidence rates. Middle left displays rising death numbers, particularly in higher SDI areas. Middle right shows varying but generally declining death rates. Bottom left shows increasing DALYs (Disability-Adjusted Life Years) numbers, especially in higher SDIs. Bottom right shows fluctuating DALY rates, with an overall decreasing trend in high SDI areas. Each line is color-coded by SDI category.

Figure 7. Epidemiological trends in the incidence, mortality, and DALYs rates of PAH in five older adults Sociodemographic Index (SDI) region from 1990 to 2021.

Figure 8
Three scatter plots (A, B, C) display data for various geographic regions overlaid with a fitted line and shaded confidence interval. Each region is represented by distinct markers and colors. Plot A shows incidence rate per 100,000 population versus SDI (Socio-Demographic Index), indicating a negative trend. Plot B depicts death rate per 100,000 population, showing a smaller variance. Plot C presents DALYs (Disability-Adjusted Life Years) rate per 100,000 population, also indicating variance. The legend identifies regions and marker types.

Figure 8. Association between the incidence, mortality, and DALYs rates of PAH in older adults and the regional incidence of PAH, mortality, and DALYs. Sociodemographic Index (SDI), 1990–2021. (A) Incidence rate. (B) Mortality rate. (C) DALYs rates.

3.3 PAH in older people: projections for 2050

3.3.1 Incidence

From 1990 to 2050, the global incidence of PAH in individuals aged 60 years and older is projected to increase significantly. By 2050, the global number of PAH cases in this age group is expected to reach 31,383 (95% CI: 17604.40, 45162.56) (Figure 9A), with an incidence rate of 1.46 (95% CI: 0.82, 2.10) per 100,000 people (Figure 9B). The highest number of new cases is projected to be in the 85–89-year age group, with 7,105 cases (95% CI: 1888.57, 12320.77) (Figure 9A). The highest incidence rate is expected to be in the 75–79-year age group, at 1.69 (95% CI: 1.21, 2.17) per 100,000 people (Figure 9B).

Figure 9
Graph A shows the projected number of incidences from 1990 to 2050, categorized by age groups starting from 60-64 to 95+ years. All groups show an upward trend over time with future projections shaded in purple. Graph B illustrates the incidence rate trends over the same period, with each age group’s rate showing fluctuations but a general increase, with future projections similarly shaded. Each graph includes a dashed line dividing past data and future projections. The legend identifies age groups and marker types.

Figure 9. Predict the total number of elderly PAH cases and the incidence rates for different age groups in 2050. (A) Number of incidence. (B) Incidence rate.

3.3.2 Mortality

The global number of PAH-related deaths in individuals aged 60 years and older is projected to reach 20,687 (95% CI: 13016.47, 28358.44) by 2050 (Figure 10A), with a death rate of 0.96 (95% CI: 0.60, 1.32) per 100,000 people (Figure 10B). The highest number of deaths is predicted to be in the 85–89-year age group, with 5,214 deaths (95% CI: 3738.05, 6689.92) (Figure 10A). The highest death rate is expected to be in the 95+ age group, at 14.50 (95% CI: 13.95, 15.05) per 100,000 people (Figure 10B).

Figure 10
Graphical data displays projected mortality figures and rates across various age groups from 1990 to 2050. Section A shows the number of deaths increasing for ages 60 years and older, with confidence intervals. Section B depicts death rates declining over time for the same age groups, showing a change in trends post-2020. Each age category, from 60–64 to 95+ years, is separately charted, emphasizing both historical and projected data with a dotted line marking the year 2020.

Figure 10. Predict the total number of elderly PAH death cases and the death rates for different age groups in 2050. (A) Number of death. (B) Death rate.

3.3.3 DALYs

The global number of PAH-related DALYs in individuals aged 60 years and older is projected to reach 302,760 (95% CI: 186486.36, 419033.63) by 2050 (Figure 11A), with a DALY rate of 14.08 (95% CI: 8.67, 19.48) per 100,000 people (Figure 11B). The highest number of DALYs is predicted to be in the 75–79-year age group, with 61,411 DALYs (95% CI: 46693.37, 76128.41) (Figure 11A). The highest DALY rate is expected to be in the 95+ age group, at 115.38 (95% CI: 112.83, 117.93) per 100,000 people (Figure 11B).

Figure 11
Graph A displays the projected number of Disability-Adjusted Life Years (DALYs) for various age groups from 1990 to 2050, showing an upward trend in most age ranges. Graph B presents the DALYs rate over the same period, illustrating a declining trend overall. Both graphs include dashed lines marking the year 2021 for reference. The projections extend beyond 2021, depicted with red points and shaded confidence intervals.

Figure 11. Predicting the total number of DALYs in older PAHs and the rate of DALYs in different age groups in 2050. (A) Number of DALYs. (B) Rate of DALYs.

4 Discussion

This study provides a comprehensive analysis of the global burden of PAH among individuals aged 60 and older from 1990 to 2021 and projects trends through 2050. Key findings indicate that during this period, global PAH incidence, mortality, and DALYs increased by 130, 130, and 100%, respectively. By 2021, there were 15,622 new cases (incidence rate: 1.43 per 100,000 people; 95% UI: 0.97, 2.05), 15,443 deaths (mortality rate: 1.51 per 100,000 people; 95% UI: 1.15, 1.80), and 248,064 DALYs (DALY rate: 23.54 per 100,000 people; 95% UI: 18.07, 27.89) globally. The age-standardized incidence rate rose from 1.447 to 1.66 per 100,000 population. The disease burden is unevenly distributed globally, with regions of medium SDI bearing the heaviest burden. China reported the highest number of cases and deaths, while Zambia had the highest incidence rate. Projections using the BAPC model indicate that the burden of PAH in the elderly population will continue to rise through 2050: the number of new cases is expected to reach 31,383 (95% CI: 17604.40, 45162.56) with an incidence rate of 1.46 per 100,000, approximately 20,687 deaths, and 302,760 DALYs. These findings underscore PAH as a significant and growing public health challenge within an increasingly aging population.

PAH is a serious disease that profoundly impacts the quality of life in the elderly and imposes a heavy burden on healthcare systems (16). The stable or slightly declining age-standardized rates of incidence and DALYs (EAPC = −0.01 for incidence, −0.23 for DALYs) indicate that the increase in absolute burden is primarily driven by population aging, while per capita risk is modulated by other factors. Lower-than-expected mortality can be attributed to significant advances in therapeutic strategies over the past two decades, including the development of targeted therapies, effective risk management, combination therapies, and improved diagnostic techniques, which collectively have enhanced survival rates among PAH patients (17). The transient decline in incidence observed between 2015 and 2018 may reflect temporary shifts in diagnostic or coding practices, warranting further investigation.

The burden of PAH varies significantly across socio-demographic regions, with the highest burden observed in areas with moderate SDI in 2021. This aligns with the complex interplay between an aging population and potentially lagging healthcare infrastructure. Despite population aging, the overall incidence trend shows a slight decline, which may be attributable to significant advances in early detection, improved screening programs, and heightened clinical awareness. The adoption of new risk assessment tools has facilitated earlier diagnosis, enabling more effective therapeutic interventions (18). Furthermore, the use of multimodal therapies has contributed to reducing mortality associated with PAH (19, 20). In contrast, high SDI regions consistently exhibit the lowest incidence rates, likely due to better integrated care and access to advanced treatments. The declining trend in low SDI regions may reflect improved public health interventions, although the possibility of undiagnosed cases and data limitations cannot be ruled out in these areas. This is evidenced by the substantial diagnostic gap between HICs and LICs within the GBD database.

Variations in the disease burden of PAH across different SDI regions may be influenced by specific national health policies, healthcare accessibility, and the pace of population aging (21). Medium-SDI regions, experiencing rapid population aging, may have healthcare systems that are not yet fully equipped to manage complex chronic diseases like PAH (22). This can lead to high diagnosis rates but limited treatment capacity, thereby increasing the overall burden. In contrast, high SDI regions typically have stronger primary care systems and specialist referral networks, which facilitate early detection and management of PAH, thus controlling its progression (8). The declining trend in low SDI regions may reflect inadequate diagnostic capabilities. A PAH diagnosis requires meeting the “hemodynamic definition of pulmonary hypertension (PH),” excluding other causes of precapillary pulmonary hypertension, and satisfying clinical/classification criteria (23). Future research should integrate specific national health policies and healthcare resource allocation to better understand the structural drivers behind these SDI disparities.

At the national level, China reported the highest number of pulmonary arterial hypertension (PAH) cases and deaths, consistent with its large and aging population. Zambia had the highest incidence rate, potentially linked to specific environmental or genetic risk factors. The significant increase in incidence in Slovakia and the marked rise in mortality in Latvia highlight the need for further investigation into local risk factors and healthcare system performance.

Projections using the BAPC model indicate that the burden of PAH in the elderly population will continue to rise through 2050. The highest incidence is projected for the 75–79 age group, while the highest mortality is anticipated in the 95+ age cohort. Increased stiffness in the cardiac and pulmonary vascular systems among the elderly elevates the risk of developing PAH (24). This underscores the need for age-specific prevention and care strategies in the context of accelerating global population aging (25).

From a gender perspective, women exhibit higher incidence, mortality, and DALYs rates than men across most age groups, particularly among those aged 60 and older. Previous studies have shown that the Y chromosome exerts a protective effect in hypoxia-induced PAH, reducing right ventricular systolic pressure and pulmonary vascular remodelling (26). It has been hypothesized that genes such as SRY and UTY may confer protection against PAH by enhancing BMP signalling and reducing proinflammatory cytokines (27, 28). However, with advancing age, the gradual loss of Y chromosome fragments in male peripheral cells or reduced expression of Y chromosome protective genes may diminish this protective effect, contributing to increased disease incidence in older males (29, 30). Conversely, estradiol has demonstrated bidirectional effects in PAH (the estrogen paradox), which may also contribute to the observed gender differences (31). Additionally, women tend to be more sensitive to early symptoms, such as shortness of breath, and are more likely to seek medical care promptly, which facilitates earlier diagnosis (32). In contrast, elderly men often attribute such symptoms to aging or comorbidities, resulting in delayed medical consultations and underdiagnosis. This disparity is further amplified by unequal access to healthcare resources. In regions with a high to medium-SDI, women achieve higher diagnosis rates due to easier access to regular check-ups. In regions with a low-SDI, some women still receive diagnoses despite widespread diagnostic limitations, while male patients remain entirely undiagnosed due to their near-total avoidance of medical care. Therefore, addressing this issue requires biomedical interventions and the implementation of gender-sensitive strategies, such as proactive screening of high-risk males, to address all contributing factors comprehensively.

Using GBD 2021, we provide a systematic, global snapshot of PAH in adults aged greater than 60 years. Our findings show that the burden is highest in middle-SDI countries; China contributes the largest absolute number of cases, while Zambia records the highest age-standardized incidence; older women consistently face greater risk than men. These epidemiological insights offer immediate, location-specific targets, such as intensified screening in middle-SDI settings and sex-tailored management for elderly women. Additionally, our BAPC projections provide actionable foresight for health-system planning toward 2050, when one in six people worldwide will be over 65.

However, this study has several limitations. The GBD estimates we used can under- or overstate true rates due to weak death registration and patchy diagnostic capacity in many low- and middle-income countries. The GBD also lacks data on air pollution, smoking, drug use, or local access to care, limiting our ability to explain why rates rise or fall in specific places. The absence of individual-level information means we cannot adjust for genetic background, comorbidities, or treatment adherence, and the clinical meaning of the estimates is limited. These data issues directly affect our trend tests. The UI provided by GBD is designed for single-year comparisons, not for tracking changes over time. We used non-overlapping UI to judge differences, but this approach ignores the serial correlation in time series and may inflate false positives. Joinpoint results depend on user choices, such as minimum observations per segment and maximum number of joinpoints, which can alter conclusions about recent trends. The EAPC assumes a constant log-linear slope from 1990 to 2021, averaging out any plateaus, rebounds, or declines, which may misrepresent trends as “stable” when they are not. For the 2050 projections, the BAPC model assumes that age, period, and cohort effects observed in only six five-year periods will remain unchanged for the next 29 years. The coarse age groups (eight five-year bands above 60) and thirteen ten-year birth cohorts smooth out shocks such as war or drug-era fluctuations, likely overstating forecast precision. Finally, our curve fitting between SDI and PAH burden uses an ecological composite index tied to the same social variables that shape healthcare access; the association is descriptive and cannot be taken as causal.

5 Conclusion

This study highlights the substantial and growing burden of PAH among the global elderly population, with a disproportionate impact on female and middle-SDI countries. Projections indicate a marked escalation by 2050, although these estimates assume stable trends and should be viewed with caution. The findings underscore the urgent need for targeted public health strategies, including enhanced early detection, sex-specific management, and stronger data systems, to mitigate PAH’s impact in an aging world.

Data availability statement

Publicly available datasets were analyzed in this study. This data can be found here: https://vizhub.healthdata.org/gbd-results/.

Author contributions

GX: Visualization, Writing – original draft. XF: Data curation, Writing – original draft. NQ: Writing – review & editing.

Funding

The author(s) declare that no financial support was received for the research and/or publication of this article.

Acknowledgments

The authors acknowledge the use of data and resources from the Global Burden of Disease (GBD) 2021 study provided by the Institute for Health Metrics and Evaluation (IHME). The authors are grateful to the GBD Collaborators for their contributions to data collection, methods development, and quality assurance.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Generative AI statement

The authors declare that no Gen AI was used in the creation of this manuscript.

Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmed.2025.1595504/full#supplementary-material

References

1. Badagliacca, R, Papa, S, Matsubara, H, Lang, IM, Poscia, R, Manzi, G, et al. The importance of right ventricular evaluation in risk assessment and therapeutic strategies: raising the bar in pulmonary arterial hypertension. Int J Cardiol. (2020) 301:183–9. doi: 10.1016/j.ijcard.2019.10.043

PubMed Abstract | Crossref Full Text | Google Scholar

2. Hassoun, P. Pulmonary arterial hypertension. N Engl J Med. (2021) 385:2361–76. doi: 10.1056/NEJMra2000348

Crossref Full Text | Google Scholar

3. Chen, Y. Etiology, diagnosis and treatments of pulmonary hypertension. Proc SPIE. (2024) 12924:1292436. doi: 10.1117/12.3013013

Crossref Full Text | Google Scholar

4. DuBrock, H, Nathan, S, Reeve, B, Kolaitis, N, Mathai, S, Classi, P, et al. Pulmonary hypertension due to interstitial lung disease or chronic obstructive pulmonary disease: a patient experience study of symptoms and their impact on quality of life. Pulm Circ. (2021) 11:20458940211005641. doi: 10.1177/20458940211005641

PubMed Abstract | Crossref Full Text | Google Scholar

5. Lau, EMT, Giannoulatou, E, Celermajer, DS, and Humbert, M. Epidemiology and treatment of pulmonary arterial hypertension. Nat Rev Cardiol. (2017) 14:603–14. doi: 10.1038/nrcardio.2017.84

PubMed Abstract | Crossref Full Text | Google Scholar

6. Yang, P, Bocobo, G, and Yu, P. Sotatercept for pulmonary arterial hypertension. N Engl J Med. (2021) 385:92–3. doi: 10.1056/NEJMc2107209

PubMed Abstract | Crossref Full Text | Google Scholar

7. Hoeper, M, Humbert, M, Souza, R, Idrees, M, Kawut, S, Sliwa-Hahnle, K, et al. A global view of pulmonary hypertension. Lancet Respir Med. (2016) 4:306–22. doi: 10.1016/S2213-2600(15)00543-3

PubMed Abstract | Crossref Full Text | Google Scholar

8. Liu, L, Li, C, Cai, J, Kong, R, Wang, Y, Wang, Y, et al. 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. Front Med. (2024) 11:1515961. doi: 10.3389/fmed.2024.1515961

PubMed Abstract | Crossref Full Text | Google Scholar

9. Moreira, E, Gall, H, Leening, M, Lahousse, L, Loth, D, Krijthe, B, et al. Prevalence of pulmonary hypertension in the general population: the Rotterdam study. PLoS One. (2015) 10:e0130072. doi: 10.1371/journal.pone.0130072

PubMed Abstract | Crossref Full Text | Google Scholar

10. GBD 2021 Pulmonary Arterial Hypertension Collaborators. Global, regional, and national burden of pulmonary arterial hypertension, 1990–2021: a systematic analysis for the Global Burden of Disease Study 2021. Lancet Respir Med. (2025) 13:69–79. doi: 10.1016/s2213-2600(24)00295-9

Crossref Full Text | Google Scholar

11. GBD 2021 Diseases and Injuries Collaborators. Global incidence, prevalence, years lived with disability (YLDs), disability-adjusted life-years (DALYs), and healthy life expectancy (HALE) for 371 diseases and injuries in 204 countries and territories and 811 subnational locations, 1990–2021: a systematic analysis for the Global Burden of Disease Study 2021. Lancet. (2024) 403:2133–61. doi: 10.1016/s0140-6736(24)00757-8

PubMed Abstract | Crossref Full Text | Google Scholar

12. GBD 2016 Healthcare Access and Quality Collaborators. Measuring performance on the healthcare access and quality index for 195 countries and territories and selected subnational locations: a systematic analysis from the Global Burden of Disease Study 2016. Lancet. (2018) 391:2236–71. doi: 10.1016/s0140-6736(18)30994-2

PubMed Abstract | Crossref Full Text | Google Scholar

13. Kim, HJ, Fay, MP, Feuer, EJ, and Midthune, DN. Permutation tests for joinpoint regression with applications to cancer rates. Stat Med. (2000) 19:335–51. doi: 10.1002/(sici)1097-0258(20000215)19:3<335::aid-sim336>3.0.co;2-z

PubMed Abstract | Crossref Full Text | Google Scholar

14. Knoll, M, Furkel, J, Debus, J, Abdollahi, A, Karch, A, and Stock, C. An R package for an integrated evaluation of statistical approaches to cancer incidence projection. BMC Med Res Methodol. (2020) 20:257. doi: 10.1186/s12874-020-01133-5

PubMed Abstract | Crossref Full Text | Google Scholar

15. Riebler, A, and Held, L. Projecting the future burden of cancer: Bayesian age-period-cohort analysis with integrated nested Laplace approximations. Biom J. (2017) 59:531–49. doi: 10.1002/bimj.201500263

PubMed Abstract | Crossref Full Text | Google Scholar

16. Chen, C-Y, Hung, C, Chiang, C, Tsa, Y-C, Fu, Y-J, Wang, C-L, et al. Pulmonary arterial hypertension in the elderly population. J Chin Med Assoc. (2021) 85:18–23. doi: 10.1097/JCMA.0000000000000658

Crossref Full Text | Google Scholar

17. Swisher, J, and Weaver, E. The evolving management and treatment options for patients with pulmonary hypertension: current evidence and challenges. Vasc Health Risk Manag. (2023) 19:103–26. doi: 10.2147/VHRM.S321025

PubMed Abstract | Crossref Full Text | Google Scholar

18. Sitbon, O, Chin, K, Channick, R, Benza, R, Di Scala, L, Gaine, S, et al. Risk assessment in pulmonary arterial hypertension: insights from the GRIPHON study. J Heart Lung Transplant. (2020) 39:300–9. doi: 10.1016/j.healun.2019.12.013

PubMed Abstract | Crossref Full Text | Google Scholar

19. Bruni, C, Tofani, L, Fretheim, H, Weber, Y, Hachulla, E, Carreira, P, et al. OP0238 immunosuppression with targeted DMARDs reduces morbidity and mortality in pre-capillary pulmonary hypertension associated with systemic sclerosis: a EUSTAR analysis. Ann Rheum Dis. (2023) 82:157–9. doi: 10.1136/ANNRHEUMDIS-2023-EULAR.3215

Crossref Full Text | Google Scholar

20. Davies, M, Miserlis, D, and Hart, J. Current status of pulmonary artery denervation. Front Cardiovasc Med. (2022) 9:972256. doi: 10.3389/fcvm.2022.972256

PubMed Abstract | Crossref Full Text | Google Scholar

21. Yang, L, Li, Y, Zeng, TT, Li, Y, Ding, L, Yue, H, et al. Global, regional, and national burden of hypertension-induced cardiorenal disease, 1990–2021 and projections to 2050: a systematic analysis for the Global Burden of Disease Study 2021. BMC Public Health. (2025) 25:2596. doi: 10.1186/s12889-025-23742-9

PubMed Abstract | Crossref Full Text | Google Scholar

22. Yang, Y, Zeng, Z, Yang, Q, Wang, H, Zhang, H, Yan, W, et al. The challenge in burden of pulmonary arterial hypertension: a perspective from the Global Burden of Disease Study. MedComm. (2025) 6:e70175. doi: 10.1002/mco2.70175

PubMed Abstract | Crossref Full Text | Google Scholar

23. Humbert, M, Kovacs, G, Hoeper, MM, Badagliacca, R, Berger, RMF, Brida, M, et al. 2022 ESC/ERS guidelines for the diagnosis and treatment of pulmonary hypertension. Eur Heart J. (2022) 43:3618–731. doi: 10.1093/eurheartj/ehac237

PubMed Abstract | Crossref Full Text | Google Scholar

24. Poor, H. Pulmonary vascular diseases in the elderly. Clin Geriatr Med. (2017) 33:553–62. doi: 10.1016/j.cger.2017.06.007

PubMed Abstract | Crossref Full Text | Google Scholar

25. Li, J, Han, X, Zhang, X, and Wang, S. Spatiotemporal evolution of global population ageing from 1960 to 2017. BMC Public Health. (2019) 19:127. doi: 10.1186/s12889-019-6465-2

PubMed Abstract | Crossref Full Text | Google Scholar

26. Umar, S, Cunningham, CM, Itoh, Y, Moazeni, S, Vaillancourt, M, Sarji, S, et al. The Y chromosome plays a protective role in experimental hypoxic pulmonary hypertension. Am J Respir Crit Care Med. (2018) 197:952–5. doi: 10.1164/rccm.201707-1345LE

PubMed Abstract | Crossref Full Text | Google Scholar

27. Cunningham, CM, Li, M, Ruffenach, G, Doshi, M, Aryan, L, Hong, J, et al. Y-chromosome gene, Uty, protects against pulmonary hypertension by reducing proinflammatory chemokines. Am J Respir Crit Care Med. (2022) 206:186–96. doi: 10.1164/rccm.202110-2309OC

PubMed Abstract | Crossref Full Text | Google Scholar

28. Wits, M, Becher, C, de Man, F, Sanchez-Duffhues, G, and Goumans, MJ. Sex-biased TGFβ signalling in pulmonary arterial hypertension. Cardiovasc Res. (2023) 119:2262–77. doi: 10.1093/cvr/cvad129

PubMed Abstract | Crossref Full Text | Google Scholar

29. Krzyżewska, A, and Kurakula, K. Sex dimorphism in pulmonary arterial hypertension associated with autoimmune diseases. Arterioscler Thromb Vasc Biol. (2024) 44:2169–90. doi: 10.1161/atvbaha.124.320886

PubMed Abstract | Crossref Full Text | Google Scholar

30. Maan, AA, Eales, J, Akbarov, A, Rowland, J, Xu, X, Jobling, MA, et al. The Y chromosome: a blueprint for men's health? Eur J Hum Genet. (2017) 25:1181–8. doi: 10.1038/ejhg.2017.128

PubMed Abstract | Crossref Full Text | Google Scholar

31. Tofovic, S, and Jackson, E. Estradiol metabolism: crossroads in pulmonary arterial hypertension. Int J Mol Sci. (2019) 21:116. doi: 10.3390/ijms21010116

PubMed Abstract | Crossref Full Text | Google Scholar

32. Mauvais-Jarvis, F, Bairey Merz, N, Barnes, PJ, Brinton, RD, Carrero, JJ, DeMeo, DL, et al. Sex and gender: modifiers of health, disease, and medicine. Lancet. (2020) 396:565–82. doi: 10.1016/s0140-6736(20)31561-0

PubMed Abstract | Crossref Full Text | Google Scholar

Abbreviations

GBD, Global Burden of Disease; PAH, Pulmonary arterial hypertension; DALYs, Disability-adjusted life years; BAPC, Bayesian age-period-cohort; EAPC, Estimated average annual percentage changes; APC, Annual percentage change; UI, Uncertainty interval; CI, Confidence interval; SDI, Sociodemographic Index.

Keywords: pulmonary arterial hypertension, Global Burden of Disease study, incidence, mortality, Sociodemographic Index

Citation: Xu G, Feng X and Qu N (2025) Global, regional, and national burden of pulmonary arterial hypertension in adults aged ≥60 years from 1990–2021: SDI-stratified trend analysis and projections to 2050. Front. Med. 12:1595504. doi: 10.3389/fmed.2025.1595504

Received: 02 May 2025; Revised: 17 October 2025; Accepted: 07 November 2025;
Published: 25 November 2025.

Edited by:

Marios Kyriazis, National Gerontology Centre, Cyprus

Reviewed by:

Sergio Cinza-Sanjurjo, University of Santiago de Compostela, Spain
Qian Guo, First Affiliated Hospital of Zhengzhou University, China
Xie Zhanpeng, Huazhong University of Science and Technology, China
Menglan Zhu, 32265 Army of Chinese People’s Liberation Army, China
Lun Liang, Guangxi Medical University, China

Copyright © 2025 Xu, Feng and Qu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Nini Qu, cXZuaWlpQDE2My5jb20=

These authors have contributed equally to this work

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.