PUBLISHER: GlobalData | PRODUCT CODE: 1761643
PUBLISHER: GlobalData | PRODUCT CODE: 1761643
Pulmonary arterial hypertension (PAH) is a rare, progressive disorder of unknown cause, characterized by vascular proliferation and remodelling of the small pulmonary arteries. A significant number of risk factors and pathophysiological conditions are suspected to play roles in disease progression (Humbert et al., 2004, 2010; Simonneau et al., 2004; Bonnet et al., 2017). In PAH, blood vessels in the lungs are narrowed, blocked, or destroyed. The damage slows blood flow through the lungs and can lead to right ventricular overload and intense right heart failure. This results in progressively increasing pulmonary vascular resistance, leading to an increase in pulmonary arterial pressure (Pugh and Hemnes, 2010; Omura et al., 2023; Mayo Clinic, 2025). The heart muscles work harder to pump blood through the lungs, eventually causing the heart muscles to become weak and fail (Mayo Clinic, 2025). PAH represents Group 1 within the World Health Organization (WHO) clinical classification for pulmonary hypertension. PAH can be idiopathic, heritable, or associated with different conditions such as connective tissue disease (CTD), congenital heart disease (CHD), human immunodeficiency virus (HIV) infection, and exposure to toxins or drugs (Simonneau et al., 2009). PAH occurs twice as frequently in women as in men (Humbert et al., 2006; Frost et al., 2011; Escribano-Subias et al., 2012; Ling et al., 2012; Farber et al., 2015; Kasahara et al., 2015; Hoeper, Huscher and Pittrow, 2016; Leber, Beaudet and Muller, 2021). Due to its unclear multifactorial mechanisms, and despite many treatment advancements over the past few decades, the long-term prognosis of patients with PAH remains poor (Galie et al., 2015; Bonnet et al., 2017; Omura et al., 2023).
In the 7MM, diagnosed incident cases of PAH are expected to decrease from 14,189 cases in 2024 to 14,154 cases in 2034, at a negative annual growth rate (AGR) of 0.02%. In 2034, the US will have the highest number of diagnosed incident cases of PAH in the 7MM, with 5,484 cases, whereas the UK will have the fewest diagnosed incident cases of PAH with 661 cases. GlobalData epidemiologists attribute the decline in the diagnosed incident cases of PAH to changes in the population dynamics, as well as the incidence rates in each market over the forecast period.
In the 7MM, diagnosed prevalent cases of PAH are expected to decrease from 76,645 cases in 2024 to 76,035 cases in 2034, at a negative AGR of 0.08%. In 2034, the US will have the highest number of diagnosed prevalent cases of PAH in the 7MM, with 29,591 cases, whereas the UK will have the fewest diagnosed prevalent cases of PAH with 3,773 cases. GlobalData epidemiologists attribute the change in the diagnosed prevalent cases of PAH to changes in population dynamics in each market over the forecast period.
The Pulmonary arterial hypertension (PAH) epidemiology series will allow you to -