The pulmonary arterial hypertension treatment market offers a ray of hope for those suffering from this uncommon but dangerous illness that affects the heart and lungs. Reduced blood flow and cardiac strain are caused by excessively high blood pressure in the arteries that connect the heart and lungs in PAH. With the development of novel medicines that focus on the disease’s fundamental causes, the landscape of PAH treatment has undergone tremendous change. Thanks to developments in personalised medicine, drug research, and our increasing knowledge of the complexity of PAH, the market is a major factor in prolonging patient life and enhancing their quality of life.
One of the hallmarks of the PAH treatment market is its focus on precision therapies that target specific pathways involved in the disease’s progression. These therapies work by dilating the blood vessels, reducing strain on the heart, and improving blood flow. By addressing the root causes of PAH, these treatments offer patients more than just symptom relief – they provide an opportunity for improved functional capacity and prolonged survival.
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Owing to non-responsive nature of several advance pharmacotherapies and high diagnosis and treatment costs, researchers and medical practitioners in the global pulmonary arterial hypertension treatment market are continually working on favorable and effective alternative treatment models and increase survival rate among the patients with pulmonary arterial hypertension.
The global pulmonary arterial hypertension treatment market is expected to reach US$ 5.7 billion by 2022. The market is expected to reach US$ 6.6 billion by 2028, growing at a healthy 2.5% CAGR.
Cancer Protein Molecules Tested for Potential Therapeutic Use- to Prevent Pulmonary Arteries ‘Scarring’
Scarring or Fibrosis, in pulmonary arterial hypertension, is an important cause of damage to pulmonary arteries, which in turn, strains the heart functions- eventually leading to breathlessness. Recently, researchers from Brigham and Women’s Hospital conducted a study using network medicine- a method of establishing correlation between proteins, pathways and more- and identified the cancer protein NEDD9 and its molecular mechanisms as a potential treatment for PAH patients. The study has identified that a specific amino acid residue in the cancer protein is expected to play a crucial role in controlling and regulating the severe consequences of scarring.
BH4- Factor Controlling Production of Nitric Oxide- Shows Promising Result on Rat Model; Results Show Lower Lung Hypertension
Researchers at Imperial College London and Bar-Ilan University, Israel explored the properties of naturally occurring tetrahydrobiopterin (BH4) and its subsequent role in effective treatment for lung hypertension and right heart failure. BH4 controls the production of endothelial nitric oxide synthase (eNOS) in the human body. eNOS produces nitric oxide which is important for healthy endothelial cells- forming the inside lining of blood vessels. Nitric oxide is responsible for dilating blood vessels, working to lower lung blood pressure.
The study- conducted on a rats first in injected with chemical triggering pulmonary hypertension and then an injection of BH4, showed signs of decreased lung pressure, stronger heart contractions and, enlarged heart. The rats were then given BH4 in food before the chemical that previously induced pulmonary hypertension. As a result of which, no thick layers of smooth muscles were developed- often leading to lung hypertension.
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After the phase 1 of clinical trials, the patients- administered BH4 orally, showed improved exercise capacity- an indicator of low pressure in lungs. It is anticipated that BH4, when given controlled measure could prove to a valuable treatment for pulmonary arterial hypertension patients who otherwise are not responsive to regular medication.
With Treatment Options, ‘Accurate Risk Measuring’ Tools is the Need of the Hour
Although measurable efforts are being made in the global pulmonary arterial hypertension treatment market, the survival rate among PAH patients continues to remain low. According to studies, the average life expectancy of PAH patient is approximately 3 years from symptom onset- being at a risk of disease progression and frequent hospitalizations. Several studies indicate that early diagnosed and ‘low-risk’ patients stand a chance of improved survival if the risk is calculated accurately. Experts have expressed the need to develop appropriate and accurate risk prediction tools improve treatment outcomes in PAH patients.
Pulmonary Arterial Hypertension Treatment Market by Category
Drug Type :
- Vasodilators
- Phosphodiesterase 5 (PDE 5) Inhibitors
- Endothelin Receptor Antagonists (ERA)
- Soluble Guanylate Cyclase (SGC) Stimulator
Distribution Channel :
- Hospital Pharmacies
- Retail Pharmacies
- Online Pharmacies
Region :
- North America
- Latin America
- Western Europe
- Eastern Europe
- Asia Pacific
- China
- Japan
- Middle East & Africa
Author By:
Sabyasachi Ghosh (Associate Vice President at Future Market Insights, Inc.) holds over 12 years of experience in the Healthcare, Medical Devices, and Pharmaceutical industries. His curious and analytical nature helped him shape his career as a researcher.
Identifying key challenges faced by clients and devising robust, hypothesis-based solutions to empower them with strategic decision-making capabilities come naturally to him. His primary expertise lies in areas such as Market Entry and Expansion Strategy, Feasibility Studies, Competitive Intelligence, and Strategic Transformation.
Holding a degree in Microbiology, Sabyasachi has authored numerous publications and has been cited in journals, including The Journal of mHealth, ITN Online, and Spinal Surgery News.
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