Pulmonary Arterial Hypertension (PAH): Causes and Types
1. Idiopathic PAH
About half of PAH cases have no known cause. When a condition’s cause is unknown, it’s called idiopathic. Idiopathic PAH is the most common type of PAH. While the exact cause of idiopathic PAH is not known, experts believe environmental triggers and genetics may play a role.
2. Connective Tissue Disease
The second most common type of PAH is caused by connective tissue disease. These conditions are autoimmune, meaning the body’s immune system attacks itself. Researchers believe that the inflammatory response of these autoimmune conditions affects the arteries in the lungs.
3. Congenital Heart Disease
Congenital heart disease is an abnormality of the heart that is present from birth. When the heart does not form properly, it can lead to abnormal blood flow in the heart and lungs.
4. Inherited PAH
Up to 20% of people with PAH have an inherited form of the disease. For example, changes in the BMPR2 gene can be passed down in families. When one parent has the mutation, the child has a 50% chance of inheriting it.
Conclusion
Pulmonary arterial hypertension (PAH) is a serious condition that can impair blood flow, causing symptoms like shortness of breath, chest pain, and light-headedness. Understanding the causes and types of PAH is essential for effective treatment and management.
FAQs
Author Bio
Dr. Angela Ryan Lee is an Ohio-based board-certified physician specializing in cardiovascular diseases and internal medicine.
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