Among the factors contributing to pulmonary hypertension, chronic obstructive pulmonary disease (COPD), particularly chronic bronchitis, is significant, occurring in 90% of smokers.
Repeated pulmonary embolisms are another common cause of pulmonary hypertension in addition to lung pathology.
Pulmonary hypertension is frequently a complication in patients with heart muscle damage due to conditions such as coronary heart disease, inflammatory myocardial diseases, and heart defects.
In individuals with congenital heart defects who are not eligible for surgical treatment, increased pressure in the pulmonary artery is the primary complication and cause of death. However, postoperative patients with congenital heart defects may also develop pulmonary hypertension.
Autoimmune pathologies, such as systemic lupus erythematosus, systemic scleroderma, and rheumatoid arthritis, are often associated with pulmonary hypertension.
Severe liver diseases leading to cirrhosis can also complicate with pulmonary hypertension. Additionally, individuals with HIV infection and hematological diseases may experience increased pressure in lung vessels.
If an examination fails to identify the cause of pulmonary hypertension, idiopathic pulmonary hypertension is diagnosed, characterized as an independent disease distinct from secondary pulmonary hypertension, which arises as a complication of various circulatory and respiratory organ diseases.
The exact causes of idiopathic pulmonary hypertension remain unknown, with genetics suspected as a contributing factor. Risk factors include the use of obesity treatment drugs, amphetamines, cocaine, tryptophan, hormonal contraceptives, smoking, and even pregnancy. Genetic factors may also play a role in the development of the disease.
Experts have identified numerous risk factors for pulmonary hypertension, including: