Pulmonary Hypertension Clinical Trial
Official title:
Evaluation of Echocardiographic Indices and Blood Biomarkers in Group 1 Pulmonary Hypertension
- To evaluate different echocardiographic indices in diagnosis and follow up of group 1
pulmonary hypertension.
- To evaluate blood biomarkers (troponin, uric acid and micro RNA) in naïve group 1
pulmonary hypertension.
Introduction:
Pulmonary hypertension is pathophysiological condition defined as increases of mean pulmonary
artery pressure above 20 mmHg as assessed by right heart catheterization (RHC) (1).
As pulmonary hypertension has a variety of causes with different clinical presentations and
characteristics; it is classified into five clinical groups (2):
- Group 1 and also called pulmonary arterial hypertension group.
- Group 2 due to left sided heart diseases.
- Group 3 caused by chronic lung diseases and hypoxemia.
- Group 4 caused by chronic pulmonary artery occlusions.
- Group 5 that has unclear and multifactorial causes. Although group 1 less common; it is
carrying significant clinical importance as early detection can improve the patient's
outcome through providing them the available vasodilator medications.
To diagnose patient in group 1 PH, the patient should have RHC (3) to obtain the definite
hemodynamic before starting treatment as advised by PH guidelines, however RHC is invasive
and expensive procedure and carrying some bad drawback (4).
Transthoracic echocardiography is less expensive, non-invasive and nonhazardous procedure and
commonly provide significant parameters before RHC (5).
several echocardiographic indices correlate significantly with RHC hemodynamic, as peak
tricuspid regurgitation velocity , right ventricular outflow acceleration time, peak early
pulmonary regurgitation velocity , peak late pulmonary regurgitation velocity, tricuspid
regurgitation time velocity integral ,and tricuspid annulus tissue Doppler image velocities.
Most of these parameters used individually to echocardiographic diagnose PH, however little
data available to integrate them together to echocardiographic diagnose PH in group1;
integrations of theses parameters might improve PH diagnosis As pulmonary arterial
hypertension is Patho biological disease, and affecting small pulmonary arteries and
arterioles, the pathologic pattern of vascular lesions is characterized by intimal
hyperplasia, medial thickness, plexiform lesions, and thrombosis in situ, and is caused by
increased migration and proliferation of smooth muscle cells (SMCs) and adventitial
fibroblasts, abnormal endothelial cell proliferation, and impaired apoptosis (6).
several biomarkers play significant role in pathogenesis and prognosis of the diseases, serum
uric acid (7,8) and serum troponin (9) may increase in PH and may affecting the clinical
severity however further studies needed to confirm this .
Also micro RNA new marker of assessing cardiovascular diseases , may have role in assessing
group 1 pulmonary hypertension(10).
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