Tag: #IdiopathicPulmonaryFibrosis

Introduction: Idiopathic Pulmonary Fibrosis (IPF) is a chronic and progressive lung disease characterized by excessive scarring of lung tissue, leading to severe respiratory complications. A recent study has highlighted a significant reduction in Alamandine, a key peptide in the Renin-Angiotensin System (RAS), in patients with IPF. Understanding this imbalance could open new avenues for treatment.…