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Idiopathic Pulmonary Fibrosis and Rare Lung Disorders
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Author(s): Parth Aphale (Dr. D.Y. Patil Homoeopathic Medical College and Research Centre, Dr. D.Y. Patil Vidyapeeth, Pune, India), Himanshu Shekhar (Dr. D.Y. Patil Homoeopathic Medical College and Research Centre, Dr. D.Y. Patil Vidyapeeth, Pune, India)and Shashank Dokania (Dr. D.Y. Patil Homoeopathic Medical College and Research Centre, Dr. D.Y. Patil Vidyapeeth, Pune, India)
Copyright: 2026
Pages: 40
Source title:
Next-Generation Bioinformatics for Pulmonary Disease Research
Source Author(s)/Editor(s): Devvret Verma (Graphic Era University, India), Debasis Mitra (Graphic Era University, India), Bhavya Mudgal (Graphic Era University, India), Suraj Vitthaloo Atram (The University of Sheffield, UK)and Rokayya Sami (Taif University, Saudi Arabia)
DOI: 10.4018/979-8-3373-4923-7.ch008
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Abstract
Idiopathic Pulmonary Fibrosis (IPF) is a chronic, progressive, and often fatal interstitial lung disease marked by fibrotic remodeling of lung tissue due to excess extracellular matrix (ECM) deposition. Cutting-edge bioinformatics is revolutionizing our understanding of IPF through “omics” technologies, uncovering hidden mechanisms, key cellular players, and disrupted signaling pathways. Advanced tools now allow cell-by-cell mapping of diseased lung tissue, while machine learning aids in earlier diagnosis and prognosis. Despite challenges like complex data, these innovations are advancing precision medicine—offering hope for targeted therapies and improved outcomes.
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