TY - JOUR
T1 - Therapeutic Approaches for the Treatment of Interstitial Lung Disease
T2 - An Exploratory Review on Molecular Mechanisms
AU - Amin, Revati
AU - Pandey, Ruchi
AU - Vaishali, K.
AU - Acharya, Vishak
AU - Sinha, Mukesh Kumar
AU - Kumar, Nitesh
N1 - Publisher Copyright:
© 2024 Bentham Science Publishers.
PY - 2024
Y1 - 2024
N2 - Background: Interstitial Lung Diseases (ILDs) are characterized by shortness of breath caused by alveolar wall inflammation and/or fibrosis. Objective: Our review aims to study the depth of various variants of ILD, diagnostic procedures, pathophysiology, molecular dysfunction and regulation, subject and objective assessment techniques, pharmacological intervention, exercise training and various modes of delivery for rehabilitation. Method: Articles are reviewed from PubMed and Scopus and search engines. Results: ILD is a rapidly progressing disease with a high mortality rate. Each variant has its own set of causal agents and expression patterns. Patients often find it challenging to self-manage due to per-sistent symptoms and a rapid rate of worsening. The present review elaborated on the pathophysiology, risk factors, molecular mechanisms, diagnostics, and therapeutic approaches for ILD will guide future requirements in the quest for innovative and tailored ILD therapies at the molecular and cellular levels. Conclusion: The review highlights the rationale for conventional and novel therapeutic approaches for better management of ILD.
AB - Background: Interstitial Lung Diseases (ILDs) are characterized by shortness of breath caused by alveolar wall inflammation and/or fibrosis. Objective: Our review aims to study the depth of various variants of ILD, diagnostic procedures, pathophysiology, molecular dysfunction and regulation, subject and objective assessment techniques, pharmacological intervention, exercise training and various modes of delivery for rehabilitation. Method: Articles are reviewed from PubMed and Scopus and search engines. Results: ILD is a rapidly progressing disease with a high mortality rate. Each variant has its own set of causal agents and expression patterns. Patients often find it challenging to self-manage due to per-sistent symptoms and a rapid rate of worsening. The present review elaborated on the pathophysiology, risk factors, molecular mechanisms, diagnostics, and therapeutic approaches for ILD will guide future requirements in the quest for innovative and tailored ILD therapies at the molecular and cellular levels. Conclusion: The review highlights the rationale for conventional and novel therapeutic approaches for better management of ILD.
UR - https://www.scopus.com/pages/publications/85185663573
UR - https://www.scopus.com/inward/citedby.url?scp=85185663573&partnerID=8YFLogxK
U2 - 10.2174/1389557523666230816090112
DO - 10.2174/1389557523666230816090112
M3 - Review article
C2 - 37587813
AN - SCOPUS:85185663573
SN - 1389-5575
VL - 24
SP - 618
EP - 633
JO - Mini-Reviews in Medicinal Chemistry
JF - Mini-Reviews in Medicinal Chemistry
IS - 6
ER -