@article{b8c74cc2370b42fe81494ce7fe2a9c6f,
title = "New Insights into Clinical and Mechanistic Heterogeneity of the Acute Respiratory Distress Syndrome Summary of the Aspen Lung Conference 2021",
abstract = "Clinical and molecular heterogeneity are common features of human disease. Understanding the basis for heterogeneity has led to major advances in therapy for many cancers and pulmonary diseases such as cystic fibrosis and asthma. Although heterogeneity of risk factors, disease severity, and outcomes in survivors are common features of the acute respiratory distress syndrome (ARDS), many challenges exist in understanding the clinical and molecular basis for disease heterogeneity and using heterogeneity to tailor therapy for individual patients. This report summarizes the proceedings of the 2021 Aspen Lung Conference, which was organized to review key issues related to understanding clinical and molecular heterogeneity in ARDS. The goals were to review new information about ARDS phenotypes, to explore multicellular and multisystem mechanisms responsible for heterogeneity, and to review how best to account for clinical and molecular heterogeneity in clinical trial design and assessment of outcomes. The report concludes with recommendations for future research to understand the clinical and basic mechanisms underlying heterogeneity in ARDS to advance the development of new treatments for this life-threatening critical illness.",
keywords = "ARDS, biological mechanisms, clinical trials, critical care",
author = "Martin, {Thomas R.} and Zemans, {Rachel L.} and Ware, {Lorraine B.} and Schmidt, {Eric P.} and Riches, {David W.H.} and Lisa Bastarache and Calfee, {Carolyn S.} and Desai, {Tushar J.} and Susanne Herold and Hough, {Catherine L.} and Looney, {Mark R.} and Matthay, {Michael A.} and Nuala Meyer and Parikh, {Samir M.} and Troy Stevens and Thompson, {B. Taylor}",
note = "Funding Information: Supported by the U.S. National Library of Medicine (R01-LM010685 [L.B.]); the National Institute on Aging (RO1AG049493 [S.M.P.]); U.S. Department of Veterans Affairs (VA 1 I01 BX003471 [D.W.H.R.]); Stanford Medical Scientist Training Program (T.J.D.); National Heart, Lung, and Blood Institute (1UO1HL123009 [B.T.T.]); German Ministry of Education and Research (BMBF and IPSELON [S.H.]); National Institute of Allergy and Infectious Diseases (AI160167 [M.R.L.]); Deutsche Forschungsgemeinschaft (Germany) (KFO309/P2,8, SFB1021/C5, and SFB-TRR84/B9 [S.H.]); National Institute of General Medical Sciences (GM125095 [E.P.S.]); Pandemeinetzwerk Hessen (Germany) (LOEWE Research Clusters Diffusible Signals and iCanX [S.H.]); U.S. Department of Defense (A130219 [L.B.W.]); and grants HL147920 and HL131608 (R.L.Z.); HL103836, HL126176, and HL135849 (L.B.W.); NHLBI 2020 R13 HL152479 and NHLBI 1R01 HL140595 (D.W.H.R.); R35 HL140026 (C.S.C.); NHLBI 5R01HL14254902 (T.J.D.); German Research Foundation (EXC2026 [S.H.]); K24HL141526 and RO1HL132232 (C.L.H.); HL134828, HL126456, and HL140026, HL143896 (M.A.M.); HL137006, HL137915, and HL155804 (N.L.M.); R35 HL139424 (S.M.P.); R35 HL161241 (M.R.L.); and HL66299, HL148069, and HL140182 (T.S.). Publisher Copyright: Copyright {\textcopyright} 2022 by the American Thoracic Society.",
year = "2022",
month = sep,
doi = "10.1165/rcmb.2022-0089WS",
language = "English (US)",
volume = "67",
pages = "284--308",
journal = "American journal of respiratory cell and molecular biology",
issn = "1044-1549",
publisher = "American Thoracic Society",
number = "3",
}