TY - JOUR
T1 - Quantification of lung PET images
T2 - Challenges and opportunities
AU - Chen, Delphine L.
AU - Cheriyan, Joseph
AU - Chilvers, Edwin R.
AU - Choudhury, Gourab
AU - Coello, Christopher
AU - Connell, Martin
AU - Fisk, Marie
AU - Groves, Ashley M.
AU - Gunn, Roger N.
AU - Holman, Beverley F.
AU - Hutton, Brian F.
AU - Lee, Sarah
AU - MacNee, William
AU - Mohan, Divya
AU - Parr, David
AU - Subramanian, Deepak
AU - Tal-Singer, Ruth
AU - Thielemans, Kris
AU - Van Beek, Edwin J.R.
AU - Vass, Laurence
AU - Wellen, Jeremy W.
AU - Wilkinson, Ian
AU - Wilson, Frederick J.
N1 - Publisher Copyright:
Copyright © 2017 SNMMI; all rights reserved.
PY - 2017/2/1
Y1 - 2017/2/1
N2 - Millions of people are affected by respiratory diseases, leading to a significant health burden globally. Because of the current insufficient knowledge of the underlying mechanisms that lead to the development and progression of respiratory diseases, treatment options remain limited. To overcome this limitation and understand the associated molecular changes, noninvasive imaging techniques such as PET and SPECT have been explored for biomarker development, with 18F-FDG PET imaging being the most studied. The quantification of pulmonary molecular imaging data remains challenging because of variations in tissue, air, blood, and water fractions within the lungs. The proportions of these components further differ depending on the lung disease. Therefore, different quantification approaches have been proposed to address these variabilities. However, no standardized approach has been developed to date. This article reviews the data evaluating 18F-FDG PET quantification approaches in lung diseases, focusing on methods to account for variations in lung components and the interpretation of the derived parameters. The diseases reviewed include acute respiratory distress syndrome, chronic obstructive pulmonary disease, and interstitial lung diseases such as idiopathic pulmonary fibrosis. Based on review of prior literature, ongoing research, and discussions among the authors, suggested considerations are presented to assist with the interpretation of the derived parameters from these approaches and the design of future studies.
AB - Millions of people are affected by respiratory diseases, leading to a significant health burden globally. Because of the current insufficient knowledge of the underlying mechanisms that lead to the development and progression of respiratory diseases, treatment options remain limited. To overcome this limitation and understand the associated molecular changes, noninvasive imaging techniques such as PET and SPECT have been explored for biomarker development, with 18F-FDG PET imaging being the most studied. The quantification of pulmonary molecular imaging data remains challenging because of variations in tissue, air, blood, and water fractions within the lungs. The proportions of these components further differ depending on the lung disease. Therefore, different quantification approaches have been proposed to address these variabilities. However, no standardized approach has been developed to date. This article reviews the data evaluating 18F-FDG PET quantification approaches in lung diseases, focusing on methods to account for variations in lung components and the interpretation of the derived parameters. The diseases reviewed include acute respiratory distress syndrome, chronic obstructive pulmonary disease, and interstitial lung diseases such as idiopathic pulmonary fibrosis. Based on review of prior literature, ongoing research, and discussions among the authors, suggested considerations are presented to assist with the interpretation of the derived parameters from these approaches and the design of future studies.
KW - Lung inflammation
KW - Molecular imaging
KW - Positron emission tomography
KW - Pulmonary
UR - http://www.scopus.com/inward/record.url?scp=85011977714&partnerID=8YFLogxK
U2 - 10.2967/jnumed.116.184796
DO - 10.2967/jnumed.116.184796
M3 - Article
C2 - 28082432
AN - SCOPUS:85011977714
SN - 0161-5505
VL - 58
SP - 201
EP - 207
JO - Journal of Nuclear Medicine
JF - Journal of Nuclear Medicine
IS - 2
ER -