TY - JOUR
T1 - Longitudinal Association Between Muscle Loss and Mortality in Ever Smokers
AU - COPDGene Investigators
AU - Mason, Stefanie E.
AU - Moreta-Martinez, Rafael
AU - Labaki, Wassim W.
AU - Strand, Matthew J.
AU - Regan, Elizabeth A.
AU - Bon, Jessica
AU - San Jose Estepar, Ruben
AU - Casaburi, Richard
AU - McDonald, Merry Lynn
AU - Rossiter, Harry B.
AU - Make, Barry
AU - Dransfield, Mark T.
AU - Han, Mei Lan K.
AU - Young, Kendra
AU - Curtis, Jeffrey L.
AU - Stringer, Kathleen
AU - Kinney, Greg
AU - Hokanson, John E.
AU - San Jose Estepar, Raul
AU - Washko, George R.
AU - Crapo, James D.
AU - Silverman, Edwin K.
AU - Cummings, Sara
AU - Madden, Kelley
AU - Make, Barry J.
AU - Nabbosa, Juliet
AU - Port, Emily
AU - Rashdi, Serine
AU - Stepp, Lori
AU - Watts, Shandi
AU - Weaver, Michael
AU - Beaty, Terri
AU - Bowler, Russell P.
AU - Lynch, David A.
AU - Anderson, Gary
AU - Bleecker, Eugene R.
AU - Coxson, Harvey O.
AU - Crystal, Ronald G.
AU - Hogg, James C.
AU - Province, Michael A.
AU - Rennard, Stephen I.
AU - Croxton, Thomas
AU - Gan, Weiniu
AU - Postow, Lisa A.
AU - Viviano, Lisa M.
AU - Costa-Davis, Corinne
AU - Malanga, Elisha
AU - Prieto, Delia
AU - Anzueto, Antonio
AU - Maselli-Caceres, Diego
N1 - Publisher Copyright:
© 2021 American College of Chest Physicians
PY - 2022/4/1
Y1 - 2022/4/1
N2 - Background: Body composition measures, specifically low weight or reduced muscle mass, are associated with mortality in COPD, but the effect of longitudinal body composition changes is undefined. Research Question: Is the longitudinal loss of fat-free mass (FFM) associated with increased mortality, including in those with initially normal or elevated body composition metrics? Study Design and Methods: Participants with complete data for at least one visit in the COPDGene study (n = 9,268) and the ECLIPSE study (n = 1,760) were included and monitored for 12 and 8 years, respectively. Pectoralis muscle area (PMA) was derived from thoracic CT scans and used as a proxy for FFM. A longitudinal mixed submodel for PMA and a Cox proportional hazards submodel for survival were fitted on a joint distribution, using a shared random intercept parameter and Markov chain Monte Carlo parameter estimation. Results: Both cohorts demonstrated a left-shifted distribution of baseline FFM, not reflected in BMI, and an increase in all-cause mortality risk associated with longitudinal loss of PMA. For each 1-cm2 PMA loss, mortality increased 3.1% (95% CI, 2.4%-3.7%; P < .001) in COPDGene, and 2.4% (95% CI, 0.9%-4.0%; P < .001) in ECLIPSE. Increased mortality risk was independent of enrollment values for BMI and disease severity [BODE (body mass, airflow obstruction, dyspnea, and exercise capacity) index quartiles] and was significant even in participants with initially greater than average PMA. Interpretation: Longitudinal loss of PMA is associated with increased all-cause mortality, regardless of BMI or initial muscle mass. Consideration of novel screening tests and further research into mechanisms contributing to muscle decline may improve risk stratification and identify novel therapeutic targets in ever smokers.
AB - Background: Body composition measures, specifically low weight or reduced muscle mass, are associated with mortality in COPD, but the effect of longitudinal body composition changes is undefined. Research Question: Is the longitudinal loss of fat-free mass (FFM) associated with increased mortality, including in those with initially normal or elevated body composition metrics? Study Design and Methods: Participants with complete data for at least one visit in the COPDGene study (n = 9,268) and the ECLIPSE study (n = 1,760) were included and monitored for 12 and 8 years, respectively. Pectoralis muscle area (PMA) was derived from thoracic CT scans and used as a proxy for FFM. A longitudinal mixed submodel for PMA and a Cox proportional hazards submodel for survival were fitted on a joint distribution, using a shared random intercept parameter and Markov chain Monte Carlo parameter estimation. Results: Both cohorts demonstrated a left-shifted distribution of baseline FFM, not reflected in BMI, and an increase in all-cause mortality risk associated with longitudinal loss of PMA. For each 1-cm2 PMA loss, mortality increased 3.1% (95% CI, 2.4%-3.7%; P < .001) in COPDGene, and 2.4% (95% CI, 0.9%-4.0%; P < .001) in ECLIPSE. Increased mortality risk was independent of enrollment values for BMI and disease severity [BODE (body mass, airflow obstruction, dyspnea, and exercise capacity) index quartiles] and was significant even in participants with initially greater than average PMA. Interpretation: Longitudinal loss of PMA is associated with increased all-cause mortality, regardless of BMI or initial muscle mass. Consideration of novel screening tests and further research into mechanisms contributing to muscle decline may improve risk stratification and identify novel therapeutic targets in ever smokers.
KW - COPD
KW - mortality
KW - muscle wasting
KW - sarcopenia
UR - http://www.scopus.com/inward/record.url?scp=85126930089&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85126930089&partnerID=8YFLogxK
U2 - 10.1016/j.chest.2021.10.047
DO - 10.1016/j.chest.2021.10.047
M3 - Article
C2 - 34785234
AN - SCOPUS:85126930089
SN - 0012-3692
VL - 161
SP - 960
EP - 970
JO - Chest
JF - Chest
IS - 4
ER -