TY - JOUR
T1 - Metformin
T2 - Experimental and clinical evidence for a potential role in emphysema treatment
AU - Polverino, Francesca
AU - Wu, Tianshi David
AU - Rojas-Quintero, Joselyn
AU - Wang, Xiaoyun
AU - Mayo, Jonathan
AU - Tomchaney, Michael
AU - Tram, Judy
AU - Packard, Samuel
AU - Zhang, Duo
AU - Cleveland, Kristan H.
AU - Cordoba-Lanus, Elizabeth
AU - Owen, Caroline A.
AU - Fawzy, Ashraf
AU - Kinney, Greg L.
AU - Hersh, Craig P.
AU - Hansel, Nadia N.
AU - Doubleday, Kevin
AU - Sauler, Maor
AU - Tesfaigzi, Yohannes
AU - Ledford, Julie G.
AU - Casanova, Ciro
AU - Zmijewski, Jaroslaw
AU - Konhilas, John
AU - Langlais, Paul R.
AU - Schnellmann, Rick G
AU - Rahman, Irfan
AU - McCormack, Meredith
AU - Celli, Bartolome
N1 - Publisher Copyright:
Copyright © 2021 by the American Thoracic Society
PY - 2021/9/15
Y1 - 2021/9/15
N2 - Rationale: Cigarette smoke (CS) inhalation triggers oxidative stress and inflammation, leading to accelerated lung aging, apoptosis, and emphysema, as well as systemic pathologies. Metformin is beneficial for protecting against aging-related diseases. Objectives: We sought to investigate whether metformin may ameliorate CS-induced pathologies of emphysematous chronic obstructive pulmonary disease (COPD). Methods: Mice were exposed chronically to CS and fed metformin-enriched chow for the second half of exposure. Lung, kidney, and muscle pathologies, lung proteostasis, endoplasmic reticulum (ER) stress, mitochondrial function, and mediators of metformin effects in vivo and/or in vitro were studied. We evaluated the association of metformin use with indices of emphysema progression over 5 years of follow-up among the COPDGene (Genetic Epidemiology of COPD) study participants. The association of metformin use with the percentage of emphysema and adjusted lung density was estimated by using a linear mixed model. Measurements and Main Results: Metformin protected against CS-induced pulmonary inflammation and airspace enlargement; small airway remodeling, glomerular shrinkage, oxidative stress, apoptosis, telomere damage, aging, dysmetabolism in vivo and in vitro; and ER stress. The AMPK (AMP-activated protein kinase) pathway was central to metformin's protective action. Within COPDGene, participants receiving metformin compared with those not receiving it had a slower progression of emphysema (20.92%; 95% confidence interval [CI], 21.7% to 20.14%; P = 0.02) and a slower adjusted lung density decrease (2.2 g/L; 95% CI, 0.43 to 4.0 g/L; P = 0.01). Conclusions: Metformin protected against CS-induced lung, renal, and muscle injury; mitochondrial dysfunction; and unfolded protein responses and ER stress in mice. In humans, metformin use was associated with lesser emphysema progression over time. Our results provide a rationale for clinical trials testing the efficacy of metformin in limiting emphysema progression and its systemic consequences.
AB - Rationale: Cigarette smoke (CS) inhalation triggers oxidative stress and inflammation, leading to accelerated lung aging, apoptosis, and emphysema, as well as systemic pathologies. Metformin is beneficial for protecting against aging-related diseases. Objectives: We sought to investigate whether metformin may ameliorate CS-induced pathologies of emphysematous chronic obstructive pulmonary disease (COPD). Methods: Mice were exposed chronically to CS and fed metformin-enriched chow for the second half of exposure. Lung, kidney, and muscle pathologies, lung proteostasis, endoplasmic reticulum (ER) stress, mitochondrial function, and mediators of metformin effects in vivo and/or in vitro were studied. We evaluated the association of metformin use with indices of emphysema progression over 5 years of follow-up among the COPDGene (Genetic Epidemiology of COPD) study participants. The association of metformin use with the percentage of emphysema and adjusted lung density was estimated by using a linear mixed model. Measurements and Main Results: Metformin protected against CS-induced pulmonary inflammation and airspace enlargement; small airway remodeling, glomerular shrinkage, oxidative stress, apoptosis, telomere damage, aging, dysmetabolism in vivo and in vitro; and ER stress. The AMPK (AMP-activated protein kinase) pathway was central to metformin's protective action. Within COPDGene, participants receiving metformin compared with those not receiving it had a slower progression of emphysema (20.92%; 95% confidence interval [CI], 21.7% to 20.14%; P = 0.02) and a slower adjusted lung density decrease (2.2 g/L; 95% CI, 0.43 to 4.0 g/L; P = 0.01). Conclusions: Metformin protected against CS-induced lung, renal, and muscle injury; mitochondrial dysfunction; and unfolded protein responses and ER stress in mice. In humans, metformin use was associated with lesser emphysema progression over time. Our results provide a rationale for clinical trials testing the efficacy of metformin in limiting emphysema progression and its systemic consequences.
KW - Aging
KW - Chronic obstructive pulmonary disease
KW - Cigarette smoke
KW - Comorbidities
KW - Metformin
UR - https://www.scopus.com/pages/publications/85114664947
UR - https://www.scopus.com/pages/publications/85114664947#tab=citedBy
U2 - 10.1164/rccm.202012-4510OC
DO - 10.1164/rccm.202012-4510OC
M3 - Article
C2 - 34033525
AN - SCOPUS:85114664947
SN - 1073-449X
VL - 204
SP - 651
EP - 666
JO - American journal of respiratory and critical care medicine
JF - American journal of respiratory and critical care medicine
IS - 6
ER -