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
AU - Rahman, Irfan
AU - McCormack, Meredith
AU - Celli, Bartolome
N1 - Funding Information:
*These authors contributed equally to this work (co–first authors). ‡These authors contributed equally to this work (co–senior authors). Supported by the Flight Attendants’ Medical Research Institute (YFAC14004), the Parker B. Francis Foundation, the Asthma and Airway Disease Research Center Funds, and the NIH/NHLBI (HL149744 and HL132523) (F.P.). COPDGene (Genetic Epidemiology of Chronic Obstructive Pulmonary Disease [COPD]) is supported by the NHLBI (U01HL89897 and U01HL089856) and by the COPD Foundation through contributions made to an Industry Advisory Board comprising AstraZeneca, Boehringer-Ingelheim, Genentech, GlaxoSmithKline, Novartis, Pfizer, Siemens, and Sunovion. T.D.W. is supported by the Department of Veterans Affairs, Veterans Health Administration, Office of Research and Development, and Center for Innovations in Quality, Effectiveness, and Safety (CIN 13-413). M.M. is supported by the National Institute of Environmental Health Sciences (P50ES018176), National Institute on Minority Health and Health Disparities (P50MD010431), and the U.S. Environmental Protection Agency (83615201 and 83615001). J.Z. is supported by the U.S. Department of Defense (W81XWH-17-1-0577) and the NIH (R01 HL139617-01).
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
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U2 - 10.1164/rccm.202012-4510OC
DO - 10.1164/rccm.202012-4510OC
M3 - Article
C2 - 34033525
AN - SCOPUS:85114664947
VL - 204
SP - 651
EP - 666
JO - American Review of Respiratory Disease
JF - American Review of Respiratory Disease
SN - 1073-449X
IS - 6
ER -