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Metformin: Experimental and Clinical Evidence for a Potential Role in Emphysema Treatment

Authors :
Xiaoyun Wang
G.L. Kinney
Maor Sauler
Duo Zhang
Michael Tomchaney
Tianshi David Wu
Bartolome R. Celli
Jaroslaw W. Zmijewski
Rick G. Schnellmann
Elizabeth Córdoba-Lanús
Kristan H. Cleveland
Jonathan Mayo
Craig P. Hersh
Judy Tram
John P. Konhilas
Paul R. Langlais
Ciro Casanova
Nadia N. Hansel
Yohannes Tesfaigzi
Samuel Packard
Joselyn Rojas-Quintero
Kevin Doubleday
Ashraf Fawzy
Meredith C. McCormack
Francesca Polverino
Irfan Rahman
Caroline A. Owen
Julie G. Ledford
Source :
American Journal of Respiratory and Critical Care Medicine, Am J Respir Crit Care Med
Publication Year :
2021
Publisher :
American Thoracic Society, 2021.

Abstract

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 (−0.92%; 95% confidence interval [CI], −1.7% to −0.14%; 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.

Details

ISSN :
15354970 and 1073449X
Volume :
204
Database :
OpenAIRE
Journal :
American Journal of Respiratory and Critical Care Medicine
Accession number :
edsair.doi.dedup.....e0f29a3fe7f3bb00367667157c72e15d
Full Text :
https://doi.org/10.1164/rccm.202012-4510oc