Metformin: Experimental and clinical evidence for a potential role in emphysema treatment

  • Francesca Polverino
  • , Tianshi David Wu
  • , Joselyn Rojas-Quintero
  • , Xiaoyun Wang
  • , Jonathan Mayo
  • , Michael Tomchaney
  • , Judy Tram
  • , Samuel Packard
  • , Duo Zhang
  • , Kristan H. Cleveland
  • , Elizabeth Cordoba-Lanus
  • , Caroline A. Owen
  • , Ashraf Fawzy
  • , Greg L. Kinney
  • , Craig P. Hersh
  • , Nadia N. Hansel
  • , Kevin Doubleday
  • , Maor Sauler
  • , Yohannes Tesfaigzi
  • , Julie G. Ledford
  • Ciro Casanova, Jaroslaw Zmijewski, John Konhilas, Paul R. Langlais, Rick G Schnellmann, Irfan Rahman, Meredith McCormack, Bartolome Celli

Research output: Contribution to journalArticlepeer-review

72 Scopus citations

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 (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.

Original languageEnglish (US)
Pages (from-to)651-666
Number of pages16
JournalAmerican journal of respiratory and critical care medicine
Volume204
Issue number6
DOIs
StatePublished - Sep 15 2021

Keywords

  • Aging
  • Chronic obstructive pulmonary disease
  • Cigarette smoke
  • Comorbidities
  • Metformin

ASJC Scopus subject areas

  • Pulmonary and Respiratory Medicine
  • Critical Care and Intensive Care Medicine

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