Unusual lung structures may raise risk of pulmonary disease
The internal anatomy of our lungs is surprisingly variable, and some of those variations are associated with a greater risk of chronic obstructive pulmonary disease (COPD), a new study led by researchers at Research Institute of the McGill University Health Centre (RI-MUHC) and the Columbia University Irving Medical Center has found.
Dr. Benjamin Smith, study's first author, who is a clinician-scientist from the Translational Research in Respiratory Diseases Program at the Research Institute of the MUHC
The variations occur in large airway branches in the lower lobes of the lungs and are readily detected with standard CT scans. The findings suggest that people with certain variations might, in the future, need more personalized treatments.
COPD is a progressive lung disease that causes airway inflammation, makes breathing more difficult, and is the fourth leading cause of death in the world. COPD usually occurs in people with a history of smoking, commonly after they have quit smoking, but is increasingly recognized in those who have never smoked.
Benjamin Smith, an assistant professor in McGill’s Department of Medicine and the study’s first author, noticed that variations in the large airways of lungs had been reported in old autopsy studies. So he and the other researchers set out to see how common those variations are in the general population, and if they were associated with COPD.
For the study, the researchers examined CT scans from more than 3,000 people in the Multi-Ethnic Study of Atherosclerosis (MESA) Lung Study.
Extra and missing branches
“We found that central airway branches of the lungs, which are believed to form early in life, do not follow the textbook pattern in one quarter of the adult population and these non-textbook variations in airway branches are associated with higher COPD prevalence among older adults,” said Smith, who is also a scientist from the Translational Research in Respiratory Diseases Program at the RI-MUHC. “Interestingly, one of the airway branch variants was associated with COPD among smokers and non-smokers. The other was associated with COPD, but only among smokers.”
About 16 percent of people possess an extra airway branch in the lung, about 6 percent are missing a branch, and another 4 percent have a combination of variants or other patterns. The results were published online Jan. 16 in the Proceedings of the National Academy of Sciences.
“The amount of lung variation high up in the airway tree was quite a surprise to us,” says R. Graham Barr, MD, DrPH, chief of general medicine at Columbia University Irving Medical Center and the study’s senior author. “These changes are occurring at a branching level equivalent to your fingers–so it’s like a quarter of us having four or six fingers instead of five.”
People with an extra airway branch were 40 percent more likely to have COPD than people with standard anatomy. And people missing a specific airway branch were almost twice as likely to have COPD, but only if they smoked. The findings were replicated in a second study of almost 3,000 patients with and without COPD.
These airway tree variations are identifiable on low-dose screening lung CT scans, which are currently indicated clinically for lung cancer screening in older patients with a history of heavy smoking in the prior 15 years. Before CT scans are used outside of this group for the identification of airway variants in clinical practice, the study authors say more research will be needed to confirm that preventive or therapeutic interventions based on the presence of airway tree variations can improve patients’ outcomes.
Quitting smoking remains best antidote
In the meantime, the researchers say they will be investigating another important finding — this one around family history. Their study identified a common airway branch variation that occurs within families and is associated with COPD among non-smokers. Smith said while other developmental events that occur within families may be involved, his research team is looking into whether there is a genetic basis for this variant. “If proven,” he said, “this would represent a novel mechanism of COPD among non-smokers.”
Smith emphasized that for all the new findings, quitting smoking remains the best antidote to COPD, and smokers trying to quit should seek professional help, if necessary, to succeed.
About the study
The study, titled “Human Airway Branch Variation and Chronic Obstructive Pulmonary Disease,” was published Jan. 16 ahead of print in Proceedings of the National Academy of Sciences.
DOI: www.pnas.org/cgi/doi/10.1073/pnas.1715564115
Other authors: Hussein Traboulsi (McGill Univ., RI-MUHC), John H.M. Austin (Columbia), Ani Manichaikul (Univ. of Virginia), Eric A. Hoffman (Univ. of Iowa), Eugene R. Bleecker (Univ. of Arizona), Wellington V. Cardoso (Columbia), Christopher Cooper (UCLA), David J. Couper (UNC-Chapel Hill), Stephen M. Dashnaw (Columbia), Jia Guo (Columbia), MeiLan K. Han (Univ. of Michigan), Nadia N. Hansel (Johns Hopkins), Emlyn W. Hughes (Columbia), David R. Jacobs Jr. (Univ. of Minnesota), Richard E. Kanner (Univ. of Utah), Joel D. Kaufman (Univ. of Washington), Eric Kleerup (UCLA), Ching-Long Lin (Univ. of Iowa), Kiang Liu (Northwestern), Christian M. Lo Cascio (Columbia), Fernando J. Martinez (Cornell Univ.), Jennifer N. Nguyen (Univ. of Virginia), Martin R. Prince (Cornell Univ.), Stephen Rennard (Univ. of Nebraska), Stephen S. Rich (Univ. of Virginia), Leora Simon (McGill Univ., RI-MUHC), Yanping Sun (Columbia), Karol E. Watson (UCLA), Prescott G. Woodruff (UCSF), and Carolyn J. Baglole (McGill Univ., RI-MUHC).
Financial support was provided by the National Institutes of Health, Research Institute of the McGill University Health Centre, and the Fonds de recherche du Québec – Santé (FRQS).
One co-author (EAH) is co-founder and shareholder in Vida Diagnostics, which was used to assess some, but not the main, lung measures in the study.
Contacts:
Cynthia Lee
McGill University, Media Relations Office
514-398-6754
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Julie Robert
McGill University Health Centre, Communications
514-971-4747
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