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Radiol 212611
Radiol 212611
Radiol 212611
Background: Global consumption of marijuana is increasing, but there is a paucity of evidence concerning associated lung imaging
findings.
Purpose: To use chest CT to investigate the effects of marijuana smoking in the lung.
Materials and Methods: This retrospective case-control study evaluated results of chest CT examinations (from October 2005 to
July 2020) in marijuana smokers, nonsmoker control patients, and tobacco-only smokers. We compared rates of emphysema,
airway changes, gynecomastia, and coronary artery calcification. Age- and sex-matched subgroups were created for comparison with
tobacco-only smokers older than 50 years. Results were analyzed using χ2 tests.
Results: A total of 56 marijuana smokers (34 male; mean age, 49 years ± 14 [SD]), 57 nonsmoker control patients (32 male; mean
age, 49 years ± 14), and 33 tobacco-only smokers (18 male; mean age, 60 years ± 6) were evaluated. Higher rates of emphysema
were seen among marijuana smokers (42 of 56 [75%]) than nonsmokers (three of 57 [5%]) (P < .001) but not tobacco-only smok-
ers (22 of 33 [67%]) (P = .40). Rates of bronchial thickening, bronchiectasis, and mucoid impaction were higher among marijuana
smokers compared with the other groups (P < .001 to P = .04). Gynecomastia was more common in marijuana smokers (13 of
34 [38%]) than in control patients (five of 32 [16%]) (P = .039) and tobacco-only smokers (two of 18 [11%]) (P = .040). In age-
matched subgroup analysis of 30 marijuana smokers (23 male), 29 nonsmoker control patients (17 male), and 33 tobacco-only
smokers (18 male), rates of bronchial thickening, bronchiectasis, and mucoid impaction were again higher in the marijuana smokers
than in the tobacco-only smokers (P < .001 to P = .006). Emphysema rates were higher in age-matched marijuana smokers
(28 of 30 [93%]) than in tobacco-only smokers (22 of 33 [67%]) (P = .009). There was no difference in rate of coronary artery
calcification between age-matched marijuana smokers (21 of 30 [70%]) and tobacco-only smokers (28 of 33 [85%]) (P = .16).
Conclusion: Airway inflammation and emphysema were more common in marijuana smokers than in nonsmokers and tobacco-only
smokers, although variable interobserver agreement and concomitant cigarette smoking among the marijuana-smoking cohort limits
our ability to draw strong conclusions.
© RSNA, 2022
The purpose of this study was to use chest CT to investigate Age- and sex-matched subgroups.—Because the tobacco smoker
the effects of marijuana smoking on the lung. We sought to de- group included only patients aged at least 50 years, similarly aged
termine if there were identifiable sequelae on chest CT images, patients in the marijuana smoker group and the nonsmoker
including emphysema and signs of airway inflammation. control group were included in the subgroup analysis.
Figure 1: Flowchart shows patient inclusion and exclusion criteria for this study. Subgroups were created by age and sex matching to the
tobacco-only cohort (who were taken from the high-risk lung cancer screening program; to qualify for screening, these patients needed to be 50
years or older). Any patients 50 years or older in the marijuana smoker or nonsmoker main groups were included in the subgroup analysis. Patients
younger than 50 years in the marijuana smoker or nonsmoker main groups were excluded from subgroup analysis.
Statistical Analyses son with those who only smoked tobacco; subgroups con-
Interobserver agreement was evaluated using the Cohen κ statis- sisted of 30 marijuana smokers (mean age, 60 years ± 6; 23
tic. Results were analyzed using χ2 tests to assess for significant male, seven female), 29 control patients (mean age, 61 years ±
differences in rates of emphysema, bronchiectasis, bronchial wall 6; 17 male, 12 female), and 33 tobacco-only smokers (mean
thickening, mucoid impaction, gynecomastia, and coronary age, 60 years ± 6; 18 male, 15 female). Patient selection crite-
artery disease between groups of marijuana smokers, tobacco ria are summarized in Figure 1, and patient characteristics are
smokers, and control patients; statistical significance was set at P summarized in Table 1.
< .05. Marijuana smokers were compared with control subjects Our ability to quantify marijuana use was limited, with a
in the main group analysis, and they were compared with both daily amount specified in only 28 of 56 patients; average mari-
tobacco smokers and control patients in the subgroup analysis. juana consumption among these patients was 1.85 g per day
The χ2 tests were performed using an online statistics calculator (range, 0.25–9.25 g per day). There were 50 of 56 marijuana-
(https://www.socscistatistics.com/). smokers who also smoked tobacco, with pack-year data specified
in only 47 patients; average smoking history was 25 pack-years
Results (range, 0–100 pack-years) (14).
For tobacco-only smokers, average smoking history was 40
Patient Characteristics pack-years (range, 25–105 pack-years).
A total of 56 marijuana smokers (mean age, 49 years ± 14
[SD]; 34 male, 22 female) and 57 control patients (mean age, Interobserver Agreement
49 years ± 14; 32 male, 25 female) were identified. Patients For the analysis of 30 patients, interobserver agreement
older than 50 years were included in subgroups for compari- between the two readers was fair for assessment of bron-
Figure 2: Airway changes in a 66-year-old male marijuana and tobacco smoker. Contrast-enhanced (A) axial and (B) coronal CT images
show cylindrical bronchiectasis and bronchial wall thickening (arrowheads) in multiple lung lobes bilaterally in a background of paraseptal (arrows)
and centrilobular emphysema.
Figure 3: Pulmonary emphysema in (A, B) marijuana and (C, D) tobacco smokers. (A) Axial and (B) coronal CT images in a 44-year-old
male marijuana smoker show paraseptal emphysema (arrowheads) in bilateral upper lobes. (C) Axial and (D) coronal CT images in a 66-year-old
female tobacco smoker with centrilobular emphysema represented by areas of centrilobular lucency (arrowheads).
chiectasis (κ = 0.27), moderate for assessment of bronchial Marijuana Smokers versus Nonsmoker Controls
wall thickening (κ = 0.49), substantial for assessment of em- There were differences in rates of emphysema (both paraseptal
physema (κ = 0.79), and strong for assessment of mucoid and centrilobular) (75% vs 5%, P < .001), bronchial thickening
impaction (κ = 0.84). (64% vs 11%, P < .001), bronchiectasis (23% vs 4%, P = .002),
Table 2: Rates of Thoracic CT Findings among Marijuana Smokers, Nonsmoker Control Patients, and Tobacco Smokers (Main Groups)
Table 3: Rates of Thoracic CT Findings among Marijuana Smokers, Nonsmoker Control Patients, and Tobacco Smokers (Age- and
Sex-matched Subgroups)
and mucoid impaction (46% vs 2%, P < .001) between mari- group analysis again demonstrated significant differences in rates
juana smokers and nonsmoker control patients, respectively. of bronchial thickening (83% vs 42%, P < .001), bronchiectasis
No patient had pneumothorax. (33% vs 6%, P = .006), and mucoid impaction (67% vs 15%,
Subgroup analysis demonstrated differences in frequency of P < .001) in marijuana smokers compared with tobacco-only
bronchial thickening (83% vs 21%, P < .001), bronchiectasis smokers. Figure 2 demonstrates CT findings of airway changes
(33% vs 7%, P = .012) and mucoid impaction (67% vs 3%, in a combined marijuana and tobacco smoker. Variable interob-
P < .001) between marijuana smokers and nonsmoker control server agreement limits our ability to draw strong conclusions
patients, respectively. about bronchial wall thickening and bronchiectasis.
Centrilobular nodules were observed in 18% of marijuana We found no difference between the overall rates of em-
smokers while no nonsmoker control patients exhibited this physema (including both paraseptal and centrilobular emphy-
finding (P < .001). Gynecomastia was significantly more sema) when comparing non–age-matched marijuana smokers
common in marijuana smokers than in nonsmoker control and tobacco-only smokers (75% vs 67%, P = .40); however,
patients (38% vs 16%, P = .04). While there was a difference in higher rates of emphysema were noted when the age-matched
coronary artery calcification rates between marijuana smokers marijuana group was compared with the tobacco-only group
and nonsmoker control patients (43% vs 26%,), this did not (93% vs 67%, P = .01). Also, a significant difference in a para-
reach statistical significance (P = .06). septal predominant pattern of emphysema was seen in the
marijuana smokers compared with the tobacco-only smokers
Marijuana Smokers versus Tobacco-only Smokers (57% vs 24%, P = .009) (Fig 3), while we found no evidence
Differences in bronchial thickening (64% vs 42%, P = .04), of a difference in the proportion of those with a centrilobular
bronchiectasis (23% vs 6%, P = .04), and mucoid impaction pattern (37% vs 39%, P = .82). Rates of the key CT findings
(46% vs 15%, P = .003) were seen in the non–age-matched in each cohort are summarized for the main group in Table 2
marijuana group compared with the tobacco-only group. Sub- and for the subgroup in Table 3.
limits our ability to draw strong conclusions about bronchial 12. Hancox RJ, Poulton R, Ely M, et al. Effects of cannabis on lung function: a
population-based cohort study. Eur Respir J 2010;35(1):42–47.
wall thickening and bronchiectasis. 13. Morris MA, Jacobson SR, Kinney GL, et al. Marijuana Use Associations with
In conclusion, our study suggests that distinct radiologic Pulmonary Symptoms and Function in Tobacco Smokers Enrolled in the
findings in the lung may be seen in marijuana smokers, including Subpopulations and Intermediate Outcome Measures in COPD Study
(SPIROMICS). Chronic Obstr Pulm Dis (Miami) 2018;5(1):46–56.
higher rates of paraseptal emphysema and airway inflammatory 14. Ridgeway G, Kilmer B. Bayesian inference for the distribution of grams of
changes, such as bronchiectasis, bronchial wall thickening, and marijuana in a joint. Drug Alcohol Depend 2016;165:175–180.
mucoid impaction when compared with nonsmoker control 15. Lynch DA, Austin JH, Hogg JC, et al. CT-Definable Subtypes of Chronic
Obstructive Pulmonary Disease: A Statement of the Fleischner Society.
patients and those who only smoke tobacco. These findings may Radiology 2015;277(1):192–205.
be related to specific inhalational techniques while smoking mari- 16. Ooi GC, Khong PL, Chan-Yeung M, et al. High-resolution CT quanti-
juana, as well as to the bronchodilatory and immunomodulatory fication of bronchiectasis: clinical and functional correlation. Radiology
2002;225(3):663–672.
properties of its components. Further larger and prospective stud- 17. Klang E, Kanana N, Grossman A, et al. Quantitative CT Assessment of
ies are necessary to confirm and further elucidate these findings, as Gynecomastia in the General Population and in Dialysis, Cirrhotic, and
marijuana use is bound to increase in the future, given the increas- Obese Patients. Acad Radiol 2018;25(5):626–635.
18. Shemesh J, Henschke CI, Shaham D, et al. Ordinal scoring of coronary artery
ing legalization of its use for medical and recreational purposes. calcifications on low-dose CT scans of the chest is predictive of death from
cardiovascular disease. Radiology 2010;257(2):541–548.
Author contributions: Guarantors of integrity of entire study, L.M., P.S., G.R.;
19. Johnson MK, Smith RP, Morrison D, Laszlo G, White RJ. Large lung
study concepts/study design or data acquisition or data analysis/interpretation, all
bullae in marijuana smokers. Thorax 2000;55(4):340–342.
authors; manuscript drafting or manuscript revision for important intellectual con-
20. Hii SW, Tam JD, Thompson BR, Naughton MT. Bullous lung disease due to
tent, all authors; approval of final version of submitted manuscript, all authors;
marijuana. Respirology 2008;13(1):122–127.
agrees to ensure any questions related to the work are appropriately resolved, all
21. Ruppert AM, Perrin J, Khalil A, et al. Effect of cannabis and tobacco on
authors; literature research, L.M., P.S., M.D.F.M., G.R.; clinical studies, G.R.; sta-
emphysema in patients with spontaneous pneumothorax. Diagn Interv
tistical analysis, L.M., J.P.S., M.D.F.M., G.R.; and manuscript editing, all authors
Imaging 2018;99(7-8):465–471.
22. Stefani A, Aramini B, Baraldi C, et al. Secondary spontaneous pneumo-
Disclosures of conflicts of interest: L.M. No relevant relationships. P.S. No thorax and bullous lung disease in cannabis and tobacco smokers: A case-
relevant relationships. J.P.S. No relevant relationships. M.D.F.M. Radiology edito- control study. PLoS One 2020;15(3):e0230419.
rial board. G.R. Legal advice for BLG firm. 23. Bisconti M, Marulli G, Pacifici R, et al. Cannabinoids Identification in
Lung Tissues of Young Cannabis Smokers Operated for Primary Sponta-
References neous Pneumothorax and Correlation with Pathologic Findings. Respira-
1. Lafaye G, Karila L, Blecha L, Benyamina A. Cannabis, cannabinoids, and tion 2019;98(6):503–511.
health. Dialogues Clin Neurosci 2017;19(3):309–316. 24. Tetrault JM, Crothers K, Moore BA, Mehra R, Concato J, Fiellin DA. Effects
2. Ribeiro LI, Ind PW. Effect of cannabis smoking on lung function and respi- of marijuana smoking on pulmonary function and respiratory complications: a
ratory symptoms: a structured literature review. NPJ Prim Care Respir Med systematic review. Arch Intern Med 2007;167(3):221–228.
2016;26(1):16071. 25. Niewoehner DE, Kleinerman J, Rice DB. Pathologic changes in
3. Rotermann M. Looking back from 2020, how cannabis use and related the peripheral airways of young cigarette smokers. N Engl J Med
behaviours changed in Canada. Health Rep 2021;32(4):3–14. 1974;291(15):755–758.
4. Kerr WC, Lui C, Ye Y. Trends and age, period and cohort effects for marijuana 26. Fraig M, Shreesha U, Savici D, Katzenstein AL. Respiratory bronchiolitis: a
use prevalence in the 1984-2015 US National Alcohol Surveys. Addiction clinicopathologic study in current smokers, ex-smokers, and never-smok-
2018;113(3):473–481. ers. Am J Surg Pathol 2002;26(5):647–653.
5. Schauer GL, King BA, Bunnell RE, Promoff G, McAfee TA. Toking, Vap- 27. Gill A. Bong lung: regular smokers of cannabis show relatively distinctive
ing, and Eating for Health or Fun: Marijuana Use Patterns in Adults, histologic changes that predispose to pneumothorax. Am J Surg Pathol
U.S., 2014. Am J Prev Med 2016;50(1):1–8. 2005;29(7):980–982.
6. Ribeiro L, Ind PW. Marijuana and the lung: hysteria or cause for concern? 28. Berkowitz EA, HenryTS, Veeraraghavan S, Staton GW Jr, Gal AA. Pulmonary
Breathe (Sheff) 2018;14(3):196–205. effects of synthetic marijuana: chest radiography and CT findings. AJR Am J
7. Aldington S, Williams M, Nowitz M, et al. Effects of cannabis on pulmonary Roentgenol 2015;204(4):750–757.
structure, function and symptoms. Thorax 2007;62(12):1058–1063. 29. Ravi D, Ghasemiesfe M, Korenstein D, Cascino T, Keyhani S. Associa-
8. Moir D, Rickert WS, Levasseur G, et al. A comparison of mainstream and tions Between Marijuana Use and Cardiovascular Risk Factors and Out-
sidestream marijuana and tobacco cigarette smoke produced under two comes: A Systematic Review. Ann Intern Med 2018;168(3):187–194.
machine smoking conditions. Chem Res Toxicol 2008;21(2):494–502. 30. Burt JR, Agha AM, Yacoub B, Zahergivar A, Pepe J. Marijuana use and
9. Martinasek MP, McGrogan JB, Maysonet A. A Systematic Review coronary artery disease in young adults. PLoS One 2020;15(1):e0228326.
of the Respiratory Effects of Inhalational Marijuana. Respir Care 31. Cheezum MK, Kim A, Bittencourt MS, et al. Association of tobacco use and
2016;61(11):1543–1551. cessation with coronary atherosclerosis. Atherosclerosis 2017;257:201–207.
10. Sarafian TA, Magallanes JA, Shau H, Tashkin D, Roth MD. Oxidative stress 32. Fonseca BM, Rebelo I. Cannabis and Cannabinoids in Reproduction and
produced by marijuana smoke. An adverse effect enhanced by cannabi- Fertility: Where We Stand. Reprod Sci 2022;29(9):2429–2439.
noids. Am J Respir Cell Mol Biol 1999;20(6):1286–1293.
11. Gong H Jr, Fligiel S, Tashkin DP, Barbers RG. Tracheobronchial changes in
habitual, heavy smokers of marijuana with and without tobacco. Am Rev
Respir Dis 1987;136(1):142–149.