Abstract
Introduction: Because of widespread use, understanding the pulmonary effects of cannabis use is important; but its role independent from tobacco smoking is yet to be elucidated. We used Mendelian randomization (MR) to assess the effect of genetic liability to lifetime cannabis use and cannabis use disorder on pulmonary function and lung cancer. Methods: We used four single nucleotide polymorphisms associated with lifetime cannabis use (p value <5 × 10−8) from a genome-wide association study (GWAS) of 184,765 individuals of European descent from the International Cannabis Consortium, 23andme, and U.K. Biobank as instrumental variables. Seven single nucleotide polymorphisms (p value <5 × 10−8) were selected as instruments for cannabis use disorder from a GWAS meta-analysis of 17,068 European ancestry cases and 357,219 controls of European descent from Psychiatric Genomics Consortium Substance Use Disorders working group, Lundbeck Foundation Initiative for Integrative PsychiatricResearch, and deCode. To assess lung function, GWAS included 79,055 study participants of the SpiroMeta Consortium, and for lung cancer GWAS from the International Lung Cancer Consortium contained 29,266 cases and 56,450 controls. Results: MR revealed that genetic liability to lifetime cannabis use was associated with increased risk of squamous cell carcinoma (OR = 1.22, 95%, confidence interval = 1.07–1.39, p value = 0.003, q value = 0.025). Pleiotropy-robust methods and positive and negative control analyses did not indicate bias in the primary analysis. Conclusions: The findings of this MR analysis suggest evidence for a potential causal association between genetic liability for cannabis use and the risk of squamous cell carcinoma. Triangulating MR and observational studies and addressing orthogonal sources of bias are necessary to confirm this finding.
Original language | English |
---|---|
Pages (from-to) | 1127-1135 |
Number of pages | 9 |
Journal | Journal of Thoracic Oncology |
Volume | 16 |
Issue number | 7 |
DOIs | |
State | Published - Jul 2021 |
Keywords
- Cannabis
- Genetic susceptibility
- Lung cancer
- Mendelian randomization
- Pulmonary function
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In: Journal of Thoracic Oncology, Vol. 16, No. 7, 07.2021, p. 1127-1135.
Research output: Contribution to journal › Article › peer-review
TY - JOUR
T1 - Cannabis Use, Pulmonary Function, and Lung Cancer Susceptibility
T2 - A Mendelian Randomization Study
AU - International Lung Cancer Consortium
AU - Baumeister, Sebastian Edgar
AU - Baurecht, Hansjörg
AU - Nolde, Michael
AU - Alayash, Zoheir
AU - Gläser, Sven
AU - Johansson, Mattias
AU - Amos, Christopher I.
AU - Johnson, Emma C.
AU - Hung, Rayjean J.
N1 - Funding Information: The authors thank the investigators of the International Cannabis Consortium, SpiroMeta Consortium, and Integrative Psychiatric Research for the genome-wide association study summary data used in this study. The Integrative Analysis of Lung Cancer Risk and Etiology (INTEGRAL) team of the International Lung Cancer Consortium (ILCCO) was supported by grants CA203654 and CA148127S1. ILCCO data harmonization is supported by the Canada Research Chair to R.J.H. The ILCCO OncoArray was supported by in-kind genotyping by the Center for Inherited Disease Research (26820120008i-0-26800068-1). ILCOO investigators include Maria Teresa Land (National Cancer Institute, Bethesda, Maryland), Victoria Stevens (Epidemiology Research Program, American Cancer Society, Atlanta, Georgia), Ying Wand (Epidemiology Research Program, American Cancer Society, Atlanta, Georgia), Demetrios Albanes (National Cancer Institute, Bethesda, Maryland), Neil Caporaso (National Cancer Institute, Bethesda, Maryland), Paul Brennan (International Agency for Research on Cancer, Lyon, France), Christopher I. Amos (Geisel School of Medicine at Dartmouth, Hanover, New Hampshire), Sanjay Shete (The University of Texas MD Anderson Cancer Center, Houston, Texas), Rayjean J. Hung (Lunenfeld-Tanenbuaum Research Institute, Sinai Health System, University of Toronto, Toronto, Ontario, Canada), Heike Bickeböller (University Medical Center Goettingen, Göttingen, Germany), Angela Risch (University of Salzburg and Cancer Cluster Salzburg, Salzburg, Germany; Translational Lung Research Center Heidelberg, Heidelberg, Germany), Richard Houlston (Institute for Cancer Research, London, United Kingdom), Stephen Lam (British Columbia Cancer Agency, Vancouver, Canada), Adonina Tardon (University of Oviedo and Center for Biomedical Research in Epidemiology and Public Health Network [CIBERESP], Oveido, Spain), Chu Chen (Fred Hutchinson Cancer Research Center, Public Health Sciences, Seattle, Washington), Stig E. Bojesen (Copenhagen General Population Study, Herlev, and Gentofte Hospital, Copenhagen, Denmark), Mattias Johansson (International Agency for Research on Cancer, Lyon, France), H-Erich Wichmann (Helmholtz Center Munich, Munich, Germany), David Christiani (Harvard School of Public Health, Boston, Massachusetts), Gadi Rennert (Carmel Medical Center, Haifa, Israel), Susanne Arnold (Markey Cancer Center, Lexington, Kentucky), John K. Field (Liverpool University, Liverpool, United Kingdom), Sanjay S. Shete (The University of Texas MD Anderson Cancer Center, Houston, Texas), Loic Le Marchand (University of Hawaii Cancer Center, Honolulu, Hawaii), Olle Melander (Department of Clinical Sciences Malmö, Lund University, Lund, Sweden), Hans Brunnström (Lund University, Lund, Sweden), Geoffrey Liu (Princess Margaret Cancer Center, Toronto, Ontario, Canada), Angeline Andrew (Norris Cotton Cancer Center, Lebanon, New Hampshire), Lambertus A. Kiemeney (Radboud University Medical Center, Nijmegen, the Netherlands), Hongbing Shen (Nanjing Medical University, Nanjing, People’s Republic of China), Shan Zienolddiny (National Institute of Occupational Health, Oslo, Norway), Kjell Grankvist (Umeå University, Umeå, Sweden), Mikael Johansson (Umeå University, Umeå, Sweden), Neil Caporaso (National Cancer Institute, Bethesda, Maryland), M. Dawn Teare (University Of Sheffield, South Yorkshire, United Kingdom), Yun-Chul Hong (Seoul National University College of Medicine, Seoul, South Korea), Jian-Min Yuan (University of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania), Philip Lazarus (Washington State University College of Pharmacy, Spokane, Washington), Matthew B. Schabath (H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida), and Melinda C. Aldrich (Vanderbilt University Medical Center, Nashville, Tennessee). Funding Information: The authors thank the investigators of the International Cannabis Consortium, SpiroMeta Consortium, and Integrative Psychiatric Research for the genome-wide association study summary data used in this study. The Integrative Analysis of Lung Cancer Risk and Etiology (INTEGRAL) team of the International Lung Cancer Consortium (ILCCO) was supported by grants CA203654 and CA148127S1. ILCCO data harmonization is supported by the Canada Research Chair to R.J.H. The ILCCO OncoArray was supported by in-kind genotyping by the Center for Inherited Disease Research (26820120008i-0-26800068-1). ILCOO investigators include Maria Teresa Land (National Cancer Institute, Bethesda, Maryland), Victoria Stevens (Epidemiology Research Program, American Cancer Society, Atlanta, Georgia), Ying Wand (Epidemiology Research Program, American Cancer Society, Atlanta, Georgia), Demetrios Albanes (National Cancer Institute, Bethesda, Maryland), Neil Caporaso (National Cancer Institute, Bethesda, Maryland), Paul Brennan (International Agency for Research on Cancer, Lyon, France), Christopher I. Amos (Geisel School of Medicine at Dartmouth, Hanover, New Hampshire), Sanjay Shete (The University of Texas MD Anderson Cancer Center, Houston, Texas), Rayjean J. Hung (Lunenfeld-Tanenbuaum Research Institute, Sinai Health System, University of Toronto, Toronto, Ontario, Canada), Heike Bickeb?ller (University Medical Center Goettingen, G?ttingen, Germany), Angela Risch (University of Salzburg and Cancer Cluster Salzburg, Salzburg, Germany; Translational Lung Research Center Heidelberg, Heidelberg, Germany), Richard Houlston (Institute for Cancer Research, London, United Kingdom), Stephen Lam (British Columbia Cancer Agency, Vancouver, Canada), Adonina Tardon (University of Oviedo and Center for Biomedical Research in Epidemiology and Public Health Network [CIBERESP], Oveido, Spain), Chu Chen (Fred Hutchinson Cancer Research Center, Public Health Sciences, Seattle, Washington), Stig E. Bojesen (Copenhagen General Population Study, Herlev, and Gentofte Hospital, Copenhagen, Denmark), Mattias Johansson (International Agency for Research on Cancer, Lyon, France), H-Erich Wichmann (Helmholtz Center Munich, Munich, Germany), David Christiani (Harvard School of Public Health, Boston, Massachusetts), Gadi Rennert (Carmel Medical Center, Haifa, Israel), Susanne Arnold (Markey Cancer Center, Lexington, Kentucky), John K. Field (Liverpool University, Liverpool, United Kingdom), Sanjay S. Shete (The University of Texas MD Anderson Cancer Center, Houston, Texas), Loic Le Marchand (University of Hawaii Cancer Center, Honolulu, Hawaii), Olle Melander (Department of Clinical Sciences Malm?, Lund University, Lund, Sweden), Hans Brunnstr?m (Lund University, Lund, Sweden), Geoffrey Liu (Princess Margaret Cancer Center, Toronto, Ontario, Canada), Angeline Andrew (Norris Cotton Cancer Center, Lebanon, New Hampshire), Lambertus A. Kiemeney (Radboud University Medical Center, Nijmegen, the Netherlands), Hongbing Shen (Nanjing Medical University, Nanjing, People's Republic of China), Shan Zienolddiny (National Institute of Occupational Health, Oslo, Norway), Kjell Grankvist (Ume? University, Ume?, Sweden), Mikael Johansson (Ume? University, Ume?, Sweden), Neil Caporaso (National Cancer Institute, Bethesda, Maryland), M. Dawn Teare (University Of Sheffield, South Yorkshire, United Kingdom), Yun-Chul Hong (Seoul National University College of Medicine, Seoul, South Korea), Jian-Min Yuan (University of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania), Philip Lazarus (Washington State University College of Pharmacy, Spokane, Washington), Matthew B. Schabath (H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida), and Melinda C. Aldrich (Vanderbilt University Medical Center, Nashville, Tennessee). Publisher Copyright: © 2021 International Association for the Study of Lung Cancer
PY - 2021/7
Y1 - 2021/7
N2 - Introduction: Because of widespread use, understanding the pulmonary effects of cannabis use is important; but its role independent from tobacco smoking is yet to be elucidated. We used Mendelian randomization (MR) to assess the effect of genetic liability to lifetime cannabis use and cannabis use disorder on pulmonary function and lung cancer. Methods: We used four single nucleotide polymorphisms associated with lifetime cannabis use (p value <5 × 10−8) from a genome-wide association study (GWAS) of 184,765 individuals of European descent from the International Cannabis Consortium, 23andme, and U.K. Biobank as instrumental variables. Seven single nucleotide polymorphisms (p value <5 × 10−8) were selected as instruments for cannabis use disorder from a GWAS meta-analysis of 17,068 European ancestry cases and 357,219 controls of European descent from Psychiatric Genomics Consortium Substance Use Disorders working group, Lundbeck Foundation Initiative for Integrative PsychiatricResearch, and deCode. To assess lung function, GWAS included 79,055 study participants of the SpiroMeta Consortium, and for lung cancer GWAS from the International Lung Cancer Consortium contained 29,266 cases and 56,450 controls. Results: MR revealed that genetic liability to lifetime cannabis use was associated with increased risk of squamous cell carcinoma (OR = 1.22, 95%, confidence interval = 1.07–1.39, p value = 0.003, q value = 0.025). Pleiotropy-robust methods and positive and negative control analyses did not indicate bias in the primary analysis. Conclusions: The findings of this MR analysis suggest evidence for a potential causal association between genetic liability for cannabis use and the risk of squamous cell carcinoma. Triangulating MR and observational studies and addressing orthogonal sources of bias are necessary to confirm this finding.
AB - Introduction: Because of widespread use, understanding the pulmonary effects of cannabis use is important; but its role independent from tobacco smoking is yet to be elucidated. We used Mendelian randomization (MR) to assess the effect of genetic liability to lifetime cannabis use and cannabis use disorder on pulmonary function and lung cancer. Methods: We used four single nucleotide polymorphisms associated with lifetime cannabis use (p value <5 × 10−8) from a genome-wide association study (GWAS) of 184,765 individuals of European descent from the International Cannabis Consortium, 23andme, and U.K. Biobank as instrumental variables. Seven single nucleotide polymorphisms (p value <5 × 10−8) were selected as instruments for cannabis use disorder from a GWAS meta-analysis of 17,068 European ancestry cases and 357,219 controls of European descent from Psychiatric Genomics Consortium Substance Use Disorders working group, Lundbeck Foundation Initiative for Integrative PsychiatricResearch, and deCode. To assess lung function, GWAS included 79,055 study participants of the SpiroMeta Consortium, and for lung cancer GWAS from the International Lung Cancer Consortium contained 29,266 cases and 56,450 controls. Results: MR revealed that genetic liability to lifetime cannabis use was associated with increased risk of squamous cell carcinoma (OR = 1.22, 95%, confidence interval = 1.07–1.39, p value = 0.003, q value = 0.025). Pleiotropy-robust methods and positive and negative control analyses did not indicate bias in the primary analysis. Conclusions: The findings of this MR analysis suggest evidence for a potential causal association between genetic liability for cannabis use and the risk of squamous cell carcinoma. Triangulating MR and observational studies and addressing orthogonal sources of bias are necessary to confirm this finding.
KW - Cannabis
KW - Genetic susceptibility
KW - Lung cancer
KW - Mendelian randomization
KW - Pulmonary function
UR - http://www.scopus.com/inward/record.url?scp=85109114791&partnerID=8YFLogxK
U2 - 10.1016/j.jtho.2021.03.025
DO - 10.1016/j.jtho.2021.03.025
M3 - Article
C2 - 33852959
AN - SCOPUS:85109114791
SN - 1556-0864
VL - 16
SP - 1127
EP - 1135
JO - Journal of Thoracic Oncology
JF - Journal of Thoracic Oncology
IS - 7
ER -