Causal association between inflammatory bowel disease and 32 site-specific extracolonic cancers: a Mendelian randomization study

被引:19
作者
Gao, Hui [1 ,2 ]
Zheng, Shuhao [1 ,2 ]
Yuan, Xin [1 ]
Xie, Jiarong [1 ]
Xu, Lei [1 ]
机构
[1] Ningbo Univ, Affiliated Hosp 1, Dept Gastroenterol, Ningbo 315010, Zhejiang, Peoples R China
[2] Ningbo Univ, Hlth Sci Ctr, Ningbo 315211, Zhejiang, Peoples R China
关键词
Mendelian randomization; Inflammatory bowel disease; Extracolonic cancer; Oral cavity cancer; Breast cancer; GENOME-WIDE ASSOCIATION; SUSCEPTIBILITY LOCI; BREAST-CANCER; ULCERATIVE-COLITIS; ANALYSES IDENTIFY; FOLLOW-UP; RISK; VARIANTS; IBD; ENDOSCOPY;
D O I
10.1186/s12916-023-03096-y
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background The risk of extracolonic cancer is increased in inflammatory bowel disease (IBD) patients, but it is not clear whether there is a causal relationship. We aimed to systematically estimate the causal relationship between IBD and extracolonic cancers.Methods Independent genetic variants strongly associated with IBD were extracted as instrumental variables from genome-wide association study (GWAS) conducted by the International IBD Genetics Consortium including 12,882 IBD patients, 5956 Crohn's disease (CD) patients, and 6968 ulcerative colitis (UC) patients. Three sources of cancer GWAS were selected as outcome data. Two-sample Mendelian randomization (MR) analysis was conducted to assess the causal effects of IBD on 32 extracolonic cancers. The meta-analysis was applied to assess the combined causal effect with multiple MR results.Results IBD, CD, and UC have potential causal associations with oral cavity cancer (IBD: OR = 1.180, 95% CI: 1.059 to 1.316, P = 0.003; CD: OR = 1.112, 95% CI: 1.008 to 1.227, P = 0.034; UC: OR = 1.158, 95% CI: 1.041 to 1.288, P = 0.007). Meta-analysis showed a significant positive causal relationship between IBD and breast cancer (OR = 1.059; 95% CI: 1.033 to 1.086; P < 0.0001) as well as a potential causal relationship between CD and breast cancer (OR = 1.029; 95% CI: 1.002 to 1.055; P = 0.032) based on combining multiple MR results.Conclusions This comprehensive MR analysis suggested that genetically predicted IBD, as well as its subtypes, may be a risk factor in the development of oral cavity and breast cancer.
引用
收藏
页数:14
相关论文
共 63 条
[21]   Endoscopy in inflammatory bowel diseases during the COVID-19 pandemic and post-pandemic period [J].
Iacucci, Marietta ;
Cannatelli, Rosanna ;
Labarile, Nunzia ;
Mao, Ren ;
Panaccione, Remo ;
Danese, Silvio ;
Kochhar, Gursimran S. ;
Ghosh, Subrata ;
Shen, Bo .
LANCET GASTROENTEROLOGY & HEPATOLOGY, 2020, 5 (06) :598-606
[22]   Quantifying the impact of between-study heterogeneity in multivariate meta-analyses [J].
Jackson, Dan ;
White, Ian R. ;
Riley, Richard D. .
STATISTICS IN MEDICINE, 2012, 31 (29) :3805-3820
[23]   Mortality and causes of death in patients with inflammatory bowel disease: A nationwide register study in Finland [J].
Jussila, Airi ;
Virta, Lauri J. ;
Pukkala, Eero ;
Farkkila, Martti A. .
JOURNAL OF CROHNS & COLITIS, 2014, 8 (09) :1088-1096
[24]   The four epidemiological stages in the global evolution of inflammatory bowel disease [J].
Kaplan, Gilaad G. ;
Windsor, Joseph W. .
NATURE REVIEWS GASTROENTEROLOGY & HEPATOLOGY, 2021, 18 (01) :56-66
[25]   The global burden of IBD: from 2015 to 2025 [J].
Kaplan, Gilaad G. .
NATURE REVIEWS GASTROENTEROLOGY & HEPATOLOGY, 2015, 12 (12) :720-727
[26]   Risk of Cancer in Patients With Inflammatory Bowel Diseases: A Nationwide Population-based Cohort Study With 30 Years of Follow-up Evaluation [J].
Kappelman, Michael D. ;
Farkas, Dora K. ;
Long, Millie D. ;
Erichsen, Rune ;
Sandler, Robert S. ;
Sorensen, Henrik T. ;
Baron, John A. .
CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2014, 12 (02) :265-+
[27]   Increased Risk of Oral Cancer in Patients With Inflammatory Bowel Diseases [J].
Katsanos, Konstantinos H. ;
Roda, Giulia ;
McBride, Russell B. ;
Cohen, Benjamin ;
Colombel, Jean-Frederic .
CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2016, 14 (03) :413-420
[28]   Sex-Dimorphic Analyses Identify Novel and Sex-Specific Genetic Associations in Inflammatory Bowel Disease [J].
Khrom, Michelle ;
Li, Dalin ;
Naito, Takeo ;
Lee, Ho-Su ;
Botwin, Gregory J. ;
Potdar, Alka A. ;
Boucher, Gabrielle ;
Yang, Shaohong ;
Mengesha, Emebet ;
Dube, Shishir ;
Song, Kyuyoung ;
Dermot, P. B. ;
Haritunians, Talin .
INFLAMMATORY BOWEL DISEASES, 2023, 29 (10) :1622-1632
[29]   Genome-Wide Association Study on Differentiated Thyroid Cancer [J].
Kohler, Aleksandra ;
Chen, Bowang ;
Gemignani, Federica ;
Elisei, Rossella ;
Romei, Cristina ;
Figlioli, Gisella ;
Cipollini, Monica ;
Cristaudo, Alfonso ;
Bambi, Franco ;
Hoffmann, Per ;
Herms, Stefan ;
Kalemba, Michal ;
Kula, Dorota ;
Harris, Shelley ;
Broderick, Peter ;
Houlston, Richard ;
Pastor, Susana ;
Marcos, Ricard ;
Velazquez, Antonia ;
Jarzab, Barbara ;
Hemminki, Kari ;
Landi, Stefano ;
Forsti, Asta .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2013, 98 (10) :E1674-E1681
[30]   British Society of Gastroenterology consensus guidelines on the management of inflammatory bowel disease in adults [J].
Lamb, Christopher Andrew ;
Kennedy, Nicholas A. ;
Raine, Tim ;
Hendy, Philip Anthony ;
Smith, Philip J. ;
Limdi, Jimmy K. ;
Hayee, Bu'Hussain ;
Lomer, Miranda C. E. ;
Parkes, Gareth C. ;
Selinger, Christian ;
Barrett, Kevin J. ;
Davies, R. Justin ;
Bennett, Cathy ;
Gittens, Stuart ;
Dunlop, Malcolm G. ;
Faiz, Omar ;
Fraser, Aileen ;
Garrick, Vikki ;
Johnston, Paul D. ;
Parkes, Miles ;
Sanderson, Jeremy ;
Terry, Helen ;
Gaya, Daniel R. ;
Iqbal, Tariq H. ;
Taylor, Stuart A. ;
Smith, Melissa ;
Brookes, Matthew ;
Hansen, Richard ;
Hawthorne, A. Barney .
GUT, 2019, 68 :S1-S106